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刺激大鼠蓝斑对胃功能的抑制作用

Inhibition of gastric functions by stimulation of rat locus coeruleus.

作者信息

Osumi Y, Ishikawa T, Okuma Y, Nagasaka Y, Fujiwara M

出版信息

Eur J Pharmacol. 1981 Oct 15;75(1):27-35. doi: 10.1016/0014-2999(81)90341-1.

DOI:10.1016/0014-2999(81)90341-1
PMID:7318897
Abstract

To investigate the possible role of central noradrenergic neurons in the regulation of gastric functions, electrical stimulation of the locus coeruleus [LC] and microinjection of noradrenaline [NA] into the ala cinerea (area of the dorsal motor nucleus of the vagi [NDV] and the nucleus tractus solitarius [NTS]) were given to urethane-anesthetized rats. Unilateral electrical stimulation of the LC decreased both the basal levels and the lateral hypothalamic area [LHA]-induced increases in gastric acid output and mucosal blood flow. Microinjection of NA 0.1 and 0.5 micrograms/animal into the ala cinerea also decreased the basal levels of these gastric parameters. From these results, combined with neuroanatomical data from the literature, it is concluded that central noradrenergic inhibitory mechanisms originating from the LC seem to be involved in the regulation of gastric functions, probably at the level of the brain-stem ala cinerea.

摘要

为研究中枢去甲肾上腺素能神经元在胃功能调节中的可能作用,对氨基甲酸乙酯麻醉的大鼠进行蓝斑[LC]电刺激以及向灰翼(迷走神经背运动核[NDV]和孤束核[NTS]所在区域)微量注射去甲肾上腺素[NA]。单侧电刺激LC可降低基础水平以及下丘脑外侧区[LHA]诱导的胃酸分泌和黏膜血流量增加。向灰翼每只动物微量注射0.1和0.5微克NA也可降低这些胃参数的基础水平。结合文献中的神经解剖学数据,从这些结果可以得出结论,源自LC的中枢去甲肾上腺素能抑制机制似乎参与胃功能的调节,可能是在脑干灰翼水平。

相似文献

1
Inhibition of gastric functions by stimulation of rat locus coeruleus.刺激大鼠蓝斑对胃功能的抑制作用
Eur J Pharmacol. 1981 Oct 15;75(1):27-35. doi: 10.1016/0014-2999(81)90341-1.
2
Central noradrenergic-cholinergic interaction in regulation of gastric acid secretion in rats.大鼠胃酸分泌调节中中枢去甲肾上腺素能-胆碱能相互作用
Life Sci. 1983 Mar 21;32(12):1363-70. doi: 10.1016/0024-3205(83)90812-3.
3
Central cholinergic descending pathway to the dorsal motor nucleus of the vagus in regulation of gastric functions.
Jpn J Pharmacol. 1986 Jul;41(3):373-9. doi: 10.1254/jjp.41.373.
4
Locus coeruleus-mediated inhibition of chemosensory responses in the rat nucleus tractus solitarius is mediated by alpha2-adrenoreceptors.蓝斑介导的对大鼠孤束核化学感受反应的抑制作用是由α2肾上腺素能受体介导的。
Neurosci Lett. 1998 Jun 12;249(1):37-40. doi: 10.1016/s0304-3940(98)00387-5.
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Nicotine applied into the dorsal motor nucleus of the vagus inhibits enhanced gastric acid output and mucosal blood flow in rats.
Eur J Pharmacol. 1986 Mar 4;121(3):313-8. doi: 10.1016/0014-2999(86)90251-7.
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The role of paraventricular nucleus of hypothalamus in stress-ulcer formation in rats.下丘脑室旁核在大鼠应激性溃疡形成中的作用。
Brain Res. 1997 Jul 4;761(2):203-9. doi: 10.1016/s0006-8993(97)00257-6.
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[Effect of neurotensin in locus coeruleus of rat on vagus-pressor response].[神经降压素对大鼠蓝斑的作用对迷走-加压反应的影响]
Sheng Li Xue Bao. 1991 Feb;43(1):84-8.
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[Effects of tofisopam on gastric functions in rats (author's transl)].托非索泮对大鼠胃功能的影响(作者译)
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Central noradrenergic inhibition of gastric mucosal blood flow and acid secretion in rats.大鼠胃黏膜血流和胃酸分泌的中枢去甲肾上腺素能抑制作用
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Dual effects of electrical stimulation of ventromedial hypothalamic neurons on gastric acid secretion in rats.
Am J Physiol. 1983 Aug;245(2):G265-9. doi: 10.1152/ajpgi.1983.245.2.G265.

引用本文的文献

1
The locus coeruleus contributes to the anorectic, nausea, and autonomic physiological effects of glucagon-like peptide-1.蓝斑核参与了胰高血糖素样肽-1 的厌食、恶心和自主生理效应。
Sci Adv. 2023 Sep 22;9(38):eadh0980. doi: 10.1126/sciadv.adh0980. Epub 2023 Sep 20.
2
Ultrastructural evidence for selective noradrenergic innervation of CNS vagal projections to the fundus of the rat.大鼠中枢神经系统迷走神经投射至胃底的去甲肾上腺素能选择性神经支配的超微结构证据。
Auton Neurosci. 2007 Oct 30;136(1-2):31-42. doi: 10.1016/j.autneu.2007.03.003. Epub 2007 Jun 14.
3
Comparison of central gastric antisecretory effects of desmethylimipramine, doxepin and pirenzepine in rats.
去甲丙咪嗪、多塞平和哌仑西平对大鼠胃中枢性抗分泌作用的比较。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Jun;326(3):210-4. doi: 10.1007/BF00505320.
4
Stimulation of central alpha-2 adrenoceptors inhibits gastric secretion in rats by releasing vasopressin.刺激中枢α-2肾上腺素能受体通过释放血管加压素抑制大鼠的胃酸分泌。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Feb;337(2):164-8. doi: 10.1007/BF00169244.