• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

曲格列酮及相关化合物:糖尿病之外的治疗潜力。

Troglitazone and related compounds: therapeutic potential beyond diabetes.

作者信息

Fujiwara T, Horikoshi H

机构信息

Pharmacology and Molecular Biol. Res. Labs., Sankyo. Co. Ltd., Tokyo, Japan.

出版信息

Life Sci. 2000 Oct 6;67(20):2405-16. doi: 10.1016/s0024-3205(00)00829-8.

DOI:10.1016/s0024-3205(00)00829-8
PMID:11065164
Abstract

Troglitazone and structurally related compounds (pioglitazone, rosiglitazone etc.) containing thiazolidinediones (TZD) are a novel class of antidiabetic agents which decrease blood glucose in diabetic animal models and in patients with Non-Insulin-Dependent Diabetes Mellitus (NIDDM) through alleviating insulin resistance. A large body of evidence is now accumulating indicating that insulin resistance and/or resulting hyperinsulinemia underlie the pathogenesis of not only diabetes but also of the clustering syndrome called "syndrome X" or "insulin resistance syndrome" which includes hypertension, dislipidemia and hypercoagulation. Therefore, TZD class of insulin sensitizers seem to have therapeutic potential to improve this clustering syndrome in addition to diabetes. Moreover, it was demonstrated that the TZD class of insulin sensitizers including troglitazone bind and activate the peroxisome proliferator-activated receptor gamma (PPARgamma), a nuclear hormone receptor. Although PPARgamma is predominantly expressed in adipose tissue, one of the target tissues for insulin, it have been subsequently found to be expressed in macrophages, vascular smooth muscle cells (VSMC), endothelial cells and several cancer cell lines. PPARgamma activation by PPARgamma agonists such as TZD class of insulin sensitizers in these cells modulates these cell functions such as the production of inflammatory cytokine by macrophages, proliferation and migration of VSMC, and growth or differentiation in cancer cells. In addition, troglitazone has potent antioxidant effect, and suppresses both L-type and receptor operated Ca2+ channel and protein kinase C. Thus since TZD class of insulin sensitizers has many kind of therapeutic effect in addition to lowering blood glucose, these agents expect to have therapeutic potential beyond diabetes.

摘要

曲格列酮以及含有噻唑烷二酮(TZD)的结构相关化合物(吡格列酮、罗格列酮等)是一类新型抗糖尿病药物,它们通过减轻胰岛素抵抗,降低糖尿病动物模型和非胰岛素依赖型糖尿病(NIDDM)患者的血糖。现在大量证据不断积累,表明胰岛素抵抗和/或由此导致的高胰岛素血症不仅是糖尿病发病机制的基础,也是被称为“X综合征”或“胰岛素抵抗综合征”的聚集综合征发病机制的基础,该综合征包括高血压、血脂异常和高凝状态。因此,TZD类胰岛素增敏剂除了对糖尿病有治疗潜力外,似乎对改善这种聚集综合征也有治疗潜力。此外,已证明包括曲格列酮在内的TZD类胰岛素增敏剂能结合并激活过氧化物酶体增殖物激活受体γ(PPARγ),一种核激素受体。尽管PPARγ主要在脂肪组织(胰岛素的靶组织之一)中表达,但随后发现它也在巨噬细胞、血管平滑肌细胞(VSMC)、内皮细胞和几种癌细胞系中表达。在这些细胞中,TZD类胰岛素增敏剂等PPARγ激动剂激活PPARγ可调节这些细胞功能,如巨噬细胞产生炎性细胞因子、VSMC的增殖和迁移以及癌细胞的生长或分化。此外,曲格列酮具有强大的抗氧化作用,并抑制L型和受体操纵的Ca2+通道以及蛋白激酶C。因此,由于TZD类胰岛素增敏剂除了降低血糖外还有多种治疗作用,这些药物有望具有超越糖尿病的治疗潜力。

相似文献

1
Troglitazone and related compounds: therapeutic potential beyond diabetes.曲格列酮及相关化合物:糖尿病之外的治疗潜力。
Life Sci. 2000 Oct 6;67(20):2405-16. doi: 10.1016/s0024-3205(00)00829-8.
2
Insulin resistance and its treatment by thiazolidinediones.胰岛素抵抗及其噻唑烷二酮类药物治疗
Recent Prog Horm Res. 2001;56:265-94. doi: 10.1210/rp.56.1.265.
3
Thiazolidinediones--tools for the research of metabolic syndrome X.噻唑烷二酮类——代谢综合征X研究的工具
Physiol Res. 1998;47(4):215-25.
4
The novel hypoglycemic agent YM440 normalizes hyperglycemia without changing body fat weight in diabetic db/db mice.新型降血糖药物YM440可使糖尿病db/db小鼠的高血糖恢复正常,且不改变体脂重量。
Metabolism. 2000 Mar;49(3):411-7. doi: 10.1016/s0026-0495(00)90440-2.
5
Thiazolidinediones, peroxisome proliferator-activated receptor gamma agonists, regulate endothelial cell growth and secretion of vasoactive peptides.噻唑烷二酮类药物,即过氧化物酶体增殖物激活受体γ激动剂,可调节内皮细胞生长及血管活性肽的分泌。
Atherosclerosis. 2001 Sep;158(1):113-9. doi: 10.1016/s0021-9150(01)00430-0.
6
[Mechanisms of action of thiazolidinediones].[噻唑烷二酮类药物的作用机制]
Diabetes Metab. 2001 Apr;27(2 Pt 2):271-8.
7
Insulin resistance, diabetes, and atherosclerosis: thiazolidinediones as therapeutic interventions.胰岛素抵抗、糖尿病与动脉粥样硬化:噻唑烷二酮类药物作为治疗干预手段
Curr Cardiol Rep. 2002 Nov;4(6):514-21. doi: 10.1007/s11886-002-0116-3.
8
Thiazolidinediones--the new insulin enhancers.噻唑烷二酮类——新型胰岛素增敏剂。
Clin Exp Hypertens. 1999 Jan-Feb;21(1-2):157-66. doi: 10.3109/10641969909068658.
9
Troglitazone: the discovery and development of a novel therapy for the treatment of Type 2 diabetes mellitus.
Adv Drug Deliv Rev. 2002 Nov 5;54(9):1173-97. doi: 10.1016/s0169-409x(02)00093-5.
10
Pharmacological profiles of a novel oral antidiabetic agent, JTT-501, an isoxazolidinedione derivative.新型口服抗糖尿病药物JTT-501(一种异恶唑烷二酮衍生物)的药理学特性
Eur J Pharmacol. 1999 Jan 8;364(2-3):211-9. doi: 10.1016/s0014-2999(98)00832-2.

引用本文的文献

1
Mechanisms underlying drug-mediated regulation of membrane protein function.药物介导的膜蛋白功能调节的机制。
Proc Natl Acad Sci U S A. 2021 Nov 16;118(46). doi: 10.1073/pnas.2113229118.
2
Patterns of use of insulin-sensitizing agents among diabetic, borderline diabetic and non-diabetic women in the National Health and Nutrition Examination Surveys.在全国健康和营养调查中,糖尿病、糖尿病前期和非糖尿病女性中胰岛素增敏剂的使用模式。
Gynecol Endocrinol. 2013 Apr;29(4):350-6. doi: 10.3109/09513590.2012.752457. Epub 2013 Jan 17.
3
Thiazolidinedione insulin sensitizers alter lipid bilayer properties and voltage-dependent sodium channel function: implications for drug discovery.
噻唑烷二酮类胰岛素增敏剂改变脂质双层性质和电压依赖性钠通道功能:对药物发现的影响。
J Gen Physiol. 2011 Aug;138(2):249-70. doi: 10.1085/jgp.201010529.
4
Rosiglitazone inhibits Kv4.3 potassium channels by open-channel block and acceleration of closed-state inactivation.罗格列酮通过开放通道阻断和加速失活状态关闭来抑制 Kv4.3 钾通道。
Br J Pharmacol. 2011 Jun;163(3):510-20. doi: 10.1111/j.1476-5381.2011.01210.x.
5
The peroxisome proliferator-activated receptor gamma agonist pioglitazone improves cardiometabolic risk and renal inflammation in murine lupus.过氧化物酶体增殖物激活受体γ激动剂吡格列酮可改善小鼠狼疮的心脏代谢风险和肾脏炎症。
J Immunol. 2009 Aug 15;183(4):2729-40. doi: 10.4049/jimmunol.0804341. Epub 2009 Jul 20.
6
The high affinity peroxisome proliferator-activated receptor-gamma agonist RS5444 inhibits both initiation and progression of colon tumors in azoxymethane-treated mice.高亲和力过氧化物酶体增殖物激活受体γ激动剂RS5444可抑制用氧化偶氮甲烷处理的小鼠结肠肿瘤的起始和进展。
Int J Cancer. 2008 Sep 1;123(5):991-7. doi: 10.1002/ijc.23640.
7
15-deoxy-(Delta12,14)-prostaglandin J2 (15d-PGJ2) induces cell death through caspase-independent mechanism in A172 human glioma cells.15-脱氧-(Δ12,14)-前列腺素J2(15d-PGJ2)通过非半胱天冬酶依赖机制诱导A172人胶质瘤细胞死亡。
Neurochem Res. 2006 Oct;31(10):1247-54. doi: 10.1007/s11064-006-9157-0.
8
mRNA expression of genes involved in lipid efflux and matrix degradation in occlusive and ectatic atherosclerotic disease.闭塞性和扩张性动脉粥样硬化疾病中参与脂质流出和基质降解的基因的mRNA表达
J Clin Pathol. 2005 Dec;58(12):1255-60. doi: 10.1136/jcp.2005.026161.
9
Inverse relationship between 15-lipoxygenase-2 and PPAR-gamma gene expression in normal epithelia compared with tumor epithelia.与肿瘤上皮相比,正常上皮中15-脂氧合酶-2和PPAR-γ基因表达呈负相关。
Neoplasia. 2005 Mar;7(3):280-93. doi: 10.1593/neo.04457.
10
Pleiotropic effects of thiazolidinediones: taking a look beyond antidiabetic activity.噻唑烷二酮类药物的多效性作用:超越抗糖尿病活性的视角
J Endocrinol Invest. 2004 Nov;27(10):982-91. doi: 10.1007/BF03347546.