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First published online March 14, 2005
Journal of Experimental Biology 208, 1117-1124 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01490
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The role of mineralized tissue in the buffering of lactic acid during anoxia and exercise in the leopard frog Rana pipiens

Daniel E. Warren* and Donald C. Jackson

Brown University, Department of Molecular Pharmacology, Physiology and Biotechnology, Box G, Providence, RI 02912, USA

* Author for correspondence (e-mail: Daniel_E_Warren{at}brown.edu)

Accepted 10 January 2005

To evaluate the role of mineralized tissues of the leopard frog in buffering acid, we analyzed the composition of femur and auditory capsule, the latter of which encloses a portion of the endolymphatic lime sacs, and investigated the extent to which these tissues are involved in buffering lactic acid after 2.5 h of anoxia and 10-19 min of strenuous exercise at 15°C. We analyzed the following tissues for lactate: plasma, heart, liver, gastrocnemius muscle, femur, auditory capsule and carcass. Plasma [Ca2+], [Mg2+], [inorganic phosphate (Pi)], [Na+] and [K+] were also measured. Femur Ca2+, Pi and CO32- compositions were similar to bone in other vertebrates. Auditory capsule had significantly more CaCO3 than femur. Lactate was significantly elevated in all tissues after anoxia and exercise, including femur and auditory capsule. Anoxia increased plasma [Ca2+], [Mg2+], [Pi] and [K+] and had no effect on plasma [Na+]. Exercise increased plasma [Mg2+], [Pi] and [K+] and had no effect on plasma [Ca2+] or [Na+]. The skeleton and endolymphatic lime sacs buffered 21% of the total lactate load during anoxia, and 9% after exercise. The exact contribution of the entire endolymphatic sac system to lactate buffering could not be determined in the present study. We conclude that the mineralized tissues function as buffers during anoxia and exercised induced lactic acidosis in amphibians.

Key words: anoxia, bone, buffering, Ca2+, exercise, lactic acid, leopard frog, Rana pipiens




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