Effects of menstrual cycle and race on peripheral vascular α-adrenergic responsiveness

Robert R. Freedman, Reda Girgis

Research output: Contribution to journalArticlepeer-review

63 Scopus citations

Abstract

Gender differences in the incidence of many cardiovascular diseases may be due to the effects of sex hormones. Both α1- and α2-adrenergic receptors produce vasoconstriction in peripheral blood vessels and have demonstrated gender effects in previous studies. In addition, race has been shown to influence the effects of some α-adrenergic stimuli. We therefore sought to determine the effects of the menstrual cycle and race on peripheral blood flow responses to the intra-arterial infusion of phenylephrine (α1- agonist) and clonidine (α2-agonist). Ten white and 8 black women were studied during the early luteal phase and the follicular phase; these phases were verified in each woman through measurements of plasma estradiol and progesterone. Plasma norepinephrine was measured with HPLC. During phenylephrine infusion, there was significantly greater vasoconstriction in the luteal phase versus the follicular phase (P<0.05). There were no differences (P>0.8) between white and black women. During clonidine infusion, white women showed significantly more vasoconstriction in the follicular phase than during the luteal phase (P<0.006). For black women, the responses for both phases did not differ (P>0.9). Blood pressures were significantly higher in the black women (diastolic P<0.005, systolic P<0.05). The luteal- phase elevation of α1-adrenergic responses may be due to elevated levels of estradiol, progesterone, or both. The lack of luteal-phase reduction in α2- adrenergic vasoconstriction in black women may contribute to their increased pressor responses to adrenergic stimuli.

Original languageEnglish (US)
Pages (from-to)795-799
Number of pages5
JournalHypertension
Volume35
Issue number3
DOIs
StatePublished - Mar 2000
Externally publishedYes

Keywords

  • Blacks
  • Blood flow
  • Estrogen
  • Gender
  • Norepinephrine
  • Race
  • Receptors, adrenergic, alpha

ASJC Scopus subject areas

  • Internal Medicine

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