Fink Klaus B, Göthert Manfred
Department of Pharmacology, Bonn University Clinic, Reuterstr. 2b, 53113 Bonn, Germany.
Pharmacol Rev. 2007 Dec;59(4):360-417. doi: 10.1124/pr.107.07103.
Serotoninergic neurons in the central nervous system impinge on many other neurons and modulate their neurotransmitter release. This review focuses on 1) the function of presynaptic 5-hydroxytryptamine (5-HT) heteroreceptors on axon terminals of central cholinergic, dopaminergic, noradrenergic, or GABAergic neurons and 2) the role of GABAergic interneurons expressing 5-HT heteroreceptors in the regulation of acetylcholine, dopamine, or noradrenaline release. In vitro studies on slices or synaptosomes and in vivo microdialysis experiments have shown that 5-HT(1A), 5-HT(1B), 5-HT(2A), 5-HT(2C), 5-HT(3), and/or 5-HT(4) heteroreceptors mediate this modulation. 5-HT(1B) receptors on neocortical cholinergic, striatal dopaminergic, or hippocampal GABAergic axon terminals are examples for release-inhibiting 5-HT heteroreceptors; 5-HT(3) receptors on hippocampal GABAergic or 5-HT(4) receptors on hippocampal cholinergic axon terminals are examples for release-facilitating 5-HT heteroreceptors. GABA released from GABAergic interneurons upon activation of facilitatory 5-HT receptors, e.g., 5-HT(2A) or 5-HT(3) receptors, mediates inhibition of the release of other neurotransmitters such as prefrontal neocortical dopamine or neocortical acetylcholine release, respectively. Conversely, attenuated GABA release in response to activation of inhibitory 5-HT heteroreceptors, e.g., 5-HT(1A) or 5-HT(1B) receptors on GABAergic interneurons is involved in paradoxical facilitation of hippocampal acetylcholine and striatal dopamine release, respectively. Such 5-HT heteroreceptors are considered potential targets for appropriate 5-HT receptor ligands which, by enhancing the release of a relevant neurotransmitter, can compensate for its hypothesized deficiency in distinct brain areas. Examples for such deficiencies are the impaired release of hippocampal or neocortical acetylcholine, striatal dopamine, and hippocampal or neocortical noradrenaline in disorders such as Alzheimer's disease, Parkinson's disease, and major depression, respectively.
中枢神经系统中的5-羟色胺能神经元作用于许多其他神经元,并调节它们的神经递质释放。本综述聚焦于:1)中枢胆碱能、多巴胺能、去甲肾上腺素能或γ-氨基丁酸能(GABA能)神经元轴突终末上的突触前5-羟色胺(5-HT)异受体的功能,以及2)表达5-HT异受体的GABA能中间神经元在调节乙酰胆碱、多巴胺或去甲肾上腺素释放中的作用。对脑片或突触体的体外研究以及体内微透析实验表明,5-HT(1A)、5-HT(1B)、5-HT(2A)、5-HT(2C)、5-HT(3)和/或5-HT(4)异受体介导这种调节作用。新皮质胆碱能、纹状体多巴胺能或海马GABA能轴突终末上的5-HT(1B)受体是释放抑制性5-HT异受体的例子;海马GABA能轴突终末上的5-HT(3)受体或海马胆碱能轴突终末上的5-HT(4)受体是释放促进性5-HT异受体的例子。当易化性5-HT受体(如5-HT(2A)或5-HT(3)受体)激活时,GABA能中间神经元释放的GABA分别介导对其他神经递质释放的抑制作用,如前额叶新皮质多巴胺释放或新皮质乙酰胆碱释放。相反,GABA能中间神经元上抑制性5-HT异受体(如5-HT(1A)或5-HT(1B)受体)激活后,GABA释放减弱,分别参与海马乙酰胆碱释放和纹状体多巴胺释放的反常易化。这类5-HT异受体被认为是合适的5-HT受体配体的潜在靶点,通过增强相关神经递质的释放,这些配体可以弥补其在不同脑区的假定缺乏。这类缺乏的例子分别是在诸如阿尔茨海默病、帕金森病和重度抑郁症等疾病中,海马或新皮质乙酰胆碱、纹状体多巴胺以及海马或新皮质去甲肾上腺素释放受损。