Pharmacological reactivity of resistance vessels in a rat PCOS model – vascular effects of parallel vitamin D₃ treatment

Abstract

The aim of this study was to clarify the effects of dihydrotestosterone (DHT)-induced polycystic ovary syndrome (PCOS) on pharmacological reactivity of a resistance vessel in a rat model and the possible modulatory role of 1,25-(OH)₂-cholecalciferol (vitamin D₃). The PCOS model was induced in adolescent female Wistar rats by a 10-week DHT treatment. Norepinephrine induced contractility and acetylcholine relaxation were tested in arterioles by pressure arteriography in control as well as DHT- and DHT plus vitamin D₃-treated (DHT+D3) animals. Decreased vasoconstriction and dilatation were detected after DHT treatment. Concomitant vitamin D₃ treatment increased the contractile response and resulted in more relaxed vessels. Endothelial dilation tested with acetylcholine was lower after DHT treatment, this effect was not depend on vitamin D₃ supplementation. In conclusion, hyperandrogenic state resulted in reduced endothelium- and smooth muscle-dependent vasorelaxation and constriction with a complete loss of nitric oxide (NO)-dependent relaxation compared with controls. These alterations caused by chronic DHT treatment were partially reversed by concomitant vitamin D₃ administration.

Keywords::

• Dihydrotestosterone
• NO
• PCOS
• relaxation
• vitamin D

Acknowledgments

The authors wish to express their gratitude to Mrs. Ildikó Murányi for her devoted efforts in solving the technical problems in the laboratory work.

Declaration of Interest: This study was sponsored by a research grant from the Hungarian Society of Hypertension. The authors declared no conflict of interest.