Suppr超能文献

用于治疗2型糖尿病和血脂异常的PPAR-β/δ激动剂:一个仍在寻找归属的被收养孤儿

PPAR-beta/delta agonists for Type 2 diabetes and dyslipidemia: an adopted orphan still looking for a home.

作者信息

Billin Andrew N

机构信息

GlaxoSmithKline, Inc., 5 Moore Drive, Research Triangle Park, NC 27709, USA.

出版信息

Expert Opin Investig Drugs. 2008 Oct;17(10):1465-71. doi: 10.1517/13543784.17.10.1465.

Abstract

BACKGROUND

The identification of small molecule agonists for the nuclear receptor peroxisome proliferator-activated receptor beta/delta (PPAR-beta/delta, NR1C2) has enabled the characterization of this receptor's functions in preclinical models. Subsequently, a number of small molecule agonists of PPAR-beta/delta have been progressed into clinical trials.

OBJECTIVE

This review will examine the major preclinical findings that underpin the hypothesis that PPAR-beta/delta agonists may be beneficial in treating dyslipidemia and Type 2 diabetes, as well as emerging clinical data with a variety of PPAR-beta/delta agonists.

METHODS

The literature concerning preclinical experiments that combine in vivo and in vitro mechanistic studies are reviewed and compared with the results of the early clinical trials.

CONCLUSIONS

Thus far, the activities of the agonists seen in the clinic are broadly similar to those seen in preclinical models. However, it is still not known if PPAR-beta/delta agonists will truly be differentiated enough from current treatments to justify their use in treating dyslipidemia or Type 2 diabetes. Major challenges for the development of PPAR-beta/delta agonists exist and the path forward is as yet undefined.

摘要

背景

核受体过氧化物酶体增殖物激活受体β/δ(PPAR-β/δ,NR1C2)小分子激动剂的鉴定,使得在临床前模型中能够对该受体的功能进行表征。随后,多种PPAR-β/δ小分子激动剂已进入临床试验阶段。

目的

本综述将探讨支持PPAR-β/δ激动剂可能有益于治疗血脂异常和2型糖尿病这一假说的主要临床前研究结果,以及多种PPAR-β/δ激动剂的最新临床数据。

方法

对结合体内和体外机制研究的临床前实验相关文献进行综述,并与早期临床试验结果进行比较。

结论

迄今为止,在临床上观察到的激动剂活性与临床前模型中所见的大致相似。然而,PPAR-β/δ激动剂是否真的能与现有治疗方法有足够差异,从而证明其在治疗血脂异常或2型糖尿病中的应用价值,目前仍不清楚。PPAR-β/δ激动剂的开发存在重大挑战,未来的发展道路尚不明确。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验