Hostname: page-component-848d4c4894-8kt4b Total loading time: 0 Render date: 2024-06-21T23:48:22.628Z Has data issue: false hasContentIssue false

TRAINING-INDUCED ALTERATIONS IN LACTATE DEHYDROGENASE REACTION KINETICS IN RATS: A RE-EXAMINATION

Published online by Cambridge University Press:  04 January 2001

TERENCE G. FAVERO
Affiliation:
Department of Biology, University of Portland, Portland, OR 97203, Department of Exercise Science, Willamette University, Salem, OR 97301, and Department of Exercise and Movement Science, University of Oregon, Eugene, OR 97403, USA
STASINOS S STAVRIANEA
Affiliation:
Department of Biology, University of Portland, Portland, OR 97203, Department of Exercise Science, Willamette University, Salem, OR 97301, and Department of Exercise and Movement Science, University of Oregon, Eugene, OR 97403, USA
and GARY A. KLUG
Affiliation:
Department of Biology, University of Portland, Portland, OR 97203, Department of Exercise Science, Willamette University, Salem, OR 97301, and Department of Exercise and Movement Science, University of Oregon, Eugene, OR 97403, USA
Get access

Abstract

The kinetics and the isozyme composition of lactate dehydrogenase (LDH) were measured in rat plantaris muscle during a 26 week endurance-training program. Alterations in the LDH isozyme pattern were detectable after 6 weeks as the percentage of the M4 isozyme was reduced from 89 to 76 % and the total percentage of M subunits compared with H subunits declined by 8 %. At 16 weeks, M4 accounted for only 62 % of the total. The replacement of M with H subunits continued when training was prolonged as M4 represented only 52 % of the total isozymes at 26 weeks. Conversely, training for 6 and 16 weeks produced no changes in either Vmax or Km. At 26 weeks, these values declined for both the forward (pyruvate to lactate) and backward reactions. The rate constants for both reactions were also reduced. These data suggest that changes in LDH isozyme pattern do not contribute significantly to the enhancement of lactate oxidation that may occur after training. They also suggest that the functional significance of alterations in LDH structure and/or function are best determined from analysis of the overall reaction kinetics as opposed to individual characteristics such as the isozyme pattern, Km or Vmax.

Type
Research Article
Copyright
The Physiological Society 1999

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)