Mollugin activates GLP-1R to improve cognitive dysfunction in type 2 diabetic mice

  • Zhuanzhuan Wang
  • , Xin Cui
  • , Wenhui Yan
  • , Na Liu
  • , Jia Shang
  • , Xinyao Yi
  • , Tingli Guo
  • , Xiaotong Wei
  • , Yuzhuo Sun
  • , Hao Hu
  • , Weina Ma
  • , Wei Cui
  • , Lina Chen

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Aims: The incidence of diabetic cognitive dysfunction is increasing year by year, and it has gradually become a research hot spot. Studies have shown that glucagon-like peptide-1 receptor (GLP-1R) agonists can improve cognitive dysfunction in diabetic patients. This study focuses on whether small molecule GLP-1R agonists from traditional Chinese medicine (TCM) can improve the diabetic cognitive dysfunction. Materials and methods: The small molecules from TCM were screened by cell membrane chromatography (CMC) with GLP-1R-HEK293 cell membrane column. MTT assay, flow cytometry, immunofluorescence cytochemistry and other methods were used to determine the effects of mollugin on the apoptosis rate and reactive oxygen species (ROS) level of high glucose (HG)/hydrogen peroxide (H2O2) induced PC12 cells. Real-Time PCR was used to detect mRNA expression in mouse cerebral cortex. Water maze test was further used to confirm the effect of mollugin on cognitive dysfunction in T2DM mice. Key findings: Mollugin bound to GLP-1R, promoted Ca2+ influx, increased insulin secretion and cAMP content in β-TC-6 cells. Mollugin enhanced the cell viability, ameliorated apoptosis, reduced intracellular ROS levels in HG/H2O2-injured PC12 cells. Mollugin reduced the T2DM mice's escape latency, improved neuronal cell damage, decreased the expression of Pik3ca, Akt1 and Mapk1 mRNA in the cerebral cortex tissue. Significance: The results suggest that mollugin could improve cognitive dysfunction in T2DM mice through activating GLP-1R/cAMP/PKA signal pathway.

Original languageEnglish
Article number122026
JournalLife Sciences
Volume331
DOIs
StatePublished - 15 Oct 2023

Keywords

  • CMC
  • Cognitive dysfunction
  • Diabetes
  • GLP-1 receptor
  • Mollugin

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