Literature DB >> 33520827

The effects of two iso-volume endurance training protocols on mitochondrial dysfunction in type 2 diabetic male mice.

Masoumeh Sadat Modaresi1, Mehrdad Fathei1, Seyed Reza Attarzadeh Hosseini1, Mohammad Mosaferi Ziaaldini1, Mohammad Reza Sadeghian Shahi2.   

Abstract

PURPOSE: Type 2diabetes(T2D) is one of the more common diseases in the world and has been widely spread. One of the suggested mechanisms in development of T2D, is mitochondrial dysfunction. The purpose of this study is to compare the effects of two endurance training protocols with low and moderate intensity on biogenesis and mitochondrial function, in Diabetic mice induced by high fat diet and Streptozotocin(STZ).
METHODS: 40 five week old mice divided to four groups including: health control (HC, n = 7), diabetic control (DC, n = 7), low endurance training (DLT, n = 7) and moderate endurance training (DMT, n = 7). DMT group ran at 5 m/min for an hour, 3 days a week on a treadmill, and DLT group ran at 3 m/min for an hour, 5 days a week on a treadmill for 8 weeks.
RESULTS: The cytosolic content of PGC1α, Tfam and mitochondrial content of citrate synthase(Cs) and cytochrome c oxidase(Cox) in DC was significantly reduced compared to HC(P˂0.05). All of the parameters except for Cs in both DLT and DMT were increased compared to DC (P˂0.05), but there was no difference between them and the HC (P˃0.05). There was no difference in Cs enzyme between the DC and the DLT(P˃0.05), but it was significantly increased in the DMT(P˂0.05). There was a significantly difference between Cs enzyme in HC and DLT(P˂0.05), but there wasn't any significant difference between HC and DMT(P˃0.05).
CONCLUSIONS: The results showed that in same volume condition, both endurance training protocols improved the proteins involved in biogenesis and mitochondrial function in T2D mice and there was no significant difference between them. © Springer Nature Switzerland AG 2020.

Entities:  

Keywords:  Citrate synthase; Cytochrome c oxidase; Mitochondrial dysfunction; PGC1α; Tfam; Type 2 Diabetes

Year:  2020        PMID: 33520827      PMCID: PMC7843807          DOI: 10.1007/s40200-020-00611-3

Source DB:  PubMed          Journal:  J Diabetes Metab Disord        ISSN: 2251-6581


  34 in total

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