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血小板活化因子和类花生酸是免疫复合物在小鼠体内诱导的局部和全身变化的介质。

Platelet-activating factor and eicosanoids are mediators of local and systemic changes induced by immune-complexes in mice.

作者信息

Steil A A, Teixeira C F, Jancar S

机构信息

Departamento de Imunologia, Universidade de São Paulo, Brazil.

出版信息

Prostaglandins Other Lipid Mediat. 1999 Jan;57(1):35-48. doi: 10.1016/s0090-6980(98)00070-7.

Abstract

A passive Arthus reaction (AR) induced in the peritoneal cavity of mice was followed by increased local vascular permeability and haemoconcentration. The intensity of the increased vasopermeability was higher in BALB/c compared with C3H/HePas mice despite the latter being 10 times more sensitive to platelet-activating factor (PAF). C3H/HePas mice however, exhibited higher levels of haemoconcentration and shock-like symptoms. Both events were inhibited by the PAF antagonist, WEB 2170. Indomethacin reduced both pathological events whereas L663,536, that inhibits leukotrienes synthesis reduced haemoconcentration but only in BALB/c mice. PAF was released into the peritoneal cavity, peak release being at 10 min after induction of AR. Prostaglandin E2 (PGE2), thromboxane B2 (TXB2), leukotriene B4 (LTB4), and leukotriene C4/D4 (LTC4/D4) were also released at this time. Similar levels of PAF and eicosanoids were found in BALB/c and C3H/HePas mice except for LTB4, which was higher in C3H/HePas. It is concluded that PAF and eicosanoids are mediators of local and systemic changes induced by immune complexes in the peritoneal cavity of mice.

摘要

在小鼠腹腔中诱导的被动阿图斯反应(AR)之后,局部血管通透性增加和血液浓缩。尽管C3H/HePas小鼠对血小板活化因子(PAF)的敏感性比BALB/c小鼠高10倍,但BALB/c小鼠中血管通透性增加的强度更高。然而,C3H/HePas小鼠表现出更高水平的血液浓缩和类似休克的症状。这两种情况都被PAF拮抗剂WEB 2170抑制。吲哚美辛减少了这两种病理情况,而抑制白三烯合成的L663,536仅在BALB/c小鼠中降低了血液浓缩。PAF释放到腹腔中,诱导AR后10分钟达到释放峰值。此时也释放了前列腺素E2(PGE2)、血栓素B2(TXB2)、白三烯B4(LTB4)和白三烯C4/D4(LTC4/D4)。在BALB/c和C3H/HePas小鼠中发现了相似水平的PAF和类花生酸,但LTB4除外,其在C3H/HePas小鼠中含量更高。得出的结论是,PAF和类花生酸是小鼠腹腔中免疫复合物诱导的局部和全身变化的介质。

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