Weinheimer G, Wagner B, Osswald H
Eur J Pharmacol. 1986 Nov 4;130(3):319-22. doi: 10.1016/0014-2999(86)90285-2.
Histamine-induced endothelium-dependent relaxation (EDR) in the pulmonary artery was inhibited in a concentration-dependent manner by the phorbolester phorbol 12,13-dibutyrate (PDBu) (IC50: 70 nM) whereas EDR occurring in response to ionophore A 23187 was not affected by PDBu. The phorbolester 4 alpha-phorbol 12,13-didecanoate (4 alpha-PDD), which does not activate protein kinase C (PKC), was without effect on receptor- or ionophore-induced EDR. The observed inhibition of signal transduction by PKC activation is suggested to reflect phosphorylation of the GTP binding protein Ni.
佛波酯佛波醇12,13 - 二丁酸酯(PDBu)以浓度依赖的方式抑制组胺诱导的肺动脉内皮依赖性舒张(EDR)(IC50:70 nM),而离子载体A 23187诱导的EDR不受PDBu影响。不激活蛋白激酶C(PKC)的佛波酯4α - 佛波醇12,13 - 二癸酸酯(4α - PDD)对受体或离子载体诱导的EDR无作用。PKC激活对信号转导的抑制作用表明反映了GTP结合蛋白Ni的磷酸化。