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Effect of the activation of central 5-HT2C receptors by the 5-HT2C agonist mCPP on blood pressure and heart rate in rats.

Abstract
In the present study we investigated the role of central 5-HT2C receptors in the control of blood pressure and heart rate in non-stressed and stressed, adult, male, Wistar rats. Third ventricle injections of the 5-HT2C agonist mCPP elicited a significant increase in blood pressure in non-stressed animals. The initial period of this hypertensive response (10-30 min after mCPP administration) was accompanied by baroreflex-mediated bradycardia, while after this period the coexistence of hypertension and tachycardia was observed. These cardiovascular effects promoted by the central administration of mCPP were blocked by pretreatment with the 5-HT2C antagonist, SDZ SER 082. The administration of SDZ SER 082 alone induced no significant changes in blood pressure or heart rate. The pharmacological stimulation of central 5-HT2C receptors by mCPP did not change the hypertensive or tachycardic responses induced by restraint stress. Conversely, the blockade of central 5-HT2C receptors by SDZ SER 082 blunted stress-induced hypertension without modifying stress-induced tachycardia. It is concluded that the activation of central 5-HT2C receptors induces hypertension in non-stressed rats and that the normal function of these receptors is essential for the rise in blood pressure that occurs in the course of restraint stress.
AuthorsHilda Silva Ferreira, Elenilda Oliveira, Thiallan Nery Faustino, Emilio de Castro E Silva, Josmara Bartolomei Fregoneze
JournalBrain research (Brain Res) Vol. 1040 Issue 1-2 Pg. 64-72 (Apr 08 2005) ISSN: 0006-8993 [Print] Netherlands
PMID15804427 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Piperazines
  • Receptor, Serotonin, 5-HT2C
  • Serotonin 5-HT2 Receptor Agonists
  • Serotonin Receptor Agonists
  • 1-(3-chlorophenyl)piperazine
Topics
  • Animals
  • Blood Pressure (drug effects, physiology)
  • Heart Rate (drug effects, physiology)
  • Male
  • Piperazines (pharmacology)
  • Rats
  • Rats, Wistar
  • Receptor, Serotonin, 5-HT2C (metabolism)
  • Serotonin 5-HT2 Receptor Agonists
  • Serotonin Receptor Agonists (pharmacology)

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