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经洗涤的兔血小板产生血小板活化因子。

Production of platelet-activating factor by washed rabbit platelets.

作者信息

Oda M, Satouchi K, Yasunaga K, Saito K

出版信息

J Lipid Res. 1985 Nov;26(11):1294-9.

PMID:3934305
Abstract

Production of platelet-activating factor by washed rabbit platelets under stimulation with the ionophore A23187 was investigated utilizing two groups of platelet preparations. The first platelet preparation contained 0.03 +/- 0.02% contaminating white cells, while the second preparation contained 0.48 +/- 0.27% white cells. The latter preparation produced platelet-activating factor, mainly 1-hexadecyl-2-acetyl-sn-glycero-3-phosphocholine, 8.3 +/- 6.3 pmol (mean +/- standard deviation) with a range of 2.6 to 21.4 pmol (n = 9), followed by small quantities of 1-octadecenyl- and 1-octadecyl-2-acetyl-sn-glycero-3-phosphocholine. In contrast, there was no production of 1-alkyl-2-acetyl-sn-glycero-3-phosphocholine by the former platelet preparation having 0.03% leukocytes. These quantitative analyses were carried out by the selected ion monitoring technique and it was concluded that it is necessary to consider the presence of contaminating white cells in studies on the production of platelet-activating factor by platelets.

摘要

利用两组血小板制剂,研究了在离子载体A23187刺激下洗涤过的兔血小板中血小板活化因子的产生情况。第一组血小板制剂含有0.03±0.02%的污染白细胞,而第二组制剂含有0.48±0.27%的白细胞。后一组制剂产生血小板活化因子,主要是1-十六烷基-2-乙酰基-sn-甘油-3-磷酸胆碱,为8.3±6.3皮摩尔(平均值±标准差),范围为2.6至21.4皮摩尔(n = 9),随后还有少量的1-十八碳烯基-和1-十八烷基-2-乙酰基-sn-甘油-3-磷酸胆碱。相比之下,含0.03%白细胞的前一组血小板制剂未产生1-烷基-2-乙酰基-sn-甘油-3-磷酸胆碱。这些定量分析采用选择离子监测技术进行,得出的结论是,在研究血小板产生血小板活化因子时,有必要考虑污染白细胞的存在。

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