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Chloride shift (also known as the Hamburger phenomenon or lineas phenomenon, named after Hartog Jakob Hamburger) is a process which occurs in a cardiovascular system and refers to the exchange of bicarbonate (HCO3−) and chloride (Cl−) across the membrane of red blood cells (RBCs).[1]
Mechanism
[edit]Carbon dioxide (CO2) is produced in tissues as a byproduct of normal aerobic metabolism. It dissolves in the solution of blood plasma and into red blood cells (RBC), where carbonic anhydrase catalyzes its hydration to carbonic acid (H2CO3). Carbonic acid then spontaneously dissociates to form bicarbonate Ions (HCO3−) and a hydrogen ion (H+). In response to the decrease in intracellular pCO2, more CO2 passively diffuses into the cell.
Cell membranes are generally impermeable to charged ions (i.e. H+, HCO3− ) but RBCs are able to exchange bicarbonate for chloride using the anion exchanger protein Band 3. Thus, the rise in intracellular bicarbonate leads to bicarbonate export and chloride intake. The term "chloride shift" refers to this exchange. Consequently, chloride concentration is lower in systemic venous blood than in systemic arterial blood: high venous pCO2 leads to bicarbonate production in RBCs, which then leaves the RBC in exchange for chloride coming in.[2]
The opposite process occurs in the pulmonary capillaries of the lungs when the PO2 rises and PCO2 falls, and the Haldane effect occurs (release of CO2 from hemoglobin during oxygenation). This releases hydrogen ions from hemoglobin, increases free H+ concentration within RBCs, and shifts the equilibrium towards CO2 and water formation from bicarbonate. The subsequent decrease in intracellular bicarbonate concentration reverses chloride-bicarbonate exchange: bicarbonate moves into the cell in exchange for chloride moving out. Inward movement of bicarbonate via the Band 3 exchanger allows carbonic anhydrase to convert it to CO2 for expiration.[3]
The chloride shift may also regulate the affinity of hemoglobin for oxygen through the chloride ion acting as an allosteric effector.[4]
Reaction
[edit]Reaction (as it occurs in the pulmonary capillaries)
RBC PLASMA HCO3− <-- <-- <-- HCO3− K+ Na+ Cl− --> --> --> --> Cl−
Bicarbonate in the red blood cell (RBC) exchanging with chloride from plasma in the lungs.
The underlying properties creating the chloride shift are the presence of carbonic anhydrase within the RBCs but not the plasma, and the permeability of the RBC membrane to carbon dioxide and bicarbonate ion but not to hydrogen ion. Continuous process of carbonic acid dissociation and outflow of bicarbonate ions would eventually lead to a change of intracellular electric potential because of lasting H+ ions. Inflow of chloride ions maintains electrical neutrality of a cell. The net direction of bicarbonate-chloride exchange (bicarbonate out of RBCs in the systemic capillaries, bicarbonate into RBCs at pulmonary capillaries) proceeds in the direction that decreases the sum of the electrochemical potentials for the chloride and bicarbonate ions being transported.
References
[edit]- ^ Crandall ED, Mathew SJ, Fleischer RS, Winter HI, Bidani A (1981). "Effects of inhibition of RBC HCO3−/Cl− exchange on CO2 excretion and downstream pH disequilibrium in isolated rat lungs". J. Clin. Invest. 68 (4): 853–62. doi:10.1172/JCI110340. PMC 370872. PMID 6793631.
- ^ Westen EA, Prange HD (2003). "A reexamination of the mechanisms underlying the arteriovenous chloride shift". Physiol. Biochem. Zool. 76 (5): 603–14. doi:10.1086/380208. PMID 14671708. S2CID 21356564.
- ^ Westen EA, Prange HD (2003). "A reexamination of the mechanisms underlying the arteriovenous chloride shift". Physiol. Biochem. Zool. 76 (5): 603–14. doi:10.1086/380208. PMID 14671708. S2CID 21356564.
- ^ Nigen AM, Manning JM, Alben JO (25 June 1980). "Oxygen-linked binding sites for inorganic anions to hemoglobin". J. Biol. Chem. 255 (12): 5525–9. doi:10.1016/S0021-9258(19)70661-9. PMID 7380825.
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