Rehm A G, Wu H, Halenda S P
Department of Pharmacology, University of Missouri School of Medicine, Columbia 65212.
FEBS Lett. 1988 Jul 18;234(2):316-20. doi: 10.1016/0014-5793(88)80107-8.
The effects of guanine nucleotides on arachidonic acid (AA) release were studied in intact and saponin-permeabilized human platelets. While GTP[S] itself caused a stimulation of AA release in permeabilized cells, GTP[S], GDP[S], GTP, ATP and other nucleotides inhibited AA release in response to thrombin and other agonists in intact, as well as permeabilized platelets. Inhibition of agonist-stimulated AA release by nucleotides was partially attenuated by addition of ADP, and was abolished by prior stimulation of platelets to discharge the ADP-containing dense granules. These results suggest: (i) that released ADP plays an important contributory role in agonist-stimulated platelet AA release, and (ii) that guanine nucleotides can modulate platelet activation through an extracellular action which is distinct from their effects on G-proteins.
在完整的和经皂角苷通透处理的人血小板中研究了鸟嘌呤核苷酸对花生四烯酸(AA)释放的影响。虽然GTP[S]本身可刺激通透处理的细胞释放AA,但GTP[S]、GDP[S]、GTP、ATP和其他核苷酸可抑制完整血小板以及通透处理的血小板中凝血酶和其他激动剂诱导的AA释放。通过添加ADP可部分减弱核苷酸对激动剂刺激的AA释放的抑制作用,而预先刺激血小板以释放含ADP的致密颗粒则可消除这种抑制作用。这些结果表明:(i)释放的ADP在激动剂刺激的血小板AA释放中起重要的促进作用,以及(ii)鸟嘌呤核苷酸可通过一种不同于其对G蛋白作用的细胞外作用来调节血小板活化。