Difference between revisions of "PH & BUFFERING-ORGAN SYSTEMS"
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==Reference(s)== | ==Reference(s)== | ||
Barrett, K.E., Barman, S.M | Barrett, K.E., Barman, S.M., Brooks, H.L., X, J. and Ganong, W.F. (2019). Ganong’s review of medical physiology. 26th ed. New York: Mcgraw-Hill Education | ||
[[Category:Ph & Buffering]] | [[Category:Ph & Buffering]] | ||
[[Category:Physiology]] | [[Category:Physiology]] |
Latest revision as of 02:30, 21 March 2023
SUMMARY
1. Respiratory system: controls pCO2 through alterations in alveolar ventilation. CO2 indirectly stimulates the central chemoreceptors of the medulla through the generation of H+ which crosses the BBB and dissolves in the CSF.
2. Kidneys: control HCO3- which is important for long-term control & compensation of acid-base disturbances.
3. Blood: through buffering by plasma proteins & haemoglobin.
4. Bone: H+ may exchange with cations in bone. Bone possesses carbonate which could be used to support plasma HCO3- levels.
5. Liver: generation of HCO3- and NH4+ (ammonia) through glutamine metabolism. Excretion of ammonia by renal tubules generates more bicarbonate.
Reference(s)
Barrett, K.E., Barman, S.M., Brooks, H.L., X, J. and Ganong, W.F. (2019). Ganong’s review of medical physiology. 26th ed. New York: Mcgraw-Hill Education