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胆碱受体和5-羟色胺3受体拮抗作用对红霉素诱导的犬肠道运动紊乱和呕吐的影响。

Effects of cholinoceptor and 5-hydroxytryptamine3 receptor antagonism on erythromycin-induced canine intestinal motility disruption and emesis.

作者信息

Qin X Y, Pilot M A, Thompson H, Scott M

机构信息

GI Science Unit, London Hospital Medical College.

出版信息

Br J Pharmacol. 1993 Jan;108(1):44-9. doi: 10.1111/j.1476-5381.1993.tb13437.x.

Abstract
  1. Erythromycin administration is associated with gastrointestinal problems, disturbed gastrointestinal motility and emesis. This study in the dog investigates the underlying mechanisms. 2. Intestinal myoelectrical activity and the occurrence and latency of emesis were recorded in eight conscious dogs. All drugs were administered intravenously. 3. Erythromycin (7 mg kg-1) increased contractions of the proximal small intestine, and caused emesis in all fasted dogs and in 5 dogs after food. Atropine (50 mg kg-1 min-1) and hexamethonium (10 mg kg-1 h-1) partially inhibited the GI motility effects but did not significantly reduce emesis. 4. Metoclopramide at a high dose (2 mg kg-1 h-1) reduced the incidence of emesis in the presence of increased intestinal motility, but a low dose (150 micrograms kg-1 h-1) was ineffective. 5. A 5-hydroxytryptamine3 (5-HT3) receptor antagonist, MDL 72222 (1 mg kg-1), reduced emesis when given alone and combined with metoclopramide (low dose). The 5-HT4 receptor agonist BRL24924 (Renzapride, 1 mg kg-1) had no effect on emesis either alone in combination with metoclopramide. 6. In conclusion, erythromycin-induced GI motility disturbances and emesis are not causally related. Whereas the increase in intestinal smooth muscle activity is possibly cholinergically mediated, emesis occurs at least in part via a 5-hydroxytryptaminergic mechanism, but does not involve the dopamine system.
摘要
  1. 给予红霉素会引发胃肠道问题、胃肠动力紊乱和呕吐。本研究以犬为对象,探究其潜在机制。2. 记录了8只清醒犬的肠肌电活动以及呕吐的发生情况和潜伏期。所有药物均通过静脉给药。3. 红霉素(7毫克/千克)可增强近端小肠的收缩,并导致所有禁食犬以及5只进食后犬呕吐。阿托品(50毫克/千克·分钟)和六甲铵(10毫克/千克·小时)部分抑制了胃肠动力效应,但并未显著减少呕吐。4. 高剂量胃复安(2毫克/千克·小时)在肠动力增强的情况下可降低呕吐发生率,但低剂量(150微克/千克·小时)无效。5. 5-羟色胺3(5-HT3)受体拮抗剂MDL 72222(1毫克/千克)单独使用或与低剂量胃复安联合使用时均可减少呕吐。5-HT4受体激动剂BRL24924(伦扎必利,1毫克/千克)单独使用或与胃复安联合使用时对呕吐均无影响。6. 总之,红霉素引起的胃肠动力紊乱与呕吐并无因果关系。肠道平滑肌活动增强可能由胆碱能介导,而呕吐至少部分通过5-羟色胺能机制发生,但不涉及多巴胺系统。

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本文引用的文献

1
Absorption and bioavailability of oral erythromycin.口服红霉素的吸收与生物利用度。
Br J Clin Pharmacol. 1981 Aug;12(2):131-40. doi: 10.1111/j.1365-2125.1981.tb01191.x.
3
Drug therapy. Metoclopramide.药物治疗。甲氧氯普胺。
N Engl J Med. 1981 Jul 2;305(1):28-33. doi: 10.1056/NEJM198107023050106.
9
Motilin receptors in rabbit stomach and small intestine.兔胃和小肠中的胃动素受体。
Regul Pept. 1986 Sep;15(2):143-53. doi: 10.1016/0167-0115(86)90084-4.

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