Urinary System (8) Flashcards
components
- aorta
- renal artery
- kidney
- ureter
- bladder
- urethra
kidney structure
- renal capsule
- cortex
- medulla
- renal column of bertin (b/t medulla pyramids)
- renal papilla
- minor calices
- major calyx
- renal pelvis
- renal sinus (fat filled space)
- hilum for all tubes/ducts/nerves
renal capsule histology
two layers
1. outer = collagen + fibroblast
2. inner = collagen + myofibroblasts
myofibrils contractile and springy
nephron components
- renal corpuscle
- proximal convoluted tubule
- distal convoluted tubue
- loops of henle w/ thin and thick ascending + descending
basic unit of kidney
cortical labyrinth
has all the curly stuff aka renal corpuscle + both convoluted tubules + connecting tubule
medullary rays
all the straight stuff aka tubules/limbs + collecting duct
extend from base of pyramid to cortex
loops of henle
short loop and long loops
longer concentrate urine more than short
uriniferous tubule
nephron + collecting duct
kidney lobes
renal pyramid (medullary) + cortical arch + columns of bertin
kidney lobule
collecting duct + all nephrons that empty into it
corpuscle development
developing glomerulus w/ afferent and efferent tubes invaginates tubule
ends with visceral layer (of Bowman’s capsule) on glomerulus + parietal layer outer
corpuscle components
- afferent arteriole = blood into cap bed, larger
- efferent arteriole = blood away, smaller since less from filtering
- urinary space = filtrate diffuses into from cap bed, aka bowmans space
- glomerulus = tufts of fenestrated capillaries surrounded by bowmans capsule
filtration barrier
corpuscle
- podocytes (primary) extend pedicels (secondary) around glomerulus for large moles
- nephrin diaphragm b/t pedicels for small moles like proteins
podocytes form visceral layer of bowman capsule
congenital nephrotic syndrome
mutation in nephrin gene so leaky diaphragm
-massive proteinuria > edema
layer histology
-glomerulus
- endothelial @inside cap bed = glycocalyx + glycoproteins
- basement membrane = basal lamina
- parietal epithelial cells = simple squamous
intraglomerular mesangial cells
phagocytic
-resorbs basal lamina and crud
@ basement membrane/basal lamina b/t capillaries
alport’s syndrome
aka hereditary glomerulonephritis
-mutation in gene for type IV collagen in glomeruli
=renal leaking, hematuria, proteinuria, progressive renal failure
proximal convoluted tubules
ultrafiltrate pass from corpuscle into lumen of PCT via urinary pole
vascular pole at other end of bowmans capsule for blood
PCT histology
cloudy looking, acidophilic cytoplasm, low mitochondria
cuboidal cells + microvilli for brush border
loops of henle
PCT > thick descending limb of loop
so has same profile as PCT
thick ascending > DCT so same profile
thick = cuboidal VS thin = simple squamous
vasa recta
arteries with RBCs that look like they have bubbles
distal convoluted tubules
DCT
has clear lumen (more white space) and smaller cuboidal epi
-fewer microvilli
-more mitochondria
-ZO tight junctions
macula densa
modified seg of distal tubule for renin secretion via juxtaglomerular cells
chemoreceptor cells sensitive to sodium chloride so imp for reg blood pressure
juxtaglomerular cells
modified smooth muscle in tunica media of afferent arteriole
have granules of renin for BP regulation
jux. apparatus = macula densa + jux cells