Progesterone treatment reduces food intake and body weight in ovariectomized female rats

Steroids. 2024 Mar:203:109367. doi: 10.1016/j.steroids.2024.109367. Epub 2024 Jan 23.

Abstract

While the effects of progesterone on body weight and appetite in pre-menopausal conditions have been well elucidated, its effects in post-menopausal conditions have not been clarified. On the contrary, the effects of estrogen on body weight and appetite in post-menopausal conditions have been well established. In this study, the effects of progesterone treatment on body weight, appetite, and fat mass in ovariectomized rats were evaluated. In addition, the central and/or peripheral levels of oxytocin (OT), leptin, and their receptors, which are potent anorectic factors, were examined. Female rats were ovariectomized and divided into control, progesterone-treated, and estrogen-treated groups. Body weight, food intake, and subcutaneous fat mass were lower in both the progesterone and estrogen groups than in the control group. The estrogen group exhibited higher serum OT levels than the control group, whereas the OT levels of the progesterone and control groups did not differ. The serum leptin levels of both the progesterone and estrogen groups were lower than those of the control group. Gene expression analysis of OT, leptin, and their receptors in the hypothalamus and adipose tissue found few significant differences among the groups. Hypothalamic neuropeptide Y (NPY) and pro-opiomelanocortin (POMC) mRNA levels involved in appetite regulation were slightly altered in the progesterone and estrogen groups. These findings suggest that progesterone treatment may have favorable effects on body weight, appetite, and fat mass regulation in post-menopausal conditions and that the mechanisms underlying these effects of progesterone differ from those underlying the effects of estrogen.

Keywords: NPY; Oxytocin; POMC; Progesterone.

MeSH terms

  • Animals
  • Body Weight
  • Carrier Proteins
  • Eating
  • Estrogens / metabolism
  • Estrogens / pharmacology
  • Female
  • Hypothalamus
  • Leptin* / metabolism
  • Pro-Opiomelanocortin / genetics
  • Pro-Opiomelanocortin / metabolism
  • Pro-Opiomelanocortin / pharmacology
  • Progesterone* / metabolism
  • Progesterone* / pharmacology
  • Rats

Substances

  • Leptin
  • Progesterone
  • Carrier Proteins
  • Estrogens
  • Pro-Opiomelanocortin