Vitamin D Deficiency and Gender Alter Vasoconstrictor and Vasodilator Reactivity in Rat Carotid Artery

Int J Mol Sci. 2021 Jul 27;22(15):8029. doi: 10.3390/ijms22158029.

Abstract

The vitamin-D-sensitivity of the cardiovascular system may show gender differences. The prevalence of vitamin D (VD) deficiency (VDD) is high, and it alters cardiovascular function and increases the risk of stroke. Our aim was to investigate the vascular reactivity and histological changes of isolated carotid artery of female and male rats in response to different VD supplies. A total of 48 male and female Wistar rats were divided into four groups: female VD supplemented, female VDD, male VD supplemented, male VDD. The vascular function of isolated carotid artery segments was examined by wire myography. Both vitamin D deficiency and male gender resulted in increased phenylephrine-induced contraction. Acetylcholine-induced relaxation decreased in male rats independently from VD status. Inhibition of prostanoid signaling by indomethacin reduced contraction in females, but increased relaxation ability in male rats. Functional changes were accompanied by VDD and gender-specific histological alterations. Elastic fiber density was significantly decreased by VDD in female rats, but not in males. Smooth muscle actin and endothelial nitric oxide synthase levels were significantly lowered, but the thromboxane receptor was elevated in VDD males. Decreased nitrative stress was detected in both male groups independently from VD supply. The observed interactions between vitamin D deficiency and sex may play a role in the gender difference of cardiovascular risk.

Keywords: cardiovascular disease; carotid artery; gender; prostanoid pathway; rat model; vascular reactivity; vitamin D; vitamin D deficiency.

MeSH terms

  • Animals
  • Carotid Arteries / metabolism
  • Carotid Arteries / physiopathology*
  • Female
  • Male
  • Rats
  • Rats, Wistar
  • Sex Characteristics*
  • Vasoconstriction*
  • Vasodilation*
  • Vitamin D Deficiency / metabolism
  • Vitamin D Deficiency / physiopathology*