• 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

相似文献

1
Combating Combination of Hypertension and Diabetes in Different Rat Models.在不同大鼠模型中对抗高血压与糖尿病的合并症
Pharmaceuticals (Basel). 2010 Mar 26;3(4):916-939. doi: 10.3390/ph3040916.
2
From molecular footprints of disease to new therapeutic interventions in diabetic nephropathy.从疾病的分子印记到糖尿病肾病的新型治疗干预措施
Ann N Y Acad Sci. 2005 Jun;1043:740-9. doi: 10.1196/annals.1333.086.
3
Oxidative stress in hypertensive,diabetic, and diabetic hypertensive rats.高血压、糖尿病及糖尿病合并高血压大鼠的氧化应激
Am J Hypertens. 2003 Dec;16(12):1049-52. doi: 10.1016/j.amjhyper.2003.07.013.
4
Effects of endothelin-1 on systemic and renal hemodynamics in hypertensive-diabetic rats (CRDH), diabetic rats (CDR), and hypertensive rats (SHR).内皮素-1对高血压糖尿病大鼠(CRDH)、糖尿病大鼠(CDR)和高血压大鼠(SHR)全身及肾脏血流动力学的影响。
J Cardiovasc Pharmacol. 2004 Nov;44 Suppl 1:S191-4. doi: 10.1097/01.fjc.0000166239.41830.3f.
5
Saga of renin-angiotensin system and calcium channels in hypertensive diabetics: does it have a therapeutic edge?高血压糖尿病患者肾素-血管紧张素系统与钙通道的研究历程:是否具有治疗优势?
Cardiovasc Drug Rev. 2005 Summer;23(2):99-114. doi: 10.1111/j.1527-3466.2005.tb00159.x.
6
Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-gamma activation.替米沙坦通过激活过氧化物酶体增殖物激活受体-γ改善非肥胖 Cohen-Rosenthal 糖尿病高血压大鼠的高血糖和代谢谱。
Metabolism. 2010 Aug;59(8):1200-9. doi: 10.1016/j.metabol.2009.11.013. Epub 2010 Jan 13.
7
Telmisartan in the treatment of Cohen-Rosenthal Diabetic Hypertensive rats: the benefit of PPAR-gamma agonism.替米沙坦治疗科恩 - 罗森塔尔糖尿病高血压大鼠:过氧化物酶体增殖物激活受体γ激动作用的益处
Clin Exp Hypertens. 2007 Aug;29(6):419-26. doi: 10.1080/10641960701578444.
8
Telmisartan is a promising cardiometabolic sartan due to its unique PPAR-gamma-inducing property.替米沙坦因其独特的诱导过氧化物酶体增殖物激活受体γ(PPAR-γ)的特性,是一种很有前景的心脏代谢类沙坦类药物。
Med Hypotheses. 2005;64(3):476-8. doi: 10.1016/j.mehy.2004.09.015.
9
Sympathoadrenergic suppression improves heart function by upregulating the ratio of sRAGE/RAGE in hypertension with metabolic syndrome.交感神经抑制通过上调代谢综合征合并高血压患者 sRAGE/RAGE 比值改善心功能。
J Mol Cell Cardiol. 2018 Sep;122:34-46. doi: 10.1016/j.yjmcc.2018.08.003. Epub 2018 Aug 7.
10
Beneficial Effect of the SGLT2 Inhibitor Empagliflozin on Glucose Homeostasis and Cardiovascular Parameters in the Cohen Rosenthal Diabetic Hypertensive (CRDH) Rat.钠-葡萄糖协同转运蛋白2抑制剂恩格列净对科恩·罗森塔尔糖尿病高血压(CRDH)大鼠血糖稳态和心血管参数的有益作用。
J Cardiovasc Pharmacol Ther. 2018 Jul;23(4):358-371. doi: 10.1177/1074248418763808. Epub 2018 Apr 8.

引用本文的文献

1
Transient receptor potential cation channel 6 contributes to kidney injury induced by diabetes and hypertension.瞬时受体电位阳离子通道 6 有助于糖尿病和高血压引起的肾脏损伤。
Am J Physiol Renal Physiol. 2022 Jan 1;322(1):F76-F88. doi: 10.1152/ajprenal.00296.2021. Epub 2021 Dec 6.
2
Type 2 diabetes mellitus in the Goto-Kakizaki rat impairs microvascular function and contributes to premature skeletal muscle fatigue.Goto-Kakizaki 大鼠的 2 型糖尿病会损害微血管功能,并导致骨骼肌过早疲劳。
J Appl Physiol (1985). 2019 Mar 1;126(3):626-637. doi: 10.1152/japplphysiol.00751.2018. Epub 2018 Dec 20.
3
Chronic atorvastatin and exercise can partially reverse established skeletal muscle microvasculopathy in metabolic syndrome.慢性阿托伐他汀和运动可以部分逆转代谢综合征中已建立的骨骼肌微血管病变。
Am J Physiol Heart Circ Physiol. 2018 Oct 1;315(4):H855-H870. doi: 10.1152/ajpheart.00193.2018. Epub 2018 Jun 22.
4
Honey: a novel antioxidant.蜂蜜:一种新型抗氧化剂。
Molecules. 2012 Apr 12;17(4):4400-23. doi: 10.3390/molecules17044400.

本文引用的文献

1
S-allyl-mercapto-captopril: a novel compound in the treatment of Cohen-Rosenthal diabetic hypertensive rats.S-烯丙基巯基卡托普利:一种治疗科恩-罗森塔尔糖尿病高血压大鼠的新型化合物。
J Clin Hypertens (Greenwich). 2010 Jun;12(6):451-5. doi: 10.1111/j.1751-7176.2010.00270.x.
2
Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-gamma activation.替米沙坦通过激活过氧化物酶体增殖物激活受体-γ改善非肥胖 Cohen-Rosenthal 糖尿病高血压大鼠的高血糖和代谢谱。
Metabolism. 2010 Aug;59(8):1200-9. doi: 10.1016/j.metabol.2009.11.013. Epub 2010 Jan 13.
3
Influence of atorvastatin on blood pressure control in treated hypertensive, normolipemic patients - An open, pilot study.阿托伐他汀对接受治疗的高血压、血脂正常患者血压控制的影响——一项开放性试点研究。
Blood Press. 2010 Aug;19(4):260-6. doi: 10.3109/08037050903576726.
4
Abstracts of the 2nd International Conference on Fixed Combination in the Treatment of Hypertension, Dyslipidemia and Diabetes Mellitus - An Ideal Approach for Improving Compliance and Combating Cardiovascular Disease. December 10-12, 2009, Valencia, Spain.第二届高血压、血脂异常及糖尿病固定复方治疗国际会议摘要——提高依从性及对抗心血管疾病的理想方法。2009年12月10 - 12日,西班牙巴伦西亚
Am J Hypertens. 2009 Nov;22 Suppl 1:1-16. doi: 10.1038/ajh.2009.197.
5
The effects of telmisartan on mechanical responses of left ventricular papillary muscle in rats with streptozotocin-induced diabetes mellitus.替米沙坦对链脲佐菌素诱导糖尿病大鼠左心室乳头肌机械反应的影响。
Acta Diabetol. 2010 Dec;47 Suppl 1:153-9. doi: 10.1007/s00592-009-0156-x. Epub 2009 Oct 24.
6
Cardioprotective actions of two bioflavonoids, quercetin and rutin, in experimental myocardial infarction in both normal and streptozotocin-induced type I diabetic rats.两种生物类黄酮,槲皮素和芦丁,在正常和链脲佐菌素诱导的 I 型糖尿病大鼠实验性心肌梗死中的心脏保护作用。
J Pharm Pharmacol. 2009 Oct;61(10):1365-74. doi: 10.1211/jpp/61.10.0014.
7
Very high doses of valsartan provide renoprotection independently of blood pressure in a type 2 diabetic nephropathy rat model.在2型糖尿病肾病大鼠模型中,非常高剂量的缬沙坦可独立于血压提供肾脏保护作用。
Nephrology (Carlton). 2009 Sep;14(6):581-7. doi: 10.1111/j.1440-1797.2009.01143.x.
8
IL-1 antagonism reduces hyperglycemia and tissue inflammation in the type 2 diabetic GK rat.白细胞介素-1拮抗剂可降低2型糖尿病GK大鼠的高血糖水平并减轻组织炎症。
Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13998-4003. doi: 10.1073/pnas.0810087106. Epub 2009 Jul 30.
9
Renoprotective effects of an angiotensin II receptor blocker in experimental model rats with hypertension and metabolic disorders.血管紧张素II受体阻滞剂对高血压合并代谢紊乱实验模型大鼠的肾脏保护作用。
Hypertens Res. 2009 Sep;32(9):807-15. doi: 10.1038/hr.2009.106. Epub 2009 Aug 7.
10
TRC4186, a novel AGE-breaker, improves diabetic cardiomyopathy and nephropathy in Ob-ZSF1 model of type 2 diabetes.新型抗晚期糖基化终末产物药物TRC4186可改善2型糖尿病Ob-ZSF1模型中的糖尿病性心肌病和肾病。
J Cardiovasc Pharmacol. 2009 Jul;54(1):72-81. doi: 10.1097/FJC.0b013e3181ac3a34.

在不同大鼠模型中对抗高血压与糖尿病的合并症

Combating Combination of Hypertension and Diabetes in Different Rat Models.

作者信息

Rosenthal Talma, Younis Firas, Alter Ariela

机构信息

Department of Physiology and Pharmacology, Sackler School of Medicine, Tel Aviv University, Israel.

出版信息

Pharmaceuticals (Basel). 2010 Mar 26;3(4):916-939. doi: 10.3390/ph3040916.

DOI:10.3390/ph3040916
PMID:27713282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4034014/
Abstract

Rat experimental models are used extensively for studying physiological mechanisms and treatments of hypertension and diabetes co-existence. Each one of these conditions is a major risk factor for cardiovascular disease (CVD), and the combination of the two conditions is a potent enhancer of CVD. Five major animal models that advanced our understanding of the mechanisms and therapeutic approaches in humans are discussed in this review: Zucker, Goto-Kakizaki, SHROB, SHR/NDmcr-cp and Cohen Rosenthal diabetic hypertensive (CRDH) rats. The use of various drugs, such as angiotensin-converting enzyme (ACE) inhibitors (ACEIs), various angiotensin receptor blockers (ARBs), and calcium channel blockers (CCBs), to combat the effects of concomitant pathologies on the combination of diabetes and hypertension, as well as the non-pharmacological approach are reviewed in detail for each rat model. Results from experiments on these models indicate that classical factors contributing to the pathology of hypertension and diabetes combination-Including hypertension, hyperglycemia, hyperinsulinemia and hyperlipidemia-can now be treated, although these treatments do not completely prevent renal complications. Animal studies have focused on several mechanisms involved in hypertension/diabetes that remain to be translated into clinical medicine, including hypoxia, oxidative stress, and advanced glycation. Several target molecules have been identified that need to be incorporated into a treatment modality. The challenge continues to be the identification and interpretation of the clinical evidence from the animal models and their application to human treatment.

摘要

大鼠实验模型被广泛用于研究高血压与糖尿病并存的生理机制及治疗方法。这两种病症中的每一种都是心血管疾病(CVD)的主要危险因素,而这两种病症并存会有力地加剧心血管疾病。本文综述了五种推进我们对人类相关机制及治疗方法理解的主要动物模型:Zucker大鼠、Goto-Kakizaki大鼠、SHROB大鼠、SHR/NDmcr-cp大鼠和科恩·罗森塔尔糖尿病高血压(CRDH)大鼠。针对每种大鼠模型,详细综述了使用各种药物(如血管紧张素转换酶(ACE)抑制剂(ACEI)、各种血管紧张素受体阻滞剂(ARB)和钙通道阻滞剂(CCB))来对抗伴随病症对糖尿病和高血压并存情况的影响,以及非药物治疗方法。对这些模型进行实验的结果表明,导致高血压与糖尿病并存病症的经典因素——包括高血压、高血糖、高胰岛素血症和高脂血症——现在可以得到治疗,尽管这些治疗并不能完全预防肾脏并发症。动物研究聚焦于高血压/糖尿病中涉及的几种尚未转化为临床医学的机制,包括缺氧、氧化应激和晚期糖基化。已经确定了几种需要纳入治疗模式的靶分子。挑战仍然在于识别和解读来自动物模型的临床证据及其在人类治疗中的应用。