Genipin improves lipid metabolism and sperm parametersin obese mice via regulation of miR-132 expression

Acta Biochim Biophys Sin (Shanghai). 2022 Sep 25;54(9):1278-1288. doi: 10.3724/abbs.2022120.

Abstract

Obesity has now surpassed malnutrition and infectious diseases as the most significant contributor to health problems worldwide. In particular, obesity is associated with several metabolic disorders, including hyperlipidemia, hepatic steatosis, and subfertility. Genipin (GNP), the aglycone of geniposide, is isolated from the extract of the traditional Chinese medicine Gardenia jasminoides Ellis and has been used in traditional oriental medicine against several inflammation-driven diseases. However, the effect and molecular mechanism of GNP on obesity-associated dyslipidemia and sperm dysfunction still need to be explored. In this study, we detect the effects of GNP on hyperlipidemia, hepatic lipid accumulation and sperm function using a high-fat diet (HFD)-induced obese mouse model. We find that obese mice treated with GNP show an improvement in body weight, serum triglyceride levels, serum hormone levels, serum inflammatory cytokines, hepatic steatosis and sperm function. At the molecular level, HFD/GNP diversely regulates the expression of miR-132 in a tissue-specific manner. miR-132 further targets and regulates the expression of SREBP-1c in liver cells, as well as the expressions of SREBP-1c and StAR in Leydig cells in the testis, thus modifying lipogenesis and steroidogenesis, respectively. Collectively, our data demonstrate that GNP shows a broad effect on the improvement of HFD-induced metabolic disorder and sperm dysfunction in male mice by tissue-specific regulation of miR-132. Our findings reveal the function GNP in ameliorating hepatic lipid metabolism and sperm function and suggest that this compound is a versatile drug to treat metabolic disorders.

Keywords: genipin; metabolic disorder; miR-132; obesity; sperm function.

MeSH terms

  • Animals
  • Diet, High-Fat / adverse effects
  • Fatty Liver* / chemically induced
  • Fatty Liver* / metabolism
  • Hyperlipidemias* / metabolism
  • Lipid Metabolism
  • Liver / metabolism
  • Male
  • Metabolic Diseases* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • MicroRNAs* / metabolism
  • Obesity / drug therapy
  • Obesity / metabolism
  • Semen / metabolism
  • Spermatozoa / metabolism
  • Sterol Regulatory Element Binding Protein 1 / metabolism

Substances

  • genipin
  • Sterol Regulatory Element Binding Protein 1
  • MicroRNAs
  • MIRN132 microRNA, mouse

Grants and funding

This work was supported by the grants from the National Natural Science Foundation of China (No. 32171407), the Development Project of Jiangsu Province TCM Science and Technology (No. YB2020024), and the Priority Academic Program Development of Jiangsu Higher Education Institutions.