COMPLEMENT SYSTEM- active transport
Dr. Smitha Madhavan
BHMS,MD(Hom)
ACTIVE TRANSPORT
Definition : Movement of solute molecules against a concentration
gradient by an energy dependent mechanism.
Two basic forms:
1. Primary active transport
2. Secondary active transport
Substances that are usually actively transported are sodium ,
potassium, calcium, urate ions , hydrogen ions , chloride ions & most
of the aminoacids. Carrier proteins have a major role in active
transport .
Primary active transport
Here energy is produced by direct hydrolysis of ATP . e.g. ; Sodium-
potassium pump
Calcium pump
Hydrogen ion transport
Sodium – potassium pump
Function :
1. It is the basis of nerve function for transmitting nerve impulses.
2. Keeping the interior of cell negatively charged & exteroir
positively charged.
3. Control of the volume of the cell : Proteins & other organic
compounds present in the interior of the cell is negatively charged .
So they have a tendency to attract positively charged particles from
outside along with water molecules. Once the cell swells , it activate
the sodium – potassium pump & which help in maintaining the volume of
cell intact .
Through the sodium – potassium pump sodium ion is transported to the
exterior of the cell & potassium ions to the interior with the help of
carrier protein . This carrier protein has three sodium ion binding
sites , two potassium ion binding sites & ATPase activity which help
in splitting up of ATP to ADP & inorganic phosphate , inturn release
energy .
Calcium pump
Calcium is transported from ICF to ECF .
Hydrogen ion transport
Occurs in,
1. Gastric glands of the stomach especially with parietal cells & is
the basis of HCl secretion in stomach
2. In late distal tubule & cortical collecting tubules of the kidney
by excreting H+ ion in urine & to maintain the appropriate H+
concentration in blood .
Applied physiology
1. Na/ K ATPase is inhibited by cardiac glycoside , digitalis which
causes Na+ accumulation inside the cell , inturn causes Ca2+
accumulation in the myocardial cells & this increases myocardial
contractility So digitalis is used in a failing heart.
2. Refrigeration of blood at 40C suppresses Na/ K ATPase activity . At
450C – denaturation of enzyme , Optimum activity is at normal body
temperature
Secondary active transport
Energy is produced by movement of one solute down concentration
gradient is used for the transport of another solute against
concentration gradient. ( energy is produced by maintaining an ionic
concentratoin gradient by primary active transport )
It is of two types
1. Co- transport
2. Counter transport
Co – transport
e.g.; Glucose & aminoacid co – transport with Na.
Concentration gradient produced by primary active transport represents
a store house of energy . There is always a tendency to move Na+ down
the concentration gradient to the cell .Under appropriate condition
this energy pull certain substance along with Na ions with the help of
carrier protein to the interior of cell .
Counter transport
Substance to be transported is inside the membrane . Na+ binds to
carrier protein at its exterior surface & the other substance to the
interior of carrier protein . Confirmational change occure in the
carrier protein & Na+ is transported to the interior of the cell &
other substance is transported to the exterior .
e.g.; Na+ / Ca2+ counter transport
Na+ / H+ counter transport
Applied physiology
1. Heriditory disorders associated with aminoacid & glucose co
transport
2. Glucose galactose malabsorption by intestine
3. Malabsorption of neutral aminoacids ( Hartnup’s disease )
4. Cystinuria : Defective reabsorption of filtered cystine , ornithine,
arginine & lysine. High concentration of cystine in urine leads to
cystine stone formation.
5. Diabetic aminoaciduria : Defect in reabsorption of lysine, arginine
, ornithine in proximal renal tubule & jejunal mucosa. Autosomal
recessive disease. Manifested as protein intolerance .
6. Lysinuria : Defect in lysine transport in proximal renal tubule –
seizures , physical & mental retardation , Autosomal recessive.
7. Hartnup’s disease: Malabsorption of neutral aminoacids in proximal
renal tubule & jejunal mucosa . Constant neutral aminoaciduria.
Intermittent symptoms of pellagra.
8. Tryptophan malabsorption: Autosomal recessive. Defect in absorption
of tryptophan in jejunal mucosa due to mutation of tryptophan
transport protein. Clinical features are indol urea, hypercalcemia and
nephrocalcinosis.
9. Methionine malabsorption : Autosomal recessive , white hair .
mental retardation , convulsions, oedema
10. Histidinuria
11. Renal glycosuria : Autosomal recessive , Defect in glucose
transport in proximal renal tubule . There is glycosuria with normal
blood glucose.
12. Bartter’s syndrome & Gitelman’s syndrome : Defect in sodium &
chloride ion co transport system , autosomal recessive.Associated with
hypokalemic metabolic alkalosis, hypermagnesuria, hypomagnesemia& low
calcium excretion.
13. Pendred syndrome : Defect in iodine & chloride ion co transport
system . Goitre with deafness, Autosomal recessive.
14. Wilson;s disease : Defect in copper transporting ATPase . Liver
and kidney is affected . Motor and psychiatric disturbances .
Hepatolenticular degeneration .
15. Congenital chloridorrhea: autosomal recessive. Defect in chloride
absorption due to mutation of chloride-hydrogen uptake pump in the
ileal and colonic mucosa. Clinical features are watery diarrhoea,
elevated faecal chloride, metabolic alkalosis and hyperaldosteronism.
16. Menke’s disease: X-linked recessive. Defect in copper transport
due to mutation of copper transporting ATPase. Clinical features
mental retardation, kinky hair( pili torti), typical facies and
arterial tortuosity.
References
Text book of medical physiology – Guyton
Physiology – Ganong
Harrison’ s principle of internal medicine
Best and Taylor’s physiological basis of Medical practice
|