Mihara S, Sakata T, Fujimoto M
Shionogi Research Laboratories, Shionogi & Co. Ltd., Osaka, Japan.
Eur J Pharmacol. 1990 Sep 18;189(2-3):233-6. doi: 10.1016/0922-4106(90)90028-v.
Recombinant rat lipocortin I increased [3H]PK 11195 binding to porcine aortic smooth muscle membranes, whereas a polyclonal anti-rat lipocortin I antiserum decreased both basal and lipocortin I-enhanced [3H]PK 11195 binding. The results suggest the possibility of lipocortin I being involved in the function of peripheral-type benzodiazepine binding sites.
重组大鼠脂皮质蛋白I增加了[3H]PK 11195与猪主动脉平滑肌膜的结合,而多克隆抗大鼠脂皮质蛋白I抗血清则降低了基础及脂皮质蛋白I增强的[3H]PK 11195结合。这些结果提示脂皮质蛋白I可能参与外周型苯二氮䓬结合位点的功能。