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excretion
toxic waste products of metabolism and substances in excess are removed from the body
carbon dioxide
decarboxylation of respiratory substrates in aerobic respiration
cells damaged if blood pH falls below normal → acidosis
ammonia
deamination of amino acids in hepatocytes. it increases cytoplasm pH and interferes with metabolic processes + receptors for neurotransmitters
urea
ornithine cycle in hepatocytes. readily diffuses into cells decreasing their water potential. causes them to absorb water by osmosis and expand until they burst
uric acid
breaking down of adenine and guanine in the liver (purines). can form crystals in joints, causing gout
bile pigments
breaking down of haem groups in liver cells. can accumulate in skin turning it yellow (jaundice)
bile
bile salts for lipid digestion, bile pigments from the breakdown of haemoglobin
hepatic artery
oxygenated blood from the heart is carried to the liver. provides oxygen for aerobic respiration, fuels metabolic activity of liver cells
hepatic portal vein
blood from digestive system - allows liver to absorb and metabolise nutrients that are absorbed into blood from small intestine
hepatic vein
deoxygenated blood exits the liver
gall bladder
stores bile, releases bile into duodenum via bile duct
sinusoids
where blood from hepatic artery and portal vein mixes within each lobule. wide capilleries
lobule
structures which the hepatocytes are arranged in. supplied with blood from hepatic artery and hepatic portal vein, also connected to a branch of hepatic vein which drains blood away into the main hepatic vein
liver functions
storage of glycogen, formation of urea, detoxification
formation of urea
deamination + ornithine cycle
deamination
NH2 is removed from each amino acid with an extra H+ atom. part of amino acid that remains is a keto acid. it can enter the Krebs cycle to be respired, be converted to glucose, be converted to glycogen, fat, storage
ornithine cycle
ammonia is converted into urea. ammonia + carbon dioxide → urea + water. it diffuses through plasma membrane of hepatocytes and transported to kidneys to be excreted
detoxification
breakdown of substances which are toxic / not required, such as alcohol, hydrogen peroxide, lactate, medicinal drugs
detoxification of alcohol
alcohol (ethanol) is absorbed in stomach and transported to hepatocytes. alcohol dehydrogenase converts ethanol into ethanal, then converted into other molecules that can be respired.
fatty liver
metabolis, of ethanol generates ATP - hepatocytes do not metabolise as much fat as usual but stores fat. causes reduces ability of hepatocytes to carry out other functions, can lead to cirrhosis (scarring of the liver)
liver histology
kidney function
osmoregulation, excretion
ureter
carries urine from kidneys to bladder
urethra
releases urine outside of body
kidney structure
surrounded by fibrous capsule. cortex contains glomerulus, bowman’s capsule, PCT, DCT. medulla contains loop of Henle + collecting duct. renal pelvis is where the ureter joins the kidney
afferent arteriole
carries blood from the renal artery to the glomerulus
efferent arteriole
leaves the glomerulus into a network of capillaries that run closely alongside rest of the nephron
ultrafiltration
small molecules (amino acids, water, glucose, urea, inorganic ions) are filtered out of the blood and into the Bowman’s capsule of the kidney nephron, forming glomerular filtrate
selective reabsorption
useful molecules are taken back from the filtrate and returned to the blood
features that aid ultrafiltration
capillary endothelium, basement membrane, epithelium of Bowman’s capsule
endothelium of capillary
gaos between the endothelial cells allow small molecules to pass
basement membrane
mesh of collagen and glycoproteins - small molecules can pass through holes in mesh
podocytes
has finger-like projections, gaps for small molecules to pass through
PCT adaptations
microvilli on luminal membrane (increases SA for reabsorption). many co transporter proteins in luminal membrane (each type of protein transports a specific solute across luminal membrane). many mitochondria (provides energy for sodium-potassium pump in basal membrane of cells). cells tightly packed together (no fluid can pass between cells)
selective reabsorption mechanism
Na+ are transported from PCT into surrounding tissue by active transport
creates electrical gradient , Cl- ions follow by diffusion
this lowers conc. of Na+ in epithelial cells, Na+ diffuse down conc gradient inot epithelial cells
Na+ move by co transporter proteins. the proteins also transport solute at the smae time
solutes diffuse down conc gradient into blood inside cells
water leaves PCT by osmosis due to reduced water potential
reabsorption of water + salts
sodium and chloride ions are pumped out of filtrate in ascending limb of loop of Henle into medulla, lowering water potential
ascending limb is IMPERMEABLE TO WATER. water is unable to leave by osmosis,
water potential of ascending limb increases as it rises back into cortex (removal of solutes, retention of water)
descending limb is PERMEABLE TO WATER. water moves out by osmosis, low permeability of ions. water potential of filtrate decreases due to loss of water, retention of ions
osmoregulation
control of water potential of body fluids. osmoreceptors detect water potential of blood.
decrease in water potential
impulse sent to posterior pituitary gland
releases ADH
ADH causes luminal membranes to become more permeable to water, increasees number of aquaporins
small vol of conc urine produced
kidney failure reasons
blood loss, high BP, diabetes, infections, drugs,
kidney failure consequences
GFR decreases, leads to a build up of toxins, electrolyte balance in blood is disrupted
excess potassium ions causes?
abdominal cramps, tiredness, muscle weakness, paralysis, continual increase causes frequency of SAN impulses to decrease, arrhythmia + cardiac arrest
build up of sodium causes?
disorientation, muscle spasms, higher blood pressure, general weakness
proteinuria
BP too high, kidney infection, blood filtration mechanism
glucouria
something wrong with functioning of insulin
ketones in urine
indicator of diabetes