Metabolism - Clinical and Experimental
Volume 59, Issue 6 , Pages 879-886, June 2010

Combination of two oxidant stressors suppresses the oxidative stress and enhances the heat shock protein 27 response in healthy humans

UMR MD2 P2COE, Faculté de Médecine, Université de la Méditerranée, 13916 cedex 20 Marseille, France

Lung Function Laboratory, North Hospital, Assistance Publique-Hôpitaux de Marseille, 13015 Marseille, France

Received 21 July 2009; accepted 13 October 2009. published online 14 December 2009.

Abstract 

We tested the hypothesis that the combination of 2 oxidant stressors (hyperoxia and fatiguing exercise) might reduce or suppress the oxidative stress. We concomitantly measured the plasma concentration of heat shock proteins (Hsp) that protect the cells against the deleterious effects of reactive oxygen species. Healthy humans breathed pure oxygen under normobaric condition for 50-minute periods during which they stayed at rest or executed maximal static handgrip sustained until exhaustion. They also repeated handgrip bouts in normoxic condition. We performed venous blood measurements of 2 markers of the oxidative stress (thiobarbituric acid reactive substances and reduced ascorbic acid) and Hsp27. Under normoxic condition, the handgrip elicited an oxidative stress and a modest increase in plasma Hsp27 level (+7.1 ± 5.4 ng/mL). Under hyperoxic condition, (1) at rest, compared with the same time schedule in normoxic condition, we measured an oxidative stress (increased thiobarbituric acid reactive substances and decreased reduced ascorbic acid levels) and the plasma Hsp27 level increased (maximal variation, +12.5 ± 6.0 ng/mL); and (2) after the handgrip, the oxidative stress rapidly disappeared. The combination of both hyperoxia and handgrip bout doubled the Hsp27 response (maximal variation, +24.8 ± 9.2 ng/mL). Thus, the combination of 2 hits eliciting an oxidative stress seems to induce an adaptive Hsp27 response that might counterbalance an excessive production of reactive oxygen species.

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 Conflict of interest statement: all authors disclose all or any potential conflicts of financial interest in the scientific project related to this manuscript.

 Institutional approval: the research was approved by our institutional ethics committee, and each subject gave an informed consent.

PII: S0026-0495(09)00437-5

doi:10.1016/j.metabol.2009.10.006

Metabolism - Clinical and Experimental
Volume 59, Issue 6 , Pages 879-886, June 2010