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Effects of monoamine receptor antagonists on nicotine-induced hypophagia in the rat
(−)-Nicotine, in doses of 0.2–0.6 mg/kg intraperitoneally (i.p.), induced a dose-dependent anorexia 1 h, 2 h and 4 h after food presentation in 20-h food-restricted male rats. The anorectic response of nicotine (0.4 mg/kg, 30 min before the test) was prevented by pretreatment with the central nicoti...
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Published in: | European journal of pharmacology 1997-02, Vol.321 (2), p.157-162 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | (−)-Nicotine, in doses of 0.2–0.6 mg/kg intraperitoneally (i.p.), induced a dose-dependent anorexia 1 h, 2 h and 4 h after food presentation in 20-h food-restricted male rats. The anorectic response of nicotine (0.4 mg/kg, 30 min before the test) was prevented by pretreatment with the central nicotine receptor antagonist mecamylamine (0.5 and 1 mg/kg). The peripheral nicotine receptor antagonist hexamethonium (5 and 10 mg/kg), the muscarinic receptor antagonist atropine (5 and 10 mg/kg), the dopamine D
2 receptor antagonist pimozide (0.5 and 1 mg/kg), the dopamine D
1 receptor antagonist SCH23390 (
R-(+)-8-chloro-2,3,4,5-tetrahydro-3-methyl-5-phenyl-1
H-3-benzazepine-7ol maleate; 0.05 and 0.1 mg/kg), the α-adrenoceptor antagonist phenoxybenzamine (5 and 10 mg/kg), and the β-adrenoceptor antagonist propranolol (5 and 10 mg/kg) amplified the nicotine response while promoting anorexia by themselves. The dopamine D
2 receptor antagonist sulpiride (25, 50 and 100 mg/kg) increased food intake and amplified the anorectic effect of nicotine. The 5-HT receptor antagonists metergoline (0.5 and 1 mg/kg) and mianserin (1 and 2 mg/kg) increased the nicotine effect. When the antagonists were used alone, metergoline did not change food intake, while mianserin increased food intake. It can be concluded that part of nicotine-induced anorexia is mediated through central nicotinic receptors. |
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ISSN: | 0014-2999 1879-0712 |
DOI: | 10.1016/S0014-2999(96)00935-1 |