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大鼠血清急性期α2-巨球蛋白水平的其他抑制剂。6-巯基嘌呤及一些脂氧合酶和环氧化酶抑制剂的作用。

Additional inhibitors of rat serum acute phase alpha 2-macroglobulin levels. Effect of 6-mercaptopurine and some lipoxygenase and cyclo-oxygenase inhibitors.

作者信息

Baldo B A

出版信息

Agents Actions. 1982 Jul;12(3):340-3. doi: 10.1007/BF01965400.

Abstract

With the use of a previously described electroimmunoassay, 4 more compounds were found to depress acute phase alpha 2-macroglobulin levels in rat serum following the injection of turpentine. The compounds, meclofenamic acid, dextropropoxyphene, 5,8,11,14-eicosatetraynoic acid and 6-mercaptopurine are thus grouped with a variety of anti-inflammatory agents, cyclo-oxygenase inhibitors, hypolipidaemics and colchicine, all of which share the property of reducing the concentration of alpha 2-macroglobulin in rat serum. Compounds with immunosuppressant properties, namely amethopterin, azathioprine, cyclophosphamide and 5-fluorouracil, the steroids, betamethasone and dexamethasone, the lipoxygenase inhibitor, nordihydroguaiaretic acid, and MK477, a compound said to stimulate prostaglandin synthesis, did not reduce serum levels of the acute phase protein. 6-Mercaptopurine, a compound known to show anti-inflammatory properties in some systems, proved to be the strongest inhibitor found so far. The rat acute phase protein electroimmunoassay may thus be an effective screen for detecting a new class of anti-inflammatory agents. Knowledge of the mechanisms of action of drugs that depress rat serum alpha 2-macroglobulin concentrations may promote understanding of the control of acute phase protein production by the liver.

摘要

使用先前描述的电免疫测定法,发现又有4种化合物在注射松节油后可降低大鼠血清中的急性期α2-巨球蛋白水平。这些化合物,即甲氯芬那酸、右丙氧芬、5,8,11,14-二十碳四炔酸和6-巯基嘌呤,因此与多种抗炎药、环氧化酶抑制剂、降血脂药和秋水仙碱归为一类,所有这些药物都具有降低大鼠血清中α2-巨球蛋白浓度的特性。具有免疫抑制特性的化合物,即氨甲蝶呤、硫唑嘌呤、环磷酰胺和5-氟尿嘧啶、类固醇、倍他米松和地塞米松、脂氧合酶抑制剂去甲二氢愈创木酸,以及据说能刺激前列腺素合成的化合物MK477,均未降低急性期蛋白的血清水平。6-巯基嘌呤,一种已知在某些系统中具有抗炎特性的化合物,被证明是迄今为止发现的最强抑制剂。因此,大鼠急性期蛋白电免疫测定法可能是检测新型抗炎药的有效筛选方法。了解降低大鼠血清α2-巨球蛋白浓度的药物的作用机制可能有助于增进对肝脏急性期蛋白产生调控的理解。

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