Lecture 16/17 = renal system Flashcards

1
Q

importance of kidneys

A

salt/water balance
reg. blood ion conc
acid/base balance
excrete waste + drugs + toxins
produce EPO (RBC prod) and renting (bp reg)
convert vit D to active form

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2
Q

gross anatomy of the kidneys

A

bean shapes
retroperitoneal
in the superior lumbar region
some protection form rib cage
right kidney is pushed down by liver
adrenal glands sit on top

concave medially = renal hilum (outside cleft) to real sinus (internal space)

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3
Q

3 layers of supportive tissue

A

renal capsule = fibrous, adheres to kidney surface, strong batter to anything infectious in Abdo cavity

perirenal fat capsule = cushions, holds kidney in place
*physical protection from damage/trauma

renal fascia = dense CT, surrounds adrenal glands and kidneys, anchoring role

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4
Q

internal anatomy

A

cortex = outer layer initial filtration of blood
blood has to go all the way to the outside and makes its way back in

medulla = medullary/renal pyramids
stripy appearance bc of collecting ducts running para to same destination
light
renal columns = in bn pyramids
used by blood to travel to cortex.

pelvis = flat funnel shaped tube
continuous with further
major/minor calicos = act as a funnel

minor = small cup like
each collects urine form a single pyramid (papillae)

major = formed by merging 3 minor calices. funnels urine into pelvis

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5
Q

propulsion of urine

A

walls of calcysces, pelvis, and ureters have smooth muscles that propel urine by peristalsis

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6
Q

circulatory pathway through kidney

A

renal artery
segmental artery
interlobar artery
arcuate artery
cortical radiate artery

afferent arteriole
efferent arteriole
peritubular capillaires / vasa recta

cortical radiate vein
arcuate vein
interlobar vein
renal vein

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7
Q

blood and nerve supply

A

arterial branches pass in bn pyramids to reach cortex, and venous branches drain back in the same route

nerve supply = renal plexus of sympathetic fibres
- reg blood flow by adjusting diameter of renal arterioles

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8
Q

the structure of a nephron, such a general overview, just the structures names

A

glomerulus
Bowmans capsule
proximal convuluted tubule
loop of henle
distal convoluted tubule
collecting duct

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9
Q

filtration components

A

renal corpuscle = glomerulus and Bowmans capsule

fenestrated glomerular endothelium podocytes = yellow structure = making inner wall of Bowmans capsule

specialized cells =
they reach out and wrap around the cappillaries of the glomerulus
key part of the filtration barrier

filtration slits = let water and small molecules out of caps but not large molecs.

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10
Q

epi in the different components of the nephron

A

glomerular capsile = single layer of epi

PCT = most of reabsorption bc of its many transports (glucose, aa, ions) + microvilli

DCT = fewer transporters, mainly salt and water

collecting duct =
1. principal cells = water/salt balance, no micovili
2. intercalated cells = acid/base balance, has microvilli

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11
Q

2 types of nephrons

A

cortical
juxtamedullary

differ = length of nephron loops

Juxta = very loop, dig deep into medullary area
super imp fro conserving water bc of water gradient (promotes having water come out of filtrate and back to blood through caps
key role = water conservation

cortisol = key role is filtration and reabsorption.

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12
Q

camels and their nephrons

A

would have a higher % of juxtamedullarry nephrons since live in dry desserts
long time w/o water, so needs more efficient water conservation

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13
Q

microcirculation of the nephron

A

glomerulus
= specialized for filtration, fed nad drained by arterioles

afferent arterioles have larger diameter arterioles are high resistance vessels

efferent bring blood to glomerulus
efferent take blood away from glomerulus

peritubular capillaries = arise from efferent
wrap around nephrons, recollect “good stuff”

vasa recta = only in juxtamedullary nephrons, more orderly array or peritubular caps, not a jumble
have a network assoc w nephron loop for maximal water reabsorption.

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14
Q

juxtaglomerular complex, simply what is it + what it regulates

A

the point where the distal convoluted tubule (DCT) loops back and touches the afferent arteriole of the same nephrons, near the glomerulus

regs. filtrate formation
systemic blood pressure

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15
Q

components of the juxtaglomerulsu

A

in the arteriole walls = granular cells = enlarged smooth muscle cells, mechanoreceptors and secrete renin = inc bp if dropped

in tubule walls = macula dense cells = chemo/osmoreceptors, monitor filtrate and adjust GFR accordingly

monitor filtrate, can release ATP when they sense that adjustments need to be made in relation to filtrate release (how quickly filtration is occurring) to assure enough time for nutrient pullback.

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16
Q

mens micturition pathway

A

peritoneum = outer wrapping

ureter carrying urine from kidney

rugae = if empty forms folds but allows it to stretch and fill

smooth muscle in walls of bladder = detrusor muscle = relax to fill, contract to empty

ureteric orifices = entry point of bladder, we don’t dump urine in from the top but from the bottom

trigone of bladder = triangle in bn the orfices, doesn’t stretch, initiates needing to go when bladder filled to a certain point
where UTI happens, where pee sits since bladder doesn’t empty EVERYTHING

then bladder neck

internal urethral sphincter = smooth muscle = involuntary control

prostatic urthera (1) = surr by prostate

external urethral sphincter = skeletal muscles = voluntary
*at level of urogenital diaphragm

urogenital diaphragm

intermediate urthera (2) = as pass bn diaphragm

goes to spongy urehtra (3) = surr by erectile tissue of penis

then to external uretthra orifice = opening to out.

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17
Q

women’s micturition pathway

A

peritoneum = outer layer

ureter = carry urine from kidney

rugae = folds when empty, but allows to stretch

detrusor muscles = relax to fill, contract to empty

cretic orifices = entry point of urine to bladder

internal urethral sphincter = Smooth muscle = no control

external urethral sphincter = skeletal = controled

urogenital diaphragm

urethra

external urethra orfiicr

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18
Q

functions of the kidney

A

A WET BED

acid base balance

water removal
erythropoiesis
toxin removal

blood bp control
electrolyte balance
vit D activation

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19
Q

main function

A

filter blood

remove toxins, waste and excess ions into urine

return materials still needed by body to bloodstream

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20
Q

filtrate vs urine

A

filtrate = plasma (blood) minus proteins

urine = filtrate minus nutrients (essentials ions and water)

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21
Q

3 step process

A

glomerular filtration
tubular reabsorption
tubular secretion

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22
Q

glomerular filtration

A

passive, non selective
fluids and soluts forced through by capillary hydrostatic P

effeieict bc mb is much more permeable than other cap mb
and bp is higher than in other cap beds.

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23
Q

3 layers in bn blood and globular capsule

A

fenestrated cappilary endothelium =
inner most
has fenestrations that let water and small solutes pass through, blocks blood and larger molecs. from leaving

basmenet mb=
- middle layer, gel like
made of - charged glycoprons , blocks large proteins and repeals (-) charged molecs.

Filtration Slits Between Podocytes
= prevents passage of most proteins
and larger molecs.

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24
Q

net filtration pressure

A

pressure responsible for filtrate
formation

what encourages filtration to happen and keep happening

NFP = HPg - (OPg + HPc)

HPg = pushes out of blood
OPg = pulls back into blood
HPc = pushes back into blood

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25
glomerular filtration rate = GFR
total amount of filtrate formed per minute by both kidneys normal value = 125 ml/min depends on = total SA for filtration *large SA so get large amounts of filtrate formed continuously damage = less SA = less filtration filtration mb permeability more permeable = pass through easily damage = dec GFR net filtration pressure = GFR is directly proportional to NFP ( the pressure pushing fluid out of te glomerulus)
26
3 regulatory influences on GFR
renal autoregulation (intrinisc) neural controls (extrensic) renin-angiotensin system (hormone - extrinsic) imp = stable filtration, proper urine formation, balance of fluids, ions and waste shared target = all reg the diameter of the afferent vessel Maintaining GFR ensures: Stable filtration of blood Proper urine formation Balance of fluids, electrolytes, and waste in the body
27
renal autoregulation
kidneys keeps GFR constant by det its own rate of flow and adjusting nephron blood flow ref diameter of afferent (little bit of efferent) more dramatic effect to reg aff. 2 controls myogenic mechanism tubuloglomerula feedback mechanism
28
myogenic mechinism
focus = afferent responds to any change in bp of blood vessels, and how much smooth muscles in vessel contract when stretched when systemic bp inc = too much stretch = contricts = lessens flow low bp = not much stretch = dilates = opens up to improve flow
29
tubuloglomerular feedback mechanism
directed by macula dense cells of JGC = monitors salt content of filtrate + rate of flow if too fast = not enough salt is being absorbed = too much salt in filtrate = releases vasoconstrictors to slow things down if too slow = too much salt is absorbed = release less ATP
30
neural control
SNS has a role during extreme stress, overrides renal autoreg nad sends blood to heart brain and muscles direct sympathetic induced vasconstricition of afferent arterioles
31
renin angiotensin mechanism activation
activated by = direct stimulation of granular cells by SNS to secret renin = macula dense cells stim granular cells whey they sense reduced salt content and flow = reduced stretch of granular cells
32
mech effects
generalized vasoconstrictor stimulates release of aldosterone = stems reabsorption of Na, water follows, inc blood volume, inc bp afferent arterioles have fewer receptors for angiotensin than efferent = has a bigger effect on efferent = blood comes in normal but leave slower so kindeys don't shut down.
33
active tubular reabsorption
substances moved against gradient, needs E, at level of basolateral mb (mb of filtrate not facing lumen). sodium pump actively pumps Na out of the tubule cell into the interdigital fluid now low conc of Na in tubule cell high conc of Na from tubule lumen wants to go to low conc in cell glucose, aa, lactate, vitamins, ions hitch a ride and get transported into the cell. passive but relies on active pumping of Na
33
tubular reabsorption
most volume filtered by kidney doesn't become urine most things reabsorbed by moving through and not In bn cells (bc of tight junctions) glucose and aa = 100% reabsorbed active of passive deg of water/ions reabsorption = hormone adjusted.
34
transport maximum
carriers are specific to what they can carry but also has a limit, when all carriers are saturated, extra substance is not reabsorbed nad shows up in urine.
35
plasma proteins in tubule
usually don't get filtered out but some my squeeze through get taken up by tubule cells from the lumen cells will hydrolyze it into aa and sent to the blood
36
question prolly gonna get asked, ex. if this is the plasma conc of glucose and the GFR is___ and the transport maximum a. how much is reabsorbed b. how much is excreted
first. T maximum is always constant no matter plasma conc 2nd. GFR will stay the same what to do. take plasma conc and multiple it by 1.25 = we get the amount filtered if amount filtered is less than transport maximum = all can be reabsorbed + non excreted if amount filtered is more than transport maximum = max of 375 will be reabsorbed = diff is excreted.
37
tubular reabsorption
intracellular and paracellular routes transcellular= - across apical mb (from lumen to tubule cells) - through cytoplasm of tubule cell - across basolateral mb - into interstitial fluid and peritubular caps. for = Glucose, aa, ions, nutrients. paracellular = between adj tubule cells through tight junctions in intersisitual fluids to caps for = water nad ions esp = in PCT, where junctions are more leaky
38
passive tubular reabsorption
diffusion, faciliated diffusion, omsosis along gradient no ATP = active reabsorption of Na pulls anions (esp Cl-) obligatory water reabsorption due to Na transport **not reg, in PCT and nephron loop due to structures and presence of aquporins as water leaves = makes gradient for reabsorption of other substances, esp if fat soluble
39
substances that are partially reabsorbed other than not at all
either no carriers, not lipid soluble, or too large N end products fo proteins and nucleic acid metabolism urea = mean N containing end product of metabolism. small enough to diffuse through pores half reclaimed creatinine = large , insoluble N waste molec. useful for measuring GFR uric acid = end product of purine metabolism = structure of DNA = some excreted some reabsorbed, too much = gout, arthritis, deposits in joints
40
diff regions of tubules and reabsorption
PCT = all glucose and aa most ions, bicarbs and water loop of hole descending = water leaves (gets reabsorbed) ascending = salt leaves (gets reabsorbed) DCT and collecting ducts only a bit of salt and water stay absorption is reg by body's needs and hydration level
41
hormones reg water reabsorption in collecting duct and DCT
antidiuretic hormone = ADH open up water channels in collecting duct as it goes deeper in gradient renin-angio tenin system (+ aldosterone) = stim secretion of aldosterone = salt reabsorbed, water follows Atrial natriuretic peptide = ANP prod in atria of cell, protect from blood V or bp getting too high allows ot get rid of extra salt and water from kidneys
42
tubular secretions secretions
kidneys get rid of unwanted substances by 1. not reabsorbin them 2. secreting them into urine usually = H, K, creatinine, NH4, uric acid, urea mostly in PCT,some in late DCT and early collecting ducts
43
4 imp functions of secretions
1. dispose of substances not in the original filtrate ( waste/drugs not dumped into filtrate in first place) 2. dispose of substances that were passively reabsorbed (get pushed back to tubule) 3. dispose of excess K ions 4. maintain blood ph, getting rid of excess H
44
countercurrent mechanism and medulla osmotic gradient
countercurrent mechanism = Process that sets up the medullary gradient (via loops of Henle & vasa recta) Medullary osmotic gradient = The salty concentration difference in the medulla used to pull water out of urine
45
descending limb
freely permeable to water, impermeable to solutes as filtrates moves down limb, water moves freely out by osmosis bc of the osmolarity of interstitial fluid. follows its conc of high to low. can reach 12000 most In juxtamedullay nephrons
46
ascending limbs
impermeable to water actively transports NaCl out Na/K/2CL transporters move ions out but water can't follow = no transporters
47
positive feedback happening in the loop
descending limb = water follows grad out (high in cell to low in IF) tubule = becomes conc in ions ascending limb = ions get pumped to into IF set up gradient make it so that water can leave and conc. and loop continues.
48
net effect of this
reduce filtrate volume absorb as much water as possible
49
formation of dilute urine
when over hydrated filtrate is dilute due to salt removal (too much water so water not reabsorbed but salts are actively pumped out. no ADH = collecting ducts remain impermeable and very dilute fine is produced (+ large volume)
50
formation of concentrated urine
when dehydrated ADH acts at collecting ducts = inc number of water channel in principal cells if don't want to lose more water in urine to maintain adeuqte bp facultative water reabsorption = reg based on body's need (hydration) + presence of ADH
51
diuretic
enhances urinary output any substances that is not reabsorbed exceeds renal reabsorption ability ex. interferes w release of ADH = less aborption of water = peeing out more than drinking in caffein and diuretic drugs ion Na reabsorption , water can't follow the gradient (cuz its not formed) = water stays in tubule = lost In urine
52
renal clearance
volume of plasma from which a substance is 100% cleared per unit time ** a measure of how effectively the kidneys remove a substance from the blood and excrete it in the urine. RC = UV/P U = substance In urine V = flow rate or urine formation P = substance in plasma
53
sampel calculation
U = 125 mg/ml P = 1 mg/ml V = 1 ml/min RC = (125 x 1)/1 RC = 125 thrfr = everything is staying In filtrate, excreted out of bodyi RC = 125 = GFR so its being filtered, not secreted not reabsorbed in the nephron = follows GFR
54
if RC of a another substance issssss
= 0 none is being excreted, like glucose and aa is higher than inulin, (higher than 120) = some is being secreted from blood to filtrate nad being excreted if lower than inulin (lower than 125) = some is being reabsorbed before being excreted
55
physical characteristics of urine color, transparcny odor ph
clear/pale to deep yellow urochorme = pigment from heme degradation deepness of yellow = conc pee cloudiness = infection, bacteria, UTI will develop ammonia our if left to stand bc of bacterial metabolism of urea affected by drugs and veggies also diseases usually ph = 6 acidic urine =diet rich in protein and whole wheat alkaline urine = diet rich in veggie
56
chemical composition
mostly water 5% solutes, in dec order = urea, Na, K, phosphate, sulphate, creatinine, uric acid much less levels of ca, mg, bicarb
57
regulation of micturition, 3 things have to happen
detrusor muscles have to contract internal urethral sphincter must open follow by the external ""
58
process
about 200 ml's in bladder stretch receptor triggers reflex arc detrusor muscles contract + pulls internal sphincter open urine flows through internal sphincter into upper part of urethra like reflex arc = now one feels urge to go external sphincter under voluntary control = relax and fo = don't relax, ignore but feeling will come back as urine accumulates.
59
incontenence
inability to control micturition voluntarily weakened pelvic floor muscles ex. pressure of pregnancy or NS problems
60
stress incontinence
when urine leaks out during physical activities that inc abdo P. pushed down on outside of bladder + distracts you cough, vomit, laughing
61
urinary retention
bladder unable to expel urine
62
renal failure
not enough functioning nephrons filtrate formation reduced or stopped nitrogenous waste accumulates = blood becomes acidic kidney not functioning = no EPO = anemia once functioning below 25% = dialysis
63
causes of renal faulure
repeated damaging kidney infections physical injury to kindeys prolonges pressure on skeletal muscle **release of a lot of proteins and creatine phosphates, clog kindeys, esp if extensive damage to muscles (like being stuck under smth heavy for long) inadequate blood delivery to tubules.
64
hemodialysis
blood is pumped outside of body to a machine, an artificial kidney, and then returned.
65
peritoneal dialysis
using the blood vessels of the peritoneal mb done at home/not at hospital a fluid -dialysate- is put into the cavity through a catheter, mostly sugar and salt encourages filtration through the peritoneum fluid and taste is drawn from the blood into the fluid which is then removed.
66
body water balance, fluid levels
Intracellular fluid compartments = w/in cells 60% of total body fluids Extracellular fluid compartments = 2 areas 40% plasma = 20% of ECF intersistual fluid (IF) = 80% of ECF ** included under IF = lymphatic fluid, CSF, fluids of the eye, synovial fluid, GI secretions. there is a constant exchange.
67
do electrolytes or non-electrolytes have greater osmotic power
electrolytes do bc they can dissociate to multiple particles Osmotic power = how much a solute can pull water The more particles in solution, the higher the osmotic pressure So electrolytes = more particles, = exert more pull on water = stronger osmotic power.
68
In ECF and ICF, chief anion/cation is ___
ECF cation = Na Anton = C ICF cation = K anion = Phosphate changes in solute conc in blood plasma will affect intracellular fluid volumes.
69
water balance
water intake must = water output intake = liquids, foods, cellular metabolism* ** = dehydration synth. as you join 2 aa to form a peptide = you form H2O output = most (60%) by kidney, fluid loss by lungs, sweat, skin, feces
70
increasing plasma osmolality
less water = more solutes = more conc blood 1. thirsty = inc water intake 2. ADH = stimulates water reabsoprtion
71
decreased plasma osmolality
too much blood = blood is dilute = thirst not stimulated ADH not stimulated/secretion
72
thirst mechanism
inc in plasma osmolality = blood becomes conc dry mouth (don't make saliva, conserve water) osmoreceptors of the hypothalamic thirst centre lose water to the hypertonic ECF (follow high to low gradient) receptors beocome irritable and depolarize = activate thirst centre = becomes aware you're thirst and pushes you to drink water dec in plasma volume = sensed as dec in bp = activates renin angiotensin mechanism = activates thirst centre once mouth becomes art = thirst feeling foes away = prevents over drinking
73
obligatory water losses
insensible water loss in lungs skin feces and urine
74
Sodium as the only solute exerting significant osmotic pressure
water follows salt if water channels are open 90-95% of ECF solute is Na + anion NaCl and NaHCO3 contribute majority Na determines blood plasma osmolaoty and blood volume Na content of the body can change but its conc in ECFC is monitors and remains stable
75
factors influencing Na, list them
aldosterone ADH ANP other hormones cardiovascular baroreceptors
76
aldosterone
most influential factor acts slowly without aldosterone = 90% in filtrate is reabsorbed in PCT and loop high aldosterone = all remaining Na actively reabsorbed by DCT and collecting ducts. if we need that extra 10%
77
2 pathways to aldosterone secretion
renin-angiotensin system = renin angiotensin mech stimulates adrenal cortex to release aldosterone which targets tubes. same thing for high K or low Na stimulates adrenal cortex to release aldosterone which effects the reabsorption and secretion of K Na/K pump. pump K into tubule (from tubule cell) as we pump Na out (into the blood)
78
renin secretion in response to
decreased filtrate osmolality = drop in Na decreased stretch = drop in bp = drop In blood volume sympathetic NS
79
Addisons disease
hyposecretion of aldosterone = loss of Na and water in urine autoimmune disease, destruction of cells in adrenal cortex resp for production of aldosterone nad cortisol both essential to life so go on hormone therapy
80
ADH effect on Na
water reabsorption in collecting ducts relies on ADH secretion + will effect plasma Na conc. osmoreceptors in hypothalamus sense: low Na = excess fluid in blood at collecting ducts = we don't want extra reabsorption = no ADH released = no channels open pee is dilute high Na = low blood V/ not enough water = blood is conc = stimulates osmoreceptors in hypo to stimulate posterior pituitary to release ADH = works on collecting ducts of kidneys = opens channels = inc water reabsorption = less urine volume (as more water is reabsorbed into blood)
81
ANP
released in atria of heart when bp is elevated is a diuretic and natriuretic hormone = inc water excretion in urine = inc excretion of Na in urine 1. inh Na reabsortpion in DCT and collecting ducts 2. dec release of ADH, renin and aldosterone 3. induces vasodilation reduce blood volume to reduce bp
82
other hormones
Estradiol: inc Na⁺ reabsorption = inc Na⁺ concentration (acts like aldosterone). Progesterone: dec Na⁺ reabsorption = inc Na excretion = dec Na⁺ concentration (blocks aldosterone) Cortisol: inc Na⁺ reabsorption = inc Na⁺ concentration (can mimic aldosterone at high levels).
83
cardiovascular baroreceptors
a pressure sensor pressure diuresis = when blood V or P increases sympathetic output to kidney dec = dilation of afferent arterioles = inc GFR = more filtrate produced = more urine = loss of water and Na = volume nad bp comes back to normal
84
Potassium balance
if conc of K is high in ECF = toxic we need to maintain mb potential in excitable cells and involved in acid/base balance within cells by moving in opposite direction of H if acidosis = too high H+ in blood, H go in, K leave to ECF = now deal w elevated K levels usually 10% in filtrate is lost but sometimes even that is more than the body needs so tubular secretion gets Na in exchange for excreting K.
85
2 factors determining rate and extend of K excretion
same as for Na but in the opposite way. if inc K plasma levels = triggers release of aldosterone = inc levels of K secretion and absorb more Na so 2. 1. plasma K conc 2. aldosterone conc.
86
calcium and phosphate balance
most of bodies Ca in bone, but imp for muscle contraction, release of NTs in neurons, and imp 2nd messenger for imp hormones in body so closely regulated
87
2 hormones,
PTH = inc blood Ca calcitonin = decrease Ca level sin children by stimulating bone deposition and inh bone respiration
88
PTH
stimulus for secretion = drop in Ca levels 3 targets 1. bone = osteoclasts dissolve bone = fastest way to get Ca in blood 2. small intestine = stim activation of vit D to stimulate absorption of calcium from meal eaten 3. kidneys = inc Ca absorption, dec phosphate reabsorption. if we pull back both, wont be free Ca, will be stuck phosphate used for bones and tissues. free Ca = Nts release, muscle contraction. w
89
normal range of blood ph alkalosis acidosis
for activity functional protein depends on depends. 7.35-7.45 alkalosis = arterial blood ph higher 7.45 acidosis = arterial blood ph lower 7.35
90
source of acid
breakdown of phosphorous containing proteins = phosphoric acid anaerobic metabolism of glucose = fermentation = lactic acid fat metabolism = fatty acids and ketone bodies loading and transport of CO2 as bicarb = makes H ions
91
blood H is reg by
chemical buffer system = carbonic acid to bicarb Na2HPO4 to Na2H2PO4 protein buffers resp centres in brain stem renal mechanism
92
renal mechanism reg blood H+ conc
biggest capacity but longest to kick in reabsorning or generating new bicard to get rid of H+ excreting bicarb = more more H+ in blood to bring pH back down
93
respiratory centre in brain stem
mid capacity, mid speed if H ions are accumulating, shift eqm to prof more CO2 t breathe more rapidly and deeply to get rid of accumulation. ie. getting getting H20 into water and out of blood
94
chemical buffer system
really fast but limited capacity carbonic to bicarb and H+ NaHPO4can soak up and extra H+ protein buffers = plasma w (-) charge can soak up H+ and buffer the changes in blood pH
95
strong vs weak acid
key diff is the extent of dissociation ex. HCl = strong dissociation, in water, only exists as H+ and Cl- H2CO3 = carbonic acid = weak dissociation, in water, exists as H+ HCO3- and H2CO3
96
renal 2 POVs honestly don't worry too much about this one, its mostly a transition slide
H+ secretion bicarb reabsoption
97
H+ secretion
tubule and collecting ducts respond to pH and alter rate of H+ secretion secreted H+ comes from carbonic acid for each H+ actively secrets into the tubule lumen, one Na+ is reabsorbed = maintained balance H+ can combine with bicarb and product CO2 and water, CO2 returns to the tubule cells and promotes more H+ secretion bicarb moves into the caps with Na
98
bicarb reabsopriton
problem = tubule cells almost completely impermeable to bicarb in filtrate solution = convert to CO2 to go in and reconvert to bicarb when in blood need to constantly replenish body's stores of bicarb = since breathing out CO2 which was initially bicarbonate in blood do it by reabsorbing it or making new ones in kidneys and move to blood Na follows
99
why do we need the generation of new bicarb ions
resorption recycles bicarb alr present and will get used up by the time you get to DCT + most H+ that you secrete in water molecules doesn't leave body since kindeys conserve most water. + new H+ enters with food so need new bicarb to maintain ph and send out H+ in urine
100
methods of generation
phosphate buffer system NH4 excretion
101
phosphate bufffer
weak base is HPO4^(-2) usually 3/4 of phosphate is reabsorbed in acidosis = will leave more in lumen to be carried out of body done in type A intercalated cells of collecting duct. CO2 inside cell combines with water, makes carbonic, dissociates to H+ (goes to lumen) and bicarb (goes to blood) phosphate will soak up H+ ions to make H2PO4 = stay in filtrate Cl- enters cell for HCO3- leaving
102
NH4 excretion
starting point = the aa glutamine is deaminated, oxygenated nad acidified result = 2 ammonia and 2 bicarb into blood H in the ammonia go to filtrate
103
bicarb ion excretion
rare occurance type B = flipped type A cells = reabsorb H+ and excrete bicarb.
104
respiratory acidosis
hypoventilation not getting rid of CO2 as quickly as you're making it more H+ bc of eqm reaction anything that interferes with lung functioning or ventilation = makes it harder to move air in/out of lungs blood becomes acidic
105
respiratory alkalosis
hyperventilation getting rid of CO2 faster than you're making it asthma, anxiety,
106
metabolic acidosis
untreated diabetes or starvation= making a lot of ketone bodies diarrhea = loosing too much bicarb In GI tract kidneys problems or too much alcohol in system
107
metabolic alkalosis
vomiting = loosing too much acid = gets too basic too much Picard sever diuretics, or too much aldosterone
108
ph = 7.6 CO2 = 24 (low) HCO3 = 23 (good)
alkalosis = ph too high cause = resp = bc PCO2 is lower than it should be getting rid of CO2 faster than making it eqm shifts to make more CO2 using H and water = blood becomes basic compensating ? = no bc HCO3 levels are normal, aren't moving in opposite directions direction
109
ph = 7.48 (high) CO2 = 46 (high) HCO3 = 33 (high)
alkalosis = ph too high is the cause resp? no, even if CO2 is high, if it were too high it would cause eqm to shift towards more H+ = make blood more acidic not basic, as we see here so cause = metabolic = inc in bicarb = push the eqm away from H+ = dec H+ = basic = alkalosis compensating? = yes bc CO2 levels are moving in opposite directions direction, trying to offset change in bicarb by holding on to more CO2
110
ph = 7.25 CO2 = 46 HCO3 = 33
acidosis = ph is too low cause = respiratory CO2 levels are out of range, too high, pushing ram towards H+ = making more acidic compensating = yes bc bicarb is also high pushing eqm away from H+ + more bicarb = more buffering to soak up H+