Criscuoli M, Subissi A, Daffonchio L, Omini C
Agents Actions. 1986 Nov;19(3-4):246-50. doi: 10.1007/BF01966213.
LG 30435 is a quaternary phenothiazinic antihistamine, endowed with bronchodilator and antiallergic activity. Since PAF-acether (PAF) is a potential mediator of asthma, LG 30435 was assayed for its ability to counteract PAF-induced platelet aggregation (PA) in rabbit platelet rich plasma and bronchoconstriction (BC) in anaesthetized guinea-pigs, in comparison with other antihistamines. LG 30435 was the most potent and selective inhibitor of PAF-induced PA (IC50: 66 microM), concentrations three and more than fifteen fold higher being needed to inhibit PA induced by collagen and arachidonic acid respectively. The other antihistamines, namely mepyramine, promethazine, mequitazine, thiazinamium methyl sulfate and ketotifen were less potent inhibitors of PAF-induced PA, while interfered at lower concentrations with collagen-induced PA. LG 30435 and thiazinamium, administered intravenously, inhibited dose-dependently PAF-induced BC, starting from the dose of 0.1 mumol/kg. The ED50 of LG 30435 was 0.28 mumol/kg, while the inhibition obtained with thiazinamium did not reach 50% even at 3 mumol/kg. Ketotifen and promethazine were partially active only at 3 mumol/kg, while mequitazine and mepyramine were inactive up to this dose. These results show that LG 30435 is endowed with a peculiar anti-PAF action, which may be advantageous in the treatment of asthma.
LG 30435是一种季铵类吩噻嗪抗组胺药,具有支气管扩张和抗过敏活性。由于血小板活化因子(PAF)是哮喘的潜在介质,与其他抗组胺药相比,对LG 30435在富含兔血小板血浆中对抗PAF诱导的血小板聚集(PA)以及在麻醉豚鼠中对抗支气管收缩(BC)的能力进行了测定。LG 30435是PAF诱导的PA最有效和最具选择性的抑制剂(IC50:66 microM),分别抑制胶原蛋白和花生四烯酸诱导的PA需要高三倍和十五倍以上的浓度。其他抗组胺药,即甲氧苄二胺、异丙嗪、美喹他嗪、甲基硫酸噻嗪铵和酮替芬对PAF诱导的PA的抑制作用较弱,而在较低浓度下会干扰胶原蛋白诱导的PA。静脉注射LG 30435和噻嗪铵,从0.1μmol/kg的剂量开始,剂量依赖性地抑制PAF诱导的BC。LG 30435的ED50为0.28μmol/kg,而即使在3μmol/kg时,噻嗪铵获得的抑制率也未达到50%。酮替芬和异丙嗪仅在3μmol/kg时部分有活性,而美喹他嗪和甲氧苄二胺在该剂量下无活性。这些结果表明,LG 30435具有独特的抗PAF作用,这在哮喘治疗中可能具有优势。