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[甲磺酸萘莫司他(FUT-175)对大鼠多形核白细胞产生活性氧的抑制作用]

[Inhibitory effect of nafamostat mesilate (FUT-175) on O2- production in rat polymorphonuclear leucocytes].

作者信息

Oda M, Ogihara M, Sato T, Kurumi M, Iwaki M

出版信息

Nihon Yakurigaku Zasshi. 1986 May;87(5):521-6. doi: 10.1254/fpj.87.521.

Abstract

Effect of nafamostat mesilate (FUT-175), a serine protease inhibitor, having anti-inflammatory effects was studied on superoxide (O2-) production in rat polymorphonuclear leucocytes (PMN) and compared with those of other serine protease inhibitors and typical anti-inflammatory agents. 1) O2- productions in rat PMN stimulated with concanavalin A (Con A) and cytochalasin B (Cyt B) were too weak to observe. With NADH, however, strong O2- production was induced by Con A and Cyt B. 2) FUT-175 at 10(-6) and 10(-5) M inhibited O2- production in rat PMN induced by Con A and Cyt B with NADH in a concentration-dependent manner. 3) The serine protease inhibitor L-tosylamido-2-phenylethyl-chloromethyl ketone (TPCK) and soybean trypsin inhibitor (SBTI) inhibited O2- production at 10(-5) M and 10(-4) M, respectively, while aprotinin, chymostatin and leupeptin did not. 4) Neither indomethacin nor dexamethasone, typical anti-inflammatory agents, inhibited O2- production. Mepacrine, a phospholipase A2 inhibitor, strongly inhibited it. 5) O2- production in PMN prepared from the rat administered FUT-175, 200 mg/kg, p.o., was significantly decreased in comparison with that of the control rat. 6) FUT-175 had no effect on O2- production by hypoxanthine-xanthine oxidase. These results showed FUT-175 had a strong inhibitory effect on O2- production in rat PMN which other typical anti-inflammatory agents did not have.

摘要

研究了具有抗炎作用的丝氨酸蛋白酶抑制剂甲磺酸萘莫司他(FUT-175)对大鼠多形核白细胞(PMN)中超氧化物(O2-)产生的影响,并与其他丝氨酸蛋白酶抑制剂和典型抗炎药进行了比较。1)用伴刀豆球蛋白A(Con A)和细胞松弛素B(Cyt B)刺激的大鼠PMN中的O2-产生太弱而无法观察到。然而,使用NADH时,Con A和Cyt B诱导了强烈的O2-产生。2)10^(-6)和10^(-5) M的FUT-175以浓度依赖性方式抑制Con A和Cyt B与NADH诱导的大鼠PMN中的O2-产生。3)丝氨酸蛋白酶抑制剂L-甲苯磺酰氨基-2-苯乙基氯甲基酮(TPCK)和大豆胰蛋白酶抑制剂(SBTI)分别在10^(-5) M和10^(-4) M时抑制O2-产生,而抑肽酶、糜蛋白酶抑制剂和亮抑蛋白酶肽则没有。4)典型抗炎药吲哚美辛和地塞米松均未抑制O2-产生。磷脂酶A2抑制剂米帕林强烈抑制了它。5)与对照大鼠相比,口服给予200 mg/kg FUT-175的大鼠制备的PMN中的O2-产生显著降低。6)FUT-175对次黄嘌呤-黄嘌呤氧化酶产生O2-没有影响。这些结果表明,FUT-175对大鼠PMN中的O2-产生具有强烈的抑制作用,而其他典型抗炎药则没有。

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