昂丹司琼的药理和止吐特性。

M B Tyers, K T Bunce, P P Humphrey
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引用次数: 0

摘要

5-HT(血清素)受体有三种主要类型。5-HT3受体位于周围和中枢神经系统的神经元组织中。昂丹司琼是这种受体类型的高选择性和强效拮抗剂。细胞毒性药物和放疗引起的严重恶心呕吐可通过甲氧氯普胺治疗减轻,但由于多巴胺受体的拮抗作用,锥体外系副作用很常见。在接受顺铂、环磷酰胺或放射治疗的雪貂中,昂丹司琼的剂量远低于甲氧氯普胺,且无相关副作用,可显著延缓呕吐的发生,减少干呕和呕吐的次数。确定昂丹司琼作用部位的实验表明,其止吐作用至少部分发生在产后区域,但也有可能发生在上消化道的外周部位。
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Pharmacological and anti-emetic properties of ondansetron.

Three main types of 5-HT (serotonin) receptor have been recognised. The 5-HT3 receptor is located on neuronal tissues in the peripheral and central nervous systems. Ondansetron is a highly selective and potent antagonist for this receptor type. The severe nausea and vomiting caused by cytotoxic agents and radiotherapy can be reduced by metoclopramide treatment, but extrapyramidal side effects are common due to antagonism of dopamine receptors. Ondansetron has been found to significantly delay the onset of emesis, and reduce the number of retches and vomits in ferrets receiving cisplatin, cyclophosphamide, or radiation, at much lower doses than metoclopramide and without the associated side effects. Experiments to define the site of action of ondansetron suggest that at least part of its antiemetic action is in the area postrema, though a peripheral site of action in the upper gastrointestinal tract is also a possibility.

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Effect of soybean feeding on experimental carcinogenesis--III. Carcinogenecity of nitrite and dibutylamine in mice: a histopathological study. Abstracts from the second annual meeting of the Danish Society for Cancer Research. 14 April 1989. International Conference on Supportive Care in Oncology. Brussels (Belgium), 23-25 August 1988. Proceedings. Proceedings of the Ondansetron Symposium. London, 30 June 1989. Pharmacological and anti-emetic properties of ondansetron.
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