Sexual dimorphism in response to repetitive bouts of acute aerobic exercise in rodents with type 1 diabetes mellitus

• Published in: PloS one 2022-09, Vol.17 (9), p.e0273701-e0273701
• Main Authors: Larocque, Jordan C, Gardy, Silar, Sammut, Mitchell, McBey, David P, Melling, C. W. James
• Format: Article
• Language: English
• Subjects: Aerobic exercises; Aerobics; Analysis; Biology and Life Sciences; Blood; Blood glucose; Blood sugar; Development and progression; Diabetes; Diabetes mellitus; Diabetes mellitus (insulin dependent); Dimorphism (Biology); Estrogens; Estrus cycle; Exercise; Fatty acids; Females; Fitness equipment; Glucose; Glycogen; Glycogens; Growth hormones; Health aspects; Homeostasis; Hyperglycemia; Hypoglycemia; Insulin; Liver; Males; Medicine and Health Sciences; Muscles; Musculoskeletal system; Oxidation; Physical fitness; Physical Sciences; Rats; Running; Sexual dimorphism; Streptozocin; Type 1 diabetes
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0273701

The purpose of this study was to examine sex-specific differences in the blood glucose (BG) response to recurrent aerobic exercise in type 1 diabetes rats. Specifically, we examined the role of peak estrogen (E2) concentrations during proestrus on BG response to prolonged repetitive aerobic exercise. To do so, nineteen Sprague-Dawley rats were assigned to four exercised groups: control female (CXF; n = 5), control male (CXM; n = 5), diabetic female (DXF, n = 5) and diabetic male (DXM, n = 4). Diabetes was induced in DX groups via subcutaneous multiple injections of low dose streptozotocin (20mg/day for 7 days). After four days of exercise, muscle and liver glycogen content, liver gluconeogenic enzyme content, muscle Beta oxidation activity and BG responses to exercise were compared. The final bout of exercise took place during proestrus when E2 concentrations were at their highest in the female rats. During days 1–3 DXM had significantly lower BG concentrations during exercise than DXF. While both T1DM and non-T1DM females demonstrated higher hepatic G6Pase expression and muscle beta oxidation activity levels on day 4 exercise, no differences in BG response between the male and female T1DM rats were evident. Further, no differences in liver and muscle glycogen content following day 4 of exercise were seen between the sexes. These results would suggest that heightened E2 levels during proestrus may not be an important factor governing glucose counter regulatory response to exercise in female T1DM rats. Rather, the pre-exercise blood glucose levels are likely to be a large determinant of the blood glucose response to exercise in both male and female rats.