Greco A V, Mancinelli R, Mingrone G, Racanicchi C
Istituto di Clinica Medica, Università Cattolica, Roma, Italy.
Experientia. 1990 May 15;46(5):452-4. doi: 10.1007/BF01954226.
The role of vasoactive intestinal peptide (VIP), as a possible neurotransmitter of the intrinsic nerve plexus in the guinea pig gallbladder, was investigated by monitoring spontaneous contractile activity. VIP receptor antagonist (4 Cl-D-Phe6, Leu 17)-VIP did not produce any effect on muscular tone and spontaneous activity, whereas (N-Ac-Tyr1, D-Phe2)-GRF-(1-29)-NH2, (14-GRF analog), which is known to stimulate digestive enzyme secretion by interacting with the VIP-preferring receptors, greatly increased the amplitude and frequency of waves as well as the muscular tone. Since VIP receptor antagonist acts selectively as a competitive antagonist for the action of VIP, we conclude that the gallbladder inhibitory intrinsic plexus neurotransmitter is not VIP, but a member of the glucagon-secretin family of peptides.
通过监测豚鼠胆囊的自发收缩活动,研究了血管活性肠肽(VIP)作为豚鼠胆囊内在神经丛可能的神经递质的作用。VIP受体拮抗剂(4-Cl-D-Phe6,Leu17)-VIP对肌张力和自发活动没有任何影响,而(N-Ac-Tyr1,D-Phe2)-GRF-(1-29)-NH2,(14-GRF类似物),已知其通过与VIP偏好受体相互作用刺激消化酶分泌,极大地增加了波的幅度和频率以及肌张力。由于VIP受体拮抗剂作为VIP作用的选择性竞争性拮抗剂起作用,我们得出结论,胆囊抑制性内在丛神经递质不是VIP,而是胰高血糖素-促胰液素肽家族的一个成员。