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Progesterone rapidly reduces arterial pressure in ewes
1Department of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville 32610-0487, USA.
The American Journal of Physiology
|January 1, 1997
Summary
Progesterone rapidly lowers blood pressure (MAP) in ewes at pregnancy-mimicking levels, suggesting a non-genomic mechanism. Higher doses did not affect MAP, indicating complex progesterone actions.
Area of Science:
- Reproductive endocrinology
- Cardiovascular physiology
- Neuroendocrinology
Background:
- Chronic progesterone treatment lowers mean arterial pressure (MAP) and expands plasma volume.
- Progesterone metabolites may exert rapid, non-genomic effects on the baroreflex.
- Understanding these rapid effects is crucial for comprehending progesterone's physiological roles.
Purpose of the Study:
- To investigate the rapid effects of progesterone on MAP, sodium levels, arginine vasopressin, and baroreflex sensitivity in ewes.
- To determine if progesterone's effects are dose-dependent and mediated by non-genomic mechanisms.
- To explore potential interactions between progesterone and the baroreflex under physiological and supraphysiological conditions.
Main Methods:
- Ewes received 2-hour infusions of vehicle or progesterone at 3 or 6 µg/kg/min.
- Measurements included MAP, plasma Na+, arginine vasopressin, and baroreflex sensitivity.
- Analysis focused on rapid changes occurring within minutes of infusion initiation.
Main Results:
- Progesterone infusion at 3 µg/kg/min, mimicking ovine pregnancy levels, significantly reduced MAP by 17 minutes.
- This rapid reduction suggests a non-genomic mechanism of action.
- Progesterone at 6 µg/kg/min (supraphysiological) did not alter MAP, and overall baroreflex sensitivity remained unchanged.
- A trend towards attenuated tachycardic response to hypotension was observed at the higher dose.
Conclusions:
- Progesterone can rapidly decrease MAP via non-genomic pathways at physiologically relevant concentrations.
- The lack of a linear dose-response suggests complex interactions involving multiple progesterone receptor populations.
- Further research is needed to elucidate the specific mechanisms and receptor subtypes involved in progesterone's rapid cardiovascular effects.