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血小板中储存化合物分泌的代谢方面。不同pH值下氟化钠对洗涤后血小板核苷酸代谢及功能的影响。

Metabolic aspects of the secretion of stored compounds from blood platelets. The effect of NaF at different pH on nucleotide metabolism and function of washed platelets.

作者信息

Mürer E H, Davenport K, Siojo E, Day H J

出版信息

Biochem J. 1981 Jan 15;194(1):187-92. doi: 10.1042/bj1940187.

Abstract

The purpose of this study was to investigate the response of human blood platelets to fluoride at different pH. The results were as follows. (1) Fluoride induced secretion faster and at a lower concentration when pH was lowered. (2) Platelets exposed to 2 mM-fluoride at 0 degrees C at pH 5.3 underwent secretion when first pH and then temperature was raised, although no secretion was seen at 2 mM-fluoride concentration in the absence of the preincubation at low pH. (3) The concentration of [14C]ATP in platelets decreased steeply in response to fluoride before induction of secretion. Addition of antimycin blocked or partly inhibited secretion. Fluoride thus exerts an inhibitory effect on platelet glycolysis before induction of secretion. (4) Fluoride accumulated in the platelet pellet by a time course that preceded secretion. The accumulation was faster and greater at pH 6 than at 7.4. These four points are taken as indirect evidence that fluoride has to penetrate to the interior of the platelet to induce secretion. The activation takes place over a wide range of acid pH in contrast with induction of platelet function via the outside of the plasma membrane. In addition evidence is presented that the salvage pathway may under special circumstances play an important role in the re-synthesis of platelet adenine nucleotides.

摘要

本研究的目的是调查人血小板在不同pH值下对氟化物的反应。结果如下:(1)当pH值降低时,氟化物诱导分泌的速度更快且所需浓度更低。(2)在pH 5.3时,于0℃下暴露于2 mM氟化物的血小板,在先是pH值然后是温度升高时会发生分泌,尽管在没有低pH值预孵育的情况下,2 mM氟化物浓度时未见分泌。(3)在诱导分泌之前,血小板中[14C]ATP的浓度因氟化物而急剧下降。添加抗霉素可阻断或部分抑制分泌。因此,氟化物在诱导分泌之前对血小板糖酵解具有抑制作用。(4)氟化物在血小板沉淀中的积累时间进程先于分泌。在pH 6时积累速度更快且积累量更大,而在pH 7.4时则不然。这四点被视为氟化物必须渗透到血小板内部才能诱导分泌的间接证据。与通过质膜外部诱导血小板功能相反,这种激活在广泛的酸性pH范围内发生。此外,有证据表明,在特殊情况下,补救途径可能在血小板腺嘌呤核苷酸的重新合成中起重要作用。

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