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结肠内甘油诱导大鼠腹部收缩:5-羟色胺3型受体的作用

Intracolonic glycerol induces abdominal contractions in rats: role of 5-HT3 receptors.

作者信息

Botella A, Fioramonti J, Eeckhout C, Bueno L

机构信息

Department of Pharmacology and Toxicology, INRA, Toulouse, France.

出版信息

Fundam Clin Pharmacol. 1998;12(6):619-23. doi: 10.1111/j.1472-8206.1998.tb00995.x.

Abstract

Serotonin and 5-HT3 receptors may be involved in the activation of nociceptive afferent pathways by rectal distension. In rats, intracolonic infusion of glycerol is able to trigger nociceptive inputs as evidenced by the occurrence of abdominal constrictions. This work was designed to evaluate the influence of 5-HT3 receptor antagonists on this reflex and to approach the site of action by comparing their relative efficacies according to the route of administration. Male Wistar rats (250-350 g) were surgically prepared for abdominal electromyography and a catheter was placed in the colonic lumen. Five days after surgery, electrical activity of abdominal muscles was recorded before and during (20 min) intracolonic infusion of glycerol (60% glycerol + 40% saline, rate 0.75 mL/h). Cilansetron was administered intraperitoneally, 15 min before glycerol infusion, at doses of 5 to 500 micrograms/kg. Granisetron, ondansetron and cilansetron were administered at the dose of 20 micrograms/kg by intraperitoneal (i.p.), intravenous (i.v.) or intracolonic (i.c.) routes. The number of abdominal spike bursts was used as an index of visceral nociception. Intracolonic infusion of glycerol increased significantly (P < 0.05) the number of abdominal spike bursts during the time of infusion compared with saline (30.6 +/- 6.6 vs 4.5 +/- 3.4 bursts). When administered i.p., cilansetron dose-dependently reduced the frequency of abdominal spike bursts from the dose of 20 micrograms/kg i.p. Administration i.p. of granisetron and ondansetron at this dose also significantly reduced the number of abdominal spikes (19.0 +/- 6.0 and 18.3 +/- 6.9 respectively). Cilansetron, ondansetron and granisetron were also effective by i.v. and i.c. routes, cilansetron was more active by the i.c. route. Serotonin, via 5-HT3 receptors, is involved in the mediation of abdominal contractions induced by intracolonic infusion of glycerol. 5-HT3 receptor antagonists are also active by i.c. route suggesting a local site of action.

摘要

血清素和5 - HT3受体可能参与直肠扩张对伤害性传入通路的激活。在大鼠中,结肠内注入甘油能够引发伤害性传入,腹部收缩的出现就证明了这一点。本研究旨在评估5 - HT3受体拮抗剂对该反射的影响,并通过比较它们根据给药途径的相对疗效来探讨作用部位。雄性Wistar大鼠(250 - 350克)接受手术准备用于腹部肌电图检查,并在结肠腔内放置一根导管。手术后5天,在结肠内注入甘油(60%甘油 + 40%盐水,速率0.75毫升/小时)之前和期间(20分钟)记录腹部肌肉的电活动。在甘油注入前15分钟,腹腔注射西兰司琼,剂量为5至500微克/千克。格拉司琼、昂丹司琼和西兰司琼以20微克/千克的剂量通过腹腔内(i.p.)、静脉内(i.v.)或结肠内(i.c.)途径给药。腹部尖峰爆发的数量用作内脏伤害感受的指标。与盐水相比,结肠内注入甘油在注入期间显著增加了腹部尖峰爆发的数量(30.6±6.6次爆发对4.5±3.4次爆发,P < 0.05)。腹腔注射时,西兰司琼从20微克/千克腹腔注射剂量开始剂量依赖性地降低腹部尖峰爆发的频率。以该剂量腹腔注射格拉司琼和昂丹司琼也显著减少了腹部尖峰的数量(分别为19.0±6.0次和18.3±6.9次)。西兰司琼、昂丹司琼和格拉司琼通过静脉内和结肠内途径也有效,西兰司琼通过结肠内途径更具活性。血清素通过5 - HT3受体参与结肠内注入甘油诱导的腹部收缩的介导。5 - HT3受体拮抗剂通过结肠内途径也具有活性,提示作用部位在局部。

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