Probiotic Escherichia coli Nissle inhibits IL-6 and MAPK-mediated cardiac hypertrophy during STZ-induced diabetes in rats

被引:14
作者
Chiang, C. J. [1 ]
Chao, Y. P. [2 ]
Ali, A. [3 ]
Day, C. H. [4 ]
Ho, T. J. [5 ,6 ,7 ]
Wang, P. N. [2 ]
Lin, S. C. [1 ]
Padma, V. V. [8 ]
Kuo, W. W. [3 ,9 ]
Huang, C. Y. [10 ,11 ,12 ,13 ,14 ]
机构
[1] China Med Univ, Dept Med Lab Sci & Biotechnol, 91 Hsueh Shih Rd, Taichung 40402, Taiwan
[2] Feng Chia Univ, Dept Chem Engn, 100 Wenhwa Rd, Taichung 40724, Taiwan
[3] China Med Univ, Dept Biol Sci & Technol, 91 Hsueh Shih Rd, Taichung 40402, Taiwan
[4] MeiHo Univ, Dept Nursing, Pingguang Rd, Pingtung 912, Taiwan
[5] Tzu Chi Univ, Hualien Tzu Chi Hosp, Buddhist Tzu Chi Med Fdn, Dept Chinese Med, 707 Sect 3 Chung Yang Rd, Hualien 97002, Taiwan
[6] Hualien Tzu Chi Hosp, Buddhist Tzu Chi Med Fdn, Integrat Ctr Tradit Chinese & Modern Med, Hualien 97002, Taiwan
[7] Tzu Chi Univ, Coll Med, Sch Postbaccalaureate Chinese Med, 701 Jhongyang Rd Sect 3, Hualien 97004, Taiwan
[8] Bharathiar Univ, Dept Biotechnol, Coimbatore, Tamil Nadu, India
[9] China Med Univ, PhD Program Biotechnol Ind, Taichung 406, Taiwan
[10] Hualien Tzu Chi Hosp, Buddhist Tzu Chi Med Fdn, Cardiovasc & Mitochondrial Related Dis Res Ctr, Hualien 97002, Taiwan
[11] China Med Univ, Grad Inst Biomed Sci, Taichung 404, Taiwan
[12] China Med Univ, China Med Univ Hosp, Dept Med Res, 91 Hsueh Shih Rd, Taichung 40402, Taiwan
[13] Asia Univ, Dept Biotechnol, 500 Liufeng Rd, Taichung 41354, Taiwan
[14] Tzu Chi Univ Sci & Technol, Buddhist Tzu Chi Med Fdn, Ctr Gen Educ, Hualien 970, Taiwan
关键词
E. coli Nissle; IL-6; hypertrophy; diabetes mellitus; GUT MICROBIOTA; HEART-FAILURE; BIOFILM FORMATION; GENE-EXPRESSION; MECHANISMS; CARDIOMYOPATHY; INFLAMMATION; MELLITUS; DISEASES; PATHWAYS;
D O I
10.3920/BM2020.0094
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Escherichia coli Nissle (EcN), a probiotic bacterium protects against several disorders. Multiple reports have studied the pathways involved in cardiac hypertrophy. However, the effects of probiotic EcN against diabetes-induced cardiac hypertrophy remain to be understood. We administered five weeks old Wistar male (271 +/- 19.4 g body weight) streptozotocin-induced diabetic rats with 10(9) cfu of EcN via oral gavage every day for 24 days followed by subjecting the rats to echocardiography to analyse the cardiac parameters. Overexpressed interleukin (IL)-6 induced the MEK5/ERK5, JAK2/STAT3, and MAPK signalling cascades in streptozotocin-induced diabetic rats. Further, the upregulation of calcineurin, NFATc3, and p-GATA4 led to the elevation of hypertrophy markers, such as atrial and B-type natriuretic peptides. In contrast, diabetic rats supplemented with probiotic EcN exhibited significant downregulated IL-6. Moreover, the MEK5/ERK5 and JAK2/STAT3 cascades involved during eccentric hypertrophy and MAPK signalling, including phosphorylated MEK, ERK, JNK, and p-38, were significantly attenuated in diabetic rats after supplementation of EcN. Western blotting and immunofluorescence revealed the significant downregulation of NFATc3 and downstream mediators, thereby resulting in the impairment of cardiac hypertrophy. Taken together, the findings demonstrate that supplementing probiotic EcN has the potential to show cardioprotective effects by inhibiting diabetes-induced cardiomyopathies.
引用
收藏
页码:283 / 293
页数:11
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