Renal Physiology Flashcards
Hallmark of glomerular disease
proteinuria
ultimate site of filtration
renal corpuscle
effective filtration pressure
50 mmHg
one of the best predictors of a poor outcome in clinical DM
decrease in podocyte number
Dissolution or attenuation of mesangial matrix and degradation of MCs by apoptosis or lysis
mesangiolysis
cessation of nephroegenesis
36th week
glomerulogenesis
8-9th week
amount of blood filtered per day by the kidney
180 L
definitive mamallian kidney is from the
metanephros
kidney situated between
12th thoracic and 3rd lumbar
difference between inner and outer medulla
absence of Thin ascending limbs in the inner medulla
splitting and basket-weave lamellae of the GBM
Alport syndrome
mutations in Laminin B2
Pierson syndrome
inhibitor of the TAL transporter NKCC2
Furosemide
NCC is expressed in what segment
Distal tubule
majority of cell type in connecting segment
CNT tubule
majority of cells in the collecting duct
principal cells
most abundant cell type in the peritubular interstitium
type 1 fibroblasts
majority of renal innervation
efferent
decline in hydraulic pressure between the renal artery and the glomerular capillaries is greatest along the
afferent arteriole
ability of the arterial smooth muscle to contract and relax in response to increases and decreases in vascular wall tension
myogenic reflex
maintain a hypertonic inferstitial gradient
medulla
Intrinsic ability of the kidney to respond to perturbations that elicits a vasoactive response, which alters renal vascular resistance in the direction that maintain RBF and GFR
renal autoregulation
macula densa cells, extraglomerular mesangium and afferent and efferent arterioles of the glomerulus
juxtaglomerular apparatus
primarily responsible for mediating tubuloglomerular feedback
adenosine
humoral response
T helper cell 2 - antibody mediated
cellular response
T helper cell 1
steroid sensitive nephrotic syndrome
MCD
steroid resistant
FSGS
Ca dependent phosphatase which dephosphorylates nuclear factor of activated T cells
calcineurin
Na K ATPase
3 Na out 2 K in
Type of transport: Na K ATPase
primary active transport
Type of transport: a-KG cotransport
secondary active transport
type of transport OAT
tertiary active transport
final urinary acidifcation
medullary CD
adaptive mechanism for preventing the exposure of cortical tubules to toxic levels of oxygen while permitting a high RBF
AV O2 shunting
most vulnerable to ischemic injury segment of the nephron
S3 proximal tubule
final pathway to progression of CKD
intrarenal hypoxia
% of NaCl reabsorbed in the proximal tubule
60%
major determinant of ecf voume
renal excretion of Na Cl
primary site of transport regulation
terminal segment of the nephron
near isosomotic reabsorption of 2/3 of the glomerular ultrafiltrate
proximal tubule
major inhibitor of proximal tubular Na Cl reabsorption
dopamine
Most abundant protein in normal human urine
Tamm Horsfall glycoprotein
target for thiazide diuretics
DCT
primary Na transport pathway in CNT and CCD
Enac
highest NaKATPase activity
DCT
loss of function mutation in ENAc; severe neonatal wasting, hypotension, acidosis, hyperkalemia
pseudohypoaldosteronism type 1
gain of function mutation ENAc, suppressed aldosterone, hypokalemia
Liddle syndrome
plays a critical role in medullary K recycling
loop of henle
primary site of distal K secretion
CNT- CCD
protein that counterbalances PTH
sclerostin
metabolic acidosis urinary calcium
increase
PTH in low calcium
increase
transport of calcium in proximal tubule
pracellular and transcellular
loss of function of claudin 16-19
renal ca and mg wasting/FHHNC
inactivating mutation in NCC
Gitelman syndrome
Bulk of reabsorption of Mg in which nephron segment
Thick ascending limb, paracellular
major site of phosphate reabsorption
proximal tubule
major site of glucose handling
kidneys
loss of function of GLUT2
fanconi bickel syndrome
basolateral glucose transporters
GLUT 1 and 2
site of greatest renal glucose reabsorption and generation
proximal tubule
major anionic transporter
OAT 1 and OAT 3
main intestinal uric acid efflux transporter
ABCG2
protons are secreted into luminal fluid by
nhe3
mutation in NBCe1
Autosomal Recessive proximal RTA
Major H+ secretory mechanism in the loop of henle
Na-H exchanger
Stimulates HCO3 reabsorption in the TAL (3)
Ang II, mineralocorticoids, hypotonicity
Inhibits Hco3 reabsorption (3)
PTH, AVP, hypertonicity
final site of HCo3 reabsorption
Collecting Duct
mutation in H-ATPase
distal RTA type 1
Cl/HCo3 exchanger
pendrin
major basolateral anion exchanger in Type A intercalated cell
kAE1
predominant titratable acid
phosphate
primary site for ammoniagenesis
proximal tubule
primary substrate for renal ammoniagenesis
glutamine
apical transporter, major NH3 reabsorption
NKCC2
major sites of parathyroid hormone–mediated calcium absorption
Thick ascending limb, DCT
final site of controlling renal acid-base regulation
collecting duct
major apical transport Na entry in thick ascending limb
NKCC2
earliest site along renal tubule where water absorption increases during antidiuresis
late distal tubule
earliest sites of distal tubular osmotic equlibration
CNT, CCD
major site of dilution
loop of henle
chief site of urine concentration
Collecting Duct