Effects of the 5-HT1C/5-5-HT2 receptor agonists DOI and alpha-methyl-5-HT on plasma glucose and insulin levels in the rat.

Abstract

Administration of the 5-HT1C/5-HT2 receptor agonist 1-(2,5-dimethoxy-4- iodophenyl)-2-aminopropane (DOI, 0.125-2.0 mg/kg i.v.) triggered dose-dependent increases in plasma glucose; plasma insulin levels remained unchanged. Pretreatment with the 5-HT1C/5-HT2 receptor antagonists LY 53857, ritanserin, or the mixed 5-HT2/alpha 1-adrenoceptor antagonist ketanserin either diminished or prevented the hyperglycemic effect of DOI (0.5 mg/kg). Administration of the mixed 5-HT1C receptor agonists/5-HT2 receptor antagonists 1-(3-chlorophenyl)-piperazine (mCPP) or 1-(3-trifluoromethyl)phenyl)piperazine level (TFMPP) did not affect plasma glucose levels. However, pretreatment with mCPP or TFMPP decreased DOI-induced hyperglycemia in a dose-dependent manner. The alpha 2-adrenoceptor antagonist idazoxan and the ganglionic blocker hexamethonium both decreased DOI-induced hyperglycemia, Whilst the alpha 1-adrenoceptor antagonist prazosin amplified the rise in plasma glucose elicited by DOI. The peripherally acting 5-HT1C/5-HT2 receptor agonist alpha-methyl-5-HT (0.5-1.0 mg/kg i.v.) triggered a rise in plasma glucose levels that was associated with an increase in plasma insulin levels. Pretreatment with LY 53857 diminished alpha-methyl-5-HT-induced hyperglycemia. These data indicate that 5-HT2 receptors, but not 5-HT1C receptors, and catecholaminergic systems, mediate DOI-induced hyperglycemia. Moreover, it is suggested that the inhibition of insulin release by DOI is centrally mediated, and that activation of peripheral 5-HT2 receptors may affect glycemia.

• Authors: F Chaouloff, D Laude, V Baudrie
• Journal: European journal of pharmacology (Eur J Pharmacol) Vol. 187 Issue 3 Pg. 435-43 (Oct 23 1990) ISSN: 0014-2999 [Print] Netherlands
• PMID: 2127400 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Amphetamines
• Blood Glucose
• Catecholamines
• Ergolines
• Insulin
• Piperazines
• Piperidines
• Receptors, Serotonin
• Ritanserin
• alpha-methylserotonin
• 1-(3-trifluoromethylphenyl)piperazine
• Serotonin
• 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid
• LY 53857
• 4-iodo-2,5-dimethoxyphenylisopropylamine

Topics

• Amphetamines (pharmacology)
• Animals
• Blood Glucose (metabolism)
• Catecholamines (blood)
• Ergolines (pharmacology)
• Hyperglycemia (blood, chemically induced)
• Insulin (blood)
• Male
• Piperazines (pharmacology)
• Piperidines (pharmacology)
• Rats
• Rats, Inbred Strains
• Receptors, Serotonin (drug effects)
• Ritanserin
• Serotonin (analogs & derivatives, pharmacology)