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外周苯二氮䓬类药物可增强花生四烯酸刺激的巨噬细胞样P388D1细胞的呼吸爆发。

Peripheral benzodiazepines enhance the respiratory burst of macrophage-like P388D1 cells stimulated by arachidonic acid.

作者信息

Zavala F, Lenfant M

出版信息

Int J Immunopharmacol. 1987;9(3):269-74. doi: 10.1016/0192-0561(87)90050-6.

Abstract

P388D1, a murine cell with macrophage properties, responds to exogenous arachidonic acid with superoxide anion production. This oxidative burst is enhanced by peripheral and mixed type benzodiazepines and this stimulation is specifically reversed by the peripheral antagonist PK 11195. In contrast, PK 11195 is unable to antagonize a stimulation caused by a non-benzodiazepine ligand such as the chemotactic peptide fMet-Leu-Phe. The optimal concentrations were close to 10 nM and corresponded to the affinities of the compounds for the peripheral benzodiazepine receptor detected on these cells. Compared to other tissues where peripheral benzodiazepines acted only at micromolar concentrations, the macrophage with its functional receptor appears as a privileged site of action for these molecules.

摘要

P388D1是一种具有巨噬细胞特性的鼠细胞,它对外源性花生四烯酸产生超氧阴离子反应。外周型和混合型苯二氮䓬类药物可增强这种氧化爆发,而外周拮抗剂PK 11195可特异性逆转这种刺激作用。相比之下,PK 11195无法拮抗由非苯二氮䓬类配体(如趋化肽fMet-Leu-Phe)引起的刺激。最佳浓度接近10 nM,这与这些化合物对在这些细胞上检测到的外周苯二氮䓬受体的亲和力相对应。与外周苯二氮䓬类药物仅在微摩尔浓度下起作用的其他组织相比,具有功能性受体的巨噬细胞似乎是这些分子的一个特殊作用位点。

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