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迈向理解催吐反射的病因学和病理生理学:抗呕吐药物的新方法。

Towards understanding the aetiology and pathophysiology of the emetic reflex: novel approaches to antiemetic drugs.

作者信息

Bountra C, Gale J D, Gardner C J, Jordan C C, Kilpatrick G J, Twissell D J, Ward P

机构信息

Division of Biology, Glaxo Research and Development Ltd., Ware, Herts., UK.

出版信息

Oncology. 1996 Jun;53 Suppl 1:102-9. doi: 10.1159/000227649.

DOI:10.1159/000227649
PMID:8692545
Abstract

The introduction of 5-HT3 antagonists, such as ondansetron, as antiemetic agents has transformed the management of patients receiving chemotherapy or radiation therapy. Studies in animal models with NK1 antagonists suggest that these represent a new class of antiemetic agents having a broader spectrum of activity than 5-HT3 antagonists. Compounds of this class may prove to be more effective in man against delayed emesis induced by cisplatin, post-operative nausea and vomiting and motion sickness. Thus, they have the potential to complement 5-HT3 antagonists and so provide a further advance in the management of nausea and vomiting.

摘要

5-羟色胺3拮抗剂(如昂丹司琼)作为止吐药的引入,改变了接受化疗或放疗患者的治疗管理。在动物模型中使用NK1拮抗剂的研究表明,这些药物代表了一类新的止吐药,其活性谱比5-羟色胺3拮抗剂更广。这类化合物在人体中可能对顺铂引起的延迟性呕吐、术后恶心和呕吐以及晕动病更有效。因此,它们有可能补充5-羟色胺3拮抗剂,从而在恶心和呕吐的治疗管理方面取得进一步进展。

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Oncology. 1996 Jun;53 Suppl 1:102-9. doi: 10.1159/000227649.
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