首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of cholinoceptor and 5-hydroxytryptamine3 receptor antagonism on erythromycin-induced canine intestinal motility disruption and emesis.
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Effects of cholinoceptor and 5-hydroxytryptamine3 receptor antagonism on erythromycin-induced canine intestinal motility disruption and emesis.

机译: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蠕动破坏和呕吐的影响。

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摘要

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.
机译:1.红霉素的给药与胃肠道问题,胃肠道蠕动和呕吐有关。对狗的这项研究调查了潜在的机制。 2.记录了八只清醒犬的肠肌电活动以及呕吐的发生和潜伏期。所有药物均静脉内给药。 3.红霉素(7 mg kg-1)增加近端小肠的收缩,并在所有禁食的狗和进食后的5只狗中引起呕吐。阿托品(50 mg kg-1 min-1)和六甲铵(10 mg kg-1 h-1)部分抑制了胃肠动力,但并未明显降低呕吐。 4.高剂量(2 mg kg-1 h-1)的甲氧氯普胺可降低肠蠕动,增加肠蠕动的发生率,但低剂量(150微克kg-1 h-1)无效。 5.一种5-羟色胺3(5-HT3)受体拮抗剂MDL 72222(1 mg kg-1),单独给予或与甲氧氯普胺(低剂量)联合使用时,呕吐减少。 5-HT4受体激动剂BRL24924(Renzapride,1 mg kg-1)单独或与甲氧氯普胺联用对呕吐无影响。 6.总之,红霉素引起的胃肠道运动障碍和呕吐与因果关系不大。肠平滑肌活动的增加可能是由胆碱介导的,而呕吐至少部分是通过5-羟色胺能机制发生的,但并不涉及多巴胺系统。

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