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Benzodiazepine receptors modulate circulating plasma vasopressin concentration
Brain Research
|December 16, 1985
Summary
Chlordiazepoxide, a benzodiazepine, reduced basal arginine-vasopressin (AVP) levels and blunted picrotoxin-induced AVP and blood pressure increases. These effects were blocked by RO 15-1788, indicating benzodiazepine receptor involvement.
Area of Science:
- Neuropharmacology
- Endocrinology
Background:
- Benzodiazepines are known to modulate neuronal activity.
- Arginine-vasopressin (AVP) plays a role in cardiovascular regulation and stress responses.
Purpose of the Study:
- To investigate the role of benzodiazepine receptors in regulating basal and evoked plasma AVP levels.
- To examine the effects of chlordiazepoxide on cardiovascular parameters and AVP release.
Main Methods:
- Administration of chlordiazepoxide or saline pretreatment in spinal animals.
- Picrotoxin challenge to induce changes in plasma AVP and blood pressure.
- Administration of RO 15-1788, a benzodiazepine receptor antagonist, to block chlordiazepoxide effects.
Main Results:
- Chlordiazepoxide pretreatment significantly decreased basal plasma AVP levels.
- Chlordiazepoxide attenuated picrotoxin-induced increases in plasma AVP and blood pressure.
- RO 15-1788 administration blocked the effects of chlordiazepoxide on both basal and evoked AVP levels and blood pressure.
Conclusions:
- Benzodiazepine receptor interactions significantly influence basal plasma AVP concentrations.
- Benzodiazepine receptors modulate the release of AVP in response to stimuli like picrotoxin.
- These findings highlight a link between benzodiazepine receptor activity and the neuroendocrine regulation of AVP.