Progesterone increases blood pressure in spontaneous gestational hypertension in rats

Leslie C. Sharkey, Sharon Kirchain, Sylvia A. McCune, Gregory I.C. Simpson, Elizabeth Z. Archambault, Naomi K. Boatright, Erin Hicks, John Fray

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Gestational hypertensive disorders are a leading cause of maternal mortality in the US, accounting for up to 10% of these deaths. During pregnancy, a new rat model (SHHF rat) has been shown to develop spontaneous hypertension with increases of more than 40 mm Hg systolic blood pressure (BP), which resolves after delivery, and which lead us to ask whether the hypertension may be triggered by increased levels of progesterone in these rats. To test this hypothesis, groups of SHHF rats were treated with progesterone (PROG), estrogen (EST), or progesterone and estrogen (PROG+EST) that correspond to levels that occur during pregnancy. Control (CON) rats received saline-filled implants and pseudopregnancy was induced in another group. Wistar-Kyoto rats served as controls for SHHF rats. By experimental day 3, progesterone caused a significantly higher systolic BP, similar to pseudopregnancy and to previously reported values during pregnancy in this strain. Blood pressure in SHHF rats given estrogen was not significantly different. RU486 reversibly prevented the increase in BP induced by progesterone. These results indicate that an anomalous response to progesterone causes dramatic increases in BP in SHHF rats during a short period of time, in contrast to the decrease in BP in response to progesterone, which has been reported in other rat models of hypertension. An abnormal pressor response to progesterone should be considered a potential mechanism contributing to the development of hypertension during pregnancy.

Original languageEnglish (US)
Pages (from-to)36-43
Number of pages8
JournalAmerican journal of hypertension
Volume18
Issue number1
DOIs
StatePublished - Jan 2005

Keywords

  • RU486
  • SHHF rat
  • intrauterine growth restriction
  • kidney and pseudopregnancy
  • preeclampsia
  • pregnancy-induced hypertension

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