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胆囊收缩素神经元系统及其与多巴胺神经元系统突触前特征的相互作用。一项形态学和神经化学分析,涉及对胆囊收缩素-8和胆囊收缩素-58作用的研究。

Cholecystokinin neuron systems and their interactions with the presynaptic features of the dopamine neuron systems. A morphometric and neurochemical analysis involving studies on the action of cholecystokinin-8 and cholecystokinin-58.

作者信息

Fuxe K, Agnati L F, Vanderhaeghen J J, Tatemoto K, Andersson K, Eneroth P, Härfstrand A, Von Euler G, Toni R, Goldstein M

出版信息

Ann N Y Acad Sci. 1985;448:231-54. doi: 10.1111/j.1749-6632.1985.tb29921.x.

DOI:10.1111/j.1749-6632.1985.tb29921.x
PMID:2862825
Abstract

A unique role for CCK-58 compared to that for CCK-8 has been demonstrated in the modulation of central catecholaminergic mechanisms and neuroendocrine functions. It is of paramount importance to localize CCK-58 immunoreactivity within the brain in order to establish if separate CCK-58- and CCK-8-immunoreactive neuron systems exist. The two most significant actions of CCK-58 are a marked lowering of TSH secretion and a selective increase of DA turnover in DA-CCK co-existing synapses in the nucleus accumbens and tuberculum olfactorium.

摘要

与CCK-8相比,CCK-58在调节中枢儿茶酚胺能机制和神经内分泌功能方面已显示出独特作用。为确定是否存在独立的CCK-58和CCK-8免疫反应性神经元系统,在脑内定位CCK-58免疫反应性至关重要。CCK-58的两个最重要作用是显著降低促甲状腺激素分泌,以及选择性增加伏隔核和嗅结节中多巴胺-CCK共存突触处的多巴胺周转率。

相似文献

1
Cholecystokinin neuron systems and their interactions with the presynaptic features of the dopamine neuron systems. A morphometric and neurochemical analysis involving studies on the action of cholecystokinin-8 and cholecystokinin-58.胆囊收缩素神经元系统及其与多巴胺神经元系统突触前特征的相互作用。一项形态学和神经化学分析,涉及对胆囊收缩素-8和胆囊收缩素-58作用的研究。
Ann N Y Acad Sci. 1985;448:231-54. doi: 10.1111/j.1749-6632.1985.tb29921.x.
2
Evidence for cholecystokinin-dopamine receptor interactions in the central nervous system of the adult and old rat. Studies on their functional meaning.成年和老年大鼠中枢神经系统中胆囊收缩素-多巴胺受体相互作用的证据。对其功能意义的研究。
Ann N Y Acad Sci. 1985;448:315-33. doi: 10.1111/j.1749-6632.1985.tb29927.x.
3
Pharmacological and mechanistic studies of cholecystokinin-facilitated [3H]dopamine efflux from rat nucleus accumbens.胆囊收缩素促进大鼠伏隔核[³H]多巴胺外流的药理学及机制研究
Neuropeptides. 1989 Jan;13(1):43-50. doi: 10.1016/0143-4179(89)90020-6.
4
Influence of cholecystokinin on central monoaminergic pathways.
Regul Pept. 1983 May;6(2):99-109. doi: 10.1016/0167-0115(83)90003-4.
5
Increases in dopamine utilization in certain limbic dopamine terminal populations after a short period of intermittent exposure of male rats to cigarette smoke.在雄性大鼠短期间歇性接触香烟烟雾后,某些边缘多巴胺终末群体中的多巴胺利用率增加。
J Neural Transm. 1986;67(1-2):15-29. doi: 10.1007/BF01243356.
6
Behavioral evidence for cholecystokinin modulation of dopamine in the mesolimbic pathway.胆囊收缩素对中脑边缘通路多巴胺调节作用的行为学证据。
Prog Clin Biol Res. 1985;192:131-8.
7
Cholecystokinin-dopamine receptor interactions as studied with cholecystokinin receptor antagonists.用胆囊收缩素受体拮抗剂研究胆囊收缩素-多巴胺受体相互作用
Prog Clin Biol Res. 1985;192:105-13.
8
Effect of cholecystokinin on acetylcholine turnover and dopamine release in the rat striatum and cortex.胆囊收缩素对大鼠纹状体和皮质中乙酰胆碱周转及多巴胺释放的影响。
Eur J Pharmacol. 1989 Jun 20;165(2-3):209-14. doi: 10.1016/0014-2999(89)90714-0.
9
Immunohistochemical studies on cholecystokinin (CCK)-immunoreactive neurons in the rat using sequence specific antisera and with special reference to the caudate nucleus and primary sensory neurons.利用序列特异性抗血清对大鼠胆囊收缩素(CCK)免疫反应性神经元进行免疫组织化学研究,并特别关注尾状核和初级感觉神经元。
J Chem Neuroanat. 1988 Jan-Feb;1(1):11-51.
10
Dopamine receptor elevation by cholecystokinin.胆囊收缩素引起的多巴胺受体升高。
Peptides. 1984 Nov-Dec;5(6):1207-12. doi: 10.1016/0196-9781(84)90189-x.

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Neuroendocrine regulation of thyrotropin-releasing hormone (TRH) in the tuberoinfundibular system.结节漏斗系统中促甲状腺激素释放激素(TRH)的神经内分泌调节。
J Endocrinol Invest. 1993 Oct;16(9):715-53. doi: 10.1007/BF03348918.
2
Cholecystokinin binding sites in the rat forebrain: effects of acute and chronic methamphetamine administration.
J Neural Transm. 1989;77(2-3):181-95. doi: 10.1007/BF01248931.
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Involvement of cholecystokinin receptors in the control of striatal dopamine autoreceptors.胆囊收缩素受体在纹状体多巴胺自身受体调控中的作用。
Naunyn Schmiedebergs Arch Pharmacol. 1990 Sep;342(3):300-4. doi: 10.1007/BF00169441.