Comparison of the Protective Effects of Nebivolol and Metoprolol against LPS-Induced Injury in H9c2 Cardiomyoblasts

被引:2
|
作者
Gul, Rukhsana [1 ]
Okla, Meshail [2 ]
Mahmood, Amer [3 ]
Nawaz, Shahid [1 ]
Fallata, Amina [1 ]
Bazighifan, Arwa [1 ]
Alfayez, Musaad [3 ]
Alfadda, Assim A. [1 ,4 ]
机构
[1] King Saud Univ, Coll Med, Obes Res Ctr, POB 2925, Riyadh 11461, Saudi Arabia
[2] King Saud Univ, Coll Appl Med Sci, Dept Community Hlth Sci, POB 22452, Riyadh 11495, Saudi Arabia
[3] King Saud Univ, Coll Med, Dept Anat, Stem Cell Unit, POB 2925, Riyadh 11461, Saudi Arabia
[4] King Saud Univ, Coll Med, Dept Med, POB 2925, Riyadh 11461, Saudi Arabia
关键词
nebivolol; metoprolol; LPS; oxidative stress; mitochondrial dysfunction; beta-blockers; IMPROVES DIASTOLIC DYSFUNCTION; OXIDATIVE STRESS; SEPTIC SHOCK; REDUCTIONS; ESMOLOL;
D O I
10.3390/cimb45110583
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here, we, for the first time, compared the cardioprotective effects of third-generation vasodilating beta-blocker nebivolol (Neb) and conventional beta-blocker metoprolol (Met) on LPS-induced injury in H9c2 cardiomyoblasts. Our findings denoted that Neb and Met pretreatment diminish LPS-mediated cytotoxicity and oxidative stress. Concomitantly, LPS-triggered inflammatory cytokines activation was significantly suppressed by Neb but not by Met. Pretreatment with either Neb or Met alleviated LPS-mediated mitochondrial impairment by enhancing the expression of genes related to its biogenesis such as PGC-1 alpha, NRF1, and TFAM. On the contrary, Neb but not Met-upregulated mitochondrial fusion-related genes such as OPA, and MFN2. In summary, our findings suggest that Neb and Met treatment significantly ameliorated the LPS-induced cytotoxicity and oxidative stress. Additionally, these findings suggest that Neb but not Met significantly down-regulates LPS-induced proinflammatory factors, probably by enhancing mitochondrial biogenesis and fusion.
引用
收藏
页码:9316 / 9327
页数:12
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