Tissue-specific metabolism during normothermy and daily torpor in deer mice (Peromyscus maniculatus).
Previous work with deer mice (Peromyscus maniculatus) has demonstrated that a significant acidosis occurs during daily torpor. In addition, carbohydrate levels are significantly lower, whereas fatty acid and ketone levels are significantly higher during torpor. The present study examined the effects of these in vivo acid-base and metabolite adjustments on in vitro 14C-glucose metabolism in tissues taken from normothermic and torpid deer mice. Glucose oxidation in liver and vastus lateralis taken from normothermic animals was reduced by a change in incubation temperature from 37 degrees C to 25 degrees C (liver, 0.44 to 0.23 mumoles/g.h; vastus, 0.66 to 0.25 mumoles/g.h), whereas heart from normothermic mice exhibited an increase from 0.57 to 0.99 mumoles/g.h at the lower temperature. Altering acid-base conditions or metabolite levels had no effect on glucose metabolism in the heart or liver. However, both of these factors significantly influenced metabolism in vastus. Vastus taken from normothermic mice had an increased glucose oxidation rate under the more acidic torpor conditions (0.25 to 0.33 mumoles/g.h), whereas a reduction in oxidation occurred when incubated with torpor substrate concentrations (0.33 to 0.22 mumoles/g.h). In vastus taken from torpid mice, changing acid-base state and metabolites to torpor levels resulted in a significant reduction in glucose oxidation (0.26 to 0.12 mumoles/g.h). Under most incubation conditions, glucose oxidation was significantly lower in tissues taken from torpid mice than in these tissues from normothermic mice, suggesting that adjustments in addition to changes in acid-base and substrate parameters may be necessary to account for metabolic modifications during daily torpor.[1]References
- Tissue-specific metabolism during normothermy and daily torpor in deer mice (Peromyscus maniculatus). Nestler, J.R. J. Exp. Zool. (1992) [Pubmed]
Annotations and hyperlinks in this abstract are from individual authors of WikiGenes or automatically generated by the WikiGenes Data Mining Engine. The abstract is from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.About WikiGenesOpen Access LicencePrivacy PolicyTerms of Useapsburg
