Gul Rukhsana, Alsalman Nouf, Alfadda Assim A
Obesity Research Center, College of Medicine, King Saud University, P.O. Box 2925, Riyadh 11461, Saudi Arabia.
Department of Medicine, College of Medicine, King Saud University, P.O. Box 2925, Riyadh 11461, Saudi Arabia.
Curr Issues Mol Biol. 2022 May 10;44(5):2139-2152. doi: 10.3390/cimb44050144.
We have recently illustrated that nebivolol can inhibit angiotensin II (Ang II)-mediated signaling in cardiomyoblasts; however, to date, the detailed mechanism for the beneficial effects of nebivolol has not been studied. Here, we investigated whether the inhibition of NO bioavailability by blocking eNOS (endothelial nitric oxide synthase) using L-NG-nitroarginine methyl ester (L-NAME) would attenuate nebivolol-mediated favorable effects on Ang II-evoked signaling in H9c2 cardiomyoblasts. Our data reveal that the nebivolol-mediated antagonistic effects on Ang II-induced oxidative stress were retreated by concurrent pretreatment with L-NAME and nebivolol. Similarly, the expressions of pro-inflammatory markers TNF-α and iNOS stimulated by Ang II were not decreased with the combination of nebivolol plus L-NAME. In contrast, the nebivolol-induced reduction in the Ang II-triggered mTORC1 pathway and the mRNA levels of hypertrophic markers ANP, BNP, and β-MHC were not reversed with the addition of L-NAME to nebivolol. In compliance with these data, the inhibition of eNOS by L-N⁵-(1-Iminoethyl) ornithine (LNIO) and its upstream regulator AMP-activated kinase (AMPK) with compound C in the presence of nebivolol showed effects similar to those of the L-NAME plus nebivolol combination on Ang II-mediated signaling. Pretreatment with either compound C plus nebivolol or LNIO plus nebivolol showed similar effects to those of the L-NAME plus nebivolol combination on Ang II-mediated signaling. In conclusion, our data indicate that the rise in NO bioavailability caused by nebivolol via the stimulation of AMPK/eNOS signaling is key for its anti-inflammatory and antioxidant properties but not for its antihypertrophic response upon Ang II stimulation.
我们最近证实奈必洛尔可抑制心肌成纤维细胞中血管紧张素II(Ang II)介导的信号传导;然而,迄今为止,尚未对奈必洛尔有益作用的详细机制进行研究。在此,我们研究了使用L-NG-硝基精氨酸甲酯(L-NAME)阻断内皮型一氧化氮合酶(eNOS)来抑制NO生物利用度是否会减弱奈必洛尔对H9c2心肌成纤维细胞中Ang II诱发信号传导的有利影响。我们的数据显示,L-NAME与奈必洛尔同时预处理可消除奈必洛尔对Ang II诱导的氧化应激的拮抗作用。同样,奈必洛尔加L-NAME的组合并未降低Ang II刺激的促炎标志物TNF-α和诱导型一氧化氮合酶(iNOS)的表达。相反,在奈必洛尔中加入L-NAME后,奈必洛尔诱导的Ang II触发的mTORC1通路的降低以及肥厚标志物心房钠尿肽(ANP)、脑钠肽(BNP)和β-肌球蛋白重链(β-MHC)的mRNA水平并未逆转。根据这些数据,在奈必洛尔存在的情况下,用L-N⁵-(1-亚氨基乙基)鸟氨酸(LNIO)及其上游调节因子AMP激活的蛋白激酶(AMPK)与化合物C抑制eNOS,对Ang II介导的信号传导显示出与L-NAME加奈必洛尔组合相似的作用。用化合物C加奈必洛尔或LNIO加奈必洛尔进行预处理,对Ang II介导的信号传导显示出与L-NAME加奈必洛尔组合相似的作用。总之,我们的数据表明,奈必洛尔通过刺激AMPK/eNOS信号传导导致的NO生物利用度升高是其抗炎和抗氧化特性的关键,但不是其对Ang II刺激的抗肥厚反应的关键。