excretion is removal of metabolic waste from the body
why do we have to excrete ?
prevent from becoming toxic and changing pH
maintain homeostasis
prevent end-product inhibition from stopping pathways
Our bodies excretes nitrogenous waste, bile pigments and carbon dioxide
nitrogenous waste is when excess amino acids cannot be stored so have to be broken down as ammonia in fish, ammonia then urea in mammals and uric acid in birds/insects
bile pigments are formed when haemoglobin from old erythrocytes is broken down by hepatocytes and then excreted in bile
too much carbon dioxide can cause pH to decrease and cause respiratory acidosis
too little carbon dioxide causes pH to increase and cause alkalosis
the liver is divided into 2 lobes and which then divided into 100,00 lobules
each lobule has 6 sides and has cylindrical in shape. Hepatocytes radiate from the central vein
hepatocyte
microvilli increase surface area which increases the toxins that can enter
big nucleus
lots of mitochondria so more ATP for reactions
dense cytoplasm with increased Golgi apparatus and smooth endoplasmic reticulum
flow through liver
oxygen rich blood enters liver via hepatic artery
capillary bed brings in nutrients and potential toxins
intestinal vein brings in deoxygenated blood and travels up hepatic portal vein
oxygen and deoxygenated blood mix in sinusoids
flows through central vein and then leaves liver back to the heart
bile canaliculi carry bile out of liver
kupffer cells line the sinusoids and resident to macrophages that breakdown bacteria and old red blood cells
why is the liver so important ?
breaks down old red blood cells and haemoglobin
stores vitamins A,D and B12
breaks down lactic acid
breaks down toxins
controls blood glucose levels
breaks down excess amino acids
when blood glucose levels are high liver cells take up excess glucose and converts to glycogen (glycogenesis)
when blood glucose levels are low, liver cells breakdown glycogen into glucose and release into the blood stream (glycogenolysis)
excess amino acids can either be transanimated or broken down in two ways :
deamination
ornithine cycle
deamination is combining amino acids with oxygen to produce keto acid and ammonia
ornithine cycle converts ammonia into urea in 4 steps
ornithine +ammonia +carbon dioxide = citruline
citruline + ammonia = arginine
arginine + water = urea +ornithine
ultrafiltration the filtration of small molecules on molecular level. Anything small enough to leave the glomerular capillaries will enter the Bowmans capsule
ultrafiltration goes from afferent arteriole into efferent arteriole
What gets out of ultrafiltration ?
hormones
water
urea
electrolytes
glucose
amino acids
drugs
vitamins
what can't get out of ultrafiltration ?
red blood cells
white blood cells
platelets
plasma proteins
ultrafiltration works in two ways ; bottleneck effect and using a 3 layer system
Bottleneck effect is when it forces the solutes out of the blood because the diameter of the afferent arteriole is larger than the efferent arteriole
the 3 layers in ultrafiltration are ; endothelium of the glomerurler capillaries, basement membrane and the epithelium of the Bowmans capsule.
basement membrane is made of collagen fibres and glycoproteins forming molecular mash. Only allows molecules of a RMM >69,000
pedocils keep podocytes away from the capillaries to create gap so solutes can get through and holds adjacent podocytes together
selective reabsorption is where useful substances are reabsorbed from glomerular filtrate back into the blood at the proximal convoluted tube
85 % of the filtrate is reabsorbed into the blood including :
glucose
most amino acids
60 % of water
some sodium, chloride, potassium
most hormones
50 % of urea
adaptations to the proximal convoluted tube
convoluted for a longer time to reabsorb
microvilli to increase surface area
may mitochondria for active transport
selective reabsorption
sodium and potassium pumps pump sodium from cell to blood and potassium from blood to cell
sodium diffused into cell via a co-transport protein that takes glucose and amino acids with it
glucose and amino acids move from cell into the blood via facilitated diffusion
water diffuses into cell via osmosis
as the water leaves the proximal convoluted tube, concentration of chloride and urea will increase so chloride and urea can diffuse into the blood
loop of henule is a countercurrent multiplier system. Its purpose is to multiply the effect of osmosis by maintaining a water potential gradient allowing water to leave the nephron and re-enter the blood
filtrate from the PCT includes 40 % of water, sodium, chloride, potassium and urea
descending limb is permeable to water, urea, sodium and chloride
ascending limp is permeable to sodium and chloride by active transport and urea. But its not permeable to water
Flow through loop of Henle
1. Sodium and chloride are pumped out of the ascending limb
2. Decreases the water potential of the medulla
3. Water leaves the descending limb by osmosis
4. Some sodium and chloride will diffuse into the descending limb
5. As filtrate moves down descending limb, water is moving out and sodium and chloride entering so the concentration of sodium and chloride will increase
6. Some sodium and chloride diffuses out of bottom of descending limb making it more salty at the bottom and maintaining the water potential gradient so water can keep moving out
7. As filtrate moves up the ascending limb, water can not get out but sodium and chloride are being pumped out so at the top of the ascending limb it has a high water potential
8. As filtrate moves down the collecting duct, water leaves by osmosis
9. As filtrate moves along the collecting duct, water leaves so concentration of urea increase so some urea diffuses out into blood and further decrease the water potential of medulla so even more water can enter medulla/blood