Difference between revisions of "PH & BUFFERING-ORGAN SYSTEMS"
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<br/>West, J.B. and Luks, A.M. (2021). West’s Pulmonary Pathophysiology. Lippincott Williams & Wilkins. | <br/>West, J.B. and Luks, A.M. (2021). West’s Pulmonary Pathophysiology. Lippincott Williams & Wilkins. | ||
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[[Category:Physiology]] | [[Category:Physiology]] |
Revision as of 11:40, 2 January 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., Boitano, S., Brooks, H.L., Weitz, M., Brian Patrick Kearns, Ganong, W.F. and Mcgraw-Hill Education (Firm (2016). Ganong’s review of medical physiology. 25th ed. New York: Mcgraw Hill Education.
Hall, J.E. and Hall, M.E. (2020). Guyton And Hall Textbook Of Medical Physiology. 14th ed. S.L.: Elsevier - Health Science.
West, J.B. and Luks, A.M. (2021). West’s Pulmonary Pathophysiology. Lippincott Williams & Wilkins.