Nucleus incertus contributes to an anxiogenic effect of buspirone in rats: Involvement of 5-HT1A receptors

NEUROPHARMACOLOGY

卷:110

Article

Kumar, Jigna Rajesh^1,2,3,4  Rajkumar, Ramamoorthy^1,2,3  Lee, Liying Corinne^1,2,3  Dawe, Gavin S.^1,2,3,4 

[1] Natl Univ Singapore, Natl Univ Hlth Syst, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore 117600, Singapore

[2] Natl Univ Singapore, Inst Life Sci, Neurobiol & Ageing Programme, Singapore 117456, Singapore

[3] Singapore Inst Neurotechnol SINAPSE, Singapore 117456, Singapore

[4] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn NGS, Singapore 117456, Singapore

关键词: Buspirone;    Nucleus incertus;    Anxiogenic;    5-HT1A receptors;    D-2 receptors;   

DOI  :  10.1016/j.neuropharm.2016.07.019

来源: Elsevier

【 摘 要 】

The nucleus incertus (NI), a brainstem structure with diverse anatomical connections, is implicated in anxiety, arousal, hippocampal theta modulation, and stress responses. It expresses a variety of neurotransmitters, neuropeptides and receptors such as 5-HT1A, D-2 and CRF1 receptors. We hypothesized that the NI may play a role in the neuropharmacology of buspirone, a clinical anxiolytic which is a 5-HT1A receptor partial agonist and a D-2 receptor antagonist. Several preclinical studies have reported a biphasic anxiety-modulating effect of buspirone but the precise mechanism and structures underlying this effect are not well-understood. The present study implicates the NI in the anxiogenic effects of a high dose of buspirone. Systemic buspirone (3 mg/kg) induced anxiogenic effects in elevated plus maze, light-dark box and open field exploration paradigms in rats and strongly activated the NI, as reflected by c-Fos expression. This anxiogenic effect was reproduced by direct infusion of buspirone (5 mu g) into the NI, but was abolished in NI-CRF-saporin-lesioned rats, indicating that the NI is present in neural circuits driving anxiogenic behaviour. Pharmacological studies with NAD 299, a selective 5-HT1A antagonist, or quinpirole, a D-2/D-3 agonist, were conducted to examine the receptor system in the NI involved in this anxiogenic effect. Opposing the 5-HT1A agonism but not the D-2 antagonism of buspirone in the NI attenuated the anxiogenic effects of systemic buspirone. In conclusion, 5-HT1A receptors in the NI contribute to the anxiogenic effect of an acute high dose of buspirone in rats and may be functionally relevant to physiological anxiety. (C) 2016 The Authors. Published by Elsevier Ltd.

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