Mukai Kazunori, Takeuchi Tadayoshi, Toyoshima Makiko, Satoh Yuji, Fujita Akikazu, Shintani Norihito, Hashimoto Hitoshi, Baba Akemichi, Hata Fumiaki
Department of Veterinary Pharmacology, Graduate School of Agriculture and Life Sciences, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan.
Regul Pept. 2006 Jan 15;133(1-3):54-61. doi: 10.1016/j.regpep.2005.09.019. Epub 2005 Oct 17.
Mediators of neurogenic responses of the gastric fundus were studied in wild type and pituitary adenylate cyclase activating peptide (PACAP) knockout mice. Electrical field stimulation (EFS) to the circular muscle strips of the wild type mouse fundus induced a tri-phasic response, rapid transient contraction and relaxation, and sustained relaxation that was prolonged for an extended period after the end of EFS. The transient relaxation and contraction were completely inhibited by N(G)-nitro-L-arginine and atropine, respectively. The sustained relaxation was completely inhibited by a PACAP receptors antagonist, PACAP(6-38). The strips prepared from PACAP knockout mice exhibited a large contraction without rapid relaxation and unexpectedly, a sustained relaxation. However, the sustained relaxation was decreased to about a half of that observed in wild type mice. Anti-peptide histidine isoleucine (PHI) serum abolished the sustained relaxation in the knockout mice. The serum partially inhibited the sustained relaxation in wild type mice and PACAP(6-38) abolished the relaxation that remained after the antiserum-treatment. PHI relaxed the strips prepared from wild type mice. The relaxation was completely inhibited by PACAP(6-38). It was concluded that PACAP and PHI separately mediate the sustained relaxation in the mouse gastric fundus, and that nitric oxide and ACh mediate transient relaxation and contraction, respectively.
在野生型和垂体腺苷酸环化酶激活肽(PACAP)基因敲除小鼠中研究了胃底神经源性反应的介质。对野生型小鼠胃底环形肌条进行电场刺激(EFS)可诱导三相反应,即快速短暂的收缩和舒张,以及在EFS结束后持续延长的舒张。短暂的舒张和收缩分别被N(G)-硝基-L-精氨酸和阿托品完全抑制。持续的舒张被PACAP受体拮抗剂PACAP(6-38)完全抑制。从PACAP基因敲除小鼠制备的肌条表现出大的收缩且无快速舒张,出乎意料的是,还有持续的舒张。然而,持续的舒张降低至野生型小鼠中观察到的约一半。抗肽组氨酸异亮氨酸(PHI)血清消除了基因敲除小鼠中的持续舒张。该血清部分抑制了野生型小鼠中的持续舒张,而PACAP(6-38)消除了抗血清处理后剩余的舒张。PHI使从野生型小鼠制备的肌条舒张。该舒张被PACAP(6-38)完全抑制。得出的结论是,PACAP和PHI分别介导小鼠胃底的持续舒张,并且一氧化氮和乙酰胆碱分别介导短暂的舒张和收缩。