Shaw J O
Prostaglandins. 1981 Apr;21(4):571-9. doi: 10.1016/0090-6980(81)90005-8.
The regulatory role of Ca2+ on the conversion of arachidonic acid (AA) into thromboxane B2 (TXB2) was examined in washed rabbit platelets, whose secretory processes are known to have requirements for extracellular Ca2+. Varying the extracellular free Ca2+ [Caf2+] concentration from less than 10(-8) M to 10(-3) M had no significant effect on the synthesis of immunoreactive TXB2 by rabbit platelets incubated with 1-4 microM AA. On the other hand, 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate (TMB-8), a putative antagonist of intracellular Ca2+ movement, inhibited AA-stimulated synthesis of TXB2 in a concentration dependent manner--an effect which could be partially overcome by increasing the AA concentration. The TMB-8 inhibition could not be reversed by increasing the [Ca2+f]. Studies examining platelet metabolism of 14C-AA and 14C-prostaglandin H2 demonstrated that TMB-8 inhibited platelet cyclooxygenase, but not thromboxane synthetase. These studies demonstrate the absence of a requirement for [Ca2+f] but suggest the presence of a TMB-8 sensitive intracellular Ca2+ pool in the rabbit platelet synthesis of TXB2 from AA.
在洗涤过的兔血小板中研究了Ca2+对花生四烯酸(AA)转化为血栓素B2(TXB2)的调节作用,已知其分泌过程需要细胞外Ca2+。将细胞外游离Ca2+[Caf2+]浓度从低于10(-8)M变化到10(-3)M,对用1-4 microM AA孵育的兔血小板合成免疫反应性TXB2没有显著影响。另一方面,8-(N,N-二乙氨基)辛基-3,4,5-三甲氧基苯甲酸酯(TMB-8),一种假定的细胞内Ca2+移动拮抗剂,以浓度依赖的方式抑制AA刺激的TXB2合成——增加AA浓度可部分克服这种效应。增加[Ca2+f]不能逆转TMB-8的抑制作用。对14C-AA和14C-前列腺素H2的血小板代谢研究表明,TMB-8抑制血小板环氧化酶,但不抑制血栓素合成酶。这些研究表明,从AA合成TXB2的过程中,兔血小板不需要[Ca2+f],但提示存在对TMB-8敏感的细胞内Ca2+池。