Chakder S, Rattan S
Department of Medicine, Jefferson Medical College, Philadelphia, Pennsylvania.
Gastroenterology. 1991 Mar;100(3):711-8. doi: 10.1016/0016-5085(91)80015-2.
The present study was carried out to investigate the effects of porcine galanin-(1-29), N-terminal fragment galanin-(1-10), C-terminal fragment galanin-(15-29), and the middle fragment galanin-(7-16) on the spontaneous tension of the opossum internal anal sphincter and on the decrease in the resting internal anal sphincter tension in response to neural stimulation by electrical field stimulation. Galanin and galanin-(1-10) caused a concentration-dependent decrease in the resting tension of internal anal sphincter and an augmentation of the percent decrease in the resting tension with electrical field stimulation. Galanin-(15-29), on the other hand, produced an increase in the resting tension of the internal anal sphincter and had no effect on the electrical field stimulation-induced decrease in the resting tension. Galanin-(7-16) produced no significant effect on the internal anal sphincter. The decrease in the internal anal sphincter tension by galanin and galanin-(1-10) was partially antagonized by tetrodotoxin, whereas the increase in the internal anal sphincter tension caused by galanin-(15-29) was not modified by tetrodotoxin. In contrast to its effect in the internal anal sphincter, galanin caused an increase in the resting tension and suppressed a decrease in the lower esophageal sphincter tension in response to electrical field stimulation. From these findings we conclude that (a) galanin exerts an inhibitory effect on the internal anal sphincter by activating galanin receptors both at the intramural inhibitory neurons and at the internal anal sphincter smooth muscle and that the N-terminal portion of galanin may be responsible for these actions; (b) the contractile action of galanin is produced by its action on the smooth muscle; and (c) the actions of galanin on the gastrointestinal tract are tissue specific.
本研究旨在探讨猪甘丙肽 -(1 - 29)、N端片段甘丙肽 -(1 - 10)、C端片段甘丙肽 -(15 - 29)以及中间片段甘丙肽 -(7 - 16)对负鼠肛门内括约肌自发张力的影响,以及对电场刺激引起的静息肛门内括约肌张力降低的影响。甘丙肽和甘丙肽 -(1 - 10)可引起肛门内括约肌静息张力呈浓度依赖性降低,并增强电场刺激引起的静息张力降低百分比。另一方面,甘丙肽 -(15 - 29)可使肛门内括约肌静息张力增加,且对电场刺激引起的静息张力降低无影响。甘丙肽 -(7 - 16)对肛门内括约肌无显著影响。甘丙肽和甘丙肽 -(1 - 10)引起的肛门内括约肌张力降低部分被河豚毒素拮抗,而甘丙肽 -(15 - 29)引起的肛门内括约肌张力增加未被河豚毒素改变。与对肛门内括约肌的作用相反,甘丙肽可引起静息张力增加,并抑制电场刺激引起的食管下括约肌张力降低。从这些发现中我们得出以下结论:(a)甘丙肽通过激活壁内抑制性神经元和肛门内括约肌平滑肌上的甘丙肽受体,对肛门内括约肌发挥抑制作用,且甘丙肽的N端部分可能负责这些作用;(b)甘丙肽的收缩作用是通过其对平滑肌的作用产生的;(c)甘丙肽对胃肠道的作用具有组织特异性。