C14: Homeostasis Flashcards

1
Q

define homeostasis

A

Homeostasis is themaintenanceof a constant internal body environment involving variousself-regulatory mechanismswithin the body.

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2
Q

examples of things regulatory mechanism control

A

body temperature, blood sugar levels, blood thyroxin levels, blood thyroxin levels, blood pressure and other internal conditions at stable levels.

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3
Q

Self-regulation in organism involve the control of biochemical processes by afeedback mechanism. what happens in a feedback mechanism

A

the products of the biochemical processes serve asregulatorsof the process itself.

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4
Q

what components do the principles of homeostasis depend on

A
  • Receptors:these are cells or specific organs in the body that are capable of detecting a stimulus, such as a change or deviation in the external and internal environment.
    • Effectors:these are tissues or organs that cause the necessary action to bring the affected condition back to a normal level after the stimulus has been received by the receptors.
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5
Q

describe negative feedback mechanism + eg in terms of blood-glucose

A

In negative feedback, the production of a certain substance inhibits the process that produces the substance, e.g. when the blood glucose level increases, the pancreas detects this change and produces the hormone insulin, which converts the excess glucose into glycogen. As the blood glucose level returns to normal, the excess insulin stops the pancreas from producing further insulin.

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6
Q

describe the positive feedback mechanism + eg Na+ ions

A

In positive feedback, the production a certain substance causes further activation of the process that produces more of the substance, e.g.during nervous transmission, the influx of Na+ ions into the membrane of the neuron, as a result of depolarization causes the membrane to become even more permeable to Na+ ions. Hence, further depolarization occurs until an action potential is generated.

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7
Q

5 differences between the endocrine and nervous systems

A
  1. endo: communication via chemical messengers transmitted in blood stream.
    nerv: via electrochemical action potentials (impulses transmitted via neurons.
  2. endo: hormones ‘broadcast’ all over the body but influence target cells and tissues only.
    nerv: action potentials are targeted on specific cells.
  3. endo: causes changes in metabolic activities.
    nerv: causes muscles to contract or glands to secrete.
  4. endo: has its effects over longer periods of time
    nerv: produced over milliseconds
  5. endo: long lasting
    nerv: short lived and/or reversible
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8
Q

when does deamination happen
and what is it
and where does it happen

A

If more proteins are eaten than required, the excess cannot be stored. To make use of the useful potential energy of amino acids, the liver removes amino groups from them
This happens in the liver cells

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9
Q

describe the process of deamination (and what happens to the products)

A
  • happens in the liver cells. together with the removal of an extra hydrogen atom.
  • Theamino groupand thehydrogen atomcombine to formammoniaand, the remaining part of the amino acid formsketo acid (Keto acid may enter the Krebs cycle and be respired, or it may be converted to glucose, or may be converted to glycogen or fat for storage)
  • Ammonia is a v soluble and toxic compound that can cause damage, this is prevented by immediately converting ammonia tourea, by combining w CO2, which is less soluble and less toxic.
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10
Q

urea is the main nitrogenous product along w …

A

-creatinine and uric acid

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11
Q

where does creatinine come from, and what happens to proportions of it

A
  • creatine is made in the liver from certain amine acids.
  • most of this is used in the muscles, in the form ofcreatine phosphate, where it acts as an energy source.
  • but some of it is converted to creatinine and is excreted.
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12
Q

how is uric acid made?
how is it removed?
whats the advantage of such removal?

A
  • Uric acid is made from the breakdown of purines from nucleotides, not from amino acids.
  • It is not toxic and is relatively insoluble so it’s removed in the form of dry pellets or thick paste.
  • This reduces water loss in animals living in dry habitats and decreases the body mass of flying animals.
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13
Q

kidneys are the major organ for what and what

A

osmoregulationandexcretionof nitrogenous waste products.

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14
Q

size of kidney

A

5cm long

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15
Q

basic unit of kidney:

A

nephron

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16
Q

describe structure of kidney from outer to inner in terms of the cross section

A

1) Fibrous Capsule: outermost layer of fibrous connective tissue covering the kidney.
2) Contains mostly the glomerulus, the Bowman’s capsule and the convoluted tubules of the nephrons. Made up of a million or so nephrons.
3) Medulla: Grouped together into renal pyramids which contain the loop of Henle and collecting ducts with a network of blood vessels. made up of many nephrons
4) Pelvis: The area where the renal pyramids project and the upper part of the ureter joins.

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17
Q

3 functions of the kidney

A
  • Excretion of metabolic waste products, e.g. urea.
    • Maintaining the balance of ions, e.g. Na+, Ca2+, K+, H+, Cl–, HCO3–.
    • Maintaining the acid-base balance of the body, thus the pH of the urine
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18
Q

function of the glomerulus + structure

A
  • blood enters from afferent, larger diameter, arteriole and leaves from the effertent, smaller diameter
  • enables the blood pressure in the glomerulus to be high so that ultrafiltration can occur.
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19
Q

function of the bowmans capsule + structure

A
  • made of a basement membrane and podocytes

- enables the molecules with a molecular mass of less than 68000 to pass through

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20
Q

function of the PCT` + structure

A
  • numerous microvilli forming a brush border along the layer of epithelial cells lining the tubule and many mitochondria
  • numerous microvilli forming a brush border along the layer of epithelial cells lining the tubule.
  • helps to provide ATP energy required during the active uptake of substances in selective reabsorption from the tubule cells into the basal channels.
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21
Q

function of the DCT +` structure

A

-has brush border and numerous mitochondri

  • Helps in active removal of substances (Na+and Cl–)
  • Helps in absorption of K+, NH4+and certain drugs into the lumen o help maintain blood’s pH.
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22
Q

function of the loop of henle + structure

A

-consisting of a narrow descending limb with water permeable walls and a wider ascending limb with water-impermeable walls.

* Helps to operate the counter current multiplier system.
* Enables water to be drawn osmotically from the D-limb to increase the concentration of glomerular filtrate.
* Enables Na+and Cl–to be actively transported out of the filtrate to decrease its concentration.
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23
Q

function of the collecting ducts + structure

A

allow water to pass through the duct into the surrounding fluid of the medulla.

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24
Q

`describe ultrafiltration (process)

A
  • Involves the forced removal of substances with a relative molecular mass of less than 68000 from blood into Bowman’s capsule.
    • passive
    • Powered by thepressure of blood. This pressure is created due to the afferent arteriole being wider than the efferent arteriole.
    • This pressure is larger than the water potential of the plasma that in turnforceswater and small soluble plasmacontents out of the capillary.
    • The glomerularcapillarieshave agreater number of fenestrationsin their walls than the capillaries located in other tissues; each endothelial cell has 1000s of holes in it.
    • Then comes thebasement membranemade up of a network of collagen and glycoproteins. it prevents large protein molecules+blood cells from escaping the glomerulus capillaries. hence is like filter.
    • Next layer is theepithelial cells (make up inner lining of Bowman’s capsule).These have many tinyfinger-like projectionswith gaps between them, and are calledpodocytes.
    • in the capsule, substances are glomerular filtrate.These includeamino acids, glucose, vitamin, ions, urea, uric acid, creatinine, water and some hormones.
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25
Q

whats Glomerular Filtrate Rate

A

The rate at which the fluid filters from the blood in the glomerular capillaries into the Bowman’s capsule and has a value of 125cm3min–in humans.

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26
Q

what determines Glomerular Filtrate Rate

A

The difference between the water potential of the plasma in the glomerular capillaries and the filtrate in Bowman’s capsule

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27
Q

PCT is thelongest sectionof the nephron and is the site wheremost of the reabsorption(more than 80%) of the filtrate takes place.WHat are the walls made of

A

The walls of the tubule are made up of asingle layerofcuboidal epithelial cells.These cells are always in contact with the filtrate

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28
Q

`adaptations of PCT

A
  1. Microvillito increase the inner surface are of the lumen.
    1. Tight junctions that hold the adjacent cells togetherso that fluid cannot pass between the cells (all substances that are reabsorbed must go through the cells).
    2. Manymitochondriato provide energy for the Na+-K+ pump proteins in the outer membrane of the cells.
    3. Transporter proteinsin the membrane facing the lumen.
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29
Q

how are amino acids, glucose and vitamins reabsorbed in PCT. describe until movement of Na+ down its gradient

A
  • capillaries very slow to the outer surface of the membrane have v less plasma than usual because they are coming from glomerulus after losing water ions etc
  • Thebasal membranes(the ones nearest to the blood and furthest from the lumen) of the cells lining the PCTactively transport Na+ions out of the cell
  • These Na+ions are then carried away in the blood hencelowering the Na+ions conc in the cell, so that they can passively diffuseinto the cell down their conc gradient, from the fluid in lumen of tubule
  • Na+ions cannot diffuse freely through the membrane and can only enter through specialco-transporter proteinsin the membrane
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30
Q

how are amino acids, glucose and vitamins reabsorbed in PCT. describe after the movement of Na+ down its gradient

A
  • passive movement of Na+ ions into the cell down their conc gradientprovides the energyto moveglucose molecules,even against a conc gradient.
  • This movement of glucose and other solutes is an example ofsecondary active transportsince energy is used in pumping the Na+ions, not in moving these solutes.
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31
Q

why is there no glucose in urine

A

All of the glucose in the glomerular filtrate is transported out of the PCT and into the blood

32
Q

`how are water molecules reabsorbed in the PCT

A
  • removal of solutes greatlyincreases tubule’s water potential.
  • movement of solutes into\ membrane cells and then into blooddecreases water potential of bloodin nearer capillaries.
  • Hence,a water potential gradient is set upbetween filtrate and blood, and water molecules move down this gradient through the cells and into blood.
  • water and the solutes are then carried away back into circulation.
33
Q

how is urea absorbed in PCT

A
  • quite a lot of it tbh about half in the filtrate
  • Urea is asmall moleculeand highly concentratedin filtrate. Hence, it diffuses passively through cells of PCT into blood.
34
Q

why are the ascending and descending limbs of the loop of henle permeable or impermeable to water, respectively

A

ascending is impermeable due to thick walls

descending is permeable because of thinner walls

35
Q

name of the blood suppy of capillaries to the loop of henle

A

vasa recta

36
Q

function of the loop of henle

A

creates and maintains high conc of Na+ and Cl- in medulla:

  • this allows a lot of water to be reabsorbed
  • therefore conserves water in body by producing conc urine
37
Q

describe how the loop of henle works (until the part where ions are getting gradually less concentrated in the ascending limb but still transported into tissue fluid)

A
  • cells lining ascending limb actively transport Na+ and Cl- into tissue fluid, thereby decreasing tissue fluid water potential and thus making water move into it down its conc gradient via osmosis from the tubule
  • at the same time the ions diffuse from the descending limb (cos lost water hence conc) via diffusion down conc gradient into lower part of ascending
  • so at bottom of hair pin fluid becomes very concentrated w little water and more ions. so it becomes easy for the ions to pass into tissue fluid so the bottom tissue fluid between the limbs can get very concentrated. going up the limb, fluid becomes less conc but still ions can be actively transported
  • and so fluid up the limb gets more dilute as it loses ions
  • urea from ascending limb and collecting duct diffuses into medulla. so when fluid passes to this region in collecting duct water again moves out by osmosis until urine wp = tissue fluid wp. how much water is controlled by ADH
38
Q

what is the mechanism of building up max solute conc inside the loop called

A

counter current mechanism

39
Q

role of the vasa recta

A

Delivers oxygen and removes carbon dioxide from the metabolically active cells of the Loop of Henle.

40
Q

what do DCT cells do

A

adjust Ph of blood by the controlledsecretion of H+ionscombined with thereabsorption of HCO3ionsin the DCT.

41
Q

how is conc of useful ions regulated by DCT

A

controlledsecretion of H+ionscombined with thereabsorption of HCO3–ionsin the DCT, and concentration ofNa+ ionsis regulated by varying the quantity of Na+ ions reabsorbed from the filtrate.

42
Q

breifly describe reabsorption/regulation in DCT and collecting duct

A
  • Na+ pumped from tubule to tissue fluid, and K+ pumped into the fluid in tubule
  • The rate at which these two ions are moved into and out of the fuid in the nephron can be varied, and helps to regulate the concentration of these ions in the blood
43
Q

what is osmoregulation

A

the control of the water potential of body fluids.

44
Q

water potential of blood is constantly monitored by _

A

sensory neurons in the hypothalamus, known as osmoreceptors

45
Q

what happens when osmoregulator neurons detect a decrease in the water potential of the blood (below set point)

A
  • Nerve impulses are sentalong the neuronsto the posterior pituitary gland.
    • These impulses stimulate the release ofADHfrom the posterior pituitary gland, where it had been stored after being secreted from the hypothalamus.
    • Molecules of ADH enter the blood capillaries and are carried all over the body.
46
Q

whats the effect of ADH

A

reduces the loss of water in urine by making the kidneys reabsorb as much water as possible.

47
Q

what are the target cells of ADH

A

collecting duct cells

48
Q

how is decreased water content in blood regulated // step 1: increasing permeability of collecting duct cells

A
  • ADH acts on the cell surface membranes of the collecting duct cells, making themmore permeable to waterthan usual
  • change in permeability is brought about byincreasing the number of water permeable channels, known asaquaporins, in the cell surface membrane
  • ADH molecules bind to receptor proteins on the cell surface membranes, which in turnactivate enzymesinside the cells
  • cells containready-made vesiclesthat have many aquaporins in their membrane and Once theenzymesin each cellare activatedby the arrival of ADH, thesevesicles move towards the cell surface membranesand fuse with them, hence increasing the membranes’permeabilityto water
49
Q

how is decreased water content in blood regulated // step 2

A
  • as the fluid flows down the collecting duct,water moleculesmove through the aquaporins,out of the tubuleandinto the tissue fluid.
  • This is because thewater potentialof the tissue fluid in themedullais very low and the water potential of the fluid in thecollecting ductis very high
  • fluid in the duct loses water and becomes more concentrated. Hence, the volume of urine, which flows from the kidneys into the bladder, will be lesser and theurine will be less concentrated
50
Q

how is increased water content in blood regulated // step 1: permeability

A
  • when anincrease in the water potentialof the blood the osmoreceptors are no longer stimulated and theneurons stop secreting ADH
  • aquaporins are moved out of the cell surface membraneof the collecting duct cells, back into the cytoplasm as part of vesicles.
  • cells impermeable to water
51
Q

how is increased water content in blood regulated // step 2:

A
  • fluid flows down the collecting duct without losing any water, so a large volume ofdilute urinecollects in the pelvis, and flows down the ureter into the bladder.
  • collecting duct cellsdon’t respond immediatelyto this reduction in ADH secretion by the posterior pituitary gland. cos it takes some time for the ADH already present in the blood to be broken down eg 30 min
  • Once ADH stop arriving at the collecting duct cells, it only takes 10-15min for the aquaporins to be removed from the cells surface membranes and taken back into the cytoplasm until they’re needed again.
52
Q

control of glucose is by 2 _ which are secreted by_ cells in _

A

hormones
islets of Langerhans
pancreas endocrine tissue

53
Q

islets cells type and product

A
  1. α cells (secreteglucagon)

2. β cells (secreteinsulin

54
Q

what do islets do

A

Act as the receptorsand thecentral controlof the homeostatic mechanism with thehormones coordinating the actions of the effectors.

55
Q

what happens when blood glucose level increases

A

α cells respond bystopping the secretion of glucagonand the β cells respond bysecreting insulininto the blood plasma

56
Q

general working of insulin (kind of molecule, permeability, how it acts) + especially what it does when glucose is increased (1. rate affecting 2. enzymes action)

A
  • Insulin is asignaling molecule.
    • It’s aproteinand cannot pass directly through the cell surface membranes.
    • Itbinds to a receptorin the cell membrane andaffects the cell indirectlythrough the mediations of intracellular messengers.

–> stimulates the cells, containing its specific receptors, toincrease the rate at which they absorb glucosefrom the blood and convert it into glycogen and use it for respiration.
OR
–> Insulin stimulates the activation of theenzyme gulcokinase, whichphosphorylates glucose. Thistraps glucose insidethe cells because phosphorylated glucose cannot pass through the transporters in the cell membrane. it also stimulates the activation of two otherenzymes, phosphofructokinase and glycogen synthase, which together add glucose molecules to glycogen. This increases the size of glycogen granules in the cell

57
Q

glucose eneters cells via what proteins

A

GLUT transporter proteins.

58
Q

types of GLUT transporter proteins.

A
  1. GLUT-1 (for brain)
    1. GLUT-2 (for liver)
    2. GLUT-4 (for muscles)
59
Q

Glut are normally kep in cytoplasm but when insulin binds… (about GLUT4, and also 1 and 2 the note about theri location)

A

When insulin molecules bind to the receptors on the muscle cells, the vesicles with GLUT-4 proteins are moved to the cell surface membrane and fused with it. Hence, they facilitate the movement of glucose into the cell\

note-GLUT 1 and GLUT 2 proteins are always in the cell membrane and their distribution is not altered by insulin.

60
Q

what happens when bood glucose level decreases (islet response, cascade ie g protein, 2ndry messenger, enzymes, product and what it does to/for glucose, muscles response to glucagon)

A
  • α cells respond bysecreting glucagon, while the β cells respond bystopping the secretion of insulin. ——-
  • Glucagon binds to different receptor molecules in the cell membranes of the liver cells.This binding activates aG-protein, that in turn activates anenzymethat catalyzes the conversion ofATP to cyclic AMP, which is asecondary messenger.
  • Cyclic AMP binds tokinase enzymeswithin the cytoplasm, which activates other enzymes. Kinase enzymesactivate enzymes by adding phosphate groupto them through a process known asphosphorylation. This enzyme cascade amplifies the original signal from glucagon
  • Glycogen phosphorylaseis the end product of theenzyme cascade, and catalyzes the breakdown of glycogen to glucose.
  • It does this byremoving glucose unitsfrom the numerous ‘ends’ of glycogen. This increases the concentration of glucose inside the cell so that it diffuses out, via the GLUT-2 transporter proteins, into the blood
  • Muscle cells don’t have receptors for glucagon and hence, don’t respond to it
61
Q

2 forms of diabetes mellitus

A

Type 1:insulin dependent

Type 2: non – insulin dependent

62
Q

what is type 1 diabetes mellitus and what are possible explantions for it

A

pancreasseemsincapable of secreting insulindue to adeficiency in the genethat codes for the production of insulin, or due to anattack on the β cellsby the body’s own immune system

63
Q

what is the effect of type 1 diabetes on a person

A

Normally, there’sno glucose in the urine, but if the glucose concentration in the blood becomes very high, the kidneys cannot reabsorb all the glucose, so that some passes out in the urine. Extra water and salts accompany this glucose. Uptake of glucose in a diabetic person is slow, even when there’s a plenty of glucose in blood

64
Q

symptoms of diabetes types 1 and 2

A

patient is hungry and thirsty

65
Q

what do cells do to cope with this inability to uptake glucose in a type 1 diabetes patient

A

cells lack glucose and so metabolize fats and proteinsasalternative energy sources. This leads to a buildup of substances in blood, calledketones (keto acids). These decrease the pH of blood (this can cause comma if accompanied with dehydration).

66
Q

how are type 1 diabetes patients treated

A

regular injectionsof insulin.

67
Q

what is type 2 diabetes mellitus and what are possible explantions for it

A
  • pancreasdoes secrete insulin, but the liver and muscle cells don’t respond to it properly
  • could be due to poor diet and obesity
68
Q

how can type 2 diabetes be treated

A

diet and, regular andfrequent exerciseto keep their blood glucose concentration within normal limits

69
Q

In urine analysis presense of glucose indicates

A

diabetes.

70
Q

In urine analysis presense of protein indicates

A

possible kidney disease arising from glomerulus membrane damage, or severe hypertension

71
Q

In urine analysis presense of ketone indicates

A

result of type-1 diabetes, or advanced type-2, but eating disorders are another possibility.

72
Q

what are dipsticks testing urine for glucose composed of

A

enzymes, glucose oxidase and peroxidaseimmobilized on a small pad on one end of the stick

73
Q

how is a test for glucose done on urine using a dipstick + mechanism

A
  • pad is immersed in urineand if the urine contain glucose.
  • glucose oxidase catalyzes a chemical reaction in whichglucose is oxidizedinto a substance calledgluconolactone. Hydrogen peroxideis also produced. Peroxidase catalyzes a reaction between hydrogen peroxide anda colorless chemicalin the pad to formabrown compound.
  • resulting color of the pad is matched against acolor chart (has colors for diff concs)
  • Larger the amount of glucose present,darker the color.
74
Q

what do and dont dipsticks indicate

A
  • whether the concentration of glucose was higher than the renal threshold in the period of time while the urine was being collected in the bladder.
  • they DONT indicate current blood glucose conc
75
Q

what do biosensors indicate

A

measure glucose level in blood

76
Q

what is a biosensor

A

device which makes use of a biological molecule to detect and measure a chemical compound. i.e. apad impregnated with glucose oxidase

77
Q

how is a biosensor used, what is the mechanism, and reading conclusion

A
  • small sample of blood is placed on the pad which is inserted into the machine.
  • glucose oxidase catalyzes the reaction toproduce gluconolactoneand at the same time, atiny electric currentis generated.
  • the current is detected by anelectrode, amplified, and read by the meter which produces a reading for blood glucose concentrationwithin seconds
  • more glucose that is present, the greater the current and the greater the reading from the biosensor.