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在炎症模型中对一种重组人锰超氧化物歧化酶的评估。

Assessment of a human recombinant manganese superoxide dismutase in models of inflammation.

作者信息

Dowling E J, Chander C L, Claxson A W, Lillie C, Blake D R

机构信息

Bone and Joint Research Unit, London Hospital Medical College, England.

出版信息

Free Radic Res Commun. 1993;18(5):291-8. doi: 10.3109/10715769309147496.

Abstract

We evaluated a novel human recombinant preparation of manganese superoxide dismutase (MnSOD) for anti-inflammatory and anti-oxidant activity compared with a copper zinc (CuZn) SOD preparation. The results showed that administration of MnSOD (50, 100 and 200 micrograms kg-1) in the Freund's Complete Adjuvant (FCA) mediated paw oedema model suppressed the inflammation at 4 hours by 43, 25 and 43% (P < 0.001, P < 0.01 and P < 0.001 at respective doses). However, 24 hours post-challenge, MnSOD (50 and 100 micrograms kg-1), suppressed the inflammation by 19% (P < 0.001). In contrast, Mn SOD at higher doses (400-800 micrograms kg-1; 2 mgkg-1) exacerbated the inflammatory response at 4 hours. This pro-inflammatory response declined progressively by 24 hours. Furthermore, CuZn SOD produced no significant effects on the inflammatory response. In the carrageenan-induced synovitis model, Mn SOD (25 and 50 micrograms; intra-articular administration) exacerbated the inflammation at 48 hours. In contrast, Mn SOD at 5 micrograms produced a significant suppression (44%, P < 0.05) in knee joint swelling at 24 hours. The CuZn SOD preparation produced marked pro-inflammatory effects in the joints whilst it lacked activity in the FCA-mediated paw oedema model. These findings support a therapeutic potential of MnSOD in inflammatory disorders, however the compound has a complex pharmaco-dynamic profile.

摘要

我们评估了一种新型的人重组锰超氧化物歧化酶(MnSOD)制剂的抗炎和抗氧化活性,并与铜锌(CuZn)超氧化物歧化酶制剂进行了比较。结果显示,在弗氏完全佐剂(FCA)介导的爪肿胀模型中,给予MnSOD(50、100和200微克/千克)在4小时时分别抑制炎症43%、25%和43%(相应剂量下P<0.001、P<0.01和P<0.001)。然而,在激发后24小时,MnSOD(50和100微克/千克)抑制炎症19%(P<0.001)。相比之下,较高剂量(400 - 800微克/千克;2毫克/千克)的MnSOD在4小时时加剧了炎症反应。这种促炎反应在24小时时逐渐下降。此外,CuZn SOD对炎症反应没有显著影响。在角叉菜胶诱导的滑膜炎模型中,MnSOD(25和50微克;关节内给药)在48小时时加剧了炎症。相比之下,5微克的MnSOD在24小时时显著抑制了膝关节肿胀(44%,P<0.05)。CuZn SOD制剂在关节中产生了明显的促炎作用,而在FCA介导的爪肿胀模型中缺乏活性。这些发现支持了MnSOD在炎症性疾病中的治疗潜力,然而该化合物具有复杂的药效学特征。

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