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拉呋替丁对大鼠胃中含降钙素基因相关肽传入神经的致敏作用。

Sensitizing effects of lafutidine on CGRP-containing afferent nerves in the rat stomach.

作者信息

Nishihara Katsushi, Nozawa Yoshihisa, Nakano Motoko, Ajioka Hirofusa, Matsuura Naosuke

机构信息

Pharmacology Research Laboratory, Taiho Pharmaceutical Co. Ltd., 224-2, Ebisuno, Hiraishi, Kawauchi-cho, Tokushima, 771-0194, Japan.

出版信息

Br J Pharmacol. 2002 Mar;135(6):1487-94. doi: 10.1038/sj.bjp.0704596.

Abstract
  1. Capsaicin sensitive afferent nerves play an important role in gastric mucosal defensive mechanisms. Capsaicin stimulates afferent nerves and enhances the release of calcitonin gene-related peptide (CGRP), which seems to be the predominant neurotransmitter of spinal afferents in the rat stomach, exerting many pharmacological effects by a direct mechanism or indirectly through second messengers such as nitric oxide (NO). 2. Lafutidine is a new type of anti-ulcer drug, possessing both an antisecretory effect, exerted via histamine H(2) receptor blockade, and gastroprotective activities. Studies with certain antagonists or chemical deafferentation techniques suggest the gastroprotective actions of lafutidine to be mediated by capsaicin sensitive afferent nerves, but this is an assumption based on indirect techniques. In order to explain the direct relation of lafutidine to afferent nerves, we conducted the following studies. 3. We determined CGRP and NO release from rat stomach and specific [(3)H]-resiniferatoxin (RTX) binding to gastric vanilloid receptor subtype 1 (VR1), which binds capsaicin, using EIA, a microdialysis system and a radioreceptor assay, respectively. 4. Lafutidine enhanced both CGRP and NO release from the rat stomach induced by a submaximal dose of capsaicin, but had no effect on specific [(3)H]-RTX and capsaicin binding to VR1. 5. In conclusion, our findings demonstrate that lafutidine modulates the activity of capsaicin sensitive afferent nerves in the rat stomach, which may be a key mechanism involved in its gastroprotective action.
摘要
  1. 辣椒素敏感传入神经在胃黏膜防御机制中起重要作用。辣椒素刺激传入神经并增强降钙素基因相关肽(CGRP)的释放,CGRP似乎是大鼠胃中脊髓传入神经的主要神经递质,通过直接机制或间接通过一氧化氮(NO)等第二信使发挥多种药理作用。2. 拉呋替丁是一种新型抗溃疡药物,具有通过组胺H2受体阻断发挥的抗分泌作用和胃保护活性。使用某些拮抗剂或化学去传入神经技术的研究表明,拉呋替丁的胃保护作用由辣椒素敏感传入神经介导,但这是基于间接技术的一种假设。为了解释拉呋替丁与传入神经的直接关系,我们进行了以下研究。3. 我们分别使用酶免疫分析(EIA)、微透析系统和放射受体分析法,测定了大鼠胃中CGRP和NO的释放以及与胃香草酸受体亚型1(VR1,可结合辣椒素)特异性结合的[3H]树脂毒素(RTX)。4. 拉呋替丁增强了次最大剂量辣椒素诱导的大鼠胃中CGRP和NO的释放,但对[3H]RTX与VR1的特异性结合以及辣椒素与VR1的结合没有影响。5. 总之,我们的研究结果表明,拉呋替丁调节大鼠胃中辣椒素敏感传入神经的活性,这可能是其胃保护作用的关键机制。

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