• 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

醛糖还原酶抑制剂依帕司他治疗24周对非胰岛素依赖型糖尿病患者周围神经病变的影响。

Effect of 24 weeks of treatment with epalrestat, an aldose reductase inhibitor, on peripheral neuropathy in patients with non-insulin-dependent diabetes mellitus.

作者信息

Uchida K, Kigoshi T, Nakano S, Ishii T, Kitazawa M, Morimoto S

机构信息

Department of Internal Medicine, Kanazawa Medical University, Ishikawa, Japan.

出版信息

Clin Ther. 1995 May-Jun;17(3):460-6. doi: 10.1016/0149-2918(95)80111-1.

DOI:10.1016/0149-2918(95)80111-1
PMID:7585850
Abstract

The effects of treatment with epalrestat, an aldose reductase inhibitor, on peripheral neuropathy were studied in 45 patients with non-insulin-dependent diabetes mellitus (NIDDM). Epalrestat 150 mg three times daily was given for 24 weeks. Subjective symptoms, such as spontaneous pain in the lower extremities and numbness and hypoesthesia of the extremities or trunk, were significantly (P < 0.001) relieved after 12 and 24 weeks of epalrestat treatment. Vibratory perception thresholds, as measured by using a tuning fork (C-128) and a vibrometer, were improved after 24 weeks of treatment. Furthermore, there were no adverse effects on glucose or lipid metabolism during treatment. These results suggest that long-term (24-week) epalrestat therapy can be used effectively to treat peripheral neuropathy in NIDDM patients without affecting glucose or lipid metabolism.

摘要

对45例非胰岛素依赖型糖尿病(NIDDM)患者研究了醛糖还原酶抑制剂依帕司他治疗周围神经病变的效果。给予依帕司他150mg,每日3次,共治疗24周。依帕司他治疗12周和24周后,下肢自发痛、肢体或躯干麻木及感觉减退等主观症状明显减轻(P<0.001)。使用音叉(C-128)和振动计测量的振动觉阈值在治疗24周后得到改善。此外,治疗期间对糖代谢或脂代谢无不良影响。这些结果表明,长期(24周)依帕司他治疗可有效用于治疗NIDDM患者的周围神经病变,且不影响糖代谢或脂代谢。

相似文献

1
Effect of 24 weeks of treatment with epalrestat, an aldose reductase inhibitor, on peripheral neuropathy in patients with non-insulin-dependent diabetes mellitus.醛糖还原酶抑制剂依帕司他治疗24周对非胰岛素依赖型糖尿病患者周围神经病变的影响。
Clin Ther. 1995 May-Jun;17(3):460-6. doi: 10.1016/0149-2918(95)80111-1.
2
Long-term clinical effects of epalrestat, an aldose reductase inhibitor, on diabetic peripheral neuropathy: the 3-year, multicenter, comparative Aldose Reductase Inhibitor-Diabetes Complications Trial.醛糖还原酶抑制剂依帕司他对糖尿病周围神经病变的长期临床疗效:为期3年的多中心、比较性醛糖还原酶抑制剂 - 糖尿病并发症试验
Diabetes Care. 2006 Jul;29(7):1538-44. doi: 10.2337/dc05-2370.
3
Effects of epalrestat, an aldose reductase inhibitor, on diabetic peripheral neuropathy in patients with type 2 diabetes, in relation to suppression of N(ɛ)-carboxymethyl lysine.醛糖还原酶抑制剂依帕司他对 2 型糖尿病患者糖尿病周围神经病变的疗效与 N(ɛ)-羧甲基赖氨酸抑制的关系。
J Diabetes Complications. 2010 Nov-Dec;24(6):424-32. doi: 10.1016/j.jdiacomp.2008.10.005. Epub 2009 Aug 27.
4
Clinical investigation of epalrestat, an aldose reductase inhibitor, on diabetic neuropathy in Japan: multicenter study. Diabetic Neuropathy Study Group in Japan.醛糖还原酶抑制剂依帕司他对日本糖尿病性神经病变的临床研究:多中心研究。日本糖尿病性神经病变研究组
J Diabetes Complications. 1996 May-Jun;10(3):168-72. doi: 10.1016/1056-8727(96)00113-4.
5
Epalrestat: an aldose reductase inhibitor for the treatment of diabetic neuropathy.依帕司他:一种用于治疗糖尿病神经病变的醛糖还原酶抑制剂。
Pharmacotherapy. 2008 May;28(5):646-55. doi: 10.1592/phco.28.5.646.
6
Long-term effect of epalrestat on cardiac autonomic neuropathy in subjects with non-insulin dependent diabetes mellitus.依帕司他对非胰岛素依赖型糖尿病患者心脏自主神经病变的长期影响。
Diabetes Res Clin Pract. 1999 Mar;43(3):193-8. doi: 10.1016/s0168-8227(99)00015-7.
7
Epalrestat. A review of its pharmacology, and therapeutic potential in late-onset complications of diabetes mellitus.依帕司他。其药理学及在糖尿病晚期并发症治疗潜力的综述。
Drugs Aging. 1993 Nov-Dec;3(6):532-55. doi: 10.2165/00002512-199303060-00007.
8
Aldose reductase inhibition ameliorates pupillary light reflex and F-wave latency in patients with mild diabetic neuropathy.醛糖还原酶抑制可改善轻度糖尿病性神经病变患者的瞳孔光反射和F波潜伏期。
Diabetes Care. 2001 Jun;24(6):1093-8. doi: 10.2337/diacare.24.6.1093.
9
[Effects of the aldose reductase inhibitor on diabetic polyneuropathy--the efficacy of F wave measurement].醛糖还原酶抑制剂对糖尿病性多发性神经病的影响——F波测量的疗效
No To Shinkei. 1998 Sep;50(9):817-20.
10
I-123 MIBG cardiac imaging in diabetic neuropathy before and after epalrestat therapy.依帕司他治疗前后糖尿病性神经病变的I-123间碘苄胍心脏显像
Clin Nucl Med. 1999 Jun;24(6):418-20. doi: 10.1097/00003072-199906000-00008.

引用本文的文献

1
-Acetylcysteine overcomes epalrestat-mediated increase of toxic 4-hydroxy-2-nonenal and potentiates the anti-arthritic effect of epalrestat in AIA model.乙酰半胱氨酸克服依帕司他介导的毒性 4-羟基-2-壬烯醛增加,并增强依帕司他在 AIA 模型中的抗关节炎作用。
Int J Biol Sci. 2023 Aug 6;19(13):4082-4102. doi: 10.7150/ijbs.85028. eCollection 2023.
2
Aldo-Keto Reductases: Multifunctional Proteins as Therapeutic Targets in Diabetes and Inflammatory Disease.醛酮还原酶:糖尿病和炎症性疾病治疗靶点的多功能蛋白。
Adv Exp Med Biol. 2018;1032:173-202. doi: 10.1007/978-3-319-98788-0_13.
3
AKR1B1 promotes basal-like breast cancer progression by a positive feedback loop that activates the EMT program.
醛酮还原酶1B1通过激活上皮-间质转化程序的正反馈回路促进基底样乳腺癌进展。
J Exp Med. 2017 Apr 3;214(4):1065-1079. doi: 10.1084/jem.20160903. Epub 2017 Mar 7.
4
Epalrestat Stimulated Oxidative Stress, Inflammation, and Fibrogenesis in Mouse Liver.依帕司他可刺激小鼠肝脏的氧化应激、炎症和纤维化。
Toxicol Sci. 2018 Jun 1;163(2):397-408. doi: 10.1093/toxsci/kfx038.
5
Efficacy, safety, and tolerability of Epalrestat compared to Methylcobalamine in patients with diabetic neuropathy.依帕司他与甲钴胺相比治疗糖尿病性神经病变患者的疗效、安全性及耐受性
Int J Diabetes Dev Ctries. 2009 Jan;29(1):28-34. doi: 10.4103/0973-3930.50712.
6
Current concepts in targeted therapies for the pathophysiology of diabetic microvascular complications.糖尿病微血管并发症病理生理学靶向治疗的当前概念
Vasc Health Risk Manag. 2007;3(6):823-32.
7
Diabetic Neuropathies.糖尿病性神经病变
Curr Treat Options Neurol. 2000 Jan;2(1):23-30. doi: 10.1007/s11940-000-0021-2.
8
[Possible genetic causes for late complications of diabetes mellitus].[糖尿病晚期并发症的可能遗传原因]
Med Klin (Munich). 2000 Jan 15;95(1):31-9. doi: 10.1007/BF03044978.