The Tricyclic Antidepressant Clomipramine Increases Plasma Glucose Levels of Mice

ABSTRACT: Effects of the tricyclic antidepressant clomipramine on plasma glucose levels in mice were studied. Clomipramine at doses ranging 5 - 20 mg/kg elicited significant hyperglycemia in mice. Hyperglycemia elicited by clomipramine was not reduced by pretreatment with the 5-hydroxytryptamine (5-...

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Main Authors: Yumi Sugimoto (Author), Kiyo Inoue (Author), Jun Yamada (Author)
Format: Book
Published: Elsevier, 2003-01-01T00:00:00Z.
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Summary:ABSTRACT: Effects of the tricyclic antidepressant clomipramine on plasma glucose levels in mice were studied. Clomipramine at doses ranging 5 - 20 mg/kg elicited significant hyperglycemia in mice. Hyperglycemia elicited by clomipramine was not reduced by pretreatment with the 5-hydroxytryptamine (5-HT) depleter p-chlorophenylalanine. The 5-HT1/2/5/7-receptor antagonist methysergide and the 5-HT2A/2B/2C-receptor antagonist LY 53857 enhanced clomipramine-induced hyperglycemia, while the 5-HT1A/1B-receptor antagonist (-)-propranolol and the 5-HT3/4-receptor antagonist tropisetron did not affect it. The 5-HT2B/2C-receptor antagonist SB 206553 facilitated hyperglycemia induced by clomipramine, although the 5-HT2A-receptor antagonist ketanserin was without effect. Clomipramine-induced hyperglycemia was reduced by prior adrenalectomy. These results suggest that clomipramine induces hyperglycemia in mice by blocking the 5-HT2B and/or 5-HT2C receptors, which results in facilitation of adrenaline release.
Item Description:1347-8613
10.1254/S1347-8613(19)32618-0