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中枢给予甘丙肽对毒蕈碱型胆碱能受体及甘丙肽受体G蛋白偶联的影响。

Effects of central galanin administration on muscarinic cholinergic and galanin receptor G protein coupling.

作者信息

Barreda-Gómez G, Giralt M T, Rodríguez-Puertas R

机构信息

Department of Pharmacology, Faculty of Medicine and Odontology, University of the Basque Country, E-48940 Leioa, Vizcaya, Spain.

出版信息

Neuropeptides. 2005 Jun;39(3):157-60. doi: 10.1016/j.npep.2004.12.020. Epub 2005 Feb 1.

DOI:10.1016/j.npep.2004.12.020
PMID:15944005
Abstract

The neuropeptide galanin is expressed in the mammalian central nervous system and has been implicated in neurotrophic actions. Central galanin administration induces cognitive deficits in rodents and inhibits the release of acetylcholine in the hippocampus. In addition, a galanin hyperinnervation of the basal forebrain cholinergic cells in Alzheimer's disease patients has been reported. To evaluate the effect of galanin treatment on galanin and muscarinic cholinergic receptor G protein coupling, galanin was administered into the lateral ventricle of rats via an implanted cannula. Galanin or muscarinic receptor functional coupling to G proteins was quantified by galanin or carbachol stimulation of guanosine 5'-(gamma-[35S]thio)triphosphate binding in rat brain slices. Guanosine 5'-(gamma-[35S]thio)triphosphate basal binding in nucleus basalis of Meynert and thalamic nuclei was increased in the vehicle treated group. This effect was reverted by galanin treatment and indicates that the surgery increased receptor functional coupling to G proteins, which is restored by a possible neurotrophic action mediated by galanin. In addition, in galanin administered animals, galanin-stimulated binding was increased in the amygdala but decreased in the diagonal band, whilst binding stimulation mediated by carbachol was found to be increased in the amygdala, thalamic nuclei and diagonal band. These findings indicate that galanin treatment modulates the coupling of galanin and muscarinic cholinergic receptors to G proteins in specific regions of the rat central nervous system.

摘要

神经肽甘丙肽在哺乳动物中枢神经系统中表达,并与神经营养作用有关。向中枢注射甘丙肽会导致啮齿动物出现认知缺陷,并抑制海马体中乙酰胆碱的释放。此外,有报道称阿尔茨海默病患者基底前脑胆碱能细胞存在甘丙肽超神经支配。为了评估甘丙肽治疗对甘丙肽和毒蕈碱胆碱能受体G蛋白偶联的影响,通过植入套管将甘丙肽注入大鼠侧脑室。通过甘丙肽或卡巴胆碱刺激大鼠脑片上鸟苷5'-(γ-[35S]硫代)三磷酸结合来定量甘丙肽或毒蕈碱受体与G蛋白的功能偶联。在溶剂处理组中,Meynert基底核和丘脑核中的鸟苷5'-(γ-[35S]硫代)三磷酸基础结合增加。甘丙肽治疗可逆转这种效应,表明手术增加了受体与G蛋白的功能偶联,而甘丙肽可能介导的神经营养作用可使其恢复。此外,在注射甘丙肽的动物中,杏仁核中甘丙肽刺激的结合增加,而在斜角带中减少,同时发现卡巴胆碱介导的结合刺激在杏仁核、丘脑核和斜角带中增加。这些发现表明,甘丙肽治疗可调节大鼠中枢神经系统特定区域中甘丙肽和毒蕈碱胆碱能受体与G蛋白的偶联。

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