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前路何方:四环素治疗关节炎类疾病的科学基础。

The road forward: the scientific basis for tetracycline treatment of arthritic disorders.

机构信息

The Division of Rheumatology, Prohealthcare Associates, LLP, Lake Success, NY, United States.

出版信息

Pharmacol Res. 2011 Dec;64(6):610-3. doi: 10.1016/j.phrs.2011.06.010. Epub 2011 Jun 21.

Abstract

The potential role of a collagenase inhibitor for treatment of arthritis was recognized almost immediately after the discovery of vertebrate collagenase. Yet despite vast efforts from the pharmaceutical industry, no such drug has been approved for such use by a regulatory agency. Although two semisynthetic antimicrobial tetracyclines, viz. minocycline and doxycycline, have been shown to have modest clinical benefits in over a dozen trials in rheumatoid arthritis, neither drug is in widespread use. The almost universal use of methotrexate and the rapid development of potent biologic agents have eclipsed the potential usage of TETs for RA. Ironically, it is in osteoarthritis, where there has only been one clinical trial which essentially failed, that the best potential exists for use of an MMP-inhibiting TET.

摘要

胶原酶抑制剂在关节炎治疗中的潜在作用在脊椎动物胶原酶被发现后几乎立即被认识到。然而,尽管制药行业做出了巨大努力,但没有一种这样的药物被监管机构批准用于这种用途。尽管两种半合成抗菌四环素,即米诺环素和多西环素,在超过 12 项类风湿关节炎临床试验中显示出适度的临床益处,但这两种药物都没有广泛使用。甲氨蝶呤的广泛应用和强有力的生物制剂的快速发展使 TET 在 RA 中的潜在用途黯然失色。具有讽刺意味的是,正是在骨关节炎中,仅有一项临床试验基本上失败了,而使用 MMP 抑制 TET 的潜力最大。

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