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从竹叶青蛇毒中纯化的一种碱性磷脂酶A2导致肥大细胞水肿形成和脱颗粒。

Edema formation and degranulation of mast cells by a basic phospholipase A2 purified from Trimeresurus mucrosquamatus snake venom.

作者信息

Chiu H F, Chen I J, Teng C M

机构信息

Department of Pharmacology, Kaohsiung Medical College, Taiwan, Republic of China.

出版信息

Toxicon. 1989;27(1):115-25. doi: 10.1016/0041-0101(89)90411-x.

Abstract

The basic phospholipase A2 (PLA2) purified from Trimeresurus mucrosquamatus snake venom was injected into the subplantar in order to induce edema formation in the rat hind paw. The maximum edema induced by PLA2 was induced at 1-2 hr after injection, and the per cent swelling curve showed a dose-dependent increase by PLA2 injection (2.5-10.0 micrograms). The rate of edema formation is different from the acute swelling induced by T. mucrosquamatus venom (TMV). Pretreatment with dexamethasone (4 mg/kg, s.c.), indomethacin (10 mg/kg, per 05) and diphenhydramine (100 mg/kg s.c.) inhibited the edema induced by the purified phospholipase A2. The injection of purified PLA2 or venom into rabbit skin resulted in an increase in vascular permeability which could be decreased by pretreatment with three antiinflammatory drugs. However, the pharmacological effect of dexamethasone (4 mg/kg) demonstrated a more effective inhibition than the other drugs in the PLA2-induced edema and vascular permeability change. Injection (i.p.) of PLA2 caused marked degranulation of mast cells in the rat mesentery which was facilitated by addition of calcium ion (10 mM) but antagonized by pretreating with three antiinflammatory agents. After incubating peritoneal mast cells with PLA2 (1.0 micrograms/ml), the release of histamine from the mast cell was approximately 36%, this effect was inhibited by preincubating the mast cell with three antiinflammatory agents.

摘要

从尖吻蝮蛇毒中纯化得到的碱性磷脂酶A2(PLA2)被注射到大鼠后爪足底皮下以诱导水肿形成。PLA2诱导的最大水肿在注射后1 - 2小时出现,肿胀百分比曲线显示PLA2注射(2.5 - 10.0微克)呈剂量依赖性增加。水肿形成速率与尖吻蝮蛇毒(TMV)诱导的急性肿胀不同。地塞米松(4毫克/千克,皮下注射)、吲哚美辛(10毫克/千克,每05)和苯海拉明(100毫克/千克,皮下注射)预处理可抑制纯化的磷脂酶A2诱导的水肿。将纯化的PLA2或蛇毒注射到兔皮肤中会导致血管通透性增加,而三种抗炎药物预处理可使其降低。然而,地塞米松(4毫克/千克)的药理作用在PLA2诱导的水肿和血管通透性变化方面比其他药物表现出更有效的抑制作用。腹腔注射PLA2会导致大鼠肠系膜中的肥大细胞明显脱颗粒,添加钙离子(10毫摩尔)可促进这一过程,但三种抗炎剂预处理可拮抗此作用。用PLA2(1.0微克/毫升)孵育腹膜肥大细胞后,肥大细胞中组胺的释放约为36%,三种抗炎剂预处理肥大细胞可抑制这一作用。

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