• 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

卡格列净和厄贝沙坦通过 TGF-β1/Smad 信号通路改善 Dahl 盐敏感性大鼠的肾纤维化。

Canagliflozin and irbesartan ameliorate renal fibrosis via the TGF-β1/Smad signaling pathway in Dahl salt-sensitive rats.

机构信息

Department of Internal Medicine, Hebei Medical University, Shijiazhuang, China.

Department of Cardiology, Hebei General Hospital, Shijiazhuang, China.

出版信息

J Int Med Res. 2023 Oct;51(10):3000605231206289. doi: 10.1177/03000605231206289.

DOI:10.1177/03000605231206289
PMID:37862678
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10590049/
Abstract

OBJECTIVES

This study assessed the antifibrotic effects of canagliflozin, with or without irbesartan, on renal injury in Dahl salt-sensitive (SS) rats fed a high-salt (HS) diet.

METHODS

After the preconditioning stage, Dahl SS rats (n = 47) were divided into five experimental groups as follows: low-salt (LS, n = 7), HS (n = 10), HS with canagliflozin (n = 10), HS with irbesartan (n = 10), and HS with canagliflozin and irbesartan (n = 10).

RESULTS

The HS diet increased systolic blood pressure (SBP), renal fibrosis, fibrotic protein expression, and transforming growth factor-β1 (TGF-β1)/Smad2/3 pathway protein expression compared with the findings in the LS group. Irbesartan reduced SBP and slowed the loss of renal function. Canagliflozin significantly reduced body weight and renal fibrosis and suppressed the TGF-β1/Smad2/3 pathway. The combined therapy exerted better renoprotective effects on all outcome parameters.

CONCLUSIONS

These results indicate that canagliflozin and irbesartan exert different effects on renal injury in SS hypertensive rats, and the combined regimen could have stronger effects than either monotherapy.

摘要

目的

本研究评估了卡格列净联合或不联合厄贝沙坦对高盐饮食喂养的 Dahl 盐敏感(SS)大鼠肾脏损伤的抗纤维化作用。

方法

在预处理阶段后,将 47 只 Dahl SS 大鼠分为五组:低盐(LS)组(n=7)、高盐(HS)组(n=10)、HS 加卡格列净组(n=10)、HS 加厄贝沙坦组(n=10)和 HS 加卡格列净和厄贝沙坦组(n=10)。

结果

与 LS 组相比,HS 饮食增加了收缩压(SBP)、肾脏纤维化、纤维蛋白表达以及转化生长因子-β1(TGF-β1)/Smad2/3 通路蛋白表达。厄贝沙坦降低了 SBP 并减缓了肾功能的丧失。卡格列净显著减轻了体重和肾脏纤维化,并抑制了 TGF-β1/Smad2/3 通路。联合治疗对所有终点参数都具有更好的肾脏保护作用。

结论

这些结果表明,卡格列净和厄贝沙坦对 SS 高血压大鼠的肾脏损伤具有不同的作用,联合治疗方案可能比单一疗法具有更强的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/90bc8f7f5df9/10.1177_03000605231206289-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/8ca45bc75559/10.1177_03000605231206289-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/e4c67149fd50/10.1177_03000605231206289-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/5f24c9c7fedc/10.1177_03000605231206289-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/8e1ce9efe7fc/10.1177_03000605231206289-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/90bc8f7f5df9/10.1177_03000605231206289-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/8ca45bc75559/10.1177_03000605231206289-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/e4c67149fd50/10.1177_03000605231206289-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/5f24c9c7fedc/10.1177_03000605231206289-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/8e1ce9efe7fc/10.1177_03000605231206289-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a24e/10590049/90bc8f7f5df9/10.1177_03000605231206289-fig5.jpg

相似文献

1
Canagliflozin and irbesartan ameliorate renal fibrosis via the TGF-β1/Smad signaling pathway in Dahl salt-sensitive rats.卡格列净和厄贝沙坦通过 TGF-β1/Smad 信号通路改善 Dahl 盐敏感性大鼠的肾纤维化。
J Int Med Res. 2023 Oct;51(10):3000605231206289. doi: 10.1177/03000605231206289.
2
Canagliflozin ameliorates epithelial-mesenchymal transition in high-salt diet-induced hypertensive renal injury through restoration of sirtuin 3 expression and the reduction of oxidative stress.卡格列净通过恢复沉默信息调节因子3的表达和减轻氧化应激,改善高盐饮食诱导的高血压肾损伤中的上皮-间质转化。
Biochem Biophys Res Commun. 2023 Apr 23;653:53-61. doi: 10.1016/j.bbrc.2023.01.084. Epub 2023 Feb 17.
3
Heterozygous knockout of transforming growth factor-β1 protects Dahl S rats against high salt-induced renal injury.转化生长因子-β1 杂合子敲除可预防 Dahl S 大鼠高盐诱导的肾损伤。
Physiol Genomics. 2013 Feb 4;45(3):110-8. doi: 10.1152/physiolgenomics.00119.2012. Epub 2012 Dec 18.
4
Recombinant Cellular Repressor of E1A-Stimulated Genes Protects against Renal Fibrosis in Dahl Salt-Sensitive Rats.重组细胞 E1A 刺激基因的转录抑制剂可预防 Dahl 盐敏感型大鼠的肾纤维化。
Am J Nephrol. 2020;51(5):401-410. doi: 10.1159/000506411. Epub 2020 Apr 22.
5
Xanthine Oxidase Inhibitor, Febuxostat Ameliorates the High Salt Intake-Induced Cardiac Hypertrophy and Fibrosis in Dahl Salt-Sensitive Rats.黄嘌呤氧化酶抑制剂非布司他可改善高盐摄入诱导的 Dahl 盐敏感大鼠心肌肥厚和纤维化。
Am J Hypertens. 2019 Jan 1;32(1):26-33. doi: 10.1093/ajh/hpy143.
6
Tempol attenuates the development of hypertensive renal injury in Dahl salt-sensitive rats.Tempol可减轻Dahl盐敏感大鼠高血压性肾损伤的发展。
Am J Hypertens. 2005 May;18(5 Pt 1):707-13. doi: 10.1016/j.amjhyper.2004.11.045.
7
Sodium-Glucose Cotransporter 2 Inhibitor Canagliflozin Antagonizes Salt-Sensitive Hypertension Through Modifying Transient Receptor Potential Channels 3 Mediated Vascular Calcium Handling.钠-葡萄糖共转运蛋白 2 抑制剂坎格列净通过调节瞬时受体电位通道 3 介导的血管钙处理拮抗盐敏感性高血压。
J Am Heart Assoc. 2022 Aug 2;11(15):e025328. doi: 10.1161/JAHA.121.025328. Epub 2022 Jul 29.
8
The Participation of Ferroptosis in Fibrosis of the Heart and Kidney Tissues in Dahl Salt-Sensitive Hypertensive Rats.铁死亡在 Dahl 盐敏感型高血压大鼠心脏和肾脏组织纤维化中的作用
Am J Hypertens. 2024 Sep 16;37(10):784-791. doi: 10.1093/ajh/hpae076.
9
Traditional Chinese medicine protects against hypertensive kidney injury in Dahl salt-sensitive rats by targeting transforming growth factor-β signaling pathway.中药通过靶向转化生长因子-β信号通路防治 Dahl 盐敏感型大鼠高血压肾损伤。
Biomed Pharmacother. 2020 Nov;131:110746. doi: 10.1016/j.biopha.2020.110746. Epub 2020 Sep 17.
10
Canagliflozin Ameliorates Ventricular Remodeling through Apelin/Angiotensin-Converting Enzyme 2 Signaling in Heart Failure with Preserved Ejection Fraction Rats.卡格列净通过心力衰竭保留射血分数大鼠中的 Apelin/血管紧张素转换酶 2 信号改善心室重构。
Pharmacology. 2023;108(5):478-491. doi: 10.1159/000533277. Epub 2023 Aug 23.

引用本文的文献

1
Oxidative Stress in Kidney Injury and Hypertension.肾脏损伤与高血压中的氧化应激
Antioxidants (Basel). 2024 Nov 27;13(12):1454. doi: 10.3390/antiox13121454.

本文引用的文献

1
Transforming growth factor-β signaling: From tissue fibrosis to therapeutic opportunities.转化生长因子-β信号传导:从组织纤维化到治疗机遇
Chem Biol Interact. 2023 Jan 5;369:110289. doi: 10.1016/j.cbi.2022.110289. Epub 2022 Nov 29.
2
Sodium-Glucose Cotransporter 2 Inhibitor Canagliflozin Antagonizes Salt-Sensitive Hypertension Through Modifying Transient Receptor Potential Channels 3 Mediated Vascular Calcium Handling.钠-葡萄糖共转运蛋白 2 抑制剂坎格列净通过调节瞬时受体电位通道 3 介导的血管钙处理拮抗盐敏感性高血压。
J Am Heart Assoc. 2022 Aug 2;11(15):e025328. doi: 10.1161/JAHA.121.025328. Epub 2022 Jul 29.
3
Head-to-head comparison of two SGLT-2 inhibitors on AKI outcomes in a rat ischemia-reperfusion model.
两种 SGLT-2 抑制剂在大鼠缺血再灌注模型中对急性肾损伤结局的头对头比较。
Biomed Pharmacother. 2022 Sep;153:113357. doi: 10.1016/j.biopha.2022.113357. Epub 2022 Jul 2.
4
Renoprotective effects of empagliflozin in type 1 and type 2 models of diabetic nephropathy superimposed with hypertension.恩格列净在合并高血压的 1 型和 2 型糖尿病肾病模型中的肾脏保护作用。
Geroscience. 2022 Dec;44(6):2845-2861. doi: 10.1007/s11357-022-00610-7. Epub 2022 Jun 29.
5
Angiotensin II up-regulates sodium-glucose co-transporter 2 expression and SGLT2 inhibitor attenuates Ang II-induced hypertensive renal injury in mice.血管紧张素 II 上调钠-葡萄糖协同转运蛋白 2 的表达,SGLT2 抑制剂可减轻血管紧张素 II 诱导的小鼠高血压肾损伤。
Clin Sci (Lond). 2021 Apr 16;135(7):943-961. doi: 10.1042/CS20210094.
6
Effects of dapagliflozin on major adverse kidney and cardiovascular events in patients with diabetic and non-diabetic chronic kidney disease: a prespecified analysis from the DAPA-CKD trial.达格列净对伴有和不伴有糖尿病的慢性肾脏病患者的主要不良肾脏和心血管事件的影响:来自 DAPA-CKD 试验的预先指定分析。
Lancet Diabetes Endocrinol. 2021 Jan;9(1):22-31. doi: 10.1016/S2213-8587(20)30369-7.
7
Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure.恩格列净治疗心力衰竭的心血管和肾脏结局。
N Engl J Med. 2020 Oct 8;383(15):1413-1424. doi: 10.1056/NEJMoa2022190. Epub 2020 Aug 28.
8
Effects of the SGLT2 inhibitor dapagliflozin on proteinuria in non-diabetic patients with chronic kidney disease (DIAMOND): a randomised, double-blind, crossover trial.达格列净对非糖尿病慢性肾脏病患者蛋白尿的影响(DIAMOND):一项随机、双盲、交叉试验。
Lancet Diabetes Endocrinol. 2020 Jul;8(7):582-593. doi: 10.1016/S2213-8587(20)30162-5.
9
Kidney outcomes associated with use of SGLT2 inhibitors in real-world clinical practice (CVD-REAL 3): a multinational observational cohort study.在真实临床实践中使用 SGLT2 抑制剂与肾脏结局的关联(CVD-REAL 3):一项多国家观察性队列研究。
Lancet Diabetes Endocrinol. 2020 Jan;8(1):27-35. doi: 10.1016/S2213-8587(19)30384-5.
10
Evaluation of the pathophysiological mechanisms of salt-sensitive hypertension.盐敏感性高血压的病理生理机制评估。
Hypertens Res. 2019 Dec;42(12):1848-1857. doi: 10.1038/s41440-019-0332-5. Epub 2019 Sep 20.