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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Elemental composition of platelets. Part III. Determination of Ag, Au, Cd, Co, Cr, Cs, Mo, Rb, Sb, and Se in normal human platelets by neutron activation analysis.
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Elemental composition of platelets. Part III. Determination of Ag, Au, Cd, Co, Cr, Cs, Mo, Rb, Sb, and Se in normal human platelets by neutron activation analysis.

机译:血小板的元素组成。第三部分通过中子活化分析测定正常人血小板中的Ag,Au,Cd,Co,Cr,Cs,Mo,Rb,Sb和Se

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摘要

The elements Ag, Au, Cd, Co, Cr, Cs, Mo, Rb, Sb, and Se were determined in platelets from seven normal donors. The results, in ng/g wet weight, for plasma-free platelets follow: "Pure" platelets: Ag = 29 +/- (18), au = 0.22 +/- (0.22), Cd = 6.2 +/- 3.4, Cs = 54.8 +/- 19.2, Cr = 6.1 +/- 2.5, Co = 7.5 +/- (5.0), Mo = 3.4 +/- 1.3, Rb = 10400 +/- 3000, Sb = 18 +/- (26), and Se = 782 +/- 127. "Impure" platelets: Au = 0.23 +/- (0.28), Cd = 6.4 +/- 2.6, Cs = 35.2 +/- 13.8, Cr = 8.2 +/- 2.9, Co = 2.9 +/- (3.0), Mo = 3.2 +/- 0.8, Rb = 8700 +/- 1700, Sb = 13.2 +/- (8.7), and Se = 679 +/- 57. To our knowledge, none of these 10 trace elements has been determined in platelets before. The selenium concentration in platelets exceeds that in other tissues (e.g., liver). We suggest that glutathione peroxidase or other unknown selenoenzymes are particularly important in platelet metabolism. Platelets are crucial for triggering thrombosis, and so may be involved as links between selenium deficiency and the concomitant increased death rate from cardiovascular disease.
机译:在七个正常供体的血小板中测定了元素Ag,Au,Cd,Co,Cr,Cs,Mo,Rb,Sb和Se。对于无血浆的血小板,以ng / g湿重为单位的结果如下:“纯”血小板:Ag = 29 +/-(18),au = 0.22 +/-(0.22),Cd = 6.2 +/- 3.4, Cs = 54.8 +/- 19.2,Cr = 6.1 +/- 2.5,Co = 7.5 +/-(5.0),Mo = 3.4 +/- 1.3,Rb = 10400 +/- 3000,Sb = 18 +/-(26 ),Se = 782 +/-127。“不纯”血小板:Au = 0.23 +/-(0.28),Cd = 6.4 +/- 2.6,Cs = 35.2 +/- 13.8,Cr = 8.2 +/- 2.9, Co = 2.9 +/-(3.0),Mo = 3.2 +/- 0.8,Rb = 8700 +/- 1700,Sb = 13.2 +/-(8.7)和Se = 679 +/-57。据我们所知这10种微量元素中的10种已经在血小板中测定过。血小板中的硒浓度超过其他组织(例如肝脏)中的硒浓度。我们建议谷胱甘肽过氧化物酶或其他未知的硒酶在血小板代谢中特别重要。血小板对于触发血栓形成至关重要,因此可能与硒缺乏与心血管疾病的死亡率增加之间的联系有关。

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