Nesfatin-1 as a crucial mediator of glucose homeostasis in the reptile, Hemidactylus flaviviridis

Sci Rep. 2024 Dec 30;14(1):31565. doi: 10.1038/s41598-024-74371-y.

Abstract

Nesfatin-1 is a crucial regulator of energy homeostasis in mammals and fishes, however, its metabolic role remains completely unexplored in amphibians, reptiles, and birds. Therefore, present study elucidates role of nesfatin-1 in glucose homeostasis in wall lizard wherein fasting stimulated hepatic nucb2/nesfatin-1, glycogen phosphorylase (glyp), phosphoenolpyruvate carboxykinase (pepck), and fructose 1,6-bisphosphatase (fbp), while feeding upregulated pancreatic nucb2/nesfatin-1 and insulin, suggesting towards tissue-specific dual role of nesfatin-1 in glucoregulation. The glycogenolytic/gluconeogenic role of nesfatin-1 was further confirmed by an increase in media glucose levels along with heightened hepatic pepck and fbp expression and concomitant decline in liver glycogen content in nesfatin-1-treated liver of wall lizard. Moreover, treatment with nesfatin-1 stimulated insulin expression in pancreas while insulin downregulated pancreatic nucb2/nesfatin-1. Further, prolonged fasting induced elevated nucb2/nesfatin-1, and lipolytic markers, adipose triglyceride lipase (atgl) and monoglyceride lipase (mgl) in adipose tissue implicate nesfatin-1 in lipolysis which is substantiated by nesfatin-1-mediated direct upregulation of atgl and mgl. Our study provides the first comprehensive overview of tissue-dependent role of nesfatin-1 in regulating energy homeostasis in a reptile.

Keywords: Carbohydrate metabolism; Glucoregulation; Lipolysis; Nesfatin-1; Wall lizard.

MeSH terms

  • Animals
  • Calcium-Binding Proteins / metabolism
  • DNA-Binding Proteins / metabolism
  • Fasting / metabolism
  • Glucose* / metabolism
  • Homeostasis*
  • Insulin / metabolism
  • Liver / metabolism
  • Lizards* / metabolism
  • Nerve Tissue Proteins / metabolism
  • Nucleobindins* / metabolism
  • Pancreas / metabolism

Substances

  • Nucleobindins
  • Glucose
  • Insulin
  • DNA-Binding Proteins
  • Nerve Tissue Proteins
  • Calcium-Binding Proteins