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过敏反应介质的释放:前列腺素合成的抑制以及过敏反应慢反应物质和组胺释放的改变。

Release of mediators of anaphylaxis: inhibition of prostaglandin synthesis and the modification of release of slow reacting substance of anaphylaxis and histamine.

作者信息

Engineer D M, Niederhauser U, Piper P J, Sirois P

出版信息

Br J Pharmacol. 1978 Jan;62(1):61-6. doi: 10.1111/j.1476-5381.1978.tb07006.x.

Abstract

1 When isolated perfused lungs from sensitized guinea-pigs were challenged with antigen, histamine, slow reacting substance of anaphylaxis (SRS-A) and prostaglandin-like substances were released into the effluent. 2 Treatment of the lungs before and during challenge with indomethacin (0.5--10 microgram/ml), sodium aspirin (1--10 microgram/ml), sodium meclofenamate (0.1--1 microgram/ml) or ketoprofen (0.5--5 microgram/ml) inhibited the release of prostaglandins while increasing the output of histamine and SRS-A between three- and five-fold. 3 Diethylcarbamazine (0.2--1 mg/ml) reduced the release of SRS-A and histamine but increased the amount of prostaglandin-like substances produced. 4 Eicosatetraynoic acid (10 microgram/ml) inhibited formation of prostaglandins but did not modify release of histamine and SRS-A. 5 The results with non-steroid anti-inflammatory drugs and diethylcarbamazine suggest that prostaglandins, or some other product of the cyclo-oxygenase system, depress the anaphylactic release of SRS-A and histamine.

摘要
  1. 当用抗原攻击致敏豚鼠的离体灌注肺时,组胺、过敏反应慢反应物质(SRS - A)和前列腺素样物质被释放到流出液中。2. 在攻击前及攻击期间用吲哚美辛(0.5 - 10微克/毫升)、阿司匹林钠(1 - 10微克/毫升)、甲氯芬那酸钠(0.1 - 1微克/毫升)或酮洛芬(0.5 - 5微克/毫升)处理肺,可抑制前列腺素的释放,同时使组胺和SRS - A的释放量增加三至五倍。3. 乙胺嗪(0.2 - 1毫克/毫升)减少SRS - A和组胺的释放,但增加前列腺素样物质的生成量。4. 二十碳四烯酸(10微克/毫升)抑制前列腺素的形成,但不改变组胺和SRS - A的释放。5. 非甾体抗炎药和乙胺嗪的结果表明,前列腺素或环氧化酶系统的其他某种产物可抑制SRS - A和组胺的过敏反应释放。

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