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新型血栓素A2(TXA2)受体拮抗剂(S-1452)对豚鼠抗原诱导的支气管收缩和气道高反应性的影响。

The effect of a novel thromboxane A2 (TXA2) receptor antagonist (S-1452) on the antigen-induced bronchoconstriction and airway hyperresponsiveness in guinea pigs.

作者信息

Nagai H, Arimura A, Yoshitake K, Iwama T, Sakurai T, Koda A

机构信息

Department of Pharmacology, Gifu Pharmaceutical University, Japan.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 1993 May;48(5):343-9. doi: 10.1016/0952-3278(93)90113-b.

Abstract

The effect of a novel thromboxane A2 (TXA2) receptor antagonist (S-1452) on antigen-induced bronchoconstriction and airway hyperresponsiveness in guinea pigs was studied. Ketotifen was used as a reference drug. S-1452 at doses of 1 and 3 mg/kg (per oral administration, 1 h before the injection of U-46619) clearly inhibited U-46619-induced pulmonary pressure increase. Ketotifen at a dose of 10 mg/kg did not affect U-46619-induced bronchoconstriction. S-1452 at doses of 3 and 10 mg/kg and ketotifen at a dose of 10 mg/kg inhibited the antigen-induced bronchoconstriction in guinea pigs which had been passively sensitized with guinea pig IgE antibody. S-1452 at a dose of 10 mg/kg inhibited repeated antigen provocation-induced airway hyperresponsiveness in guinea pigs. The accumulation of inflammatory cells by antigen provocation in bronchial alveolar lavage fluid (BALF) was inhibited by ketotifen but not by S-1452. These results indicate the efficacy of S-1452 on antigen-induced bronchoconstriction and antigen-induced airway hyperresponsiveness in guinea pigs.

摘要

研究了一种新型血栓素A2(TXA2)受体拮抗剂(S - 1452)对豚鼠抗原诱导的支气管收缩和气道高反应性的影响。酮替芬用作对照药物。剂量为1和3毫克/千克的S - 1452(口服给药,在注射U - 46619前1小时)明显抑制U - 46619诱导的肺压力升高。剂量为10毫克/千克的酮替芬不影响U - 46619诱导的支气管收缩。剂量为3和10毫克/千克的S - 1452以及剂量为10毫克/千克的酮替芬抑制了用豚鼠IgE抗体被动致敏的豚鼠的抗原诱导的支气管收缩。剂量为10毫克/千克的S - 1452抑制了豚鼠反复抗原激发诱导的气道高反应性。酮替芬抑制了抗原激发在支气管肺泡灌洗液(BALF)中引起的炎症细胞积聚,但S - 1452没有。这些结果表明S - 1452对豚鼠抗原诱导的支气管收缩和抗原诱导的气道高反应性有效。

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