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抗炎药对眼镜蛇毒磷脂酶A2所致大鼠后爪肿胀的影响。

Effects of anti-inflammatory drugs on rat hind-paw swelling caused by phospholipase A2 from Naja naja atra venom.

作者信息

Wang J P, Teng C M

机构信息

Department of Medical Research, Taichung Veterans General Hospital, ROC.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1991 Sep;344(3):377-81. doi: 10.1007/BF00183014.

Abstract

Rat hind-paw swelling was induced dose-dependently by subplantar injection of acidic phospholipase A2 (NNAVPLA2) from Naja naja atra venom. Diphenhydramine and methysergide pretreatment greatly reduced the swelling effect caused by NNAVPLA2. Several doses of compound 48/80 given to deplete the histamine content of rat hind paw, also greatly suppressed NNAVPLA2-induced paw swelling. The paw swelling caused by NNAVPLA2 was reduced following pretreatment with BW 755C, a dual inhibitor of cyclooxygenase/lipoxygenase, or subplantar co-injection with FPL 55712, a SRS-A antagonist, while pretreatment with acetylsalicylic acid had no effect. Captopril significantly potentiated the NNAVPLA2-induced paw swelling. The recovered myeloperoxidase activity was increased within 1 h and still elevated in the rat paw 3 to 6 h after subplantar injection of NNAVPLA2. In isolated peripheral PMN leukocyte suspension, NNAVPLA2 caused a release of superoxide radical. Subplantar co-injection with superoxide dismutase/catalase significantly inhibited NNAVPLA2-induced paw swelling. NNAVPLA2 did not trigger platelet aggregation either in platelet-rich plasma or in washed platelet suspension. NNAVPLA2-induced hind-paw swelling was also suppressed by the pretreatment with isoprenaline or terbutaline, while this response was not affected by co-injection with BN 52021, a PAF antagonist, into the paw. It is concluded that the hind-paw swelling caused by NNAVPLA2 is mainly due to histamine and serotonin released from mast cells and partly due to the formed kinins and SRS-A in the inflammatory area, and superoxide radical from PMN leukocytes.

摘要

通过足底注射眼镜蛇毒中的酸性磷脂酶A2(NNAVPLA2),大鼠后爪肿胀呈剂量依赖性诱导。苯海拉明和甲基麦角新碱预处理可大大降低NNAVPLA2引起的肿胀效应。给予几剂化合物48/80以耗尽大鼠后爪的组胺含量,也可大大抑制NNAVPLA2诱导的爪肿胀。在用环氧化酶/脂氧合酶双重抑制剂BW 755C预处理后,或与SRS-A拮抗剂FPL 55712足底联合注射后,NNAVPLA2引起的爪肿胀减轻,而乙酰水杨酸预处理则无效果。卡托普利显著增强了NNAVPLA2诱导的爪肿胀。足底注射NNAVPLA2后1小时内,恢复的髓过氧化物酶活性增加,在大鼠爪中3至6小时仍升高。在分离的外周PMN白细胞悬液中,NNAVPLA2导致超氧阴离子释放。与超氧化物歧化酶/过氧化氢酶足底联合注射可显著抑制NNAVPLA2诱导的爪肿胀。NNAVPLA2在富血小板血浆或洗涤血小板悬液中均未引发血小板聚集。用异丙肾上腺素或特布他林预处理也可抑制NNAVPLA2诱导的后爪肿胀,而将PAF拮抗剂BN 52021注入爪中对该反应无影响。结论是,NNAVPLA2引起的后爪肿胀主要是由于肥大细胞释放的组胺和5-羟色胺,部分是由于炎症区域形成的激肽和SRS-A,以及PMN白细胞产生的超氧阴离子。

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