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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Differential action of anti-emetic drugs on defecation and emesis induced by prostaglandin E2 in the ferret.
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Differential action of anti-emetic drugs on defecation and emesis induced by prostaglandin E2 in the ferret.

机译:止吐药对白鼬中前列腺素E2诱导的排便和呕吐的差异作用。

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摘要

In the present studies we investigated the mechanism of action of prostaglandin E2 (1 mg/kg, i.p.) to induce emesis and defecation and/or tenesmus in the ferret. The emesis was antagonized significantly (P<0.05) by ondansetron (0.3 and 1 mg/kg, i.p.) and (+)-(2S,3S)-3-(2-methoxybenzylamino)-2-phenlypiperidine hydrochloride (CP-99,994; 10 mg/kg, i.p.), but neither compound reduced defecations and/or tenesmus, with ondansetron (0.3 mg/kg) actually producing a slight increase (P<0.05). Droperidol (1 and 3 mg/kg), metoclopramide (0.3 and 3 mg/kg), domperidone (0.3 and 3 mg/kg), promethazine (0.3 and 3 mg/kg) and scopolamine (0.3 and 3 mg/kg) failed to reduce prostaglandin E2 induced emesis. However, droperidol (1 and 3 mg/kg) and scopolamine (0.3 and 3 mg/kg) reduced significantly the defecatory and/or tenesmus response (P<0.05). Bilateral abdominal vagotomy was ineffective to reduce emesis and defecations and/or tenesmus. The data suggests that 5-HT3 receptor and NK1 tachykinin receptor antagonists could be useful in the clinic to prevent emesis but not defecations induced by prostaglandin E2.
机译:在本研究中,我们研究了前列腺素E2(1 mg / kg,腹腔注射)在雪貂中引起呕吐,排便和/或里急后重的作用机理。恩丹西酮(0.3和1 mg / kg,ip)和(+)-(2S,3S)-3-(2-甲氧基苄氨基)-2-苯哌啶盐酸盐(CP-99,994; 10 mg / kg,腹腔注射),但两种化合物均不能减少排便和/或里急后重,而昂丹司琼(0.3 mg / kg)实际上会略有增加(P <0.05)。氟哌利多(1和3 mg / kg),甲氧氯普胺(0.3和3 mg / kg),多潘立酮(0.3和3 mg / kg),异丙嗪(0.3和3 mg / kg)和东pol碱(0.3和3 mg / kg)失败减少前列腺素E2引起的呕吐。但是,氟哌利多(1和3 mg / kg)和东pol碱(0.3和3 mg / kg)显着降低了排便和/或里急后重的反应(P <0.05)。双侧腹部迷走神经切断术不能有效减少呕吐,排便和/或里急后重。数据表明5-HT3受体和NK1速激肽受体拮抗剂可在临床上用于预防呕吐,但不能预防前列腺素E2引起的排便。

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