Effect of high intensity interval training under hypoxic conditions in a normobaric environment on moderately trained university students’ antioxidant status
Yazarlar (2)
Doç. Dr. Mustafa Şakir AKGÜL Kastamonu Üniversitesi, Türkiye
Mitat Koz
Ankara Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale (ESCI dergilerinde yayınlanan tam makale)
Dergi Adı PHYSICAL EDUCATION OF STUDENTS
Dergi ISSN 2075-5279 Wos Dergi
Dergi Tarandığı Indeksler ESCI
Makale Dili İngilizce Basım Tarihi 01-2019
Cilt / Sayı / Sayfa 23 / 5 / 217–222 DOI 10.15561/20755279.2019.0501
Makale Linki https://sportedu.org.ua/index.php/PES/article/view/939
Özet
Purpose The effects of high intensity interval exercises on antioxidant defence system are not clear. Since there is an evident lack of studies focused on oxidative stress in moderately trained males following high intensity interval training, we investigated oxidative stress markers (malondialdehyde [MDA], catalase [CAT], glutathione peroxidase [GPX], superoxide dismutase [SOD]) by completing a high intensity interval training program (HIITP) under hypoxic and normoxic conditions in a normobaric environment. Material The study was carried out on moderately trained university students who had regular exercising habits. The participants completed 8-week wingate based high intensity interval training under normoxic and hypoxic conditions (2500 m.) in the normobaric environment. They were instructed to maintain their normal dietary practices during the study not to take any antioxidant containing vitamin tablets. Results The interaction effect (time× group) for SOD (p= 0.230), CAT (p= 0.736), GPX (p= 0.517), and MDA (p= 0.596), revealed no significant change in repeated response. Conclusions Although 8 weeks of high-intensity interval training significantly affected only SOD and GPX (p< 0.05), the normoxic and hypoxic conditions did not present any significant change between treatments.
Anahtar Kelimeler
interval training | superoxide dismutase | catalase | glutathione peroxidase | malondialdehyde