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S-腺苷同型半胱氨酸水解酶抑制剂3-去氮腺苷的免疫抑制作用

Immunosuppressive effects of the S-adenosylhomocysteine hydrolase inhibitor, 3-deazaadenosine.

作者信息

Medzihradsky J L, Zimmerman T P, Wolberg G, Elion G B

出版信息

J Immunopharmacol. 1982;4(1-2):29-41. doi: 10.3109/08923978209031073.

Abstract

Immunosuppressive effects of 3-deazaadenosine (3-DAA), an inhibitor of S-adenosylhomocysteine hydrolase, were tested in vivo in immune assays against sheep red blood cells (SRBC), involving serum titrations for hemagglutinins and hemolysins, cellular cytotoxicity tests and the direct plaque-forming cell assay. At daily doses up to 100 mg/kg, the compound was suppressive when injected before antigen and the effect appeared to be dose-dependent (ED50 = 52.6 +/- 4.9 mg/kg). When doses of 25 mg/kg of 3-DAA were given before antigen, co-injections of 250 mg/kg of L-homocysteine (L-HC) potentiated the suppressive effect, although L-HC alone was inactive. Daily administration of 100 mg/kg of 3-DAA or 250 mg/kg of L-HC alone was not suppressive when given after the antigen; however, in combination they were able to induce suppression. The possible biochemical mechanisms of the suppression, particularly those involving the inhibition of S-adenosylmethionine-dependent methylation reactions, are discussed.

摘要

S-腺苷同型半胱氨酸水解酶抑制剂3-脱氮腺苷(3-DAA)的免疫抑制作用在针对绵羊红细胞(SRBC)的体内免疫试验中进行了测试,这些试验包括血凝素和溶血素的血清滴定、细胞毒性试验以及直接空斑形成细胞试验。在每日剂量高达100 mg/kg时,该化合物在抗原注射前注射具有抑制作用,且这种作用似乎呈剂量依赖性(半数有效剂量 = 52.6 ± 4.9 mg/kg)。当在抗原前给予25 mg/kg的3-DAA剂量时,共同注射250 mg/kg的L-同型半胱氨酸(L-HC)可增强抑制作用,尽管单独的L-HC没有活性。当在抗原后给予时,每日给予100 mg/kg的3-DAA或单独给予250 mg/kg的L-HC没有抑制作用;然而,联合使用时它们能够诱导抑制作用。文中讨论了抑制作用可能的生化机制,特别是那些涉及抑制S-腺苷甲硫氨酸依赖性甲基化反应的机制。

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