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Article type: Research Article
Authors: Chanda, Makamasa | Nantakomol, Duangdaoa | Suksom, Daroonwanb | Palasuwan, Attakorna; *
Affiliations: [a] Molecular Hematology Research Unit, Department of Clinical Microscopy, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand | [b] Faculty of Sports Science, Chulalongkorn University, Bangkok, Thailand
Correspondence: [*] Corresponding author: Attakorn Palasuwan, Ph.D., Department of Clinical Microscopy, Faculty of Allied Health Sciences, Chulalongkorn University, Phayathai road, Pathumwan, Bangkok 10330, Thailand. Tel.: +66 2 218 1069; Fax: +66 2 218 3771; E-mails: Attakorn.P@chula.ac.th, attakornp@yahoo.com.
Abstract: Glucose-6-phospate dehydrogenase (G6PD) deficient cells are sensitive to oxidative damage leading to the formation of microparticles (MPs). Therefore, we examined the concentration of MPs and changes in the antioxidant balance after an acute strenuous exercise (SEx) and moderate-intensity exercise (MEx). Eighteen healthy females (18–24 years) with G6PD normal and eighteen age-matched females with G6PD Viangchan (871G>A) were tested by running on a treadmill at their maximal oxygen uptake for SEx and at 75% of their maximal heart rate for MEx. It was found that SEx triggered the release of total microparticles (TTMPs) above baseline levels and remained significantly higher 45 minutes after the exercise in G6PD normal individuals. However, SEx-induced increase in TTMPs was significantly higher in G6PD Viangchan as compared to G6PD normal. In contrast, MEx did not to alter the release of TTMPs in both G6PD normal and Viangchan. Moreover, TTMPs concentrations were inversely correlated with G6PD activity (r =−0.82, P < 0.05) but positively correlated with MDA concentrations (r = 0.74, P < 0.05). Using cell specific antibodies, we determined that MPs were mainly derived from platelets and erythrocytes. Altogether, the present study indicates that G6PD Viangchan may participate in MEx without higher MPs concentration and oxidative stress compared with G6PD normal.
Keywords: G6PD, antioxidant status, oxidative stress
DOI: 10.3233/CH-141865
Journal: Clinical Hemorheology and Microcirculation, vol. 60, no. 2, pp. 241-251, 2015
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