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促胰液素和血管活性肠肽可激活交感神经末梢中的酪氨酸羟化酶。

Secretin and vasoactive intestinal peptide activate tyrosine hydroxylase in sympathetic nerve endings.

作者信息

Schwarzschild M A, Zigmond R E

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Neurosci. 1989 Jan;9(1):160-6. doi: 10.1523/JNEUROSCI.09-01-00160.1989.

Abstract

Secretin and vasoactive intestinal peptide (VIP) are known to stimulate tyrosine hydroxylase (TH) activity acutely in the rat superior cervical ganglion (SCG). Because TH-containing neurons in the SCG innervate the iris, submaxillary gland, and pineal gland, we examined the effects of secretin and VIP in these 3 autonomic end organs in vitro. Both peptides stimulated TH activity in each tissue. These stimulations resembled those in the SCG in that (1) secretin displayed a higher potency than VIP in all 3 end organs, (2) the peptide effects were unchanged when calcium was excluded from the incubation medium, and (3) they were mimicked by activators of the cyclic adenosine monophosphate (cAMP) pathway. These findings indicate that secretin and VIP can regulate transmitter metabolism in both the cell bodies and axon terminals of neurons originating in the SCG. Furthermore, the data raise the possibility that catecholamine synthesis in sympathetic nerve terminals is modulated by peptides released by other, nearby nerve endings.

摘要

已知促胰液素和血管活性肠肽(VIP)可在大鼠颈上神经节(SCG)中急性刺激酪氨酸羟化酶(TH)的活性。由于SCG中含TH的神经元支配虹膜、颌下腺和松果体,我们在体外研究了促胰液素和VIP对这3个自主神经终末器官的影响。两种肽均刺激了每个组织中的TH活性。这些刺激与SCG中的刺激相似,表现为:(1)在所有3个终末器官中,促胰液素的效力均高于VIP;(2)当孵育培养基中不含钙时,肽的作用不变;(3)它们被环磷酸腺苷(cAMP)途径的激活剂模拟。这些发现表明,促胰液素和VIP可调节起源于SCG的神经元的细胞体和轴突终末中的递质代谢。此外,这些数据增加了一种可能性,即交感神经终末中的儿茶酚胺合成受到其他附近神经末梢释放的肽的调节。

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