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芬那酸盐及类似作用药物对豚鼠中由缓激肽或抗原诱导的支气管收缩的拮抗作用。

Antagonism by fenamates and like-acting drugs of bronchoconstriction induced by bradykinin or antigen in the guinea-pig.

作者信息

Collier H O, James G W, Piper P J

出版信息

Br J Pharmacol. 1968 Sep;34(1):76-87. doi: 10.1111/j.1476-5381.1968.tb07952.x.

DOI:10.1111/j.1476-5381.1968.tb07952.x
PMID:5676040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1703405/
Abstract
  1. Nine non-steroidal anti-inflammatory drugs were tested for antagonism of bradykinin-induced bronchoconstriction in guinea-pig lungs in vivo. Only one, benzydamine, was inactive.2. The descending order of potency of the active anti-inflammatory drugs was meclofenamate = Scha 306>Scha 87/2>indoxole>Mi85>indomethacin>glafenine>ibufenac.3. Of eight other drugs tested, chlorpromazine, phenoxybenzamine and four others were inactive, whereas phenelzine and mebanazine possessed activity.4. In tests at two dose-levels of meclofenamate, the dose-ratio of bradykinin increased proportionately with the dose of meclofenamate.5. The anti-bradykinin effect of meclofenamate was still observed after destruction of the brain and spinal cord, after bilateral adrenalectomy or after blockade of beta-receptors for adrenaline.6. Meclofenamate did not release catecholamines from the adrenal medulla or prevent such a release by bradykinin given intra-arterially.7. The fenamates and like-acting drugs reduced the intensity of anaphylactic bronchoconstriction in guinea-pigs treated with mepyramine or propranolol. The descending order of potency was meclofenamate>flufenamate>mefenamate.8. Dose / response curves for the antagonism of anaphylactic bronchoconstriction by the fenamates, in the presence of propranolol, turned downwards at high doses.9. These findings suggest that the fenamates may find a useful place in the treatment of bronchial asthma or other conditions involving allergic ventilatory impairment.
摘要
  1. 对九种非甾体抗炎药进行了测试,以观察其对豚鼠体内缓激肽诱导的支气管收缩的拮抗作用。只有一种药物,即苄达明,没有活性。

  2. 活性抗炎药的效力由高到低依次为甲氯芬那酸 = Scha 306>Scha 87/2>吲哚洛尔>Mi85>吲哚美辛>格拉非宁>异丁苯丙酸。

  3. 在测试的其他八种药物中,氯丙嗪、酚苄明和其他四种药物没有活性,而苯乙肼和甲苄肼具有活性。

  4. 在甲氯芬那酸的两个剂量水平测试中,缓激肽的剂量比随甲氯芬那酸的剂量成比例增加。

  5. 在破坏脑和脊髓后、双侧肾上腺切除术后或阻断肾上腺素β受体后,仍可观察到甲氯芬那酸的抗缓激肽作用。

  6. 甲氯芬那酸不会从肾上腺髓质释放儿茶酚胺,也不会阻止动脉内注射缓激肽引起的这种释放。

  7. 邻氨基苯甲酸酯类药物和类似作用的药物降低了用美吡拉敏或普萘洛尔治疗的豚鼠过敏性支气管收缩的强度。效力由高到低依次为甲氯芬那酸>氟芬那酸>甲芬那酸。

  8. 在普萘洛尔存在的情况下,邻氨基苯甲酸酯类药物对过敏性支气管收缩的拮抗作用的剂量/反应曲线在高剂量时向下弯曲。

  9. 这些发现表明,邻氨基苯甲酸酯类药物在治疗支气管哮喘或其他涉及过敏性通气障碍的疾病中可能会有一席之地。

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Antagonism by fenamates and like-acting drugs of bronchoconstriction induced by bradykinin or antigen in the guinea-pig.芬那酸盐及类似作用药物对豚鼠中由缓激肽或抗原诱导的支气管收缩的拮抗作用。
Br J Pharmacol. 1968 Sep;34(1):76-87. doi: 10.1111/j.1476-5381.1968.tb07952.x.
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Arch Int Pharmacodyn Ther. 1967 Feb;165(2):291-301.
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Br J Pharmacol. 1972 Sep;46(1):56-65. doi: 10.1111/j.1476-5381.1972.tb06848.x.
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Fenamates as antagonists of bronchoconstriction and nociception induced by bradykinin and other substances.非甾体抗炎芬那酸类药物作为缓激肽及其他物质诱导的支气管收缩和伤害性感受的拮抗剂。
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Br Med J. 1971 May 29;2(5760):494-6. doi: 10.1136/bmj.2.5760.494.
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本文引用的文献

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ANTI-INFLAMMATORY AND ANTIPYRETIC PROPERTIES OF N-(2,6-DICHLORO-M-TOLYL)ANTHRANILIC ACID (CI-583).N-(2,6-二氯间甲苯基)邻氨基苯甲酸(CI-583)的抗炎和解热特性
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Br J Pharmacol Chemother. 1960 Jun;15(2):290-7. doi: 10.1111/j.1476-5381.1960.tb01247.x.
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Analgesic antipyretic drugs as antagonists of bradykinin.作为缓激肽拮抗剂的解热镇痛药。
Br J Pharmacol Chemother. 1960 Dec;15(4):601-10. doi: 10.1111/j.1476-5381.1960.tb00288.x.
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The pharmacology of 2,3-bis-(p-methoxyphenyl)-indole (indoxole).
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Pharmacological research on benzydamine-a new analgesic-anti-inflammatory drug.新型镇痛抗炎药苄达明的药理学研究
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The influence of analgesic antipyretic drugs on the responses of guinea-pig lungs to bradykinin.解热镇痛药对豚鼠肺脏对缓激肽反应的影响。
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