Islets of Langerhans phenotype alterations induced by fatty diet and physical activity levels in Wistar rats

Nutrition. 2020 Nov-Dec:79-80:110838. doi: 10.1016/j.nut.2020.110838. Epub 2020 Apr 19.

Abstract

Objectives: Physical inactivity (PIn) and a fatty diet (FD) are closely linked to development of metabolic syndrome (MetS), overloading the endocrine pancreas seeking energy homeostasis. However, the relative contribution of FD and PIn to the pancreatic overload is unknown. The aim of this study was to verify the isolated and conjugated influence of FD and PIn in the islets of Langer hans (islets) structure and function related to overload in Wistar rats.

Methods: Male Wistar rats were divided into four groups (n = 10/group): active groups, fed with fat (AFD) or standard (ASD) diet; and physically inactive groups, fed with fat (SFD) or standard (SSD) diet for 21 wk. Glucose tolerance (GT) and insulin sensitivity (IS) were assessed before sacrifice. Retroperitoneal adipose tissue and pancreas were weighted (PW), and pancreas samples processed for histologic analyses.

Results: Only the FD-fed animals presented MS. Compared with standard diet, FD impaired GT and IS, decreased PW, and enlarged islets dimensions, with islets cellular death, inflammatory response, and enhanced collagen content, which were attenuated in AFD. Independent of the diet, PIn groups presented higher amounts of islets connective tissue, but without influence on inflammatory reaction and cellular death. The GT impairment was higher in the FD-fed groups, whereas the decreased IS was more pronounced in the PIn groups.

Conclusion: FD induced MS with detrimental effects on pancreas overload, inducing islets morphologic and functional maladaptation, which were attenuated in active animals. Physical activity was not able to prevent FD-induced MS. FD showed a negative influence on GT, whereas PIn mainly affected IS.

Keywords: Glucose tolerance; Histology; Inflammation; Insulin sensitivity; Metabolic syndrome; Pancreas overload.

MeSH terms

  • Animals
  • Diet
  • Insulin*
  • Islets of Langerhans*
  • Male
  • Phenotype
  • Rats
  • Rats, Wistar

Substances

  • Insulin