All posts by medical

‘Grey’s Anatomy’ Creator Shonda Rhimes Shares How She Was Inspired by Oprah Winfrey – Showbiz Cheat Sheet

Media mogul Shonda Rhimes is known for her blockbuster prime time shows including Greys Anatomy, Scandal, and How To Get Away With Murder. After inking a multi-million dollar deal with Netflix, the famous producer is now creating a suite of shows for the mega popular streaming service.

Rhimes has shared that she had a love for storytelling when she was a child, though there werent many people in the television industry to whom she could relate. The Private Practice creator revealed that talk show icon Oprah Winfrey provided Rhimes with the inspiration and hope she needed.

In June, Rhimes spoke with Variety on the milestone Greys Anatomy hit in becoming the longest running medical drama in television history. The TV producer credited the shows loyal fans for staying tuned since the series premiere.

Its surreal. I mean it truly is a surreal feeling to know that that shows been going for as long as its been going, Rhimes told Variety. Ellen Pompeo [who portrays Meredith Grey] and I talk about that every once in a while. This idea that something that we thought maybe would go a season is still strong, I feel incredibly lucky. Those fans have been amazing.

Rhimes is known for creating strong female characters in all of her shows, hoping to portray women in a realistic and empowering light. When asked if she considers herself a feminist, Rhimes focused more on the importance of equality rather than labels.

I dont even know if I can answer that question, she said. I think that given the fact that a feminist is a woman who believes that men and women should be treated equally, I think Ive probably been a feminist since the day I was born. Thats not really a consideration in the household I was raised in.

While Rhimes had early aspirations of creating stories, she couldnt relate to anyone in the spotlight when she was growing up.

I always knew I wanted to be a writer, she explained. I always knew I wanted to be a storyteller, but there was nobody out there who seemed anything like me.

The Scandal creator shared that she saw media icon Oprah Winfrey as a trailblazer for her. I gave a speech once at the Television Academy where I talked about the only woman I saw in television who looked a little bit different, who had a different body type, was Oprah when I was growing up, Rhimes recalled. And that was the one image of somebody who made me feel like, Oh, theres somebody out there. You can be something different.

As the mom of three daughters, Rhimes knows the demands of motherhood and the importance of being present. Experiencing the challenges of being a working mother first-hand, Rhimes is mindful to give her female cast members with kids the flexibility they need.

I think its important because women work and obviously were expecting women to have children and women to have lives, she told Variety. And we live in a society right now where its not an obvious thing where men are having children and staying home. So women have to figure out a way to be mothers and working mothers at the same time.

Rhimes believes in treating her cast members with the same respect she treats herself when it comes to the demands of parenting. Im a working mother. So Im not going to create a world in which its simpler for me than it is for the people that I work with, she said.

Rhimes show Bridgerton is set to be released this year on Netflix.

Here is the original post:
'Grey's Anatomy' Creator Shonda Rhimes Shares How She Was Inspired by Oprah Winfrey - Showbiz Cheat Sheet

Grey’s Anatomy: 10 People Owen Hunt Should End Up With (Instead Of Teddy) – Screen Rant

It's been over a week since the season finale ofGrey's Anatomy and fans still can't get over that cliffhanger. While fans know nothing remains a secret forever, no one expected that Owen would find out about Teddy's infidelity over a voicemail. On the day of their wedding.Talk about a mood killer.

While Owen hasn't always been the perfect partner, most fans will agree that he deserves better and wouldn't blame him if he walked away. Especially since it's clear how Teddy isn't right for him. Want to know who is? Keep reading to discover 10 other people from Grey's AnatomywhoOwen should end up with instead!

One of the more obvious choices as to who Owen should end up with is Meredith. Although the General surgeon would never cross that boundary out of loyalty to Cristina (and Amelia), it wouldn't be a complete surprise. After all, the pair did become close friends in the aftermath of the plane crash, with Mere being one of the first people to find out about Megan.

If fans also take a closer look at the two, they will realize they have a lot more in common. They are both family-orientated, passionate about their careers, and have gone through their fair share of tragedy. It wouldn't be the worst thing if Mere chose Owen in the end.

This is a long shot but one romance that would have been interesting to watch would have been Owen and Izzie. Although the surgeons never spent much time together after the incident in "Life During Wartime," this is also a reason why they should have been paired up.

Izzie needed someone to show her that she couldn't always be in control. There were going to be moments that required spontaneity and quick thinking. Owen also needed someone likeIzzie who could help to bring him out of his depression. A missed opportunity, really.

Considering that he almost destroyed his marriage because of it, wouldn't it be interesting to find out what happened to the other woman? After all, he must have felt some sort of connection to her if it meant cheating on Cristina.

Although fans wouldn't be happy since it would be the ultimate betrayal to Cristina, it would make for some interesting TV if Owen and this mysterious third party met up again... especially if Meredith discovered that he was dating the woman he cheated with. Who knows, maybe they could have a lot more in common than we all think?

It's no secret that April and Owen shared a special bond. While their relationship started as a mentor-mentee, they soon developed a strong friendship after serving a tour in Iraq. After coming back from the war zone, April and Owen became each other's confidants, especially during April's second pregnancy.

What made Owen and April's relationship so special was how it was built on mutual understanding and respect. They got to know each other on a level nobody else could understand. If April wasn't happy with Matthew, a romance between her and Owen would have been interesting.

When Owen decided to take a job at Seattle-Grace, fans got to know his character more. One of the first things they learned was that he had been engaged to a school teacher, Beth Whitman. However, it was revealed that Owen had called off their engagement while he was on tour in Iraq.

RELATED:Grey's Anatomy: Why April & Owen Aren't Real Friends

While many have suspected that it was due to his PTSD, Owen is now in a different place so it may be worth him trying to reconnect. After all, she wouldn't be the same woman he saw 13 years ago.

One of the most surprising hook-ups had to be Owen and Carina's in Season 14. As Carina was finding her footing in Seattle, the OB/GYN caught the eye of many other surgeons - including Owen. First meeting at the intern mixer, the viewers find out that Owen and Carina spent the night together after Amelia walked in on them having breakfast.

However, nothing came of it as Carina shortly began a relationship with Arizona. While Carina is now in a relationship withStation 19's Maya Bishop, there's still a possibility the writers may revisit (depending on how many seasons are left).

Inhindsight, one of the worst mistakes Owen ever made was breaking up with Emma. For a brief couple of months, Owen was in a serious and committed relationship with Emma, who he met at the hospital's fundraiser. They were so serious that they even contemplated marriage and getting a place together.

However, they soon broke up when Owen claimed they wanted different things (when the truth was, he cheated on her with Cristina). It was a shame, especially as Emma wanted to start a family and become a stay-at-home mom. With Teddy and Owen on the verge of breaking up, maybe now is the time for them to reconnect.

While Amelia is happily in a relationship with Link, there was a time where she and Owen were too. Although their relationship started as a spur-in-moment, there were some times where they were happy too. Especially in season 14 and 15 when they decided to give their relationship another shot.

Amelia would have still been raising Leo with Owen if it wasn't for Teddy revealing her own pregnancy. Now that Amelia has changed her mind about her own future goals, maybe they will find their way back to one another down the line. That is if Amelia and Link don't work out.

Fans may not have considered it but Callie could have also been another love interest for Owen. If someone decided to rewatch the series again, they will notice that Callie and Owen were closer than we think. When Owen first arrived at Grey-Sloan, Callie took an instant liking to the trauma surgeon's brazen attitude.

Not only did the two have a successful work partnership, with them creating limbs for army veterans, but they also became close friends after their marriages broke down. If they had decided to get together, they could have been happy.

If there is one person Owen should end up with, it's Cristina. While the pair never seem to have gotten it right due to their different life-goals and ambitions, who's to say they couldn't make it work in twenty years? After all, Owen has achieved one of his dreams, raising Allison and Leo with Teddy and Amelia.

Cristina's career, too, has flourished in Switzerland. Who's to say they couldn't reunite when they both retire and the kids are grown. It's not like they ended on a bad note.

NEXT:Grey's Anatomy: Why Meredith & Cristina Aren't Real Friends

Next10 Obscure (But Awesome) Sci-Fi Movies You can Stream Today On Amazon Prime

A writer, reader and tv fanatic, Kayleigh enjoys reading movie news and your film reviews. She has attained an Undergraduate degree in Creative Writing and is also the creator of the film and television blog 'The Critics' Corner'.

See original here:
Grey's Anatomy: 10 People Owen Hunt Should End Up With (Instead Of Teddy) - Screen Rant

Chemical tool developed to examine lipids in living cells – Drug Target Review

A new method has been developed by researchers using chemical tools activated by light to influence lipid concentration in living cells.

So far, it has been difficult for researchers to analyse the functions of lipids in living cells. Now, scientists at the Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG) and the Leibniz Research Institute for Molecular Pharmacology (FMP), both in Germany, have now developed chemical tools that can be activated by light and used to influence lipid concentration in living cells.

According to the researchers, this approach could enable medical doctors to work with biochemists to identify what molecules within a cell actually do.

Every cell can create thousands of different lipids (fats). However, little is known about how this chemical lipid diversity contributes to the transport of messages within the cell. This is mainly due to the lack of methods to quantitatively study lipid function in living cells. An understanding of how lipids work is very important because they control the function of proteins throughout the cell and are involved in bringing important substances into the cell through the cell membrane.

The research groups developed chemical tools to control the concentration of lipids in living cells, which can be activated by light. Milena Schuhmacher, the lead author of the study, explained: Lipids are actually not individual molecular structures, but differ in tiny chemical details. For example, some have longer fatty acid chains and some have slightly shorter ones. Using sophisticated microscopy in living cells and mathematical modelling approaches, we were able to show that the cells are actually able to recognise these tiny changes through special effector proteins and thus possibly use them to transmit information. It was important that we were able to control exactly how much of each individual lipid was involved.

Molecular probes (in blue) for the analysis of lipid messengers [credit: Schuhmacher et al., MPI-CBG].

Andr Nadler, who supervised the study, added: These results indicate the existence of a lipid code that cells use to re-encode information, detected on the outside of the cell, on the inner side of the cell.

The results of the study could enable membrane biophysicists and lipid biochemists to verify their results with quantitative data from living cells, say the researchers.

Andr Nadler concluded: Clinicians could also benefit from our newly developed method. In diseases such as diabetes and high blood pressure, more lipids that act as biomarkers are found in the blood. This can be visualised with a lipid profile. With the help of our method, doctors could now see exactly what the lipids are doing in the body. That was not possible before.

The study was published in the journal PNAS.

Original post:
Chemical tool developed to examine lipids in living cells - Drug Target Review

Global Live Cell Imaging Market : Industry Analysis and Forecast (2018-2026) – Research Columnist

Global Live Cell Imaging Marketwas valued at US$ 1.5Bn in 2017 and is expected to reach US$ XX Bn by 2026, at a CAGR of XX% during a forecast period.

The report study has analyzed revenue impact of covid-19 pandemic on the sales revenue of market leaders, market followers and disrupters in the report and same is reflected in our analysis.

REQUEST FOR FREE SAMPLE REPORT:https://www.maximizemarketresearch.com/request-sample/28816/

Global live cell imaging market is majorly influenced by the growing incidence of chronic diseases and the consistent need for swift diagnostic techniques. Availability of exact and accurate live cell imaging techniques also help in accelerating drug discovery processes and other biotechnology research.

Growth in expenditure and funding for the development of advanced cell imaging is further expected to boost the live cell imaging market in the future. It is also observed that collaborations of market players with research and academic institutions to develop and introduce breakthrough products have recently gained pace. Small players are being increasingly acquired by large incumbents for procurement of breakthrough technologies to secure their stronghold in the market.

Fluorescence recovery after photobleaching is the most commonly used technique for live cell imaging. The technique has found rapid adoption in genetic targeting peptides and appropriately offers a determination of spatial proximity at a protein level that is not possible through fluorescence microscopy. Rapid introduction of FRET systems with an insight to offer better cell imaging techniques will so determine the major market trends.

Cell biology segment is leading the application owing to the increasing number of researchers working on molecular interaction networks. Innovations, for instance, filter techniques and advanced illumination devices further enable the procedure. Cell biologists use live cell imaging to understand the fundamental cellular structures and their interaction on the tissue level. Benefits are clarity of structural components and spatial heterogeneity of a cell offered by live cell imaging are expected to further boost the market.

North America dominated by market share in 2017 closely followed by Europe. Substantial investments and funding available for research in this field is the key driver in the North America region. The growing adoption of live cell imaging by research laboratories and academic institutions, particularly in the U.S. is one of the major factors driving market growth in this region.

One of the recent acquisition in the industry was done in March 2017 by Sartorius who agreed to buy Essen Bioscience in a transaction worth US$ 320Mn. Essen was energetic in developing equipment, reagents, and software.

DO INQUIRY BEFORE PURCHASING REPORT HERE:https://www.maximizemarketresearch.com/inquiry-before-buying/28816/

Nikon Corporation Company has strategic partnerships with research groups to gain professional expertise. They have established imaging centers and offer microscopes, automation, software, and support to various institutes, for instance, Harvard Medical School.

The objective of the report is to present a comprehensive assessment of the market and contains thoughtful insights, facts, historical data, industry-validated market data and projections with a suitable set of assumptions and methodology. The report also helps in understanding Global Live Cell Imaging Market dynamics, structure by identifying and analyzing the market segments and project the global market size.

Further, the report also focuses on the competitive analysis of key players by product, price, financial position, product portfolio, growth strategies, and regional presence. The report also provides PEST analysis, PORTERs analysis, SWOT analysis to address the question of shareholders to prioritizing the efforts and investment in the near future to the emerging segment in the Global Live Cell Imaging Market.Scope of Global Live Cell Imaging Market

Global Live Cell Imaging Market, by Product & Service

Instruments Consumables Software ServicesGlobal Live Cell Imaging Market, by Application

Cell Biology Stem Cells Developmental Biology Drug DiscoverGlobal Live Cell Imaging Market, by End User

Pharmaceutical & Biotechnology Companies Academic & Research Institutes Contract Research OrganizationsGlobal Live Cell Imaging Market, by Region

North America Europe Asia Pacific Middle East and Africa South AmericaKey players operating in Global Live Cell Imaging Market

Danaher Corporation Carl Zeiss AG Nikon Corporation Olympus Corporation Perkinelmer GE Healthcare Bruker Thermo Fisher Scientific Sartorius AG Biotek Instruments Etaluma Cytosmart Technologies Nanoentek

MAJOR TOC OF THE REPORT

Chapter One: Live Cell Imaging Market Overview

Chapter Two: Manufacturers Profiles

Chapter Three: Global Live Cell Imaging Market Competition, by Players

Chapter Four: Global Live Cell Imaging Market Size by Regions

Chapter Five: North America Live Cell Imaging Revenue by Countries

Chapter Six: Europe Live Cell Imaging Revenue by Countries

Chapter Seven: Asia-Pacific Live Cell Imaging Revenue by Countries

Chapter Eight: South America Live Cell Imaging Revenue by Countries

Chapter Nine: Middle East and Africa Revenue Live Cell Imaging by Countries

Chapter Ten: Global Live Cell Imaging Market Segment by Type

Chapter Eleven: Global Live Cell Imaging Market Segment by Application

Chapter Twelve: Global Live Cell Imaging Market Size Forecast (2019-2026)

Browse Full Report with Facts and Figures of Live Cell Imaging Market Report at:https://www.maximizemarketresearch.com/market-report/global-live-cell-imaging-market/28816/

About Us:

Maximize Market Research provides B2B and B2C market research on 20,000 high growth emerging technologies & opportunities in Chemical, Healthcare, Pharmaceuticals, Electronics & Communications, Internet of Things, Food and Beverages, Aerospace and Defense and other manufacturing sectors.

Contact info:

Name: Lumawant Godage

Organization: MAXIMIZE MARKET RESEARCH PVT. LTD.

Email: sales@maximizemarketresearch.com

Contact: +919607065656/ +919607195908

Website: http://www.maximizemarketresearch.com

Continue reading here:
Global Live Cell Imaging Market : Industry Analysis and Forecast (2018-2026) - Research Columnist

Interdisciplinary Physiology Graduate Program

Physiology is an integrative area in the biological sciences that employs a systems-based approach. It is important for students to integrate information about the entire biological system from across all the biological-related sciences.

Admissions Update Amid COVID-19 Pandemic:

We are still accepting applications for the Summer and Fall 2020 semesters, as well as semesters beyond(Spring 2021, etc.).

All admissions interviews will be conducted via Skype or Zoom and we will still evaluate applications submitted by April 15, 2020. We will also add a new application evaluation date of May 15, 2020. As of today, our final applicationdeadline is June 15, 2020 for Fall 2020.

Important Note for Summer 2020 and Fall 2020 Applicants:

We have recently updated our testing requirementsand will now accept an MCAT or DAT score report in lieuof the GRE. A practice test score for the GRE, MCAT or DAT will not count as meeting this requirement.

NC State is the best college for the money in North Carolina, according to a national ranking of more than 700 schools.Moneymagazines annual survey,2017 Best Colleges for Your Money, is based on enrollment data and student outcomes collected from the top colleges and universities in the United States.

Originally posted here:
Interdisciplinary Physiology Graduate Program

Physiology of the Kidneys | Boundless Anatomy and Physiology

Overview of Urine Formation

Urine is formed in three steps: filtration, reabsorption, and secretion.

Summarize the steps in urine formation

Urine is a waste byproduct formed from excess water and metabolic waste molecules during the process of renal system filtration. The primary function of the renal system is to regulate blood volume and plasma osmolarity, and waste removal via urine is essentially a convenient way that the body performs many functions using one process.Urine formation occurs during three processes:

During filtration, blood enters the afferent arteriole and flows into the glomerulus where filterable blood components, such as water and nitrogenous waste, will move towards the inside of the glomerulus, and nonfilterable components, such as cells and serum albumins, will exit via the efferent arteriole. These filterable components accumulate in the glomerulus to form the glomerular filtrate.

Normally, about 20% of the total blood pumped by the heart each minute will enter the kidneys to undergo filtration; this is called the filtration fraction. The remaining 80% of the blood flows through the rest of the body to facilitate tissue perfusion and gas exchange.

The next step is reabsorption, during which molecules and ions will be reabsorbed into the circulatory system. The fluid passes through the components of the nephron (the proximal/distal convoluted tubules, loop of Henle, the collecting duct) as water and ions are removed as the fluid osmolarity (ion concentration) changes. In the collecting duct, secretion will occur before the fluid leaves the ureter in the form of urine.

During secretion some substancessuch as hydrogen ions, creatinine, and drugswill be removed from the blood through the peritubular capillary network into the collecting duct. The end product of all these processes is urine, which is essentially a collection of substances that has not been reabsorbed during glomerular filtration or tubular reabsorbtion.

Urine is mainly composed of water that has not been reabsorbed, which is the way in which the body lowers blood volume, by increasing the amount of water that becomes urine instead of becoming reabsorbed. The other main component of urine is urea, a highly soluble molecule composed of ammonia and carbon dioxide, and provides a way for nitrogen (found in ammonia) to be removed from the body. Urine also contains many salts and other waste components. Red blood cells and sugar are not normally found in urine but may indicate glomerulus injury and diabetes mellitus respectively.

Normal kidney physiology: This illustration demonstrates the normal kidney physiology, showing where some types of diuretics act, and what they do.

Glomerular filtration is the renal process whereby fluid in the blood is filtered across the capillaries of the glomerulus.

Explain the process of glomerular filtration in the kidneys

Glomerular filtration is the first step in urine formation and constitutes the basic physiologic function of the kidneys. It describes the process of blood filtration in the kidney, in which fluid, ions, glucose, and waste products are removed from the glomerular capillaries.

Many of these materials are reabsorbed by the body as the fluid travels through the various parts of the nephron, but those that are not reabsorbed leave the body in the form of urine.

Glomerulus structure: A diagram showing the afferent and efferent arterioles bringing blood in and out of the Bowmans capsule, a cup-like sac at the beginning of the tubular component of a nephron.

Blood plasma enters the afferent arteriole and flows into the glomerulus, a cluster of intertwined capillaries. The Bowmans capsule (also called the glomerular capsule) surrounds the glomerulus and is composed of visceral (simple squamous epithelial cellsinner) and parietal (simple squamous epithelial cellsouter) layers.

The visceral layer lies just beneath the thickened glomerular basement membrane and is made of podocytes that form small slits in which the fluid passes through into the nephron. The size of the filtration slits restricts the passage of large molecules (such as albumin) and cells (such as red blood cells and platelets) that are the non-filterable components of blood.

These then leave the glomerulus through the efferent arteriole, which becomes capillaries meant for kidneyoxygen exchange and reabsorption before becoming venous circulation. The positively charged podocytes will impede the filtration of negatively charged particles as well (such as albumins).

The process by which glomerular filtration occurs is called renal ultrafiltration. The force of hydrostatic pressure in the glomerulus (the force of pressure exerted from the pressure of the blood vessel itself) is the driving force that pushes filtrate out of the capillaries and into the slits in the nephron.

Osmotic pressure (the pulling force exerted by the albumins) works against the greater force of hydrostatic pressure, and the difference between the two determines the effective pressure of the glomerulus that determines the force by which molecules are filtered. These factors will influence the glomeruluar filtration rate, along with a few other factors.

Regulation of GFR requires both a mechanism of detecting an inappropriate GFR as well as an effector mechanism that corrects it.

List the conditions that can affect the glomerular filtration rate (GFR) in kidneys and the manner of its regulation

Glomerular filtration rate (GFR) is the measure that describes the total amount of filtrate formed by all the renal corpuscles in both kidneys per minute. The glomerular filtration rate is directly proportional to the pressure gradient in the glomerulus, so changes in pressure will change GFR.

GFR is also an indicator of urine production, increased GFR will increase urine production, and vice versa.

The Starling equation for GFR is:

GFR=Filtration Constant (Hydrostatic Glomerulus PressureHydrostatic Bowmans Capsule Pressure)(Osmotic Glomerulus Pressure+Osmotic Bowmans Capsule Pressure)

The filtration constant is based on the surface area of the glomerular capillaries, and thehydrostatic pressure is a pushing force exerted from the flow of a fluid itself; osmotic pressure is the pulling force exerted by proteins. Changes in either the hydrostatic or osmotic pressure in the glomerulus or Bowmans capsule will change GFR.

Many factors can change GFR through changes in hydrostatic pressure, in terms of the flow of blood to the glomerulus. GFR is most sensitive to hydrostatic pressure changes within the glomerulus. A notable body-wide example is blood volume.

Due to Starlings law of the heart, increased blood volume will increase blood pressure throughout the body. The increased blood volume with its higher blood pressure will go into the afferent arteriole and into the glomerulus, resulting in increased GFR. Conversely, those with low blood volume due to dehydration will have a decreased GFR.

Pressure changes within the afferent and efferent arterioles that go into and out of the glomerulus itself will also impact GFR. Vasodilation in the afferent arteriole and vasconstriction in the efferent arteriole will increase blood flow (and hydrostatic pressure) in the glomerulus and will increase GFR. Conversely, vasoconstriction in the afferent arteriole and vasodilation in the efferent arteriole will decrease GFR.

The Bowmans capsule space exerts hydrostatic pressure of its own that pushes against the glomerulus. Increased Bowmans capsule hydrostatic pressure will decrease GFR, while decreased Bowmans capsule hydrostatic pressure will increase GFR.

An example of this is a ureter obstruction to the flow of urine that gradually causes a fluid buildup within the nephrons. An obstruction will increase the Bowmans capsule hydrostatic pressure and will consequently decrease GFR.

Osmotic pressure is the force exerted by proteins and works against filtration because the proteins draw water in. Increased osmotic pressure in the glomerulus is due to increased serum albumin in the bloodstream and decreases GFR, and vice versa.

Under normal conditions, albumins cannot be filtered into the Bowmans capsule, so the osmotic pressure in the Bowmans space is generally not present, and is removed from the GFR equation. In certain kidney diseases, the basement membrane may be damaged (becoming leaky to proteins), which results in decreased GFR due to the increased Bowmans capsule osmotic pressure.

Glomeruluar filtration: The glomerulus (red) filters fluid into the Bowmans capsule (blue) that sends fluid through the nephron (yellow). GFR is the rate at which is this filtration occurs.

GFR is one of the many ways in which homeostasis of blood volume and blood pressure may occur. In particular, low GFR is one of the variables that will activate the reninangiotensin feedback system, a complex process that will increase blood volume, blood pressure, and GFR. This system is also activated by low blood pressure itself, and sympathetic nervous stimulation, in addition to low GFR.

Tubular reabsorption is the process by which solutes and water are removed from the tubular fluid and transported into the blood.

Describe the process of tubular reabsorption in kidney physiology

The fluid filtered from blood, called filtrate, passes through the nephron, much of the filtrate and its contents are reabsorbed into the body. Reabsorption is a finely tuned process that is altered to maintain homeostasis of blood volume, blood pressure, plasma osmolarity, and blood pH. Reabsorbed fluids, ions, and molecules are returned to the bloodstream through the peri-tubular capillaries, and are not excreted as urine.

Tubular secretion: Diagram showing the basic physiologic mechanisms of the kidney and the three steps involved in urine formation. Namely filtration, reabsorption, secretion, and excretion.

Reabsorption in the nephron may be either a passive or active process, and the specific permeability of the each part of the nephron varies considerably in terms of the amount and type of substance reabsorbed. The mechanisms of reabsorption into the peri-tubular capillaries include:

These processes involve the substance passing though the luminal barrier and the basolateral membrane, two plasma membranes of the kidney epithelial cells, and into the peri-tubular capillaries on the other side. Some substances can also pass through tiny spaces in between the renal epithelial cells, called tight junctions.

As filtrate passes through the nephron, its osmolarity (ion concentration) changes as ions and water are reabsorbed. The filtrate entering the proximal convoluted tubule is 300 mOsm/L, which is the same osmolarity as normal plasma osmolarity.

In the proximal convoluted tubules, all the glucose in the filtrate is reabsorbed, along with an equal concentration of ions and water (through cotransport), so that the filtrate is still 300 mOsm/L as it leaves the tubule. The filtrate osmolarity drops to 1200 mOsm/L as water leaves through the descending loop of Henle, which is impermeable to ions. In the ascending loop of Henle, which is permeable to ions but not water, osmolarity falls to 100200 mOsm/L.

Finally, in the distal convoluted tubule and collecting duct, a variable amount of ions and water are reabsorbed depending on hormonal stimulus. The final osmolarity of urine is therefore dependent on whether or not the final collecting tubules and ducts are permeable to water or not, which is regulated by homeostasis.

Reabsorption throughout the nephron: A diagram of the nephron that shows the mechanisms of reabsorption.

Hydrogen, creatinine, and drugs are removed from the blood and into the collecting duct through the peritubular capillary network.

Describe the purpose of tubular secretion in kidney physiology

Tubular secretion is the transfer of materials from peritubular capillaries to the renal tubular lumen; it is the opposite process of reabsorption. This secretion is caused mainly by active transport and passive diffusion.

Usually only a few substances are secreted, and are typically waste products. Urine is the substance leftover in the collecting duct following reabsorption and secretion.

The mechanisms by which secretion occurs are similar to those of reabsorption, however these processes occur in the opposite direction.

Renal secretion is different from reabsorption because it deals with filtering and cleaning substances from the blood, rather than retaining them. The substances that are secreted into the tubular fluid for removal from the body include:

Tubular secretion: Diagram showing the basic physiologic mechanisms of the kidney and the three steps involved in urine formation.

Many pharmaceutical drugs are protein-bound molecules thatDiagram showing the basic physiologic mechanisms of the kidney and the three steps involved in urine formation. amely filtration, reabsorption, secretion, and excretion. are easily secreted, which is why urine testing can detect the exposure to many types of drugs. Tubular secretion occurs throughout the different parts of the nephron, from the proximal convoluted tubule to the collecting duct at the end of the nephron.

The tubular secretion of H+ and NH4+ from the blood into the tubular fluid is involved in blood pH regulation. The movement of these ions also helps to conserve sodium bicarbonate (NaHCO3). The typical pH of urine is about 6.0, while it is ideally 7.35 to 7.45 for blood.

pH regulation is primarily a respiratory system process, due to the exchange of carbon dioxide (a component of carbonic acid in blood), however tubular secretion assists in pH homeostasis as well.

Urine that is formed via the three processes of filtration, reabsorption, and secretion leaves the kidney through the ureter, and is stored in the bladder before being removed through the urethra. At this final stage it is only approximately one percent of the originally filtered volume, consisting mostly of water with highly diluted amounts of urea, creatinine, and variable concentrations of ions.

Read more:
Physiology of the Kidneys | Boundless Anatomy and Physiology

What are the effects of COVID-19 on the lungs? – Medical News Today

How does the body respond when the SARS-CoV-2 virus infects it? Which physiological processes help or hinder us in getting rid of the virus, and which processes ensure that we have a mild form of COVID-19, the disease that the virus causes? In this Special Feature, we investigate.

The more we learn about COVID-19, the more we have to question our assumptions about it.

Early on in the COVID-19 pandemic, our information about the disease came from clinical case reports of COVID-19 and what we knew about influenza pandemics and the severe acute respiratory syndrome (SARS) resulting from SARS-CoV.

SARS-CoV is a coronavirus that shares 82% of its genome with SARS-CoV-2. In 2003, it caused an international SARS epidemic.

Stay informed with live updates on the current COVID-19 outbreak and visit our coronavirus hub for more advice on prevention and treatment.

It quickly became clear that COVID-19 was very different than seasonal influenza, with higher mortality and infectivity, but it took longer to realize that there were important differences and similarities with SARS.

For instance, COVID-19 is infectious even during the presymptomatic phase. Also, physiological processes that are harmful in one phase of the disease may become helpful later. For example, the angiotensin converting enzyme 2 (ACE2) receptor, which allows the virus to enter the body, may also be key to the protection of the lungs in the later phases of the disease.

This feature describes what we know so far about COVID-19. To explain the different processes that occur within the body, we have split the disease into four separate phases that roughly match the different levels of severity: mild, moderate, severe, and critical.

However, in reality, the physiological processes underlying these phases overlap. People with COVID-19 may or may not show features of earlier or later phases.

Both SARS-CoV-2 and SARS-CoV gain entry via a receptor called ACE2.

More commonly known for their role in controlling blood pressure and electrolytes, these receptors are also present in the lungs, back of the throat, gut, heart muscle, and kidneys.

In 2004, researchers from the University Medical Center Groningen in the Netherlands reported that ACE2 receptor cells were not present on the surface layer of cells in the nose and were, therefore, not an important site for SARS-CoV viral replication.

In SARS, there are hardly any upper respiratory tract symptoms, and viral units are rarely present outside the lungs. This fact initially took the focus away from continuing to look for ACE2 receptors in the nose.

Recently, an international team of researchers has found the ACE2 receptors on goblet (secretory) cells in and on ciliated (hairy) cells in the nose.

More recently, scientists have found ACE2 receptors in the mouth and tongue, potentially indicating a hand-to-mouth route of transmission.

Researchers also found a plentiful supply of a protease called TMPRSS2, which chemically splits off the top of the coronavirus spike to allow the SARS-CoV-2 RNA to enter into the nasal cells.

Once inside the cell, the viruss genetic material directs the cell to manufacture millions of new copies of itself.

According to a paper that has not yet undergone peer review, the protease TMPRSS2 can act more easily to remove the top section of the coronavirus spike because a genetic difference between SARS-CoV and SARS-CoV-2 means that there is now an easily broken section known as the furin-cleavage site.

As a result, SARS-CoV-2 can bind 10 times more tightly to insert its RNA into the cell, starting to explain why COVID-19 spreads so rapidly.

A small but very careful study of viral samples from nine people admitted to hospital following contact tracing as part of a cluster of COVID-19 cases in Germany has shown the importance of replication in the nose for the early spread of the virus.

On average, there were 676,000 copies of the virus per swab from the upper respiratory tract during the first 5 days of symptoms. The levels of the virus in six out of the nine participants were undetectable in the nose and throat by day 10. Samples were available from day 1 of symptoms.

In all but one of the nine individuals, the viral load in the upper respiratory tract swabs was dropping from day 1, suggesting that the peak preceded the onset of symptoms. This has clear implications for preventing the transmission of the virus.

In a preliminary report by Menni and colleagues, which has yet to go through peer review, loss of sense of smell occurred 6.6 times more commonly in people with other symptoms of COVID-19 who went on to have a positive COVID-19 PCR test (59%) than in those who had symptoms of COVID-19 but tested negative (18%).

The ACE2 receptors and the protease TMPRSS2 have also been found in the supporting structures for the sheet of nerve cells in the upper part of the nose, which transmit signals about smell to the brain.

This is the first research to provide a potential explanation for this important symptom of COVID-19. However, this study is also awaiting peer review.

According to Mennis study, loss of smell was the most commonly reported upper respiratory tract symptom in those testing positive for COVID-19, affecting 59% of people. It was more common than a persistent cough (58%) or a hoarse voice (32.3%).

Interestingly, data from the first description of 99 people who tested positive for COVID-19 in Wuhan, China, suggests that some symptoms you might expect to see from a respiratory virus are not that common in COVID-19. For instance, only 4% had a runny nose, and 5% had a sore throat.

The viral load study in Germany showed that active viral replication occurs in the upper respiratory tract. Seven out of nine participants listed a cough among their initial symptoms.

In contrast to the falling numbers of viral units in the upper respiratory tract, numbers in sputum rose for most of the participants.

In two individuals with some signs of lung infection, the virus in sputum peaked at day 1011. It was present in the sputum up to day 28 in one person. Across all participants, there was an average of 7 million units in 1 milliliter (about 35 million units in a teaspoon). This amount is about 1,000 times more than that in people with SARS.

In the lung, the ACE2 receptor sits on top of lung cells called pneumocytes. These have an important role in producing surfactant a compound that coats the air sacs (alveoli), thus helping maintain enough surface tension to keep the sacs open for the exchange of oxygen and carbon dioxide.

As soon as the body recognizes a foreign protein, it mounts the first response. One part of the bodys immune response the lymphocytes begin to produce the first defense IgM-type antibodies and then the longer term specific neutralizing antibodies (the IgG type).

In the German viral study, 50% of the participants had IgM or IgG antibodies by day 7, and they all had these antibodies by day 14. The amount of antibodies did not predict the clinical course of the disease.

80% of people with COVID-19 will have mild or asymptomatic disease, with common symptoms including fever, cough, and loss of sense of smell. Most will only have phase 1 or 2 physiological responses to SARS-CoV-2 infection.

Approximately 13.8% of people with COVID-19 will have severe disease and will require hospitalization as they become short of breath. Of these individuals, 75% will have evidence of bilateral pneumonia.

Pneumonia in COVID-19 occurs when parts of the lung consolidate and collapse. Reduced surfactant in the alveoli from the viral destruction of pneumocytes makes it difficult for the lungs to keep the alveoli open.

As part of the immune response, white blood cells, such as neutrophils and macrophages, rush into the alveoli. Meanwhile, blood vessels around the air sacs become leaky in response to inflammatory chemicals that the white blood cells release.

This fluid puts pressure on the alveoli from outside and, in combination with the lack of surfactant, causes them to collapse.

As a result, breathing becomes difficult, and the surface area in the lung where oxygen transfer usually takes place becomes reduced, leading to breathlessness.

The body attempts to heal itself by promoting inflammatory and immune responses. The World Health Organization (WHO) advise against the use of glucocorticosteroids during this phase, as they could prevent the natural healing response. The evidence seems to refute this position, but this is a fast developing field, and findings are subject to change.

Most patients will recover at this stage with supportive intravenous fluids and oxygen via a mask or an external positive pressure mask.

The most common time for the onset of critical disease is 10 days, and it can come on suddenly in a small proportion of people with mild or moderate disease.

In severe acute respiratory distress syndrome (ARDS), the inflammation stage gives way to the fibrosis stage. Fibrin clots form in the alveoli, and fibrin-platelet microthrombi (small blood clots) pepper the small blood vessels in the lung that are responsible for gas exchange with the alveoli.

There is hope that drugs already licensed for anticlotting action in strokes could be helpful at this stage.

Cytokines are chemical mediators that white blood cells such as macrophages release, and they can engulf infected cells. These cytokines which have names such as IL1, IL6, and TNF have actions that include dilating the vessel walls and making them more permeable. In extreme circumstances, this can lead to a collapse of the cardiovascular system.

Estrogen in mouse cells suppresses the release of cytokines from macrophages. Although animal studies often fail to translate into important findings in humans, this could be one explanation for worse outcomes from COVID-19 in males.

While smaller numbers of ACE2 receptors are protective in phase 1, as there are fewer landing sites for the virus, by the time we reach phase 4, these receptors may become protective.

ACE2 receptors in health play an important regulating role for the activities of angiotensin converting enzyme 1 (ACE1).

In response to infection, ACE1 creates excess angiotensin 2 from angiotensin 1.

Angiotensin 2 directly damages the lungs, causes blood vessel constriction, and makes the blood vessels leaky. Drugs that doctors typically use in the treatment of hypertension (ACE inhibitors and ARBs) may be helpful at this stage.

The role of ACE2 inhibitors in treating COVID-19 is a complex one. As some authors note, on the one hand, using them may lead to a higher risk of SARS-CoV-2 infection. On the other hand, ACE inhibitors may reduce the lung damage that this infection causes.

Furthermore, it is noteworthy that the protective role of ACE2 in the respiratory system is supported by ample evidence, whereas the increased danger of infection is still a hypothesis.

This is why more research is necessary to understand the physiology of this challenging new disease.

For live updates on the latest developments regarding the novel coronavirus and COVID-19, click here.

Go here to see the original:
What are the effects of COVID-19 on the lungs? - Medical News Today

Wild Turkey Anatomy and Physiology – OutdoorHub

Turkeys are always a challenge to hunt, but their anatomy and physiology is just as intriguing. Some think they are ugly, while others appreciate the array of colors and behavior. Heck, they were almost our national bird. So, as you gear up to chase these illusive birds in their natural habitat, take some time to familiarize yourself with some basic wild turkey anatomy and physiology.

The head of a turkey is a colorful cornucopia. Composed of the caruncles, wattles, snood and dewlap, all are used for different purposes. The changing of color and shape in males emanates aggression, sexual arousal and overall mood. It is a signpost for other turkeys. There are also tiny hairs and feathers around the ear to aid in hearing.

The main fighting tool of a tom is the spur. Since they do all the fighting for the right to breed, they are only present in males. Gobblers jump and use their spurs as daggers to attempt to injure the competition. Spur length is good teller of age, too. Toms with spurs longer than an inch are mature birds, while toms with spurs an inch or less are usually two-year old birds.

A turkeys beard is made from the same material as a rhinoceros hornkeratin. Keratinized epithelial cells are cells filled with the protein keratin. In this case, feathers in toms (and in some hens) keratinize and form the beard. So, a beard is essentially a collection of specialized feathers.

Archibald Rutledge once said, the turkeys eyes are such that he can see a bumblebee turn a somersault on the verge of the horizon. Turkeys can see as a human would while using 8-10x zoom on a pair of binoculars. They also do not have to focus in on objects. If they can see it, it is always in focus. Being able to see in a 300-degree range helps, too. The only spot they cannot see without turning their heads is directly behind them.

Oh, and unlike deer they can see color very well. Good luck.

A turkeys breast is what we call white meat, while its thighs and legs are dark meat. Why is this? White meat is made of light muscle. These muscles are meant for short burst of energy and lack a lot of hemoglobin to sustain activity for too long. Dark meat is composed of dark muscle, which contains high levels of hemoglobin and help sustain a lot of activity for long periods of time. Turkeys walk way more than they fly, so that is why the meat of the legs is dark and the breast is white. (This is why the breast of migratory birds like ducks is dark, FYI).

What interesting things have you noticed about a turkeys anatomy and physiology?

Read the original here:
Wild Turkey Anatomy and Physiology - OutdoorHub

The Doctor Game: Is home confinement a good time to fast? – The Westerly Sun

Today, nearly all of us are in enforced home confinement due to an invisible foe, the coronavirus. So, how do we amuse ourselves? Some pick up books theyve always wanted to read. Others get household chores done. But how about some of us losing weight? If typical busy schedules have interfered with your efforts in the past, could the current context support a concentrated effort on fasting to shed pounds? And what are the best ways to fast?

Fasting diets have generated considerable buzz among diet gurus in the media, not only as an approach to weight loss but also as a way to improve overall health. But do facts back it up?

Researchers say that animals and humans share some comment elements in the evolutionary process. One of these is that neither animals nor humans have always had the good fortune of enjoying three meals a day. Over long eras when our ancestors needed to scrounge for food, humans developed physiology capable of enduring periods without food. So the question arises, is it possible that the occasional fast might be good for us?

That seems to be true for animals. Studies show that fasting produces health benefits in laboratory animals. For instance, restrictive diet experiments involving rats and mice have delayed the progression of chronic conditions such as diabetes, cardiovascular diseases, cancer and neurological disorders.

Research suggests humans derive benefits too. For example, many studies look at the health impact of fasting by large numbers of people during Ramadan. Results show a reduction in inflammation biomarkers, and this in turn can help prevent a wide range of illness, including neurodegenerative conditions. Other benefits include reduced coronary artery disease and a lower risk of diabetes. Several studies have demonstrated that fasting can decrease blood sugar levels, improve blood sugar control, and reduce insulin resistance, facilitating efforts by those with diabetes to keep levels steady and prevent spikes and crashes.

If you decide to fast during home confinement, how should you do it? Some diets involve a complete fast, allowing only water for a period of time. But many people prefer intermittent fasting. This involves eating at only certain times of the day and fasting the rest of the day. Still other fasts involve drastically reducing food intake for two or three days of the week. Remember, fasting is about calorie restriction, and this is only advantageous if there is no overeating when breaking the fast.

Dr. Sai Krupa Das of the Human Nutrition Research Center on Aging says, In terms of weight loss and improvement on body composition, intermittent fasting can work, but there is not sufficient evidence to say it is superior to overall calorie restriction. In fact, the two methods appear to be pretty comparable.

A report in the journal Aging Research Reviews looked at various forms of calorie restriction. Researchers concluded that all forms of calorie restriction in overweight human subjects have shown improvement in multiple health indicators.

But Dr. Dariush Mozaffarian, dean of Tufts Friedman School of Nutrition Science and Policy, has sound advice. He says, Avoiding refined starches, grains, avoiding added sugars and other hyper-processed foods, and eating plenty of minimally processed foods such as nuts, seeds, beans, fruits, vegetables, fish, yogurt, healthy fats, and plant oils activates many natural weight controlling pathways.

The bottom line is to eat and diet in a way that works for you. Many complicated factors, including inherited genetics and socioeconomic context, make it difficult for some of us to maintain a healthy weight. But for too many of us, the problem is not genetic or societal. It is a lack of individual will and poor lifestyle choices that result in overconsumption of too many calories. This, combined with not enough exercise and confinement at home, is a recipe for trouble.

Dr. W. Gifford-Jones, aka Ken Walker, is a graduate of the University of Toronto and Harvard Medical School. You can reach him online at his website, docgiff.com, or via email at info@ docgiff.com.

See the article here:
The Doctor Game: Is home confinement a good time to fast? - The Westerly Sun

William Frankland obituary – The Guardian

When Bill Frankland began practising in the 1940s, allergy medicine was barely a discipline. The allergist Adam Fox said: To say Bill Frankland was the grandfather of allergy medicine doesnt do it justice. He wasnt the grandfather in the sense of being the oldest but in the sense of being the originator of the speciality. He did the original trials and founded the British society. He was still practising in his 90s and 100s, and remained the doctor people wanted to see.

On his release from a Japanese prisoner of war camp in 1945, Frankland, who has died aged 108, returned to St Marys hospital, Paddington, in London, where he had trained. He had suffered with hay fever since he was nine, and when he saw an advertisement for a part-time assistant in the allergy department, he applied. In February 1946 he became full-time and for the next 70 years was gripped by allergy medicine, which he said was like a fascinating detective story.

Frankland worked at the allergy clinic at St Marys hospital for more than 30 years, and was its director from 1958 until he retired in 1977. A few years later it was renamed the Frankland Allergy Clinic. It was the busiest in the country, and it is estimated that Frankland oversaw the desensitisation treatment of around 30,000 hay fever patients. At the same time, he also ran the hospitals pollen farm near Woking, Surrey, until it closed in 1970.

In 1948 the British Association of Allergists was formed with 30 members and Frankland as its secretary. It grew rapidly as it widened its scope to include immunology, becoming the British Society for Allergy and Clinical Immunology (BSACI) in 1973. Frankland was its president from 1963 to 1966 and remained at its heart all his life.

When he began his career in the late 1940s antihistamines had recently come on stream to treat allergies. Frankland was involved in several trials, demonstrating that two antihistamines reduced hay fever symptoms but were not effective for asthma.

Allergen desensitisation for hay fever had been used since 1911, but had not been properly evaluated. Frankland had read about double-blind placebo-controlled trials and wanted to apply them to his discipline. Patients at that time were injected with a grass-pollen extract called Pollaccine to desensitise them.

Frankland was concerned that it contained material that gave unwanted side-effects and wanted to determine exactly which part of the pollen extract was effective. In 1953 he recruited 200 hay fever patients and showed that a purified pollen protein worked just as well as Pollaccine. His paper, published in 1954, was a milestone: the first double-blind randomised clinical trial in immunotherapy; 65 years later, Frankland was gratified to see it celebrated on the 2018 cover of the journal Allergy.

In the 40s and 50s it was difficult for hay fever patients to control their symptoms without information on what type of pollen and how much of it was in the air. Frankland knew that atmospheric levels of pollen were being measured in Cardiff and wanted to do the same in London. In 1953 he installed a Hirst spore trap on the roof of the nurses home at St Marys and recruited a biologist (whose name he was amused to recount was Miss Hay) to provide daily pollen counts and analyse the prevalence of different pollens. Initially the information went out once a week to members of the British Association of Allergists, but, to disseminate it further, in 1963 Frankland persuaded the Times and the Daily Telegraph to print a daily pollen count. (It is now part of the weather forecast and coordinated by the Met Office.)

As well as his other duties at St Marys, in the 40s Frankland spent two years as Sir Alexander Flemings clinical assistant. He took care of Flemings patients, reporting on their progress every morning at 10am even though Fleming preferred to discuss other subjects.

Frankland said: He just wasnt interested in clinical medicine once he looked down a microscope, he continued looking down a microscope

In 1948 the publisher Butterworths asked for a new chapter on sensitivities in Flemings bestseller Penicillin: Its Practical Application, and Fleming tasked Frankland with writing it. Fleming himself did not accept that people could be allergic to penicillin, saying adverse reactions must be the result of drug impurities. When he read Franklands draft, he crossed out the last sentence: With the increasing use of penicillin, it is to be expected that allergic reactions will become more common, substituting: With the increasing use of penicillin, reactions due to impurities will become less common. Frankland disagreed, but did not feel he should argue with the Nobel prize winner.

In his long career Frankland treated many patients including, in 1979, Saddam Hussein, whose symptoms were caused by cigarettes rather than asthma. He told him: If youre not eating, sleeping or praying, youre smoking. If you carry on, you wont be president in two years time. Saddam heeded the advice and later flew Frankland out to Baghdad for a celebratory lunch.

As well as asthma and hay fever, Frankland was interested in many different allergies, and, in the now no longer permissible tradition of self-experimentation, in 1955 allowed the South American insect Rhodnius prolixus to bite him weekly so he could observe the reaction. He got the insect from the London School of Hygiene and Tropical Medicine and kept it in the glove compartment of his car. After eight weeks, he had a severe anaphylactic reaction and was saved by two injections of adrenaline. Three hours later, he helped a nurse push her car. The strenuous exercise brought on anaphylaxis again, requiring a third shot of adrenaline. This experience led to his interest in the delay that is possible in allergic reactions.

Frankland was born near Bexhill-on-Sea, East Sussex. His father, Henry, was a vicar and his mother, Rose (nee West), a musician. He was an identical twin and nearly didnt survive because he was born prematurely and was tiny, weighing just over 3lb (1.4kg). The family moved to Cumberland (now Cumbria), in north-west England, and Frankland remembered getting postcards from his father who was away during the first world war.

When he was nine he caught tuberculosis, and was unimpressed with the doctor treating him, deciding he could do a better job and should study medicine. He went to St Bees school in the county and then to Queens College, Oxford, to study natural sciences. His studies were interrupted for six months when he returned home to care for his elder sister Ella, who had scarlet fever. She died in October 1933 and he returned to Oxford before moving to St Marys hospital, qualifying as a doctor in 1938.

Two days before the second world war was declared in September 1939, Frankland volunteered as a civilian medical practitioner in the army. He was shipped out to Singapore, where his life was saved a second time. Another doctor and I decided to spin a coin to determine our assignments, he said. I called heads and won. The man who lost went to [the] Alexandra hospital where he was brutally murdered by Japanese forces in 1942.

Frankland, however, was captured and became a Japanese PoW. In 1943 he was moved to Pulau Blakang Mati (now Sentosa Island), off Singapores southern coast, where his two days of tropical medicine training were scant preparation for the array of malnutrition, malaria, dengue and beri-beri he faced. He was nearly bayoneted to death during a punishment bashing from Japanese soldiers, and his life was saved yet again when the Americans dropped atomic bombs on Hiroshima and Nagasaki in 1945, ending the war and preventing mass shooting of PoWs.

Frankland returned home in October of that year. He had married Pauline Jackson, an optometrist, in 1941, and had treasured her letters. When he arrived in Liverpool, he was asked if he wanted to see a psychiatrist and replied: No. I want to see my wife.

Frankland decided not to talk about his experiences to Pauline or to his family. He said: When I got back, I thought Im alive and this is marvellous. Im going to forget everything Ive gone through. When he was nearly 100, he told a colleague he watched a TV programme about VE Day and had his first flashback. Thereafter he was amenable to talking about his experiences.

When Frankland left St Marys in 1977, he became an honorary consultant at Guys hospital in London, where he saw patients into his 90s. He also worked as an expert witness in court cases, and continued to write papers and attend conferences. Each year he presented the BSACI William Frankland award. He had a wide circle of friends and a great zest for life, remembered by one colleague as enjoying tea at the Ritz and riding a dodgem car aged 103.

Pauline died in 2002, and two years ago Frankland moved from his flat in Marylebone to accommodation in the Charterhouse, central London. When asked about his life, Frankland said: I have been very lucky.

He is survived by two sons and two daughters, 10 grandchildren and six great-grandchildren.

Alfred William Frankland, immunologist, born 19 March 1912; died 2 April 2020

Read the original post:
William Frankland obituary - The Guardian