Homeostasis Flashcards

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1
Q

Homeostasis

A
  • Maintenance of internal environment within restricted limits in organisms
  • Involves trying to maintain chemical make-up, volume and other features of blood and tissue fluid within limits
  • Also ensures that cells are in an environment that meets their requirements and allows them to function normally despite external changes
  • This doesn’t mean their are no changes-continuous fluctuations brought by variations in external and internal conditions e.g. temperature, pH
  • These changes occur around optimum point
  • Homeostasis is the ability to return to that optimum point and maintain organisms in balanced equilibrium
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2
Q

Internal environment

A
  • Made up of tissue fluids that bathe each cell, supplying nutrients and removing wastes
  • Maintaining feautures of fluid at optimum levels projects cells from changes in external environment
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3
Q

Importance of homeostasis

A
  • Important to maintain right core body temperature and blood pH
  • This is because temperature and pH affect enzyme activity, and enzymes control the rate of metabolic reactions
  • Also important to maintain right blood glucose concentration because cells need glucose for energy and blood glucose concentration affects the water potential of blood
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4
Q

Effect of temperature on homeostasis

A
  • Rate of metabolic reactions increases when the temperature’s increased
  • More heat means more kinetic energy, so molecules move faster
  • Makes the substrate molecules more likely to collide with the enzymes’ active sites
  • Energy of these collisions also increases, which means each collision is more likely to result in a reaction
  • If temperature gets too high, reaction essentially stops
  • Rise in temperature makes enzyme’s molecules vibrate more
  • If temperature goes above a certain level, this vibration breaks some of the hydrogen bonds that hold the enzyme in its 3D shape
  • Active site changes shape and enzyme and substrate no longer fit (enzyme has denatured-no longer functions as a catalyst)
  • If body temperature is too low, enzyme activity is reduced, slowing rate of metabolic reactions
  • Highest rate happens at optimum temperature (37 C in humans)
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5
Q

Effect of pH on homeostasis

A
  • If blood pH is too high or low (highly alkaline or acidic) enzymes become denatured
  • When an enzyme is denatured the reaction can still happen but too slow for body’s needs
  • Ionic and hydrogen bonds that hold them in their 3D shape are broken, so shape of enzyme’s active site is changed and no longer works as a catalyst
  • Highest rate of enzyme activity happens at their optimum pH (so metabolic reactions are fastest)
  • Optimum usually around 7 but some enzymes work best at other pHs
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6
Q

Logarithmic Scale

A
  • pH calculated based on concentration of hydrogen ions in the environment
  • Scale uses logarithm number instead of number itself
  • Each value on scale is 10 times larger than the value before-so a solution of pH 3 contains 10 times more H+ ions than a solution of pH 4
  • This is because the concentration of H+ can vary enormously and so it’s easier to compare values
  • Converting values to logarithmic scale also makes it easier to plot both very small and large values on the same axis
  • pH= -log10 [H+]
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7
Q

Blood glucose concentration

A

Too high

  • Water potential of blood is reduced to a point where water molecules diffuse out of cells into blood by osmosis
  • High to low water potential across a partially permeable membrane
  • Causes cells to shrivel up and die
  • Maintenance of blood glucose concentration ensures constant water potential and glucose for respiration by cells

Too low

  • Cells are unable to carry out normal activities because their isn’t enough glucose for respiration to provide energy
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8
Q

Respiratory substrate

A

Substance that can be broken down during respiration to release energy (glucose)

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9
Q

Negative Feedback

A
  • When change produced by control system leads to a change in stimulus detected by receptor and turns system off
  • Reversal of a change (high or low level) in the environment to return to the optimum position
  • Receptor detects the change
  • Communication systems (hormonal/nervous) inform the effectors
  • The effector reacts to reverse the change to bring the level back to normal
  • Only works within certain limits (if change is too big, effectors may not be able to counteract it)
  • Normal level-level changes from normal-receptors detect change-communication(hormonal or nervous)-effectors respond
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10
Q

Multiple negative feedback mechanisms

A
  • Having more than one mechanism gives more control over changes in your internal environment than just having one negative feedback mechanism
  • Also means you can actively increase or decrease a level so it returns to normal
  • If you had one negative feedback mechanism, all you could do would be turn it on or off
  • You’d only be able to actively change a level in one direction so it returns to normal
  • Only one negative feedback mechanism means a slower response and less control
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11
Q

Positive Feedback

A
  • Response causes change to increase (amplifies change)
  • Effectors respond to further increase level away from normal level
  • Destabilizes the system
  • Usually more harmful
  • Does not lead to homeostasis
  • Can be useful in certain situations (can rapidly activate processes in the body)
  • Can also happen when a homeostatic system breaks down
  • Normal level-level changes from normal-receptors detect change-communication(hormonal or nervous)-effectors respond
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12
Q

Feedback mechanism

A
  • Optimum point=point at which system operates best. This is monitored by a…
  • Receptor=detects any deviation from optimum point and informs the…
  • Coordinator=which coordinates information from receptors and sends instructions to the right…
  • Effector=often muscle or gland, which brings about changes needed to return the system to the optimum point. This return to normality creates a…
  • Feedback mechanism=by which a receptor responds to a stimulus created by the change to the system brought about by the effector
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13
Q

Glucose concentration in the blood

A
  • All cells need a constant supply of energy to work-so blood glucose concentration must be controlled
  • Concentration of glucose is monitored by cells in the pancreas and rises after eating food containing carbohydrate
  • Falls after exercise, as more glucose is used in respiration to release energy
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14
Q

Hormonal control of blood glucose concentration

A
  • Hormonal system controls concentration using hormones insulin and glucagon
    • Insulin and glucagon are chemical messengers that travel in the blood to their target cells (effectors)
    • Both secreted by clusters of cells in the pancreas called the islets of Langerhans
    • islets of Langerhans contain beta and alpha cells
    • Beta cells secrete insulin into the blood and alpha cells secrete glucagon
    • Insulin and glucagon act on effectors, which respond to restore the blood glucose concentration to the normal level
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15
Q

Insulin

A
  • (globular protein) Lowers blood glucose concentration when it’s too high
  • Binds to specific receptors on the cell membranes of muscle cells and liver cells (hepatocytes)
  • It increases the permeability of muscle-cell membranes to glucose, so cells take up more glucose
  • This involves increasing the number of channel proteins in the cell membranes
  • Tertiary structure of glucose transport carrier proteins changes, allowing more glucose into cells by facilitated diffusion
  • Glucose transport channels activate enzymes converting glucose to glycogen and fat
  • Insulin also activates enzymes in muscle and liver cells that convert glucose into glycogen
  • The cells are able to store glycogen in their cytoplasm, as an energy source
  • Process of forming glycogen from glucose is called glycogenesis
  • Insulin also increases the rate of respiration of glucose, especially in muscle cells
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16
Q

What happens when blood glucose concentration is lowered?

A
  • Increased rate of absorption of glucose into cells (especially muscle)
  • Increasing respiratory rate of cells that use up glucose
  • Increased rate of glycogenesis
  • Increased rate of coversion of glucose to fat
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17
Q

Glucagon

A
  • Raises blood glucose concentration when it’s too low
  • Binds to specific receptors on cell membranes of liver cells and activates enzymes that break down glycogen into glucose
  • Process of breaking down glycogen is called glycogenolysis
  • Glucagon also activates enzymes involved in the formation of glucose from glycerol and amino acids
  • Forming glucose from non-carbohydrates is called gluconeogenesis
  • Glucagon decreases the rate of respiration of glucose in cells
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18
Q

Hormones and the system

A
  • Travel in the blood to their target cells, so responses produced by hormones are slower than those produced by nervous impulses
  • Responses to hormones can occur all over the body if their target cells are widespread, unlike nervous impulses that are localised to one area
  • Hormones are not broken down as quickly as neurotransmitters though, so their effects tend to last for longer
  • Hormones are effective in low concentrations, widespread, longlasting, produced by glands, carried to target cells
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19
Q

Negative Feedback

A
  • Occurs when the stimulus causes the corrective measures to be turned off
  • In doing so this tends to return the system to its original (optimum) level (prevents any overshoot)
  • There are separate negative feedback mechanisms to regulate departures from the norm in each direction
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20
Q

Rise in blood glucose concentration (negative feedback)

A
  • When the pancreas detects blood glucose concentration is too high, the beta cells secrete insulin and the alpha cells stop secreting glucagon
  • Insulin binds to receptors on liver and muscle cells (effectors)
  • The liver and muscle cells respond to decrease the blood glucose concentration e.g. glycogenesis is activated
  • Blood glucose concentration returns to normal
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21
Q

Fall in blood glucose concentration (negative feedback)

A
  • When the pancreas detects blood glucose concentration is too low, the alpha cells secrete glucagon and the beta cells stop secreting insulin
  • Glucagon then binds to receptors on liver cells (effector)
  • Liver cells respond to increase the blood glucose concentration e.g. glycogenolysis is activated
  • Blood glucose concentration returns to normal
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22
Q

Glucose transporters

A
  • Channels proteins which allow glucose to be transported across a cell membrane
  • Skeletal and cardiac muscle cells contain a glucose transporter called GLUT4
  • When insulin levels are low, GLUT4 is stored in vesicles in the cytoplasm of cells, but when insulin binds to receptors on the cell-surface membrane, it triggers the movement of GLUT4 to the membrane
  • Glucose can then be transported into the cell through the GLUT4 protein by facilitated diffusion
  • Concentration of glucose is not constant but fluctuates around optimum point
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23
Q

Adrenaline

A
  • Hormone that’s secreted from your adrenal glands (found just above kidneys)
  • Secreted when there’s a low concentration of glucose in your blood, when your stressed and when your exercising
  • Adrenaline binds to receptors in the cell membrane of liver cells and does these things to increase blood glucose concentration:
  • Activates glycogenolysis (caused by activation of enzymes)
  • Inhibits glycogenesis
  • Attaches to protein receptors on target cells
  • Also activates glucagon secretion and inhibits insulin secretion, which increases glucose concentration
  • Adrenaline gets the body ready for action by making more glucose available for muscles to respire
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24
Q

Adrenaline (second messengers)

A
  • Both adrenaline and glucagon can activate glycogenolysis inside a cell even though they binds to receptors on the outside of the cell
  • Do this by the second messenger model- binding of hormone to cell receptors which changes it’s shape (on liver cell) activates an enzyme on the inside of the cell membrane, which then produces a chemical known as a second messenger
  • Second messenger activates other enzymes in the cell to bring about a response
  • Receptors for adrenaline and glucagon have specific tertiary structures that make them complementary in shape to their respective hormones
  • To activate glycogenolysis, adrenaline and glucagon bind to their receptors and activate an enzyme called adenylate cyclase
  • Activated adenylate cyclase converts ATP into a chemical called cyclic AMP (cAMP), which is a second messenger
  • cAMP activates an enzyme called protein kinase A by changing it’s shape
  • Protein kinase A activates a cascade (chain of reactions) that breaks down glycogen into glucose (glycogenolysis)
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25
Q

Factors that influence blood glucose concentration

A
  • Diet- hydrolysis of carbohydrates like starch, maltose and lactose
  • From hydrolysis in small intestine of glycogen- glycogenolysis stored in liver and muscle cells
  • From gluconeogenesis- production of glucose from sources other than carbohydrate
  • As animals do not eat continuously and diet varies, intake of glucose fluctuates glucose used in respiration
26
Q

Control Systems

A
  • Normally have many receptors and effectors (allows greater degree of control)
  • Important to ensure that the information provided by receptors is analysed by the coordinator before action is taken e.g. temperature of skin is cold, but hypothalamus might indicate blood temperature above normal so body temperature shouldn’t be raised (happens during exercise, sweating cools skin but blood temperature raised)
27
Q

What is diabetes?

A
  • Blood glucose concentration can’t be controlled properly
  • Person can’t metabolise carbohydrate, especially glucose
  • Due to lack of insulin or loss of responsiveness to insulin
28
Q

Type I Diabetes

A
  • Immune system attacks beta cells in the islets of Langerhans so they can’t produce any insulin
  • After eating, the blood glucose level rises and stays high (called hyperglycaemia and can result in death if untreated)
  • Kidneys can’t reabsorb all this glucose, so some of it’s excreted in the urine
  • Most people need regular insulin injections throughout the day, but some people use an insulin pump to deliver insulin continuously instead
  • Insulin therapy has to be carefully controlled because too much can produce a dangerous drop in blood glucose levels (hypoglycaemia)
  • Eating regularly and controlling simple carbohydrate intake (intake of sugars) helps to avoid a sudden rise in glucose
  • Develops quickly
  • No one knows exact cause (think it’s due to a genetic predisposition or triggered by a viral infection)
  • Insulin can’t be taken by mouth (protein) as it will break down
29
Q

Type II Diabetes

A
  • Normally due to loss of glycoprotein receptors on body cells or inadequate supply of insulin from pancreas
  • Usually acquired in later life than type I
  • Often linked with obesity and is more likely in people with family history of the condition
  • Other risk factors are lack of exercise, age, poor diet
  • Type II occurs when B-cells don’t produce enough insulin or when the body’s cells don’t respond properly to insulin
  • Cells don’t respond properly because insulin receptors on their membranes don’t work properly, so cells don’t take up enough glucose
  • Means blood glucose concentration is higher than normal
  • Can be treated by eating a healthy, balanced diet, losing weight (if necessary) and regular exercise
  • Glucose lowering medication can be taken if diet and exercise can’t control it (insulin injections may be needed)
30
Q

Response to type II Diabetes

A
  • Can cause additional problems like visual impairment and kidney failure (important to educate people about this)
  • Health advisors reccommend that people eat a diet that’s low in fat, sugar and salt
  • Also regularly exercise and lose weight if needed
  • Campaigns like NHS Change4Life aims to educate people to reduce risk of diabetes and other problems
  • Food industry needs to reduce advertising junk food (particularly to kids), use clearer labelling and improve nutrional value of products
  • Industry has attempted this by using sugar alternatives and reducing fat and salt content (although sweeteners are linked to weight gain too)
  • However, their is pressure on companies to increase profits (reluctant to spend money on developing new and healthy products if unhealthy products are popular and generate a profit)
31
Q

Glucose in urine

A

High concentrations of glucose in the blood may indicate diabetes (blood test confirms it)

32
Q

Ureter

A

Tube that carries urine to the bladder

33
Q

Renal artery

A

Supplies the kidney with blood from the heart via aorta

34
Q

Renal vein

A

Returns blood to the heart via vena cava

35
Q

Renal (Bowman’s) Capsule

A
  • Cup-shaped and surrounds a mass of blood capillaries known as the glomerulus
  • Inner layer of renal capsule is made up of specialised cells called podocytes
36
Q

Collecting Duct

A
  • Tube into which a number of DC tubules from a number of nephrons empty
  • It is lined by epithelial cells and becomes increasingly wide as it empties into the pelvis of the kidney
37
Q

Afferent arteriole

A
  • Tiny vessel that arises from the renal artery and supplies the nephron with blood
  • It enters the renal capsule of the nephron where it forms the glomerulus
38
Q

Glomerulus

A
  • Many-branched knot of capillaries from which fluid is forced out of the blood
  • Glomerulus capillaries recombine to form efferent arteriole
39
Q

Efferent arteriole

A
  • Tiny vessel that leaves the renal capsule
  • Smaller diameter than afferent and so causes increase of blood pressure within glomerulus
  • Carries blood away from renal capsule and later branches to form blood capillaries
40
Q

Blood capillaries in kidneys

A
  • Concentrated network of capillaries that surrounds the PCT, loop of Henle and DCT and from where they reabsorb mineral salts, glucose and water
  • Capillaries merge into venules (tiny veins) to form renal vein
41
Q

Excretion of waste products

A
  • Blood enters the kidney through the renal artery and then passes through capillaries in the cortex (outer layer) of the kidneys
  • As blood passes through capillaries in the cortex, substances are filtered out of the blood and into long tubules that surround the capillaries (ultrafiltration)
  • Useful substances, such as glucose and the right amount of water, are then reabsorbed back into the blood (selective reabsorption)
  • Remaining unwanted substances pass along to the bladder and are excreted as urine
42
Q

Nephrons

A

Long tubules along with bundles of capillaries where blood is filtered (around one million in each kidney)

43
Q

Where does ultrafiltration take place?

A
  • Blood from the renal artery enters small arterioles in the cortex of the kidney
  • Each arteriole splits into a structure called a glomerulus-bundle of capillaries looped inside a hollow ball called a Bowman’s capsule
44
Q

Ultrafiltration

A
  • The arteriole that takes blood into each glomerulus is called the afferent arteriole
  • Arteriole that takes filtered blood away from the glomerulus is called the efferent arteriole
  • Efferent is smaller in diameter than afferent, so blood in glomerulus is under high pressure
  • High hydrostatic pressure forces liquid and small molecules in the blood out of the capillary and into the Bowman’s capsule
  • Liquid and small molecules pass through 3 layers to get into the Bowman’s capsule and enter the nephron tubules
  • Capillary endothelium, basement membrane and epithelium of Bowman’s capsule
  • Larger molecules like proteins and blood cells can’t pass through so stay in the blood
  • Substances that enter the Bowman’s capsule are known as glomerular filtrate (water, glucose and mineral ions squeezed out due to hydrostatic pressure)
  • Glomerular filtrate passes along the rest of the nephron and useful substances are reabsorbed along the way
  • Finally, filtrate flows through collecting duct and passes out of the kidney along the ureter
45
Q

What is movement of filtrate out of glomerulus resisted by?

A
  • Capillary epithelial cells
  • Connective tissue and epithelial cells of blood capillary
  • Epithelial cells of renal capsule
  • Hydrostatic pressure of fluid in renal capsule
  • Low water potential of blood in glomerulus
  • Total resistance would be sufficient to prevent filtrate leaving the glomerular capillaries
46
Q

Podocytes

A
  • Inner layer of renal capsule is made up of highly specialised cells called podocytes (have spaces between them)
  • This allows filtrate to pass beneath them and through gaps between their branches
  • Filtrate passes between these cells rather than through them
  • As a result, hydrostatic pressure of blood in glomerulus is sufficient to overcome the resistance and so filtrate passes from blood to renal capsule
47
Q

Where does selective reabsorption occur?

A
  • Takes place as the glomerular filtrate flows along the proximal convoluted tubule (PCT), through the loop of Henle, and along the distal convoluted tubule (DCT)
  • Useful substances leave the tubules of the nephrons and enter the capillary network that’s wrapped around them
48
Q

Selective Reabsorption

A
  • Epithelium of the wall of the PCT has microvilli to provide a large surface area for the reabsorption of useful materials from the glomerular filtrate (in the tubules) into the blood (in the capillaries)
  • Infoldings at their bases give a large surface area to transfer reabsorbed substances in blood capillaries and high density of mitochondria to provide ATP for active transport
  • Useful solutes, like glucose, are reabsorbed along the PCT by active transport and facilitated diffusion
  • Water enters the blood by osmosis because the water potential of the blood is lower than that of the filtrate
  • Water is reabsorbed from the PCT, loop of Henle, DCT and the collecting duct
  • The filtrate that remains is urine, which passes along the ureter to the bladder
49
Q

Urine

A
  • Usually made up of water and dissolved salts, urea and other substances such as hormones and excess vitamins
  • Doesn’t usually contain proteins or blood cells as they’re too big to be filtered out of the blood
  • Glucose is actively reabsorbed back into the blood, so it’s not usually found in the urine either
50
Q

Reabsorption of glucose and water by PCT in Selective Reabsorption

A
  • Sodium ions are actively transported out of the cells lining the PCT into blood capillaries which carry them away
  • Sodium ion concentration of these cells is therefore lowered
  • Sodium ions now diffuse down a concentration gradient from the lumen of PCT into epithelial lining cells but only through special carrier proteins by facilitated diffusion
  • These carrier proteins are of specific types, each of which carries another molecule (glucose,amino acids, Cl-) along with sodium ions (known as co-transport)
  • The molecules which have been co-transported into the cells of the PCT then diffuse into the blood
  • As a result, all glucose and most other valuable molecules are reabsorbed as well as water (most of reabsorption of water occurs in PCT and remainder from collecting duct)
51
Q

Regulation of water content

A
  • Water is essential for body functioning so content in blood needs to be constant
  • Mammals excrete urea and other waste products in solution, which means water is lost during excretion and sweat
  • Kidneys regulate water potential of blood and urine so body has right amount of water (osmoregulation)
  • If the water potential of the blood is too low (the body is dehydrated), more water is reabsorbed by osmosis into the blood from the tubules of the nephrons
  • Means urine is more concentrated, so less water is lost during excretion
  • If the water potential of the blood is too high (body is too hydrated), less water is reabsorbed by osmosis into the blood from the tubules of the nephrons
  • Means urine is more dilute, so more water is lost during excretion
  • Water is reabsorbed into the blood along almost all of the nephron, but regulation of water potential mainly takes place in the loop of Henle, DCT and collecting duct
  • Volume of water reabsorbed by the DCT and collecting duct is controlled by hormones
52
Q

Causes of low water potential

A
  • Little water consumption
  • Sweating loads
  • Large amount of ions being taken in
53
Q

Causes of fall in solute concentration

A
  • More water consumption
  • Salts used in metabolism or excreted (not being replaced in diet)
54
Q

loop of Henle

A
  • Located in the medulla (inner layer) of the kidneys
  • Made up of 2 limbs-the descending limb and the ascending limb
  • The limbs control the movement of sodium ions so that water can be reabsorbed by the blood
55
Q

Maintenance of a gradient of sodium ions by the loop of Henle

A
  • Sodium ions are actively transported out of the ascending limb (near the top) using ATP provided by mitochondria
  • This creates a low water potential (high ion concentration) in the region of the medulla between the 2 limbs (interstitial space)
  • Ascending limb is impermeable to water, so water stays inside tubule
  • Because there’s a lower water potential in the medulla than in the descending limb, water moves out of the descending limb (which is permeable to water) into the medulla by osmosis
  • This makes the glomerular filtrate more concentrated (ions can’t diffuse out-descending limb isn’t permeable to them)
  • Water in the medulla is reabsorbed into the blood through the capillary network
  • Near the bottom of the ascending limb, Na+ ions diffuse out into the medulla, further lowering the water potential in the medulla (ascending limb is impermeable to water, so it stays in the tubule)
  • Water moves out of the DCT by osmosis and is reabsorbed into the blood
  • These stages increase the ion concentration in the medulla, which lowers the water potential
  • This causes water to move out of the collecting duct by osmosis
  • Does this through channel proteins specific to water (aquaporins)
  • ADH can alter number of channels and control water loss
  • By the time filtrate (now urine) leaves the collecting duct on it’s way to the bladder, it has lost most of it’s water and so has a lower water potential than the blood
  • As before, the water in the medulla is reabsorbed into the blood through the capillary network
  • The volume of water reabsorbed into the capillaries is controlled by changing the permeability of the DCT and the collecting duct
56
Q

Counter-current multiplier

A
  • If 2 liquids flow in opposite directions past one another, exchange of substances greater
  • For loop of Henle, counter-current flow means that the filtrate in the collecting duct with a lower water potential meets interstitial fluid that has an even lower water potential
  • If 2 flows were same direction, less water would enter blood
57
Q

DCT functions

A
  • Cells that make up DCT walls have microvilli and many mitochondria that allow them to reabsorb material rapidly from the filtrate, by active transport
  • DCT makes final changes to water and salts reabsorbed and to control pH of blood by selecting which ions to reabsorb
  • To achieve this, the permeability of it’s walls becomes altered under the influence of various hormones
58
Q

Antidiuretic Hormone (ADH)

A
  • Water potential of the blood is monitored by cells called osmoreceptors in a part of the brain called the hypothalamus
  • When the water potential of the blood decreases, water will move out of the osmoreceptor cells by osmosis
  • This causes the cells to shrink
  • This then sends a signal to other cells in the hypothalamus, which send a signal to the posterior pituitary gland
  • This causes the posterior pituitary to release a hormone called ADH into the blood
  • ADH molecules bind to receptors on the plasma membranes of cells in the DCT and the collecting duct
  • When this happens, protein channels called aquaporins are inserted into the plasma membrane
  • These channels allow water to pass through via osmosis, making the walls of the DCT and collecting duct more permeable to water
  • This means more water is reabsorbed from these tubules into the medulla and into the blood by osmosis
  • A small amount of concentrated urine is produced, which means less water is lost from the body
  • ADH changes the water content of the blood when it’s too low or too high
59
Q

Role of ADH in dehydration-blood water content is too low

A
  • Water content of blood drops, so water potential drops
  • This is detected by osmoreceptors in the hypothalamus
  • The posterior pituitary gland is stimulated to release more ADH into the blood
  • More ADH means that the DCT and collecting duct are more permeable, so more water is reabsorbed into the blood by osmosis
  • Osmoreceptors detect brain to drink water
  • A small amount of highly concentrated urine is produced and less water is lost
60
Q

Role of ADH in hydration-blood water content is too high

A
  • The water content of the blood rises, so it’s water potential rises
  • This is detected by the osmoreceptors in the hypothalamus
  • The posterior pituitary gland releases less ADH into the blood
  • Less ADH means that the DCT and collecting duct are less permeable, so less water is reabsorbed into the blood by osmosis
  • A large amount of dilute urine is produced and more water is lost
  • When water potential returned to normal, osmoreceptors in hypothalamus cause pituitary gland to raise ADH release back to normal
  • ADH is a protein (once it’s had its effect, broken down by liver)