Oxytocin antagonist disrupts hypotension-evoked renin secretion and other responses in conscious rats
1Department of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
Abstract:
Previous experiments have indicated that arterial hypotension increases plasma oxytocin (OT) levels in rats and that OT infused intravenously causes an increase in plasma renin activity (PRA). The goal of the present study was to determine whether systemic administration of an OT receptor antagonist would attenuate the increase in PRA that is normally evoked by arterial hypotension in rats. In conscious male rats, intravenous injection of hydralazine or diazoxide produced sustained hypotension and evoked a significant increase in PRA, as expected. Intravenous infusion of an OT receptor antagonist did not alter the hypotension induced by hydralazine or diazoxide, but it did markedly blunt the induced increase in PRA. The OT receptor antagonist also blunted the hypotension-evoked increase in heart rate and plasma vasopressin levels, suggesting that the antagonist may have generally disrupted afferent signaling of hypotension. Thus hypotension-evoked OT secretion may contribute to cardiovascular homeostasis by enhancing baroreceptor signals that stimulate increases in renin secretion, vasopressin secretion, and heart rate during arterial hypotension in rats.
Insights
Arterial hypotension increases oxytocin (OT) levels, which may help maintain cardiovascular homeostasis. Blocking OT receptors blunts the rise in renin activity and other responses to hypotension in rats.
Area of Science:
- Cardiovascular Physiology
- Endocrinology
- Renal Physiology
Background:
- Arterial hypotension is known to increase plasma oxytocin (OT) levels in rats.
- Intravenous OT infusion can elevate plasma renin activity (PRA).
Purpose of the Study:
- To investigate if blocking oxytocin receptors attenuates the increase in plasma renin activity during arterial hypotension in rats.
Main Methods:
- Conscious male rats were subjected to hypotension using hydralazine or diazoxide.
- An oxytocin receptor antagonist was administered intravenously.
- Plasma renin activity, heart rate, and vasopressin levels were measured.
Main Results:
- Hypotension induced by hydralazine or diazoxide significantly increased PRA.
- The oxytocin receptor antagonist blunted the increase in PRA without affecting the induced hypotension.
- The antagonist also reduced hypotension-evoked increases in heart rate and plasma vasopressin.
Conclusions:
- Hypotension-evoked oxytocin secretion may contribute to cardiovascular homeostasis.
- Oxytocin might enhance baroreceptor signals, stimulating renin, vasopressin, and heart rate responses during hypotension.
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