Renal/Male GU Flashcards
kidney functions include
removal of waste products, maintenance of fluid balance/volume, regulation of electrolytes, regulation of plasma osmolality, regulation of BP, regulation of acid/base, regulation of RBC production (EPO), maintenance of hormone levels, vitamin D activation, and gluconeogenesis (converting amino acids into glucose)
renal hilum
includes the renal artery, vein, lymphatics, nerves, and the ureter
location of kidneys within the body
retroperitoneal around the level of L1-L3 where the left kidney is slightly higher than the right, surrounded by a fibrous capsule and embedded in renal fat (perinephric and paranephric) and fascia (anterior and posterior) which holds the kidney in place
renal cortex
extends between renal pyramids as columns and contains the glomeruli, the proximal tubule, and some of the distal tubule
renal medulla
contains 8-10 renal pyramids which taper at the papilla, contents from the papilla then drain into the minor calyces followed by the major calyces of the renal pelvis which ultimately drains into the ureter
number of nephrons within the kidney
1.2 million nephrons/kidney which do not regenerate (after age 40, people lose about 10% every 10 years)
renal blood supply
renal arteries which come off the aorta divide into anterior and posterior branches at the hilum, then into segmental arteries, interlobar arteries, arcuate arteries, cortical radiate arteries, afferent arterioles, glomerular capillaries, efferent arterioles, peritubular capillaries, and vasa recta within the kidneys
percentage of cardiac output going to the kidneys
20-25% of CO
location of arcuate artery/vein within the kidney
runs along the cortical-medullary junction
nephron blood supply
arcuate artery branches into the afferent arteriole, the glomerular capillaries, the efferent arteriole, the peritubular capillaries, the vasa recta network, and then into renal venous circulation
part of the kidney that enhances the regulation of hydrostatic pressure
its 2 sets of capillary beds - the glomerular and peritubular which are separated by efferent arterioles
functional unit of the kidney
the nephron which filters and concentrates urine
location of the renal corpuscle
within the renal cortex
location of the loop of Henle
the descending limb (thin segment) travels down within the renal pyramid/medulla whereas the ascending limb travels back up from the medulla into the cortex (thick segment)
renal corpuscle
includes the glomerulus, Bowman’s capsule, and the mesangial cells
glomerulus
contains capillaries that loop together within Bowman’s capsule covered with modified epithelial cells referred to as podocytes
Bowman’s capsule
composed of 2 layers - the visceral epithelial layer which contains podocytes and is tight around the glomerular capillaries, forming a network of intracellular clefts (moderates filtration), and the parietal layer which is the capsular outer layer
glomerular filtration membrane
includes the capillary endothelium, basement membrane (negatively charged), and podocytes which help with filtration and prevent large proteins and RBCs from passing through into the urine
medullary collecting duct
where 8-10 cortical collecting ducts come together (each collects urine from about 4,000 nephrons)
proximal convoluted tubule (PCT)
contains cuboidal cells with brush border microvilli and is continuous with Bowman’s capsule, attaching to the descending loop of Henle
PCT function
reabsorbs 90% of HCO3- into peritubular capillaries, actively reabsorbs sodium (which helps with the cotransport of other electrolytes), and reabsorbs glucose and amino acids, this area also secretes urate and creatinine
urea formation
amino acids are broken down into carbohydrates through deamination and release ammonia (NH3) which is converted to urea within the mitochondria of the liver, urea is then excreted within the urine
loop of Henle function
the location where urine concentration is primarily determined (in addition to the distal tubule), includes the thin descending limb which is passively permeable to H2O, the thin ascending limb which is permeable to ions but not H2O, and the thick ascending limb which actively transports ions including NaCl
distal convoluted tubule (DCT) function
extends from the macula densa to the collecting duct and is poorly permeable to H2O unless ADH is present, allowing reabsorption of ions including potassium (determined based on aldosterone) diluting the urine and regulating calcium excretion
renal pelvis function
contains contractile properties which push urine to the bladder for storage
ureter function
smooth muscle bundles that are 33 mm in diameter and 25-35 cm in length which will generate peristalsis when stretched (innerved by sympathetic and parasympathetic systems), function to carry urine from the kidney to the bladder, during micturition the bladder muscles close the ureters to prevent urine reflux
blood supply to ureters
renal arteries, iliac arteries, abdominal aorta, gonadal arteries, and internal iliac arteries
ureter sensory innervation
10th thoracic nerve root which sends pain to umbilicus
location of bladder within the body
“basket weave” of smooth muscle (detrusor) that sits within the pelvis in adults but above the pubic symphysis in children, fills with urine passively and will stimulate micturition reflex (autonomic spinal cord reflex) when above the volume threshold which can be inhibited by cerebral cortex or brain stem
location of ureter insertion into bladder
posterior and inferior on either side of the trigone muscle
urethra
3-4 cm in women and 18-20 cm in men, lined by uroepithelium and contains glands that secrete mucous
bladder innervation
the detrusor muscle and internal urethral sphincter are under involuntary control and innervated by the parasympathetic nervous system, the trigone muscle is innervated by the sympathetic nervous system (L2), and the external urethral sphincter is made of skeletal muscle and innervated by the pudendal nerve whereas it is under voluntary control
juxtaglomerular apparatus
includes granular cells (or JG cells), which are smooth muscle cells that sense stretch, the macula densa, and the mesangial cells and is the area in which the afferent arteriole comes in contact with the thick ascending limb of Henle and the DCT
juxtaglomerular apparatus function
functions to sense blood pressure or perfusion pressure as well as sodium concentration in urine, regulate renin release, and cause afferent vasoconstriction
juxtaglomerular apparatus response to increased urine sodium
inhibits renin release from JG cells and causes afferent vasoconstriction
macula densa
composed of modified epithelial cells that have chemoreceptor function which marks the end of the ascending thick limb of Henle and the beginning of the DCT
macula densa function
monitors NaCl concentration in the DCT, releasing adenosine, which causes vasoconstriction of the afferent arteriole to decrease GFR, and inhibiting renin release from JG cells if NaCl concentration is high, if NaCl concentration is low (sensed by macula densa) or BP is low (sensed by JG cells), it stimulates renin release from JG cells and nitric oxide increases vasodilation of both the afferent and efferent arterioles
systemic and renal effects of angiotensin II
causes systemic vasoconstriction to elevate BP and constricts the efferent arteriole to increase glomerular capillary pressure and maintain GFR, increases reabsorption of sodium and H2O in the PCT to increase intravascular volume
immediate effect of systemic drop in BP on the kidney
drop in BP will stimulate baroreceptor stimulation and release of catecholamines which causes afferent arteriole vasoconstriction leading to decrease renal blood flow and decreased GFR
creatinine
filtered readily by the glomerulus and should remain constant but will go up with increased creatinine creation (muscle breakdown, PO intake) or decreased excretion
blood urea nitrogen (BUN)
not as reliable as creatinine and indicates the amount of systemic urea, either from consumption, hydration status, tissue breakdown, or decreased excretion - 50% of urea is passively absorbed in PCT (goes up with dehydration)
GFR
typically an estimated measurement most commonly calculated from creatinine using a formula that takes age and sex into consideration (Cockcroft-Gault equation), normal GFR = 120 mL/min
volume filtered by glomeruli per day
180 L/day (99% of filtrate reabsorbed), typically 30 mL urine produced per hour
components of urine
water and urea are the main components, typically no glucose or RBCs, specific gravity of 1.001 - 1.035, contains trace proteins primarily uromodulin (Tamm-Horsfall proteins) which is made in the loop of Henle and binds uropathogens preventing stone formation
pH of urine
4.6 - 8, typically acidic
total body water includes
intracellular fluid (2/3), interstitial fluid, plasma (both interstitial and plasma = 1/3), and insensible fluid (fluid lost by sweating, exhaling, urinating, and bowel movement) where water is able to readily pass between compartments via osmotic and hydrostatic forces
primary driver of osmosis within the body
osmolality = the number of osmoles of solute per kilogram of fluid
primary driver of fluid movement in ECF
sodium
primary driver of fluid movement in ICF
potassium
primary driver of intravascular fluid
albumin
tonicity
the ability of a solution to affect the fluid volume and pressure in a cell which determines cellular size
tonicity is maintained by
intact thirst, functioning GFR, a functioning loop of Henle and DCT, appropriate functioning of ADH, and an appropriate response of the kidney to ADH
tonicity is determined by
extracellular sodium level and osmolality whereas when it is increased, ADH is released stimulating increased H2O retention and increased thirst
normal EC potassium range
3.5 - 5
normal chloride range
95 - 105
normal bicarbonate range
22 - 26
normal glucose range
90 - 120
normal calcium range
8.5 - 10
normal EC magnesium range
1.4 - 2.1
normal urea nitrogen range
10 - 20
normal IC potassium range
130 - 140
normal IC magnesium
20
normal EC sodium range
135 - 145
major drivers of fluid shift from intravascular to interstitial space
plasma or interstitial hydrostatic pressure (BP) and oncotic pressure (osmolality)
renal clearance
removal of waste (400 mL/day minimum), excess ions, urea, creatinine, hydrophobic drugs, and some hormones where there is a lower concentration of waste products within the renal venous system compared to the arterial system
creatinine clearance (CrCl)
a measure of GFR and helps to indicate the functional status of the kidneys
effect of low BP on the kidney
JG cells release renin which stimulates RAAS
effect of low BP on the liver
releases angiotensinogen which is converted to angiotensin I by renin (released from the kidney)
effect of low BP on the adrenals
angiotensin II stimulates release of aldosterone which causes increased sodium reabsorption in the collecting duct and DCT
effect of low BP on the brain
releases ADH which stimulates sodium and H2O reabsorption in the collecting duct and DCT
effect of low BP on the heart
decreases production on ANP (BNP)
effect of low BP on the lungs
release angiotensin-converting enzyme (ACE) that converts angiotensin I to angiotensin II causing stimulation of the brain to release ADH and increased sodium reabsorption in the PCT
percentage of plasma entering Bowman’s capsule as filtrate
20%
normal urinary output
30 mL/hour (determined by renal blood flow)
juxtaglomerular cell function (JG cells)
release renin in response to low urine osmolality and EPO in response to low circulating oxygen
effect of angiotensin II on glomerulus
stimulates vasoconstriction of the efferent arteriole to increase GFR in response to low renal blood flow (decreased GFR)
carbon dioxide (CO2)
a result of the cellular metabolism of carbs and fat which is 20X more soluble than O2 and will diffuse very quickly, the primary trigger for central chemoreceptors - increases with an increase in cellular metabolism (on average we produce 200 mL/min
bicarbonate (HCO3-)
made in the kidneys to buffer acids, for every molecule of HCO3- made in the kidney, one molecule on H+ is eliminated in the urine, HCO3- is reabsorbed in the PCT
normal CO2 range
35 - 45
processes requiring pH balance
metabolic functioning, protein structure, enzymatic functioning, and cell wall integrity, etc.
effects of acidosis on the cardiovascular system
decreased cardiac output and LV contraction leading to compensatory tachycardia, vasodilation leading to hypotension, increased ectopic rhythms from unstable cellular function, and hyperkalemia (peaked T waves, P wave flattening, PR prolongation, and wide QRS complexes)
effects of alkalosis on the cardiovascular system
cardiac excitability, ventricular tachyarrhythmias, SVT, and hypokalemia (T wave inversions, ST depression, and prominent U waves)
effects of acidosis on the respiratory system
tachypnea, a drop in CO2 to about 10 at the lowest point, and a right shift in oxyhemoglobin
effects of alkalosis on the respiratory system
low respiratory rate and a left shift in oxyhemoglobin
effects of acidosis on the CNS
decreased neurotransmitter release, decreased mental status, and lethargy
effects of alkalosis on the CNS
increased action potentials, seizures, and tetany