关于胡椒碱对小牛胸腺 DNA 荧光淬灭效应的研究:人类乳腺癌细胞系研究中的 Caspase 激活。

DNA and cell biology Pub Date : 2024-01-01 Epub Date: 2023-12-11 DOI:10.1089/dna.2023.0269
Sakineh Rezaei, Hoda-Sadat Meftah, Yasamin Ebtehajpour, Hamid Reza Rahimi, Jamshidkhan Chamani
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引用次数: 0

摘要

在这项研究中,我们测定了哌啶与小牛胸腺 DNA(ct DNA)在 pH = 6.8 的 Tris-HCl 缓冲溶液中的相互作用,并通过多光谱技术数据以及热熔和粘度测量评估了其结合机制。荧光淬灭的结果证实了胡椒碱与ctDNA之间存在相互作用,并指出了胡椒碱作为淬灭剂的作用。此外,在 298、303 和 308 K 三种不同温度下测得的 KSV 值分别为 4.5 × 107 M-1、5.65 × 107 M-1 和 9.36 × 107 M-1,这表明哌啶-ctDNA 的荧光淬灭以动态机制为主。热力学参数表明ctDNA与哌啶的相互作用中疏水作用力占主导地位。根据共振光散射数据,哌啶与ctDNA之间形成的复合物导致了较大颗粒的产生。溴化乙锭(EB)和吖啶橙(AO)置换研究以及 NaCl 和 KI 评估的离子效应证实了哌啶-ctDNA 通过沟结合模式发生相互作用。加入哌啶浓度后,ctDNA 的熔化温度检测表明哌啶可能与ctDNA 形成沟结合,相对粘度测量也证实了这一点。CD 研究的圆二色性(CD)光谱未检测到任何变化,这证实了沟结合机制的特征,同时也证实了哌啶-ctDNA 复合物结合的所有实验结果。除了观察到哌啶对 MDA-MB-231 细胞具有浓度和时间依赖性的细胞毒性外,还注意到哌啶对增加脂质过氧化和降低超氧化物歧化酶活性的影响。显然,胡椒碱还能诱导 Caspase-3 的活性。
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Investigation on the Effect of Fluorescence Quenching of Calf Thymus DNA by Piperine: Caspase Activation in the Human Breast Cancer Cell Line Studies.

In this study, we determined the interaction of piperine and calf thymus DNA (ct DNA) in Tris-HCl buffer solution at pH = 6.8 and also evaluated the binding mechanism through the data of multi-spectroscopic techniques along with thermal melting and viscosity measurements. The outcomes of fluorescence quenching confirmed the occurrence of interactions between piperine and ctDNA and pointed out the role of piperine as the quencher. In addition, the KSV values were measured at three different temperatures of 298, 303, and 308 K to be 4.5 × 107 M-1, 5.65 × 107 M-1, and 9.36 × 107 M-1, respectively, which suggested the dominance of dynamic mechanism as the fluorescence quenching of piperine-ctDNA. The thermodynamic parameters revealed the predominance of hydrophobic forces in the interaction of ctDNA with piperine. According to the resonance light scattering data, the formation of a complex between piperine and ctDNA led to the creation of a larger particle. Ethidium bromide (EB) and acridine orange (AO) displacement studies, along with the ionic effects of NaCl and KI assessments, confirmed the interaction of piperine-ctDNA through a groove binding mode. The melting temperature assay of ctDNA upon the addition of piperine concentration indicated the probable groove binding of piperine to ctDNA, which was affirmed by relative viscosity measurement as well. The lack of detecting any alterations in the circular dichroism (CD) spectrum of CD investigation verified as a characteristic sign of groove binding mechanism and also confirmed all the experimental results with regard to the binding of piperine-ctDNA complex. Next to observing a concentration and time-dependent cytotoxicity in MDA-MB-231 cells, the impact of piperine on increasing lipid peroxidation and decreasing the activity of superoxide dismutase was also noticed. Apparently, piperine is capable of inducing caspase-3 activity as well.

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