Metformin improves depressive-like behavior in experimental Parkinson's disease by inducing autophagy in the substantia nigra and hippocampus

Inflammopharmacology. 2022 Oct;30(5):1705-1716. doi: 10.1007/s10787-022-01043-6. Epub 2022 Aug 6.

Abstract

Parkinson's disease (PD) remains a disease of little known etiology. In addition to the motor symptoms, depression is present in about 40% of patients, contributing to the loss of quality of life. Recently, the involvement of the autophagy mechanism in the pathogenesis of depression has been studied, in addition to its involvement in PD as well. In this study, we tested the effects of metformin, an antidiabetic drug also with antidepressant effects, on depressive-like behavior in a rotenone-induced PD model and on the autophagy process. Mice 8-week-old male C57BL/6 were induced with rotenone for 20 consecutive days (2.5 mg/kg/day) and treated with metformin (200 mg/kg/day) from the 5th day of induction. All the animals were submitted to rotarod, sucrose preference and tail suspension tests. After euthanasia, the substantia nigra and hippocampus were removed for analysis by western blotting or fixed and analyzed by immunofluorescence. The results show that there was an impairment of autophagy in animals induced by rotenone both in nigral and extranigral regions as well as a depressive-like behavior. Metformin was able to inhibit depressive-like behavior and increase signaling pathway proteins, transcription factors and autophagosome-forming proteins, thus inducing autophagy in both the hippocampus and the substantia nigra. In conclusion, we show that metformin has an antidepressant effect in a rotenone-induced PD model, which may result, at least in part, from the induction of the autophagy process.

Keywords: Autophagy; Depression; Metformin; Parkinson’s disease; Rotenone.

MeSH terms

  • Animals
  • Antidepressive Agents / pharmacology
  • Autophagy
  • Disease Models, Animal
  • Hippocampus / metabolism
  • Hypoglycemic Agents / metabolism
  • Hypoglycemic Agents / pharmacology
  • Male
  • Metformin* / pharmacology
  • Mice
  • Mice, Inbred C57BL
  • Parkinson Disease* / drug therapy
  • Parkinson Disease* / metabolism
  • Quality of Life
  • Rotenone / pharmacology
  • Substantia Nigra
  • Sucrose / metabolism
  • Sucrose / pharmacology
  • Transcription Factors / metabolism
  • Transcription Factors / pharmacology

Substances

  • Antidepressive Agents
  • Hypoglycemic Agents
  • Transcription Factors
  • Rotenone
  • Sucrose
  • Metformin