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血管活性肠肽和垂体腺苷酸环化酶激活肽介导的大鼠远端结肠纵行肌非肾上腺素能、非胆碱能抑制作用:与大蝎毒素和蜂毒明肽敏感钾通道激活的关系

VIP- and PACAP-mediated nonadrenergic, noncholinergic inhibition in longitudinal muscle of rat distal colon: involvement of activation of charybdotoxin- and apamin-sensitive K+ channels.

作者信息

Kishi M, Takeuchi T, Suthamnatpong N, Ishii T, Nishio H, Hata F, Takewaki T

机构信息

Department of Veterinary Pharmacology, College of Agriculture, Osaka Prefecture University, Sakai, Japan.

出版信息

Br J Pharmacol. 1996 Oct;119(4):623-30. doi: 10.1111/j.1476-5381.1996.tb15719.x.

Abstract
  1. The mediators of nonadrenergic, noncholinergic (NANC) inhibitory responses in longitudinal muscle of rat distal colon were studied. 2. An antagonist of pituitary adenylate cyclase activating peptide (PACAP) receptors, PACAP6-38, concentration-dependently inhibited the rapid relaxation of the longitudinal muscle induced by electrical field stimulation (EFS), resulting in a maximal inhibition of 47% at 3 microM. 3. PACAP6-38 inhibited the relaxation by 75% in the presence of the vasoactive intestinal peptide (VIP) receptor antagonist, VIP10-28 at 3 microM, which inhibited the relaxation by 44%. 4. An antagonist of large conductance Ca(2+)-activated K+ channels, charybdotoxin, concentration-dependently inhibited the rapid relaxation of the longitudinal muscle, resulting in a maximal inhibition of 58% at 100 nM. 5. An antagonist of small conductance Ca(2+)-activated K+ channels, apamin, concentration-dependently inhibited the relaxation (58% at 1 microM). 6. Treatment with both K+ channel antagonists resulted in 84% inhibition of the EFS-induced relaxation, which is comparable to the extent of inhibition induced by PACAP6-38 plus VIP10-28. 7. The inhibitory effect of VIP10-28 and of apamin, but not of charybdotoxin was additive: the same applied to PACAP6-38 and charybdotoxin, but not apamin. 8. Exogenously added VIP (100 nM 1 microM) induced a slow gradual relaxation of the longitudinal muscle. Charybdotoxin, but not apamin significantly inhibited the VIP-induced relaxation VIP10-28, but not PACAP6-38 selectively inhibited the VIP-induced relaxation. 9. Exogenously added PACAP (10-100 nM) also induced slow relaxation. Apamin and to a lesser extent, charybdotoxin, inhibited the PACAP-induced relaxation. PACAP6-38, but not VIP10-28 selectively inhibited the PACAP-induced relaxation. 10. Apamin at 100 nM inhibited inhibitory junction potentials (i.j.ps) induced by a single pulse of EFS Apamin also inhibited a rapid phase, but not a delayed phase of i.j.ps induced by two pulses at 10 Hz. VIP10-28 did not inhibit i.j.ps induced by a single pulse, but significantly inhibited the delayed phase at two pulses. A combination of apamin and VIP10-28 abolished the i.j.ps induced by two pulses. 11. Both VIP and PACAP induced slow hyperpolarization of the cell membrane of the longitudinal muscle. Apamin inhibited the PACAP-, but not VIP-induced hyperpolarization. 12. From these findings it is suggested that VIP and PACAP are involved in NANC inhibitory responses of longitudinal muscle of the rat distal colon via activation of charybdotoxin- and apamin-sensitive K+ channels, respectively.
摘要
  1. 对大鼠远端结肠纵行肌中非肾上腺素能、非胆碱能(NANC)抑制反应的介质进行了研究。2. 垂体腺苷酸环化酶激活肽(PACAP)受体拮抗剂PACAP6 - 38浓度依赖性地抑制电场刺激(EFS)诱导的纵行肌快速舒张,在3 μM时最大抑制率达47%。3. 在存在3 μM血管活性肠肽(VIP)受体拮抗剂VIP10 - 28的情况下,PACAP6 - 38使舒张抑制75%,而VIP10 - 28使舒张抑制44%。4. 大电导钙激活钾通道拮抗剂蝎毒素浓度依赖性地抑制纵行肌快速舒张,在100 nM时最大抑制率达58%。5. 小电导钙激活钾通道拮抗剂蜂毒明肽浓度依赖性地抑制舒张(在1 μM时为58%)。6. 两种钾通道拮抗剂联合使用对EFS诱导的舒张的抑制率达84%,这与PACAP6 - 38加VIP10 - 28诱导的抑制程度相当。7. VIP10 - 28和蜂毒明肽的抑制作用具有相加性,但蝎毒素的抑制作用不具有相加性;PACAP6 - 38和蝎毒素的抑制作用具有相加性,但蜂毒明肽的抑制作用不具有相加性。8. 外源性添加VIP(100 nM至1 μM)诱导纵行肌缓慢渐进性舒张。蝎毒素可显著抑制VIP诱导的舒张,但蜂毒明肽不能;VIP10 - 28可选择性抑制VIP诱导的舒张,但PACAP6 - 38不能。9. 外源性添加PACAP(10 - 100 nM)也诱导缓慢舒张。蜂毒明肽以及程度稍轻的蝎毒素可抑制PACAP诱导的舒张。PACAP6 - 38可选择性抑制PACAP诱导的舒张,但VIP10 - 28不能。10. 100 nM的蜂毒明肽抑制单个EFS脉冲诱导的抑制性接头电位(i.j.ps)。蜂毒明肽也抑制10 Hz两个脉冲诱导的i.j.ps的快速相,但不抑制延迟相。VIP10 - 28不抑制单个脉冲诱导的i.j.ps,但显著抑制两个脉冲时的延迟相。蜂毒明肽和VIP10 - 28联合使用可消除两个脉冲诱导的i.j.ps。11. VIP和PACAP均诱导纵行肌细胞膜缓慢超极化。蜂毒明肽抑制PACAP诱导的超极化,但不抑制VIP诱导的超极化。12. 从这些发现提示,VIP和PACAP分别通过激活对蝎毒素和蜂毒明肽敏感的钾通道参与大鼠远端结肠纵行肌的NANC抑制反应。

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