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血管活性肠肽作为大鼠胃底舒张的可能介质。

Vasoactive intestinal polypeptide as possible mediator of relaxation in the rat gastric fundus.

作者信息

De Beurme F A, Lefebvre R A

机构信息

Heymans Institute of Pharmacology, University of Gent Medical School, Belgium.

出版信息

J Pharm Pharmacol. 1988 Oct;40(10):711-5. doi: 10.1111/j.2042-7158.1988.tb07000.x.

Abstract

Relaxations were induced in longitudinal muscle strips of the rat gastric fundus by stimulation of non-adrenergic non-cholinergic (NANC) neurons and by administration of vasoactive intestinal polypeptide (VIP) or isoprenaline. The effect of antiserum against vasoactive intestinal polypeptide (VIP antiserum) and of control serum on these relaxations was investigated. Incubation with VIP antiserum (dilution 1/50) for 1 h almost completely prevented the relaxation by VIP. It partially prevented the relaxation evoked by electrical stimulation while the relaxation induced by isoprenaline was not influenced. Control serum decreased the VIP- and stimulation-induced relaxations much less than did VIP antiserum. In addition, the effect of the putative VIP antagonist (4Cl-D-Phe6, Leu17) VIP was studied on the relaxations induced by NANC neuron stimulation and by VIP. The VIP antagonist (3 x 10(-5) M, incubation time 10 min) had a relaxatory effect itself but had no influence on either VIP- or stimulation-induced relaxations. The results with VIP antiserum confirm the involvement of VIP in the inhibitory NANC neurotransmission of the rat gastric fundus.

摘要

通过刺激非肾上腺素能非胆碱能(NANC)神经元以及给予血管活性肠肽(VIP)或异丙肾上腺素,可诱导大鼠胃底纵行肌条产生舒张。研究了抗血管活性肠肽抗血清(VIP抗血清)和对照血清对这些舒张作用的影响。用VIP抗血清(稀释度1/50)孵育1小时几乎完全阻断了VIP引起的舒张。它部分阻断了电刺激诱发的舒张,而异丙肾上腺素诱导的舒张则不受影响。对照血清对VIP和刺激诱导的舒张的降低作用远小于VIP抗血清。此外,研究了假定的VIP拮抗剂(4Cl-D-Phe6,Leu17)VIP对NANC神经元刺激和VIP诱导的舒张的影响。VIP拮抗剂(3×10⁻⁵ M,孵育时间10分钟)本身具有舒张作用,但对VIP或刺激诱导的舒张均无影响。VIP抗血清的结果证实了VIP参与大鼠胃底抑制性NANC神经传递。

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