Abstract

The effects of exposure to hyperbaric oxygen on the oxidative capacity of the skeletal muscles in mice at different ages were investigated. We exposed 5-, 34-, 55-, and 88-week-old mice to 36% oxygen at 950 mmHg for 6 hours per day for 2 weeks. The activities of succinate dehydrogenase (SDH), which is a mitochondrial marker enzyme, of the tibialis anterior muscle in hyperbaric mice were compared with those in age-matched mice under normobaric conditions (21% oxygen at 760 mmHg). Furthermore, the SDH activities of type IIA and type IIB fibers in the muscle were determined using quantitative histochemical analysis. The SDH activity of the muscle in normobaric mice decreased with age. Similar results were observed in both type IIA and type IIB fibers in the muscle. The decrease in the SDH activity of the muscle was reduced in hyperbaric mice at 57 and 90 weeks. The decreased SDH activities of type IIA and type IIB fibers were reduced in hyperbaric mice at 90 weeks and at 57 and 90 weeks, respectively. We conclude that exposure to hyperbaric oxygen used in this study reduces the age-related decrease in the oxidative capacity of skeletal muscles.

Highlights

  • A reduction in skeletal muscle mass is one of the most striking features of the aging process

  • An elevation in atmospheric pressure accompanied by high oxygen concentration enhances the partial pressure of oxygen and increases the concentration of dissolved oxygen in the plasma [20, 21]

  • An increase in atmospheric pressure and oxygen concentration increases carbon dioxide concentration, which in turn facilitates the release of oxygen from hemoglobin and causes the dilation of blood vessels

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Summary

Introduction

A reduction in skeletal muscle mass is one of the most striking features of the aging process. A reduction in the number and volume of type II fibers in skeletal muscles of rats can be observed in the initial stages of the aging process [6, 7]. These changes in type II fibers are considered to be due to a transition of fiber types from type II to type I, selective loss and atrophy of type II fibers, and/or degeneration in the neuromuscular junction, which are induced by age-related disuse of type II fibers. A decrease in the number and volume of both type I and type II fibers in skeletal muscles of rats can be observed in the late stages of the aging process [6,7,8]. A decrease in the oxidative enzyme activity of skeletal muscles in rats was observed with increasing age [9,10,11]

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