Protective effects of combining SERMs with estrogen on metabolic parameters in postmenopausal diabetic cardiovascular dysfunction: The role of cytokines and angiotensin II

Steroids. 2022 Jul:183:109023. doi: 10.1016/j.steroids.2022.109023. Epub 2022 Mar 28.

Abstract

Introduction: The beneficial effects of the administration of selective estrogen receptor modulators (SERMs) and estrogen (E2), alone or in combination with each other, have been reported in postmenopausal diabetic cardiovascular dysfunction. In the present study, we determined the mechanism of action of SERMs and E2 on inflammatory balance, angiotensin II (Ang II) serum levels, and glycemic profile in a postmenopausal diabetic rat model.

Methods: Ovariectomized rats with type 2 diabetes received daily SERMs (tamoxifen and raloxifene) and E2 for one month. After treatment, cardiovascular risk indices, glycemic profile, and serum Ang II, TNF-α and IL-10 levels were measured.

Results: Type 2 diabetes caused an abnormal glycemic profile, which was exacerbated by ovariectomy. All treatments inhibited the effects of diabetes and ovariectomy on the glycemic profile, with combined treatments (SERMs + E2) showing stronger effects. Cardiovascular risk indices that became abnormal by diabetes and worsened by ovariectomy were improved in all treatment modalities. Also, combined treatment reduced serum Ang II, TNF-α, and the ratio of TNF-α to IL-10, indicating an improvement in inflammatory balance.

Conclusion: Our study showed the administration of SERMs and E2, alone or in combination, could be an effective alternative in the treatment of menopausal diabetes, and generally, the beneficial effects of combined treatments were more effective than the effects of E2 or SERMs alone. It appears that E2 or SERMs benefit the cardiovascular system by improving inflammatory balance and reducing Ang II levels.

Keywords: Angiotensin II; Cytokines; Estrogen; Raloxifene; Tamoxifen; Type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II
  • Animals
  • Cytokines
  • Diabetes Mellitus, Type 2* / complications
  • Diabetes Mellitus, Type 2* / drug therapy
  • Estrogens / metabolism
  • Female
  • Interleukin-10
  • Postmenopause
  • Raloxifene Hydrochloride / pharmacology
  • Rats
  • Selective Estrogen Receptor Modulators* / pharmacology
  • Tamoxifen / pharmacology
  • Tumor Necrosis Factor-alpha

Substances

  • Cytokines
  • Estrogens
  • Selective Estrogen Receptor Modulators
  • Tumor Necrosis Factor-alpha
  • Tamoxifen
  • Angiotensin II
  • Interleukin-10
  • Raloxifene Hydrochloride