Margalit A, Sofer Y, Grossman S, Reynaud D, Pace-Asciak C R, Livne A A
Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2589-92. doi: 10.1073/pnas.90.7.2589.
When human blood platelets are exposed to hypotonic medium they swell first but, shortly thereafter, revert toward their original volume in a process termed regulatory volume decrease (RVD). RVD is the result of an enhanced efflux of K+ and Cl- ions and associated water. Platelet RVD is controlled by a short-lived lipoxygenase-derived product (LP). By using a combination of high-performance liquid chromatography, gas chromatography-mass spectrometry, and RVD reconstitution bioassay, we show that LP is identical with hepoxilin A3. In addition we demonstrate that authentic hepoxilin A3 possesses the same biological properties on RVD reconstitution as LP and that the activity of both compounds is amplified through epoxide hydrolase inhibition with 3,3,3-trichloropropene-1,2-oxide. Therefore, we report here that volume expansion causes the formation and release of hepoxilin A3 from intact human platelets and that this hepoxilin plays a major role in volume regulation.
当人体血小板暴露于低渗介质中时,它们首先会肿胀,但此后不久,会通过一种称为调节性容积减小(RVD)的过程恢复到原始体积。RVD是K⁺和Cl⁻离子以及相关水分外流增加的结果。血小板RVD由一种寿命短暂的脂氧合酶衍生产物(LP)控制。通过结合使用高效液相色谱、气相色谱-质谱联用以及RVD重建生物测定法,我们发现LP与hepoxilin A3相同。此外,我们证明了纯正的hepoxilin A3在RVD重建方面具有与LP相同的生物学特性,并且这两种化合物的活性通过用3,3,3-三氯丙烯-1,2-氧化物抑制环氧水解酶而增强。因此,我们在此报告,容积扩张会导致完整人体血小板形成并释放hepoxilin A3,并且这种hepoxilin在容积调节中起主要作用。