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Features of kidneys
Homeostatic organs, filter and maintain 200L fluid/day (all blood 40x/day), remove toxins/wastes/excess ions, regulate fluid volume/pH/salts, endocrine function, produce renin (regulates BP) and erythropoietin (stimulates RBC production), metabolize/activate vitamin D
Anatomy of kidneys
Hilus: vertical cleft on medical surface, entry site for blood vessels, lymphatics, nerves
Cortex: outer granular tissue
Medulla: red/brown cone-shaped masses/pyramids, appear striped due to parallel bundles of tubules
Columns: cortical tissue between pyramids
Lobe: pyramid+surrounding tissue, 8
Pelvis: Funnel-shaped tube continuous with ureter, branches into major→minor calyces, enclose papillae/apex of pyramid
Calyces: peristalsis propels urine to pelvis→ureter→bladder
Renal artery
Delivers 25% of total cardiac output/min, 5 segmental arteries→interlobar arteries between pyramids→arcuate arteries→cortical cradiate arteries
Renal plexus
Kidney nerve network controlled by sympathetic fibers
Features of nephrons
1 million per kidney, forms urine, several connect to 1 collecting duct
Consist of glomerulus, renal tubule, renal corpuscle
Endothelium of glomerulus
Fenestrated to allow large volumes of fluid (60mmHg) to filter from blood into glomerular capsule, filtrate=unprocessed urine, gets processed in kidney tubules to urine
Endothelium of glomerular capsule
Outer parietal layer is simple squamous epithelium, inner visceral layer has unique epithelial cells- podocytes: legs/pedicles, interdigitate with pedicles of adjacent podocytes with filtration slits/pores in between
Glomerulus filtrate
Fluid/filtrate comes out
RBCs, WBCs, platelets, and proteins don’t come out bc too big
Proximal convoluted tubule
Cuboidal epithelial cells, actively reabsorb solutes, secrete molecules, dense microvilli
Loop of Henle thin segment
Simple squamous epithelia, freely permeable to water
Loop of Henle thick segment and distal convoluted tubule
Cuboidal, no microvilli, secrete solutions into filtrate, little solute absorption
Cortical nephrons
85% of nephrons in kidneys, located in cortex except for tip of loop of Henle
Juxtamedullary nephrons
Located close to medulla, loop of Henle goes deep into medulla, very long thin segments, role is to concentrate urine
Afferent arterioles
Arise from interlobar arteries, feeds glomerulus, high bp, easily forces fluids and solutes out of glomerulus
Peritubular capilaries
Arise from efferent arterioles draining glomeruli, cling to renal tubules, adapted for absorption, low pressure, porous, readily absorb solutes and water, reclaims most filtrate produced by glomerulus
Vasa recta
Formed by efferent nephrons from juxtamedullary nephrons, important role in forming concentrated urine, reclaims most filtrate produced by glomerulus
Juxtaglomerular apparatus
Portion of the distal tubule is nestles between afferent and efferent arterioles of glomerulus
In the walls of arterioles are JG cells: large smooth muscle cells containing renin, sense bp in afferent arteriole (diameter controlled by lack of ATP)
Renin increases bp
Glomerular filtration rate
Normal level=60mmHg
High=lose too much fluid/increased urine production
Low=retain waste/not filtering blood
Macula densa
Columnar cells in distal tubule next to JG cells, chemoreceptors, sense filtrate flow, regulate rate of filtration in kidneys
Urine formation processes
Glomerular filtration, tubular reabsorption, secretion
Unprocessed filtrate is like plasma but without proteins, as it percolates through tubules,most water/nutrients/ions/glucose are reclaimed, regulated by renal and hormonal controls
Urine formation- glomerular filtration
Passive, non-selective, due to high hydrostatic pressure (55mmHg)
Rate depends on forces that increase/decrease filtration: glomerular hydrostatic pressure increases it, osmotic pressure of blood and hydrostatic pressure in glomerular capsule decrease it (back pressures)
Glomerular filtration pressure
Determined by net effect of HPg (55mmHg), OPg (30mmHg), and HPc (15mmHg)=55mmHg-(33mmHg and 15mmHg)=10mmHg=GFR 180L/day
15% drop in HPg stops filtration
Regulation of glomerular filtration
Greater filtrate form- increase flow through tubules, substances can’t be reabsorbed fast enough
Reduced filtration form- decrease flow, many substances including waste reabsorbed
Autoregulation regulates diameter of afferent arterioles
Myogenic regulation and tubuloglomerular feedback are intrinsic mechanisms that directly regulate GFR despite moderate changes in bp (80mmHg-180mmHg mean arterial pressure)
Myogenic regulation
Smooth muscle contracts when stretched
If bp increases→vessels stretch→vasoconstriction→decrease flow→maintain GFR
If bp decreases→decreased blood flow→decrease stretch of vessels→vasodilation→increase flow→maintain GFR
Tubuloglomerular feedback
Macula densa cells detect filtrate flow and osmotic levels
If filtrate has low flow or osmolarity→macula densa cells don’t release vasoconstrictive chemical ATP→vasodilation of afferent arteriole→more blood enters glomerulus→increase GFR
If filtrate has high flow or osmolarity→macula densa cells release vasoconstrictive chemical ATP→vasoconstriction of afferent arteriole→less blood enters glomerulus→decrease GFR
Renin
Angiotensin mechanism, vasoconstriction restores GFR, aldosterone lowers osmolarity
Sympathetic nervous system control of renal flow
Only during extreme stress (shock), vasoconstriction, shunts blood to vital organs, reduces fluid loss, helps maintain bp
Tubular reabsorption- primary convoluted tubule
Mostly transcellular, Na+ most abundant ion in filtrate, actively transported from tubule cell by Na+/K+ ATPase pumps (produces electrochemical gradient that pulls Na+ into cells from filtrate), inside of tubule cell left with small negative charge, obligatory water reabsorption by diffusion/osmosis
Molecules in primary convoluted tubule concentration gradient
Cations, fatty acids, urea, lipid-soluble drugs and environmental toxins
Gradient created by Na+/K+ pump draws glucose, amino acids, lactate, vitamins, and cations across tubule cells luminal membrane by symport
Transcellular route across proximal convoluted tubule
Transport across apical membrane, diffusion through cytosol, transport across basolateral membrane (involves lateral intercellular spaces), movement through interstitial fluid and into capillary
Paracellular route across proximal convoluted tubule
Movement through leaky tight junctions, movement through interstitial fluid and into capillary
Loop of Henle- water
Water reabsorbed by osmosis, can leave descending limb only (increase concentration 300-1200mOsm), solutes can leave ascending limb (decreases concentration 1200-100mOsm) only via sodium/potassium/2chloride symporter
Vasa recta gradient
Highly permeable to water and solutes, countercurrent exchanges occur between each section and its surrounding fluid, blood remains isosmotic with surrounding fluid, able to reabsorb water and solutes into general circulation without undoing osmotic gradient created by countercurrent multiplier
Distal convoluted tubule and collecting ducts
Na/Cl symporters reabsorb Na and Cl, water also reabsorbed, most reabsorption regulated by hormones, water controlled by ADH released from posterior pituitary when blood is too concentrated/high osmolarity, ADH makes collecting ducts more permeable to water, Na reabsorption controlled by aldosterone from adrenal cortex, targets collecting ducts t open more Na channels to increase Na reabsorption→increase BV and bp
Tubular secretion
Some substances (H, K, creatinine, ammonium ions, penicillin, phenobarbital) move from blood of peritubular capillaries into filtrate, most secretion occurs in primary convoluted tubule, important for excreting K ions, controlling blood pH
Concentrating urine
Kidneys must keep solute concentration around 300mOsm, regulate urine concentration via countercurrent mechanism: filtrate flows in 1 direction through loop of Henle and flows in opposite direction through vasa recta, establishes and maintains osmotic gradient
Mechanism for concentrating urine