Basic tubular function Flashcards
(19 cards)
Osmolarity
A measure of the osmotic pressure exerted by a solution across a perfect semi-permeable membrane
All the concentrations of the different solutes (measured in mmol/l) added together. Each ion is “counted” separately
Osmolarity dependent on?
Dependent on the number of particles in a solution and NOT the nature of the particles
Any solute present at equal concentrations either side of a semi-permeable membrane…?
No net effect on water movement
Types of transport in tubules
Effect of rate as solute concentration increases for each of these?
Passive movement- protein independent transport (lipophilic)
Incease conc.= increase rate (directly proportional)
Passive movement- protein dependent transport (hydrophilic molecules)
Increase conc= increase rate but then plateaus
Active movement- directly coupled to ATP hydrolysis
Increase conc= increase rate but then plateaus
Active movement- indirectly coupled to ATP hydrolysis
Increase conc= increase rate but then plateaus
2 types of H2O transport
Paracellular
Transcellular
Regulation of passive uptake system?
Storage of protein channels inside cell- moved to surface when needed
Protein reabsorption that gets into primary urine
- Receptors have low specificity+ high capacity for binding to protein
- Receptor binds to protein+ gets endocytosed
- Receptor dissociates from protein by dropping pH of vesicle
- Releases receptor + protein from each other= receptor can be used again
- Pump protons in endosome= decreased pH= increased +ve charge
- Harder to pump H+ in because of positive charge so Cl- transporter required to decreased charge so more H+ can be pumped in (2Cl- exhcnaged for one H+)
Example of transport maxima?
Glucose
After a certain solute conc, limit to how much solute can be in the reabsorbed solution= increase glucose in urine
What causes glucose in urine?
Diabetes mellitus
Ingestion of large quantities of vitamins B and C
Where does most of reabsorption occur?
Proximal convoluted tubule
Largest brush border
Where is reabsorption regulated the most?
Collecting duct
Least active part of the nephron?
Descending limb of loop of Henle
Water passively reabsorbed because osmolarity of IF fluid= high; Draws in Sodium and Potassium
Bicarbonate absorption process?
Reabsorption of bicarbonate= indirectly coupled to Na transport
- Pumping proton out in exchange for Na in neutralizes bicarbonate
- Bicarbonate in the presence of carbonic anhydrase outside cell turns to H20 and CO2 which cross membrane
- Inside the cell carbonic anhydrase activity converts the H20 and CO2 back into H2CO3
- H2CO3 dissociates into H+ and HCO3-
- H+ is used on Na+/H+ exchange to start the process again
- HCO3- moves out of the basolateral membrane by simple diffusion.
Why is net secretion in PCT important?
Route of excretion for some substances
Some drugs enter tubular fluid here + act further down nephron.
Ascending limb?
Chloride actively reabsorbed
Sodium passively reabsorbed with it (because pumping on basolateral side)
Bicarbonate reabsorbed
Impermeable to water (very tight junctions+ no aquaporins
Thiazide mechanism?
Blockage with thiazide= increased plasma Ca2+
- Under normal conditions when pumping out sodium= low Na conc. In cell
- Na passively enters into cell either through Na/Cl- co transport on apical membrane or 3Na+/ Ca2+ exchange (counter transport) on basolateral membrane
- Thiazide blocks Na/Cl- co transport protein= only way to bring Na in is through countertransport
- Decreased Ca in cell
- More Ca comes in through passive system on apical membrane
Types of cells in collecting duct + distal part of distal convoluted tubule
Dependent on?
Principal Cell: important in sodium, potassium and water balance (mediated via Na/K ATP pump)
Dependent on vasopressin
Intercalated Cell: important in acid-base balance (mediate via H-ATP pump)- imp in regulating acid-base balance
Single gene defects that affect tubular function
Caused by?
Leads to?
Renal tubule acidosis
Caused by acidosis is in blood (metabolic acidosis) because of failure of getting protons out into lumen (not excreting protons) OR carbonic anhydrase problems
Less acidic urine + Leads to impaired growth+ hypokalaemia
Antenatal Bartter syndrome
Caused by excessive electrolyte secretion, mutation in Na/2Cl-/K+ uptake process
Premature birth, polyhydramnios (increased aminiotic fluid)
Severe salt loss
Moderate metabolic alkalosis
Hypokalemia
Renin and aldosterone hypersecretion
Fanconi syndrome (Dent’s disease)
Cause= can’t separate protein from receptor because can’t acidify endosome (mutation in 2Cl-/ H+ exchanger)= can’t recirculate carrier/ receptor
Increased excretion of uric acid, glucose, phosphate, bicarbonate
Increased excretion of low MW protein
Which ion transporter is found on the apical side of the ascending limb of the loop of Henle?
Na+/ 2Cl-/ K+ triple transporter