Obstetrics & Gynecology

The Department of Obstetrics and Gynecology at the Medical College of Georgia at Augusta University is a comprehensive clinical service and educational department, specializing in the healthcare of women both on a primary and referral basis. We provide quality clinical services in following areas: General Obstetrics and Gynecology, Gynecologic Oncology, Maternal-Fetal Medicine, Reproductive Endocrinology, Infertility, and Genetics, and Urogynecology and Pelvic Surgery.

General Obstetrics and Gynecology provides a full range of general obstetrical and gynecological services ranging from outpatient care to surgery, and from routine visits to complicated consultations. In addition to normal obstetrical and gynecological services, our specialized research and interest areas include urodynamics, dysmenorrhea, menorrhagia, pelvic pain, menopause, and others.

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Obstetrics & Gynecology

Anatomy and Physiology – McGraw Hill Education

Glossary Click here to go to Prefixes and Suffixes.

Most of the words in this glossary are followed by a phonetic spelling that serves as a guide to pronunciation. The phonetic spellings reflect standard scientific usage and can be easily interpreted following a few basic rules.

abduction (ab-dukshun) The movement of a body part away from the axis or midline of the body; movement of a digit away from the axis of the limb.

ABO system The most common system of classification for red blood cell antigens. On the basis of antigens on the red blood cell surface, individuals can be type A, type B, type AB, or type O.

absorption (ab-sorpshun) The transport of molecules across epithelial membranes into the body fluids.

accessory organs (ak-sesuo-re) Organs that assist with the functioning of other organs within a system.

accommodation (ua-komuo-dashun) A process whereby the focal length of the eye is changed by automatic adjustment of the curvature of the lens to bring images of objects from various distances into focus on the retina.

acetabulum (asue-tabyuu-lum) A socket in the lateral surface of the hipbone (os coxa) with which the head of the femur articulates.

acetone (asue-t=on) A ketone body produced as a result of the oxidation of fats.

acetyl coenzyme A (acetyl CoA) (asue-tl, ua-setl) A coenzyme derivative in the metabolism of glucose and fatty acids that contributes substrates to the Krebs cycle.

acetylcholine (ACh) (ua-setl-kol=en) An acetic acid ester of choline-a substance that functions as a neurotransmitter in somatic motor nerve and parasympathetic nerve fibers.

acetylcholinesterase (ua-setl-kolu1-nestue-r=as) An enzyme in the membrane of postsynaptic cells that catalyzes the conversion of ACh into choline and acetic acid. This enzymatic reaction inactivates the neurotransmitter.

Achilles tendon (ua-kil=ez) See tendo calcaneous.

acid (asid) A substance that releases hydrogen ions when ionized in water.

acidosis (asu1-dosis) An abnormal increase in the H+ concentration of the blood that lowers the arterial pH to below 7.35.

acromegaly (akro-megua-le) A condition caused by the hypersecretion of growth hormone from the pituitary gland after maturity and characterized by enlargement of the extremities, such as the nose, jaws, fingers, and toes.

actin (aktin) A protein in muscle fibers that together with myosin is responsible for contraction.

action potential An all-or-none electrical event in an axon or muscle fiber in which the polarity of the membrane potential is rapidly reversed and reestablished.

active immunity (u1-myoonu1-te) Immunity involving sensitization, in which antibody production is stimulated by prior exposure to an antigen.

active transport The movement of molecules or ions across the cell membranes of epithelial cells by membrane carriers. An expenditure of cellular energy (ATP) is required.

adduction (au-dukshun) The movement of a body part toward the axis or midline of the body; movement of a digit toward the axis of the limb.

adenohypophysis (adn-o-hi-pofu1-sis) The anterior, glandular lobe of the pituitary gland that secretes FSH (follicle-stimulating hormone), LH (luteinizing hormone), ACTH (adrenocorticotropic hormone), TSH (thyroid-stimulating hormone), GH (growth hormone), and prolactin. Secretions of the adenohypophysis are controlled by hormones produced by the hypothalamus.

adenoids (adue-noidz) The tonsils located in the nasopharynx; pharyngeal tonsils.

adenylate cyclase (ua-denl-it sikl=as) An enzyme found in cell membranes that catalyzes the conversion of ATP to cyclic AMP and pyrophosphate (PP1). This enzyme is activated by an interaction between a specific hormone and its membrane receptor protein.

ADH Antidiuretic hormone; a hormone produced by the hypothalamus and released by the posterior pituitary that acts on the kidneys to promote water reabsorption; also known as vasopressin.

ADP Adenosine diphosphate; a molecule that together with inorganic phosphate is used to make ATP (adenosine triphosphate).

adrenal cortex (ua-drenal korteks) The outer part of the adrenal gland. Derived from embryonic mesoderm, the adrenal cortex secretes corticosteroid hormones (such as aldosterone and hydrocortisone).

adrenal medulla (mue-dulua) The inner part of the adrenal gland. Derived from embryonic postganglionic sympathetic neurons, the adrenal medulla secretes catecholamine hormones-epinephrine and (to a lesser degree) norepinephrine.

adrenergic (adreu-nerjik) A term used to describe the actions of epinephrine, norepinephrine, or other molecules with similar activity (as in adrenergic receptor and adrenergic stimulation).

adventitia (adven-tishua) The outermost epithelial layer of a visceral organ; also called serosa.

afferent (afer-ent) Conveying or transmitting to.

afferent arteriole (ar-tire-=ol) A blood vessel within the kidney that supplies blood to the glomerulus.

afferent neuron (nooron) See sensory neuron.

agglutinate (ua-glootn-=at) A clump of cells (usually erythrocytes) formed as a result of specific chemical interaction between surface antigens and antibodies.

agranular leukocytes (ua-granyuu-lar loo kuo-s1=tz) White blood cells (leukocytes) that do not contain cytoplasmic granules; specifically, lymphocytes and monocytes.

albumin (al-byoomin) A water-soluble protein produced in the liver; the major component of the plasma proteins.

aldosterone (al-doster-=on) The principal corticosteroid hormone involved in the regulation of electrolyte balance (mineralocorticoid).

alimentary canal The tubular portion of the digestive tract. See also gastrointestinal tract (GI tract).

allantois (ua-lanto-is) An extraembryonic membranous sac involved in the formation of blood cells. It gives rise to the fetal umbilical arteries and vein and also contributes to the formation of the urinary bladder.

allergens (aler-jenz) Antigens that evoke an allergic response rather than a normal immune response.

allergy (aler-je) A state of hypersensitivity caused by exposure to allergens. It results in the liberation of histamine and other molecules with histaminelike effects.

all-or-none principle The statement of the fact that muscle fibers of a motor unit contract to their maximum extent when exposed to a stimulus of threshold strength.

allosteric (aluo-sterik) A term used with reference to the alteration of an enzyme's activity as a result of its combination with a regulator molecule. Allosteric inhibition by an end product represents negative feedback control of an enzyme's activity.

alveolar sacs (al-veuo-lar) A cluster of alveoli that share a common chamber or central atrium.

alveolus (al-veuo-lus) 1.An individual air capsule within the lung. The alveoli are the basic functional units of respiration. 2.The socket that secures a tooth(tooth socket).

amniocentesis (amne-o-sen-tesis) A procedure in which a sample of amniotic fluid is aspirated to examine suspended cells for various genetic diseases.

amnion (amne-on) A developmental membrane surrounding the fetus that contains amniotic fluid.

amphiarthrosis (amfe-ar-throsis) A slightly movable articulation in a functional classification of joints.

amphoteric (am-fo-terik) Having both acidic and basic characteristics; used to denote a molecule that can be positively or negatively charged, depending on the pH of its environment.

ampulla (am-poolua) A saclike enlargement of a duct or tube.

ampulla of Vater (Fuater) See hepatopancreatic ampulla.

anabolic steroids (anua-bolik steroidz) Steroids with androgenlike stimulatory effects on protein synthesis.

anabolism (ua-nabuo-lizem) A phase of metabolism involving chemical reactions within cells that result in the production of larger molecules from smaller ones; specifically, the synthesis of protein, glycogen, and fat.

anaerobic respiration (an-ua-robik respu1-rashun) A form of cell respiration involving the conversion of glucose to lactic acid in which energy is obtained without the use of molecular oxygen.

anal canal (anal) The terminal tubular portion of the large intestine that opens through the anus of the GI tract.

anaphylaxis (anua-fu1-laksis) An unusually severe allergic reaction that can result in cardiovascular shock and death.

anastomosis (ua-nastuo-mosis) An interconnecting aggregation of blood vessels or nerves that form a network plexus.

anatomical position (anua-tomu1-kal) An erect body stance with the eyes directed interior, the arms at the sides, the palms of the hands facing interior, and the fingers pointing straight down.

anatomy (ua-natuo-me) The branch of science concerned with the structure of the body and the relationship of its organs.

androgens (andruo-jenz) Steroids containing 18 carbons that have masculinizing effects; primarily those hormones(such as testosterone) secreted by the testes, although weaker androgens are also secreted by the adrenal cortex.

anemia (ua-neme-ua) An abnormal reduction in the red blood cell count, hemoglobin concentration, or hematocrit, or any combination of these measurements. This condition is associated with a decreased ability of the blood to carry oxygen.

angina pectoris (an-jinua pektuo-ris) A thoracic pain, often referred to the left pectoral and arm area, caused by myocardial ischemia.

angiotensin II (anje-o-tensin) An 8-amino-acid polypeptide formed from angiotensin I(a 10-amino-acid precursor), which in turn is formed from cleavage of a protein(angiotensinogen) by the action of renin(an enzyme secreted by the kidneys). Angiotensin II is a powerful vasoconstrictor and a stimulator of aldosterone secretion from the adrenal cortex.

anions (ani-onz) Ions that are negatively charged, such as chloride, bicarbonate, and phosphate.

antagonist (an-taguo-nist) A muscle that acts in opposition to another muscle.

antebrachium (ante-brake-em) The forearm.

anterior (ventral) Toward the front; the opposite of posterior, or dorsal.

anterior pituitary (pu1-toou1-ter-e) See adenohypophysis.

anterior root The anterior projection of the spinal cord, composed of axons of motor neurons.

antibodies (antu1-bod=ez) Immunoglobin proteins secreted by B lymphocytes that have transformed into plasma cells. Antibodies are responsible for humoral immunity. Their synthesis is induced by specific antigens, and they combine with these specific antigens but not with unrelated antigens.

anticodon (antu1-kodon) A base triplet provided by three nucleotides within a loop of transfer RNA that is complementary in its base-pairing properties to a triplet(the codon) in mRNA. The matching of codon to anticodon provides the mechanism for translating the genetic code into a specific sequence of amino acids.

antigen (antu1-jen) A molecule that can induce the production of antibodies and react in a specific manner with antibodies.

antigenic determinant site (an-tu1-jenik) The region of an antigen molecule that specifically reacts with particular antibodies. A large antigen molecule may have a number of such sites.

antiserum (antu1-sirum) A serum that contains specific antibodies.

anus (anus) The terminal opening of the GI tract.

aorta (a-ortua) The major systemic vessel of the arterial system of the body, emerging from the left ventricle.

aortic arch The superior left bend of the aorta between the ascending and descending portions.

apex (apeks) The tip or pointed end of a conical structure.

aphasia (ua-fazhua) Defects in speech, writing, or in the comprehension of spoken or written language caused by brain damage or disease.

apneustic center (ap-noostik) A collection of nuclei(nerve cell bodies) in the brain stem that participates in the rhythmic control of breathing.

apocrine gland (apuo-krin) A type of sweat gland that functions in evaporative cooling. It may respond during periods of emotional stress.

aponeurosis (apuo-noo-rosis) A fibrous or membranous sheetlike tendon.

appendix A short pouch that attaches to the cecum.

aqueous humor (akwe-us) The watery fluid that fills the anterior and posterior chambers of the eye.

arachnoid mater (ua-raknoid) The weblike middle covering(meninx) of the central nervous system.

arbor vitae (arbor vite) The branching arrangement of white matter within the cerebellum.

arm (brachium) The portion of the upper extremity from the shoulder to the elbow.

arrector pili muscle (ah-rektor pihle) The smooth muscle attached to a hair follicle that, upon contraction, pulls the hair into a more vertical position, resulting in "goose bumps."

arteriole (ar-tire-=ol) A minute arterial branch.

arteriosclerosis (ar-tire-o-sklue-rosis) Any one of a group of diseases characterized by thickening and hardening of the artery wall and in the narrowing of its lumen.

arteriovenous anastomoses (ar-tire-o-venus ua-nastuo-mos=ez) Direct connections between arteries and veins that bypass capillary beds.

artery (artue-re) A blood vessel that carries blood away from the heart.

arthrology (ar-throluo-je) The scientific study of the structure and function of joints.

articular cartilage (ar-tikyuu-lar kartu1-lij) A hyaline cartilaginous covering over the articulating surface of the bones of synovial joints.

articulation (ar-tikyuu-lashun) A joint.

arytenoid cartilages (arue-tenoid) A pair of small cartilages located on the superior aspect of the larynx.

ascending colon (kolon) The portion of the large intestine between the cecum and the hepatic flexure.

association neuron (nooron) A nerve cell located completely within the central nervous system. It conveys impulses in an arc from sensory to motor neurons; also called interneuron or internuncial neuron.

astigmatism (ua-stigmua-tizem) Unequal curvature of the refractive surfaces of the eye (cornea and/or lens), so that light entering the eye along certain meridians does not focus on the retina.

atherosclerosis (athue-ro-sklue-rosis) A common type of arteriosclerosis found in medium and larger arteries in which raised areas within the tunica intima are formed from smooth muscle cells, cholesterol, and other lipids. These plaques occlude arteries and serve as sites for the formation of thrombi.

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Anatomy and Physiology - McGraw Hill Education

New Human Physiology Ch 21 – zuniv.net

This Chapter is written following discussions with my colleague, Leif Vanggaard, MD, Arctic Institute, Copenhagen.

Study Objectives

To define body core and body shell, heat balance, heat exchange (conduction, conversion, evaporation and radiation), hyperthermia, hypothermia, mean body temperature, heat capacity, and thermal steady state.

To describe fever (pyrogens), benignant and malignant hyperthermia, heat exhaustion, heat syncope, heat stroke, sun stroke, and hypothermia.

To describe radiation sickness.

To calculate one thermal variable, when relevant variables are given.

To explain the concepts heat exchange, thermogenesis by food and shivering, the human temperature control system and its function at different environmental temperatures.

To use the above concepts in problem solving and case histories.

Principles

Newtons law of cooling: The dry heat loss is proportional to the temperature difference between the human body (shell) and the surroundings.

The total energy of a system is conserved in an interaction, not the kinetic energy or the mass (Einstein). If the mass changes during an interaction, there is a resultant change in kinetic energy, so that the total energy remains constant. Heat energy is proportional to molecular movement rates heat energy equals movement.

Stefan-Boltzmanns rule: The higher the temperature of an object, the more it radiates. The energy radiated from an object is proportional to the fourth power of its Kelvin temperature. The energy radiating from an object and received by the human body is proportional to the temperature difference between the object and the skin (see Eq. 21-4). This is because human life implies relatively small temperature gradients.

Definitions

Body core consists of the thermoregulated deeper parts of the body and the proximal extremity portions of warm-blooded animals including man.

Body shell refers to those outer parts of the body (skin and subcutaneous tissue) that change temperature at cold exposure.

Conductance changes of the shell are used as a measure of skin bloodflow.

Conductive heat loss describes a direct transfer of heat energy by contact between two bodies of different temperature (eg, skin and objects).

Convective heat loss is defined as the heat loss by contact between the surface (skin) and a moving medium (air or water).

Evaporative heat loss is defined as the heat loss by evaporation from the body surface or lungs.

Fever occurs when the core temperature of the body is raised above normal steady state levels. The body reacts as if it is too cold. Fever implies a disorder resulting in shivering combined with vasoconstriction, headache, dedolation, and general discomfort (eg, malaria).

Heat flow is defined as energy exchanged due to a temperature difference. Heat flow is transmitted along a temperature gradient.

Heat capacity is the amount of heat required to produce a temperature increase for a given amount of substance.

Heat energy balance in a resting person is a condition, where the heat production is equal to the heat loss. Thus the body temperature is constant and the heat storage is zero (thermal steady state). Usually, there is no internal heat energy flux between body core and shell.

Hyperthermia is an increase in core temperature above normal.

Hypothermia refers to a clinical condition with a lowered core temperature (below 35 oC).

Mean body temperature is defined according to Eq. 21-1 (see end of Chapter).

Non-shivering thermogenesis is a rise in metabolism, which is not related to muscular activity (shivering or exercise).

Insensible perspiration (leakage of the skin) is the small cutaneous evaporation loss, which is unrelated to sweat gland function.

Insulation refers to resistance to heat transfer.

Radiative heat loss is a transfer of heat energy between 2 separate objects at different temperature. Heat energy is transferred via electromagnetic waves (photons). This heat transfer does not require a medium, and the temperature of any intervening medium is immaterial.

Shell temperature is the temperature of the outer parts of the body (measured on the skin surface) and related to cold environments.

Shivering is a reflex myogenic response to cold with asynchronous or balanced muscle contractions performing no external work.

Specific heat capacity is the relationship between heat energy exchanged per weight unit of a substance and the corresponding temperature change. The specific heat capacity of water is 4.18 and of the human body (blood and tissues) 3.49 kJ kg-1 oC-1, respectively. The specific heat capacity of atmospheric air is 1.3 kJ (m3)-1 oC-1.

Temperature is the measurement of heat energy content.

Essentials

This paragraph deals with

1. The temperatures of the body, 2. Body responses to cold, 3. Body responses to heat, 4. Emotional sweating, 5. Metabolic Rate and environmental temperature, 6. Temperature control, 7. The human thermo-control system, and 8. Thermoregulatory effectors.

1. The temperatures of the body

The human body consists of a peripheral shell and a central core (Fig. 21-1). The heat content (H or enthalpy) of the human body is reflected by its temperature. By definition a thermometer only measures the temperature of the thermometer, so its location is essential. The mean core temperature is 37 oC in healthy adults at rest, but small children have larger diurnal variations.

The skin is the main heat exchanger of the body. The skin temperature is determined by the core temperature and by the environment (temperature, humidity, air velocity). Thus the shell temperature is governed by the needs of the body to exchange heat energy.

Fig. 21-1: Heat transfers, body cores and shells temperatures of a naked person standing in cold and warm air, respectively.

The shell temperature is measured on the skin surface and at the hands and feet to approach the room temperature of 19oC in a person standing in a cold room for hours (Fig. 21-1, left). The shell temperature is several degrees lower than the temperature in the central core. The limbs have both a longitudinal and a radial temperature gradient. The shell temperature and the size of the shell vary with the environmental temperature and the termal state of the person. A naked person, standing on a cold floor in 19oC air has a small core and a thick shell compared to the same person in a warm environment (Fig. 21-1). The shell temperature of the skin and distal extremities is difficult to evaluate. The best estimate is measurement of the infrared heat radiation flux with a radiometer.

The core temperature is the rather constant temperature in the deeper parts of the body and in the proximal extremity portions (see the red stippled lines of Fig. 21-1). However, the core temperature may vary several Centigrades between different regions depending on the cellular activity. The brain has a radial temperature gradient between its deep and superficial parts. In a sense, the temperature of the mixed venous blood represents an essential core temperature.

The rectal temperature

A high core temperature is found to be constant in the rectum about 10-15 cm from the anus. When measuring the rectal temperature a standard depth of 5-10 cm is used clinically. The venous plexus around the rectum communicate with the cutaneous blood in the anal region. The rectal temperature falls when the feet are cold, because cold blood passes the rectum in the veins from the legs for the same reason. The rectal temperature rises during heavy work involving the legs.

Parents should be advised to measure the rectal temperature in disease suspect children. The rectal temperature is a reliable estimate of the core temperature in resting persons.

Sublingual (oral) or axillary temperatures are unreliable measures of the core temperature - often more than half a degree lower than the rectal temperature.

The cranial temperature (tympanic and nasal)

The main control of temperature is performed by the anterior hypothalamus, which has a high bloodflow. Within the cranium the hypothalamus lies over the Circle of Willis, which supplies it with blood, and close to the cavernous sinus which drains it. Hypothalamus elicits heat loss responses when stimulated by heat. The tympanic membrane and areas in the nasal cavity (the anterior ethmoidal region, part of the sphenoid sinus) are supplied with blood from the internal carotid artery just like the hypothalamus. These cranial locations then serve as a substitute for the measurement of the inaccessible hypothalamic temperature.

Intake of 250 g of ice releases an abrupt fall in the nasal temperature in a warm person, whereas the change in rectal temperature is smaller and delayed (Fig. 21-2). The cranial core temperature is more dynamic than the rectal.

Fig. 21-2: Intake of ice reduces the temperature in a warm person resting at 45oC.

In sports and in surgical hypothermia dynamic measurements of core temperature are essential. The cranial temperature is often preferred. During forceful movements the thermistor may be displaced. In such situations an oesophageal location is applied at heart level. This is an approximative measure of the temperature of the mixed venous blood of the right heart located close to the thermistor.

The mean body temperature is defined according to Eq. 21-1. The storage of heat energy in the body can be calculated according to its heat capacity (3.49 kJ* kg-1*oC-1), the body weight (kg) and the change in mean body temperature in the period (Eq. 21-2).

According to the first law of thermodynamics, the storage of heat energy equals the metabolic energy change minus the heat loss (Eq. 21-3). Quantification of thermodynamics in humans is possible using equations 21-1 to 21-7 (later in this chapter).

The body is in heat energy balance, when the storage is zero. However, the core temperature may change with internal fluxes of heat energy between core and shell without storage or loss of heat energy at a constant activity.

Venous blood draining active muscles and the liver is likely to be warmer than pulmonary venous blood, since this has undergone evaporative cooling in the alveoli. A patient with high fever can be in thermal steady state, with a high constant heat production, if both core- and shell-temperatures are constant, and no internal energy flux occurs.

Warm-blooded animals, homeotherms such as humans, can change their metabolism in order to keep their heat production equal to the heat loss. Such animals have a temperature control system and thereby maintain a rather constant core temperature. Warm-blooded animals live with the advantage of an unchanged cell activity and temperature in their core. However, the human core temperature falls during the oestrogen phase of the menstrual cycle and during sleep (circadian rhythm). The lowest temperature is between 18 at night and 6 oclock in the morning (Fig. 21-3). The temperature cycle is part of the circadian periodicity. Our biological clock seems to be synchronised with the rotation of the globe. Also meals, light and temperature plays a role.

Ovulation releases a sharp rise in morning temperature. Progesterone effects seem to explain the higher temperature in the last phase of the menstrual cycle (Fig. 21-3).

Fig. 21-3: Variations of the core temperature during 24 hour (above), and variations related to phases of the menstrual cycle (below).

Cold-blooded animals (poikilotherms) live with a behavioural temperature rhythm, but have no autonomic temperature control. The core- and shell-temperatures vary with the environment and the cellular activity. Reptiles, premature and low weight-premature newborn babies are cold-blooded. These babies have no thermoregulation (see later). However, their capacity for heat production is 5-10 times as great per unit weight as that of adults.

Humans have a warm-blooded (homeothermic) coreand a cold-blooded (poikilothermic) shell in a cold environment.

Persons exposed to general anaesthesia, alcohol, and certain drugs lose the autonomic thermoregulation. Cold-blooded animals must live with varying core and shell temperature, whereby the rate of their cellular activities varies with the surrounding temperature (Fig. 21-4).

Fig. 21-4: The body core temperature and the environmental body temperature for a warm-blooded animal (cat) and a cold-blooded animal (lizard).

a) Convection. The convective heat loss is calculated by Eq. 21-7. A healthy person in sports clothes experiences thermal comfort at three times the resting metabolic rate (3 MET), when the surrounding temperature is 20oC, the humidity is 50% and the wind velocity is 0.5 m*s-1.

Diving (water has a high thermal conductivity) illustrates the importance of conduction andconvection in heat energy transfer.

The dry diving suit excludes water from contact with the skin and traps low-conductance air in insulating clothing worn inside the watertight sealing.

The wet suit traps water next to the skin but prevents its circulation. The water is warmed through contact with the skin, and the high insulation of the foam rubber wet diving suit, with its many pockets of trapped air, minimises the rate of heat energy loss to the surrounding water. Air is a poor heat conductor and thus a good insulator. During deep diving high pressures compress these air pockets and thus reduce the insulation properties of wet diving suits.

b) Radiation describes a transfer of energy between objects in the form of electromagnetic waves (photons). This includes ultraviolet and visible (sun light) radiation from the outside and from the body infrared or warm heat radiation.

Radiative heat transfer can be calculated for a naked person according to Eq. 21-4.

When the skin temperature (Tskin) is less than the temperature of the surrounding objects, heat is gained by radiation.

At wintertime, heat can be lost through a window glass by radiation from the body to the cold environment irrespective of the room temperature. This is because the skin temperature is higher than the outside temperature.

c) Conduction. Sitting on a cold stone is a typical example of conduction loss, just as standing on a cold floor (Fig. 21-1). Conduction heat can also be gained, although it is really possible to walk on glowing coals with speed and a thick epidermal horn layer.

d) Evaporative heat loss- see sweat secretion below.

2. Body-responses to cold

Cutaneous vasoconstriction lowers skin temperature, and thereby reduces the conductive-convective heat loss that is determined by the temperature gradient from the skin surface to the environment. Cutaneous vasoconstriction directs the peripheral venous blood back to the body core through the deep veins and the commitant veins. These veins are located around the arteries with warm blood, so that the venous blood receives part of the heat energy from the arterial blood - so-called counter current heat exchange (Fig. 21-5). The vasoconstriction is so effective, that the bloodflow through the arterio-venous anastomoses in the fingers and toes can fall to below one percent of the flow at normal temperature. The cooling of the shell is immediate, and the size of the shell increases (Fig. 21-1). Obviously, the shell is large for a naked person in cold air. The resistance vessels of the hands may open periodically to nourish the tissues, but the high viscosity of the cold blood can endanger the tissue nutrition and result in trench foot.

The arterio-venous shunts of the hands and feet are closed, so the bloodflow to the limbs is a nutritive minimum.

The deep arteries and veins of the limbs lie in parallel, so the arterial bloodflow loses heat to the incoming venous blood partially surrounding the arteries (Fig. 21-5). This is a typical counter-current heat exchange. In a cold environment, where vasoconstriction and heat exchange produces cold extremities, the total insulation is increased at the expense of reduced neuromuscular efficiency.

Fig. 21-5: Counter-current exchange in a human arm conserving heat energy in a cold climate (left). Superficial venous cooling ribs eliminate heat energy in a warm climate (right).

In a warm climate the high bloodflow of the extremities ensures an optimal temperature of the deeper structures (eg, the neuromuscular system). The temperature of the arterial blood is maintained (Fig. 21-5, right) and the arterio-venous anastomoses are wide open conveying warm blood to the superficial veins. The superficial veins also act as cooling ribs and transfer large amounts of heat to the skin surface, where it is eliminated from the body by convection, conduction and evaporation (Fig. 21-5, right).

Shivering is a reflex myogenic response to cold with asynchronous or balanced muscle contractions elicited from the hypothalamus via cutaneous receptors. The activity in agonist and antagonist muscles balance, so there is no external work. Without outside work, all energy is liberated as metabolic heat energy. Heat production is also increased by thyroid gland activity and by release of catecholamines from the adrenal medulla.

External work, such as running, is helpful in maintaining body temperature when feeling cold. Cold increases the motivation for warm-up exercises and illustrates the voluntary, cortical (feedforward influence) on temperature homeostasis. The core temperature increases proportionally to the work intensity during prolonged steady state work (Fig. 21-6). The mean skin temperature falls with increasing work intensity at 20oC, because the sweat evaporation cools the skin.

Fig. 21-6: Muscular and oesophageal temperature during steady state exercise. The levels of exercise range from zero to 100% of the maximum oxygen uptake.

The temperature in the active muscles determines the level of the rectal temperature. Following marathon rectal temperatures of more than 41oC have been measured and heat strokes have occurred. A marathon is even more difficult to accomplish in warm, humid environments and strong sun may cause sunstroke (see later).

People may adapt to prolonged exposure to cold by increasing their basal metabolic rate up to 50% higher than normal. This metabolic adaptation is found in Inuits (Eskimos) and other people continuously subject to cold.

The environmental temperature, where we maintain our autonomic temperature control, is in the range of zero to 45oC. Below and above this range we adapt to the environment by behaviour (adding or removing clothing, warm or cold bath, sun or shadow). A core temperature above 44oC starts protein denaturation in all cells and is incompatible with life. Below 32oC humans lose consciousness and below 28oC the frequency of malignant cardiac arrhythmias is increasing, ending with ventricular fibrillation and death at a core temperature below 23 oC (Fig. 21-7).

Fig. 21-7: Environmental temperature variations and temperature control. Lack of vital signs in the clinic (respiration, heart rate, EEG) must not be taken as death. Treatment must be instituted until death signs are developed.

3. Body-responses to heat

Sweat secretion. Three million sweat glands produce sweat at a rate of up to 2 litres per hour or more during exercise in extreme warm conditions. If not compensated by drinking, such high sweat rates lead to circulatory failure and shock. Sweat resembles a dilute ultrafiltrate of plasma. Healthy humans cannot maintain their body temperature, if the environmental air reaches body temperature and the air is saturated with water vapour. Primary sweat is secreted as an isosmotic fluid into the sweat duct, and subsequent NaCl reabsorption results in the final hypo-osmotic sweat. Thermal sweating is abolished by atropine, proving that the postganglionic fibres are cholinergic. Cholinergic drugs provoke sweating just as adrenergic agonists do. Evaporation of water on the body surface eliminates 2428-2436 J g-1 at mean shell temperatures of 30-32oC. Evaporation of a large volume of sweat per time unit (Vsweat) implies a substantial loss of heat according to Eq. 21-5.

Normally, the skin temperature falls with increasing work intensity, because the sweat evaporation cools the skin (Fig. 21-6). Danger occurs when the average skin temperature and the body core temperature converge towards the same value.

Condensation of water on the skin gains heat energy, which is stored in the body. This is what happens in a Sauna.

Vasodilatation of skin vessels in warm environments results in increased cardiac output. The arterio-venous anastomoses in the hands and feet are open, and the bloodflow can rise up to at least 10 folds. The shell is minimal, when a naked person is in warm air (Fig. 21-1, right). The skin bloodflow, mainly in the extremities, determines the amount of heat energy, which is carried from the body core to be lost on the surface. The heat energy is transported from the large body core to the skin by convection in the blood. A substantial part of the heat energy is lost through the superficial veins of the extremities acting as cooling ribs (Fig. 21-5). The blood of the superficial veins is thus arterialized, when the person is warm.

A piece of steak has the same composition as human skin but of course no blood flow and no sweat evaporation. Thus the steak will be cooked at an air temperature that humans can survive. A person can stay in a room with dry air at 128oC for up to 10 min during which time the steak is partially cooked.

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New Human Physiology Ch 21 - zuniv.net

History of neuroscience – Wikipedia

From the ancient Egyptian mummifications to 18th century scientific research on "globules" and neurons, there is evidence of neuroscience practice throughout the early periods of history. The early civilizations lacked adequate means to obtain knowledge about the human brain. Their assumptions about the inner workings of the mind, therefore, were not accurate. Early views on the function of the brain regarded it to be a form of "cranial stuffing" of sorts. In ancient Egypt, from the late Middle Kingdom onwards, in preparation for mummification, the brain was regularly removed, for it was the heart that was assumed to be the seat of intelligence. According to Herodotus, during the first step of mummification: "The most perfect practice is to extract as much of the brain as possible with an iron hook, and what the hook cannot reach is mixed with drugs." Over the next five thousand years, this view came to be reversed; the brain is now known to be the seat of intelligence, although colloquial variations of the former remain as in "memorizing something by heart".

The Edwin Smith Surgical Papyrus, written in the 17th century BC, contains the earliest recorded reference to the brain. The hieroglyph for brain, occurring eight times in this papyrus, describes the symptoms, diagnosis, and prognosis of two patients, wounded in the head, who had compound fractures of the skull. The assessments of the author (a battlefield surgeon) of the papyrus allude to ancient Egyptians having a vague recognition of the effects of head trauma. While the symptoms are well written and detailed, the absence of a medical precedent is apparent. The author of the passage notes "the pulsations of the exposed brain" and compared the surface of the brain to the rippling surface of copper slag (which indeed has a gyral-sulcal pattern). The laterality of injury was related to the laterality of symptom, and both aphasia ("he speaks not to thee") and seizures ("he shutters exceedingly") after head injury were described. Observations by ancient civilizations of the human brain suggest only a relative understanding of the basic mechanics and the importance of cranial security. Furthermore, considering the general consensus of medical practice pertaining to human anatomy was based on myths and superstition, the thoughts of the battlefield surgeon appear to be empirical and based on logical deduction and simple observation.[1][2]

During the second half of the first millennium BC, the Ancient Greeks developed differing views on the function of the brain. However, due to the fact that Hippocratic doctors did not practice dissection, because the human body was considered sacred, Greek views of brain function were generally uninformed by anatomical study. It is said that it was the Pythagorean Alcmaeon of Croton (6th and 5th centuries BC) who first considered the brain to be the place where the mind was located. According to ancient authorities, "he believed the seat of sensations is in the brain. This contains the governing faculty. All the senses are connected in some way with the brain; consequently they are incapable of action if the brain is disturbed...the power of the brain to synthesize sensations makes it also the seat of thought: The storing up of perceptions gives memory and belief and when these are stabilized you get knowledge."[2] In the 4th century BC Hippocrates, believed the brain to be the seat of intelligence (based, among others before him, on Alcmaeon's work). During the 4th century BC Aristotle thought that, while the heart was the seat of intelligence, the brain was a cooling mechanism for the blood. He reasoned that humans are more rational than the beasts because, among other reasons, they have a larger brain to cool their hot-bloodedness.[3]

In contrast to Greek thought regarding the sanctity of the human body, the Egyptians had been embalming their dead for centuries, and went about the systematic study of the human body. During the Hellenistic period, Herophilus of Chalcedon (c.335/330280/250 BC) and Erasistratus of Ceos (c. 300240 BC) made fundamental contributions not only to brain and nervous systems' anatomy and physiology, but to many other fields of the bio-sciences. Herophilus not only distinguished the cerebrum and the cerebellum, but provided the first clear description of the ventricles. Erasistratus used practical application by experimenting on the living brain. Their works are now mostly lost, and we know about their achievements due mostly to secondary sources. Some of their discoveries had to be re-discovered a millennium after their death.[2]

During the Roman Empire, the Greek anatomist Galen dissected the brains of sheep, monkeys, dogs, swine, among other non-human mammals. He concluded that, as the cerebellum was denser than the brain, it must control the muscles, while as the cerebrum was soft, it must be where the senses were processed. Galen further theorized that the brain functioned by movement of animal spirits through the ventricles. "Further, his studies of the cranial nerves and spinal cord were outstanding. He noted that specific spinal nerves controlled specific muscles, and had the idea of the reciprocal action of muscles. For the next advance in understanding spinal function we must await Bell and Magendie in the 19th Century."[2][3]

Andreas Vesalius noted many structural characteristics of both the brain and general nervous system during his dissections of human cadavers.[4] In addition to recording many anatomical features such as the putamen and corpus collusum, Vesalius proposed that the brain was made up of seven pairs of 'brain nerves', each with a specialized function. Other scientists including Leonardo da Vinci furthered Vesalius' work by adding their own detailed sketches of the human brain. Ren Descartes also studied the physiology of the brain, proposing the theory of dualism to tackle the issue of the brain's relation to the mind. He suggested that the pineal gland was where the mind interacted with the body after recording the brain mechanisms responsible for circulating cerebrospinal fluid.[5]Thomas Willis studied the brain, nerves, and behavior to develop neurologic treatments. He described in great detail the structure of the brainstem, the cerebellum, the ventricles, and the cerebral hemispheres.

The role of electricity in nerves was first observed in dissected frogs by Luigi Galvani in the second half of the 18th century. In the 1820s, Jean Pierre Flourens pioneered the experimental method of carrying out localized lesions of the brain in animals describing their effects on motricity, sensibility and behavior. Richard Caton presented his findings in 1875 about electrical phenomena of the cerebral hemispheres of rabbits and monkeys. Studies of the brain became more sophisticated after the invention of the microscope and the development of a staining procedure by Camillo Golgi during the late 1890s that used a silver chromate salt to reveal the intricate structures of single neurons. His technique was used by Santiago Ramn y Cajal and led to the formation of the neuron doctrine, the hypothesis that the functional unit of the brain is the neuron. Golgi and Ramn y Cajal shared the Nobel Prize in Physiology or Medicine in 1906 for their extensive observations, descriptions and categorizations of neurons throughout the brain. The hypotheses of the neuron doctrine were supported by experiments following Galvani's pioneering work in the electrical excitability of muscles and neurons. In the late 19th century, Emil du Bois-Reymond, Johannes Peter Mller, and Hermann von Helmholtz showed neurons were electrically excitable and that their activity predictably affected the electrical state of adjacent neurons.

In parallel with this research, work with brain-damaged patients by Paul Broca suggested that certain regions of the brain were responsible for certain functions.[6]

Neuroscience during the twentieth century began to be recognized as a distinct unified academic discipline, rather than studies of the nervous system being a factor of science belonging to a variety of disciplines.

Broca's hypothesis was supported by observations of epileptic patients conducted by John Hughlings Jackson, who correctly deduced the organization of motor cortex by watching the progression of seizures through the body. Carl Wernicke further developed the theory of the specialization of specific brain structures in language comprehension and production. Modern research still uses the Korbinian Brodmann's cytoarchitectonic (referring to study of cell structure) anatomical definitions from this era in continuing to show that distinct areas of the cortex are activated in the execution of specific tasks.[6]Eric Kandel and collaborators have cited David Rioch, Francis O. Schmitt, and Stephen Kuffler as having played critical roles in establishing the field.[7] Rioch originated the integration of basic anatomical and physiological research with clinical psychiatry at the Walter Reed Army Institute of Research, starting in the 1950s. During the same period, Schmitt established a neuroscience research program within the Biology Department at the Massachusetts Institute of Technology, bringing together biology, chemistry, physics, and mathematics. The first freestanding neuroscience department (then called Psychobiology) was founded in 1964 at the University of California, Irvine by James L. McGaugh. Kuffler started the Department of Neuroscience at Harvard Medical School in 1966.

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History of neuroscience - Wikipedia

Molecular Biology of the Cell

Molecular Biology of the Cell (MBoC) is an online journal published twice monthly and owned by the American Society for Cell Biology (ASCB). Unredacted accepted manuscripts are freely accessible immediately through MBoC in Press. Final published versions are freely accessible two months after publication at http://www.molbiolcell.org. MBoC is also available online through PubMed Central, sponsored by the U.S. National Library of Medicine. Access earlier than two months is available through subscription or membership in the ASCB.

Last updated: December 5, 2016

January 1992 - December 2016

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Molecular Biology of the Cell

Biochemistry

Welcome to the home page of one of the fastest growing departments of biochemistry in the U.S., where our faculty have developed superb educational and research programs. Learn more about our department.

Charles Brenner, PhD Chair and DEO, Department of Biochemistry

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Biochemistry

Genetics | Answers in Genesis

Scientists have discovered an unmistakable language within all living things. Like a miniature library, DNA stores piles of information in extraordinary molecules that specify the details of everything from the shape of flower petals to the color of your eyes. A supremely intelligent Author and Life-Giver left His indelible message in every living thing.

The species on earth today descend from the original created kinds of Genesis 1. The many inter-species breedings that are possible today (e.g., zonkeys, wholphins), as well as the close similarities within biological groups (e.g., the canine group) that are distinct from one another, remind us of this fact. But exactly why the created kinds have fractured into many incompatible species has only been answered indirectly by creationists.

Successful evolution requires the addition of new information and new genes that produce new proteins that are found in new organs and systems. Losing structures, or misplacing their development, should not be equated with the increased information that is needed to form novel structures and cellular systems.

Minimal genomes is the number of genes considered essential for a bacterium to survive in a nutrient-rich, stress-free and competitor-free environment in the lab. Evolutionists believe if the genes universal to all life can be determined then its just a matter of tinkering with the existing genetic information via mutations to go from goo to you.

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Genetics | Answers in Genesis

ST genetics

Females calving heifers in their first two pregnancies produce up to 981 lbs. more milk over the two lactations than females calving back-to-back males.

(Hinde K, et al, (2014), Holsteins Favor Heifers, Not Bulls: Biased Milk Production Programmed during Pregnancy as a Function of Fetal Sex. PLoS ONE 9(2): e86169. doi:10.1371/journal.pone.0086169)

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ST genetics

Molecular and Human Genetics | Baylor College of Medicine …

Top-Ranked Genetics Department

The Department of Molecular and Human Genetics at Baylor College of Medicine is ranked first in the countryin grants and funding from the National Institutes of Health.

The Department has launched Consultagene, a newand innovative virtual platform for genetics services.Find out more about it here.

Baylor Miraca Genetics Laboratories, a joint venture of Baylor College of Medicine and Miraca Holdings, Inc., has rebranded as Baylor Genetics.

Baylor College of Medicine centers, ledby Drs. Richard Gibbs, James Lupski, and Suzanne Leal, will receivefunding as a result of programslaunched today by the National Human Genome Research Institute.

The Department of Molecular and Human Genetics is participating in anNIH-sponsored, multi-center study called the Undiagnosed Disease Network. The program is currently accepting online applications.

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Molecular and Human Genetics | Baylor College of Medicine ...

Genetics – Advocate Health Care

The Division of Genetics at Advocate Medical Group offers a team of genetic specialists to help individuals and families navigate the complex arena of genetics and genomics. We are committed to the diagnosis, management, and treatment of patients with genetic disorders.

Our specially trained clinical geneticists and genetic counselors provide a full range of services including:

We guide families facing hereditary and genetic disorders through complicated genetic issues in an easy-to-understand manner and provide educational resources helpful to your understanding of a genetic disorder. Our specialists can also help you identify support groups and social services, and coordinate and refer you to appropriate specialty providers based on your diagnosis.

The Division of Genetics offers comprehensive care that extends beyond genetic counseling and diagnosis. Our patients have access to multidisciplinary clinics that offer exceptional, compassionate care to children and adults with a variety of genetic disorders. Individuals in these multidisciplinary clinics have the opportunity to be evaluated by an experienced treatment team which includes multiple specialists from different healthcare disciplines.

Our specialists will determine which genetic tests are most appropriate for your particular situation. We discuss the risks, benefits, and limitations of genetic testing, as well as the emotional issues of a diagnosis and knowing your risk.

The Advocate Medical Group Genetics offers a range of services.

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Genetics - Advocate Health Care