Rahman Khalid, Lowe Gordon M, Smith Sarah
School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom
School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom.
J Nutr. 2016 Feb;146(2):410S-415S. doi: 10.3945/jn.114.202408. Epub 2016 Jan 13.
Increased platelet aggregation plays a pivotal role in the etiology of cardiovascular disease. Upon platelet aggregation, an increase in free cytoplasmic Ca(2+) results in the inhibition of soluble guanylyl cyclase (sGC) and adenylyl cyclase (AC), leading to a decrease in cyclic guaninosine-5'-monophosphate (cGMP) and cAMP, respectively. This leads to the activation of the glycoprotein IIb/IIIa (GPIIb/IIIa) fibrinogen receptor, resulting in platelet shape change. Aged garlic extract (AGE) decreases platelet aggregation; however, the mechanisms involved are not clearly defined.
Our objective was to investigate the effects of AGE on intraplatelet cell signaling and platelet shape change.
Platelets from 14 participants were studied. Platelet aggregation was induced by ADP in the presence of AGE up to a concentration of 6.25% (vol:vol) alone or in combination with 3-morpholinosydnonimine (Sin-1), a nitric oxide donor. The experiments with AGE were repeated in the presence of 3-isobutyl-1-methylxanthine (IBMX), a phosphodiesterase inhibitor. In a series of separate experiments, platelet aggregation was induced in the presence of either 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), an sGC inhibitor, or 9-(tetrahydro-2-furanyl)-9H-purin-6-amine (SQ22536), an AC inhibitor, or a combination of both in the presence of IBMX and AGE. Intraplatelet cGMP and cAMP were measured. The platelets were also subjected to scanning electron microscopic analysis, and their binding to fibrinogen was determined.
AGE decreased platelet aggregation at all concentrations tested; this decrease was more marked in the presence of Sin-1 and ranged between 15% and 67%.The presence of IBMX also led to a decrease (17-35%) in platelet aggregation at all AGE concentrations and a significant decrease in the amounts of cGMP (24-41%) and cAMP (19-70%), respectively, in the presence of ODQ and SQ22536. The presence of AGE significantly inhibited the binding of activated platelets to fibrinogen, preventing changes in platelet shape.
These results indicate that AGE inhibits platelet aggregation by increasing cyclic nucleotides and inhibiting fibrinogen binding and platelet shape change.
血小板聚集增加在心血管疾病的病因中起关键作用。血小板聚集时,游离细胞质Ca(2+)增加会导致可溶性鸟苷酸环化酶(sGC)和腺苷酸环化酶(AC)受到抑制,分别导致环磷酸鸟苷(cGMP)和环磷酸腺苷(cAMP)减少。这会导致糖蛋白IIb/IIIa(GPIIb/IIIa)纤维蛋白原受体活化,引起血小板形状改变。 aged garlic extract(AGE)可减少血小板聚集;然而,其涉及的机制尚不清楚。
我们的目的是研究AGE对血小板内细胞信号传导和血小板形状改变的影响。
研究了14名参与者的血小板。在单独存在高达6.25%(体积:体积)的AGE或与一氧化氮供体3-吗啉代辛二亚胺(Sin-1)联合存在的情况下,用ADP诱导血小板聚集。在磷酸二酯酶抑制剂3-异丁基-1-甲基黄嘌呤(IBMX)存在的情况下重复进行AGE实验。在一系列单独的实验中,在IBMX和AGE存在的情况下,分别用sGC抑制剂1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ)或AC抑制剂9-(四氢-2-呋喃基)-9H-嘌呤-6-胺(SQ22536)或两者的组合诱导血小板聚集。测量血小板内的cGMP和cAMP。还对血小板进行了扫描电子显微镜分析,并测定了它们与纤维蛋白原的结合。
在所有测试浓度下,AGE均降低了血小板聚集;在Sin-1存在的情况下,这种降低更为明显,范围在15%至67%之间。IBMX的存在也导致在所有AGE浓度下血小板聚集减少(17 - 35%),并且在ODQ和SQ22536存在的情况下,cGMP(24 - 41%)和cAMP(19 - 70%)的量分别显著减少。AGE的存在显著抑制了活化血小板与纤维蛋白原的结合,防止了血小板形状的改变。
这些结果表明,AGE通过增加环核苷酸并抑制纤维蛋白原结合和血小板形状改变来抑制血小板聚集。