Decreased glucose tolerance but normal blood glucose levels in the field in the caviomorph rodent Ctenomys talarum: The role of stress and physical activity

Hystricomorph rodents have a divergent insulin molecule with only 1–10% of the biological activity in comparison to other mammalian species. In this study, we used the subterranean rodent Ctenomys talarum as a model and performed blood glucose tolerance tests (GTTs) with trained and untrained indivi...

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Published inComparative biochemistry and physiology. Part A, Molecular & integrative physiology Vol. 151; no. 2; pp. 232 - 238
Main Authors Vera, Federico, Zenuto, Roxana R., Antenucci, C. Daniel
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2008
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Summary:Hystricomorph rodents have a divergent insulin molecule with only 1–10% of the biological activity in comparison to other mammalian species. In this study, we used the subterranean rodent Ctenomys talarum as a model and performed blood glucose tolerance tests (GTTs) with trained and untrained individuals to evaluate blood glucose regulation and the possible role of physical activity as a compensatory mechanism. Additionally, we evaluated the variations in blood glucose during acute and chronic stress and gathered data in the field to evaluate natural-occurring variations in blood glucose levels. The GTTs showed that C. talarum have a diminished capacity of regulating blood glucose levels in comparison to other mammals and suggest that unexplored differences in the compensatory mechanisms, insulin structure and/or glucose transporters exist within species of hystricomorph rodents. However, blood glucose levels in the field stayed within the normal mammalian range. Physical activity did not prove to be a compensatory mechanism for blood glucose regulation. The individuals did not display important increases in blood glucose after acute stressors and managed to adequately regulate blood glucose during chronic stress. We suggest that the species may not face a selective pressure favoring a more tightly, mammalian like, capacity of regulating blood glucose levels.
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ISSN:1095-6433
1531-4332
DOI:10.1016/j.cbpa.2008.06.030