Geniposide prevents rotenone-induced apoptosis in primary cultured neurons.

Lin Li, Juan Zhao, Ke Liu, Guang-Lai Li, Yan-Qing Han, Yue-Ze Liu
Author Information
  1. Lin Li: Key Laboratory of Cellular Physiology, Shanxi Medical University, Taiyuan, Shanxi Province, China.
  2. Juan Zhao: Key Laboratory of Cellular Physiology, Shanxi Medical University, Taiyuan, Shanxi Province, China.
  3. Ke Liu: Key Laboratory of Cellular Physiology, Shanxi Medical University, Taiyuan, Shanxi Province, China.
  4. Guang-Lai Li: Second Hospital, Shanxi Medical University, Taiyuan, Shanxi Province, China.
  5. Yan-Qing Han: Second Hospital, Shanxi Medical University, Taiyuan, Shanxi Province, China.
  6. Yue-Ze Liu: Second Hospital, Shanxi Medical University, Taiyuan, Shanxi Province, China. ORCID

Abstract

Geniposide, a monomer extracted from gardenia and widely used in Chinese medicine, is a novel agonist at the glucagon-like peptide-1 receptor. This receptor is involved in neuroprotection. In the present study, we sought to identify an anti-apoptotic mechanism for the treatment of neurodegenerative diseases. Primary cultured neurons were treated with different concentrations of rotenone for 48 hours. Morphological observation, cell counting kit-8 assay, lactate dehydrogenase detection and western blot assay demonstrated that 0.5 nM rotenone increased lactate dehydrogenase release, decreased the expression of procaspase-3 and Bcl-2, and increased cleaved caspase-3 expression in normal neurons. All these effects were prevented by geniposide. Our results indicate that geniposide diminished rotenone-induced injury in primary neurons by suppressing apoptosis. This may be one of the molecular mechanisms underlying the efficacy of geniposide in the treatment of neurodegenerative diseases.

Keywords

References

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