Poeckel Daniel, Tausch Lars, Altmann Anja, Feisst Christian, Klinkhardt Ute, Graff Jochen, Harder Sebastian, Werz Oliver
Institute of Pharmaceutical Chemistry, University of Frankfurt, Marie-Curie-Str. 9, Frankfurt D-60439, Germany.
Br J Pharmacol. 2005 Oct;146(4):514-24. doi: 10.1038/sj.bjp.0706366.
We have recently shown that in polymorphonuclear leukocytes, 11-keto boswellic acids (KBAs) induce Ca2+ mobilisation and activation of mitogen-activated protein kinases (MAPK). Here we addressed the effects of BAs on central signalling pathways in human platelets and on various platelet functions. We found that beta-BA (10 microM), the 11-methylene analogue of KBA, caused a pronounced mobilisation of Ca2+ from internal stores and induced the phosphorylation of p38 MAPK, extracellular signal-regulated kinase (ERK)2, and Akt. These effects of beta-BA were concentration dependent, and the magnitude of the responses was comparable to those obtained after platelet stimulation with thrombin or collagen. Based on inhibitor studies, beta-BA triggers Ca2+ mobilisation via the phospholipase (PL)C/inositol-1,4,5-trisphosphate pathway, and involves Src family kinase signalling. Investigation of platelet functions revealed that beta-BA (> or =10 microM) strongly stimulates the platelet-induced generation of thrombin in an ex-vivo in-vitro model, the liberation of arachidonic acid (AA), and induces platelet aggregation in a Ca2+-dependent manner. In contrast to beta-BA, the 11-keto-BAs (KBA or AKBA) evoke only moderate Ca2+ mobilisation and activate p38 MAPK, but fail to induce phosphorylation of ERK2 or Akt, and do not cause aggregation or significant generation of thrombin. In summary, beta-BA potently induces Ca2+ mobilisation as well as the activation of pivotal protein kinases, and elicits functional platelet responses such as thrombin generation, liberation of AA, and aggregation.
我们最近发现,在多形核白细胞中,11-酮基乳香酸(KBA)可诱导钙离子动员及丝裂原活化蛋白激酶(MAPK)激活。在此,我们研究了乳香酸(BA)对人血小板中中心信号通路及各种血小板功能的影响。我们发现,β-BA(10微摩尔),即KBA的11-亚甲基类似物,可引起细胞内钙离子的显著动员,并诱导p38 MAPK、细胞外信号调节激酶(ERK)2及Akt的磷酸化。β-BA的这些作用具有浓度依赖性,其反应强度与用凝血酶或胶原刺激血小板后获得的反应相当。基于抑制剂研究,β-BA通过磷脂酶(PL)C/肌醇-1,4,5-三磷酸途径触发钙离子动员,并涉及Src家族激酶信号传导。对血小板功能的研究表明,β-BA(≥10微摩尔)在体外模型中强烈刺激血小板诱导的凝血酶生成、花生四烯酸(AA)释放,并以钙离子依赖的方式诱导血小板聚集。与β-BA相反,11-酮基乳香酸(KBA或AKBA)仅引起适度的钙离子动员并激活p38 MAPK,但不能诱导ERK2或Akt的磷酸化,也不会引起聚集或显著的凝血酶生成。总之,β-BA可有效诱导钙离子动员以及关键蛋白激酶的激活,并引发血小板的功能性反应,如凝血酶生成、AA释放和聚集。