TRAINING-INDUCED ALTERATIONS IN LACTATE DEHYDROGENASE REACTION KINETICS IN RATS: A RE-EXAMINATION
Terence G. Favero, Stasinos S Stavrianea, and GARY A. KLUG
Abstract
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Terence G. Favero, Stasinos S Stavrianea, and GARY A. KLUG
Abstract
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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.
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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.
Key concepts: Isozyme, Lactate dehydrogenase, Kinetics, Biochemistry, Enzyme kinetics, Internal medicine, Chemistry, Endocrinology