a Computational Biology and Molecular Simulations Laboratory, Department of Biophysics , School of Medicine, Bahcesehir University , Istanbul , Turkey.
b Department of Medicinal and Aromatic Plants , Vocational School of Technical Sciences , Aksaray , Turkey.
J Biomol Struct Dyn. 2018 Feb;36(3):609-620. doi: 10.1080/07391102.2017.1288660. Epub 2017 Feb 15.
The objective of the present study was to evaluate the effects of propolis, pollen, and caffeic acid phenethyl ester (CAPE) on tyrosine hydroxylase (TH) activity and total RNA levels of Nω-nitro-L-arginine methyl ester (L-NAME) inhibition of nitric oxide synthase in the heart, adrenal medulla, and hypothalamus of hypertensive male Sprague dawley rats. The TH activity in the adrenal medulla, heart, and hypothalamus of the rats was significantly increased in the L-NAME group vs. control (p < 0.05). Treatment with L-NAME led to a significant increase in blood pressure (BP) in the L-NAME group compared to control (p < 0.05). These data suggest that propolis, pollen, and CAPE may mediate diminished TH activity in the heart, adrenal medulla, and hypothalamus in hypertensive rats. The decreased TH activity may be due to the modulation and synthesis of catecholamines and BP effects. In addition, the binding mechanism of CAPE within the catalytic domain of TH was investigated by means of molecular modeling approaches. These data suggest that the amino acid residues, Glu429 and Ser354 of TH may play a pivotal role in the stabilization of CAPE within the active site as evaluated by molecular dynamics (MD) simulations. Gibbs binding free energy (ΔG) of CAPE in complex with TH was also determined by post-processing MD analysis approaches (i.e. Poisson-Boltzmann Surface Area (MM-PBSA) method).
本研究旨在评估蜂胶、花粉和咖啡酸苯乙酯(CAPE)对酪氨酸羟化酶(TH)活性的影响,以及 Nω-硝基-L-精氨酸甲酯(L-NAME)抑制高血压雄性 Sprague dawley 大鼠心脏、肾上腺髓质和下丘脑一氧化氮合酶总 RNA 水平的影响。与对照组相比,L-NAME 组大鼠肾上腺髓质、心脏和下丘脑的 TH 活性显著升高(p<0.05)。与对照组相比,L-NAME 组大鼠的血压(BP)显著升高(p<0.05)。这些数据表明,蜂胶、花粉和 CAPE 可能介导高血压大鼠心脏、肾上腺髓质和下丘脑 TH 活性降低。TH 活性降低可能是由于儿茶酚胺的调节和合成以及 BP 作用。此外,还通过分子建模方法研究了 CAPE 在 TH 催化结构域内的结合机制。这些数据表明,TH 的氨基酸残基 Glu429 和 Ser354 可能在 MD 模拟评估的 CAPE 稳定在活性位点中发挥关键作用。还通过后处理 MD 分析方法(即泊松-玻尔兹曼表面积(MM-PBSA)方法)确定了 CAPE 与 TH 复合物的吉布斯结合自由能(ΔG)。