Takayasu-Okishio M, Terashita Z, Kondo K
Research and Development Division, Takeda Chemical Industries Ltd, Osaka, Japan.
Biochem Pharmacol. 1990 Dec 15;40(12):2713-7. doi: 10.1016/0006-2952(90)90592-9.
The effect of endothelin-1 (ET-1) on the release of thromboxane A2 (TXA2) was examined in cultured rat vascular smooth muscle cells (VSMC). ET-1 (10(-11) to 10(-6) M) significantly stimulated the release of thromboxane B2 (TXB2), a stable metabolite of TXA2. These effects of ET-1 were blocked by a cyclooxygenase inhibitor (indomethacin), a TXA2 synthetase inhibitor (CV-1451) and a specific platelet activating factor (PAF) antagonist (CV-6209). Additionally, PAF (10(-11) to 10(-6) M) stimulated the TXB2 release. Pretreatment with the phospholipase A2 inhibitor dexamethasone potently inhibited both ET-1 and PAF-induced elevation of cytosolic free Ca2+ concentrations [( Ca2+]i) in fura-2-loaded VSMC. These results clearly demonstrate that both ET-1 and PAF stimulate TXA2 biosynthesis in cultured rat VSMC, and TXA2 may contribute to the elevation of [Ca2+]i induced by ET-1 or PAF in VSMC. Furthermore, the stimulation of TXA2 biosynthesis may be a result of PLA2 activation by not only ET-1 but also PAF.
在培养的大鼠血管平滑肌细胞(VSMC)中研究了内皮素 -1(ET -1)对血栓素A2(TXA2)释放的影响。ET -1(10^(-11)至10^(-6) M)显著刺激了TXA2的稳定代谢产物血栓素B2(TXB2)的释放。ET -1的这些作用被环氧化酶抑制剂(吲哚美辛)、TXA2合成酶抑制剂(CV -1451)和特异性血小板活化因子(PAF)拮抗剂(CV -6209)所阻断。此外,PAF(10^(-11)至10^(-6) M)刺激了TXB2的释放。用磷脂酶A2抑制剂地塞米松预处理可有效抑制ET -1和PAF诱导的用fura -2负载的VSMC中胞质游离Ca2+浓度[Ca2+]i的升高。这些结果清楚地表明,ET -1和PAF均刺激培养的大鼠VSMC中TXA2的生物合成,并且TXA2可能有助于ET -1或PAF诱导的VSMC中[Ca2+]i的升高。此外,TXA2生物合成的刺激可能是不仅ET -1而且PAF激活PLA2的结果。