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乙酰胆碱通过激活毒蕈碱受体和烟碱受体刺激青蛙垂体黑素细胞刺激素释放。

Acetylcholine stimulates alpha-melanocyte-stimulating hormone release from frog pituitary melanotrophs through activation of muscarinic and nicotinic receptors.

作者信息

Lamacz M, Tonon M C, Louiset E, Cazin L, Strosberg D, Vaudry H

机构信息

Groupe de Recherche en Endocrinologie Moléculaire, CNRS URA 650, Unité Affiliée à l'INSERM, Université de Rouen, Mont-Saint-Aignan, France.

出版信息

Endocrinology. 1989 Aug;125(2):707-14. doi: 10.1210/endo-125-2-707.

Abstract

The release of alpha MSH from the pars intermedia of amphibians is regulated by multiple factors, including classical neurotransmitters and neuropeptides. In this study we have examined the possible involvement of acetylcholine (ACh) in the regulation of alpha MSH secretion from the pars intermedia of the frog (Rana ridibunda) using the perifusion technique. When intact neurointermediate lobes (NIL) were exposed to graded doses of ACh (3 X 10(-7) to 3 X 10(-4) M), a dose-dependent stimulation of alpha MSH release was observed. Repeated administration of ACh (10(-4) M) induced reproducible responses of NIL without any desensitization phenomenon. ACh was also capable of stimulating alpha MSH release from dispersed intermediate lobe cells, indicating that the neurotransmitter exerts its effect by acting directly on frog melanotrophs. Using the monoclonal antibody M-35 against calf muscarinic receptors we have visualized, by the immunofluorescence technique, the presence of muscarinic receptor-like immunoreactivity in the frog pars intermedia. The stimulatory action of ACh was mimicked by both nicotine and muscarine (10(-5) M each). Nicotine-induced stimulation of alpha MSH release was partially abolished by alpha-bungarotoxin (10(-6) M) and hexamethonium (10(-4) M). The stimulatory effect of muscarine was suppressed by atropine and the M1-muscarinic antagonist pirenzepine (10(-5) M), but not by the M2-muscarinic antagonist gallamine. We have investigated the effect of ACh during administration of specific nicotinic and muscarinic antagonists. While hexomethonium or atropine could block only part of the stimulatory effect of ACh, concomitant administration of these antagonists totally abolished the response of NIL to ACh. Finally, the stimulatory effect of ACh was not impaired during prolonged administration of the beta-adrenergic antagonist propranolol. These data show that ACh stimulates in vitro alpha MSH secretion by frog NIL. Our results also indicate that amphibian pars intermedia cells possess two types of cholinergic receptors, an M1-muscarinic receptor sensitive to pirenzepine and nicotinic receptors sensitive to hexamethonium and alpha-bungarotoxin.

摘要

两栖动物垂体中间叶α-促黑素(α-MSH)的释放受多种因素调节,包括经典神经递质和神经肽。在本研究中,我们使用灌流技术研究了乙酰胆碱(ACh)在调节青蛙(泽蛙)垂体中间叶α-MSH分泌中可能的作用。当完整的神经中间叶(NIL)暴露于不同剂量的ACh(3×10⁻⁷至3×10⁻⁴M)时,观察到α-MSH释放呈剂量依赖性刺激。重复给予ACh(10⁻⁴M)可诱导NIL产生可重复的反应,且无任何脱敏现象。ACh还能够刺激分散的中间叶细胞释放α-MSH,表明该神经递质通过直接作用于青蛙黑素细胞发挥作用。使用针对小牛毒蕈碱受体的单克隆抗体M-35,我们通过免疫荧光技术观察到青蛙垂体中间叶存在毒蕈碱受体样免疫反应性。尼古丁和毒蕈碱(各10⁻⁵M)均可模拟ACh的刺激作用。α-银环蛇毒素(10⁻⁶M)和六甲铵(10⁻⁴M)可部分消除尼古丁诱导的α-MSH释放刺激。毒蕈碱的刺激作用被阿托品和M1型毒蕈碱拮抗剂哌仑西平(10⁻⁵M)抑制,但不受M2型毒蕈碱拮抗剂加拉明抑制。我们研究了在给予特定烟碱和毒蕈碱拮抗剂期间ACh的作用。虽然六甲铵或阿托品只能阻断ACh部分刺激作用,但同时给予这些拮抗剂可完全消除NIL对ACh的反应。最后,在长期给予β-肾上腺素能拮抗剂普萘洛尔期间,ACh的刺激作用未受损害。这些数据表明,ACh在体外刺激青蛙NIL分泌α-MSH。我们的结果还表明,两栖动物垂体中间叶细胞具有两种胆碱能受体,一种是对哌仑西平敏感的M1型毒蕈碱受体,另一种是对六甲铵和α-银环蛇毒素敏感的烟碱受体。

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