The Effect of Different Exercise Modalities on Sertoli-germ Cells Metabolic Interactions in High-fat Diet-induced Obesity Rat Models: Implication on Glucose and Lactate Transport, Igf1, and Igf1R-dependent Pathways

Reprod Sci. 2024 Aug;31(8):2246-2260. doi: 10.1007/s43032-024-01533-8. Epub 2024 Apr 17.

Abstract

The study aimed to uncover a unique aspect of obesity-related metabolic disorders in the testicles induced by a high-fat diet (HFD) and explored the potential mitigating effects of exercise modalities on male fertility. Thirty mature male Wistar rats were randomly assigned to control, HFD-sole, moderate-intensity exercise with HFD (HFD+MICT), high-intensity continuous exercise with HFD (HFD+HICT), and high-intensity interval exercise with HFD (HFD+HIIT) groups (n=6/group). Intracytoplasmic carbohydrate (ICC) storage, expression levels of GLUT-1, GLUT-3, MCT-4, Igf1, and Igf1R, and testicular lactate and lactate dehydrogenase (LDH) levels were assessed. ICC storage significantly decreased in HFD-sole rats, along with decreased mRNA and protein levels of GLUT-1, GLUT-3, MCT-4, Igf1, and Igf1R. The HFD-sole group exhibited a notable reduction in testicular lactate and LDH levels (p<0.05). Conversely, exercise, particularly HIIT, upregulated ICC storage, expression levels of GLUT-1, GLUT-3, MCT-4, Igf1, and Igf1R, and enhanced testicular lactate and LDH levels. These results confirm that exercise, especially HIIT, has the potential to mitigate the adverse effects of HFD-induced obesity on testicular metabolism and male fertility. The upregulation of metabolite transporters, LDH, lactate levels, Igf1, and Igf1R expression may contribute to maintaining metabolic interactions and improving the glucose/lactate conversion process. These findings underscore the potential benefits of exercise in preventing and managing obesity-related male fertility issues.

Keywords: Exercise; High-fat diet; Metabolic interactions; Spermatogenesis.

MeSH terms

  • Animals
  • Diet, High-Fat* / adverse effects
  • Disease Models, Animal
  • Glucose* / metabolism
  • Insulin-Like Growth Factor I* / metabolism
  • Lactic Acid / metabolism
  • Male
  • Obesity* / metabolism
  • Physical Conditioning, Animal* / physiology
  • Rats
  • Rats, Wistar*
  • Receptor, IGF Type 1* / metabolism
  • Sertoli Cells* / metabolism
  • Signal Transduction
  • Testis / metabolism

Substances

  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1
  • insulin-like growth factor-1, rat
  • Glucose
  • Igf1r protein, rat
  • Lactic Acid