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利那格列汀抑制二肽基肽酶-4(DPP-4)可降低西方饮食诱导的雌性小鼠心肌TRAF3IP2表达、炎症和纤维化。

Dipeptidyl peptidase-4 (DPP-4) inhibition with linagliptin reduces western diet-induced myocardial TRAF3IP2 expression, inflammation and fibrosis in female mice.

作者信息

Aroor Annayya R, Habibi Javad, Kandikattu Hemanth Kumar, Garro-Kacher Mona, Barron Brady, Chen Dongqing, Hayden Melvin R, Whaley-Connell Adam, Bender Shawn B, Klein Thomas, Padilla Jaume, Sowers James R, Chandrasekar Bysani, DeMarco Vincent G

机构信息

Diabetes and Cardiovascular Center, Department of Medicine, University of Missouri, Columbia, MO, USA.

Research Service, Harry S. Truman Memorial Veterans' Hospital, Columbia, MO, USA.

出版信息

Cardiovasc Diabetol. 2017 May 5;16(1):61. doi: 10.1186/s12933-017-0544-4.

Abstract

BACKGROUND

Diastolic dysfunction (DD), a hallmark of obesity and primary defect in heart failure with preserved ejection fraction, is a predictor of future cardiovascular events. We previously reported that linagliptin, a dipeptidyl peptidase-4 inhibitor, improved DD in Zucker Obese rats, a genetic model of obesity and hypertension. Here we investigated the cardioprotective effects of linagliptin on development of DD in western diet (WD)-fed mice, a clinically relevant model of overnutrition and activation of the renin-angiotensin-aldosterone system.

METHODS

Female C56Bl/6 J mice were fed an obesogenic WD high in fat and simple sugars, and supplemented or not with linagliptin for 16 weeks.

RESULTS

WD induced oxidative stress, inflammation, upregulation of Angiotensin II type 1 receptor and mineralocorticoid receptor (MR) expression, interstitial fibrosis, ultrastructural abnormalities and DD. Linagliptin inhibited cardiac DPP-4 activity and prevented molecular impairments and associated functional and structural abnormalities. Further, WD upregulated the expression of TRAF3IP2, a cytoplasmic adapter molecule and a regulator of multiple inflammatory mediators. Linagliptin inhibited its expression, activation of its downstream signaling intermediates NF-κB, AP-1 and p38-MAPK, and induction of multiple inflammatory mediators and growth factors that are known to contribute to development and progression of hypertrophy, fibrosis and contractile dysfunction. Linagliptin also inhibited WD-induced collagens I and III expression. Supporting these in vivo observations, linagliptin inhibited aldosterone-mediated MR-dependent oxidative stress, upregulation of TRAF3IP2, proinflammatory cytokine, and growth factor expression, and collagen induction in cultured primary cardiac fibroblasts. More importantly, linagliptin inhibited aldosterone-induced fibroblast activation and migration.

CONCLUSIONS

Together, these in vivo and in vitro results suggest that inhibition of DPP-4 activity by linagliptin reverses WD-induced DD, possibly by targeting TRAF3IP2 expression and its downstream inflammatory signaling.

摘要

背景

舒张功能障碍(DD)是肥胖的一个标志,也是射血分数保留的心力衰竭的主要缺陷,是未来心血管事件的一个预测指标。我们之前报道过,二肽基肽酶-4抑制剂利格列汀可改善肥胖和高血压的遗传模型——Zucker肥胖大鼠的舒张功能障碍。在此,我们研究了利格列汀对西式饮食(WD)喂养小鼠舒张功能障碍发展的心脏保护作用,WD喂养小鼠是一种与临床相关的营养过剩和肾素-血管紧张素-醛固酮系统激活的模型。

方法

对雌性C56Bl/6 J小鼠喂食富含脂肪和单糖的致肥胖WD,并补充或不补充利格列汀,持续16周。

结果

WD诱导氧化应激、炎症、血管紧张素II 1型受体和盐皮质激素受体(MR)表达上调、间质纤维化、超微结构异常和舒张功能障碍。利格列汀抑制心脏二肽基肽酶-4活性,预防分子损伤以及相关的功能和结构异常。此外,WD上调了TRAF3IP2的表达,TRAF3IP2是一种细胞质衔接分子,也是多种炎症介质的调节剂。利格列汀抑制其表达、其下游信号中间体NF-κB、AP-1和p38-丝裂原活化蛋白激酶的激活,以及多种炎症介质和生长因子的诱导,这些炎症介质和生长因子已知会促进肥大、纤维化和收缩功能障碍的发展和进展。利格列汀还抑制WD诱导的I型和III型胶原蛋白表达。支持这些体内观察结果的是,利格列汀抑制醛固酮介导的MR依赖性氧化应激、TRAF3IP2上调、促炎细胞因子和生长因子表达,以及原代培养心脏成纤维细胞中的胶原蛋白诱导。更重要的是,利格列汀抑制醛固酮诱导的成纤维细胞活化和迁移。

结论

总之,这些体内和体外结果表明,利格列汀抑制二肽基肽酶-4活性可能通过靶向TRAF3IP2表达及其下游炎症信号传导来逆转WD诱导的舒张功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b01f/5420102/936909c72f90/12933_2017_544_Fig1_HTML.jpg

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