Transcriptomic changes in the hypothalamus of ovariectomized mice: Data from RNA-seq analysis

Ann Anat. 2022 Apr:241:151886. doi: 10.1016/j.aanat.2022.151886. Epub 2022 Jan 12.

Abstract

Background: Menopausal symptoms can affect the physical and mental health of females and are often related to abnormal function of the hypothalamus. In this study, we evaluated changes in the hypothalamus transcriptome in ovariectomized mice to identify key mRNAs, and systematically elucidated the possible molecular mechanisms underlying the menopausal syndrome to provide a theoretical basis for clinical diagnosis and treatment.

Methods: Forty-six adult female C57BL/6 J mice were randomly divided into SHAM and OVX groups, 23 mice per group. Eight weeks after the procedure, differentially expressed genes (DEGs) in the hypothalamus were identified through RNA-sequencing. DEGs were analyzed using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genome (KEGG) analyses. Key DEGs were then evaluated using quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and immunohistochemical staining.

Results: Compared with SHAM group, 7295 genes were upregulated, and 8979 genes were downregulated in the hypothalamus of OVX mice with a fold change of 1.5 (log2 fold change ≥0.585). GO and KEGG analyses suggested these key genes were involved in thermoregulation, food intake, glucose and lipid metabolism, cardiovascular regulation, biological rhythm, and endocrine regulation.

Conclusions: Differential expression of genes in the hypothalamus of OVX mice involved in thermoregulation, eating, sleeping, homeostasis, and endocrine regulation 8 weeks after ovariectomy suggest potential roles in the pathogenesis of climacteric syndrome.

Keywords: Food intake; Hot flush; Menopause; Obesity; Ovariectomy; RNA-seq; Thermoregulation.

Publication types

  • Randomized Controlled Trial, Veterinary

MeSH terms

  • Animals
  • Female
  • Gene Expression Profiling*
  • Hypothalamus
  • Mice
  • Mice, Inbred C57BL
  • Sequence Analysis, RNA
  • Transcriptome*