辣木与雌激素受体α对接可改善应激大鼠胎盘和脑损伤。

Q3 Biochemistry, Genetics and Molecular Biology
Odochi O Chukwu, Cordilia Iyare, Anthony C U Ezimah, Albert E Okorocha, Nwaeze G Konyefom, Nnaemeka T Asogwa, Nancy P Igwe
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引用次数: 0

摘要

背景:妊娠期应激对子代早期生理编程有显著影响。孕妇经常使用草药来增强她们的健康。辣木叶提取物(Moringa oleifera Leaf Extract, MoLE)被认为具有抗应激和抗氧化的双重特性,可以作为选择性雌激素受体调节剂(Selective Estrogen Receptor Modulator, SERM)调节雌激素的活性,对不同的组织有不同的作用。本研究的目的是对妊娠应激过程中moore靶向雌激素受体α (Estrogen receptor -α, ER-α)的植物化学物质进行分子对接分析,并评估给药对母鼠和胎儿脑组织及胎盘的影响。方法:采用气相色谱-质谱联用法测定其植物化学性质。采用分子对接技术,利用autodock工具预测植物活性化合物在ER-α蛋白位点的相互作用和结合亲和能。将30只明显健康的妊娠期白化wistar大鼠随机分为6组,每组5只,分别进行2周的慢性不可预知应激(Chronic Unpredictable Stress, CUS)试验:ⅰ组(随意饮水和正常鼠粮)、ⅱ组(仅进行CUS试验)、ⅲ组(5 mg/kg体重/day mol)、ⅳ组(10 mg/kg体重/day mol)、ⅴ组(CUS试验+5 mg/kg体重/day mol)、ⅵ组(CUS试验+10 mg/kg体重/day mol)。结果:本研究发现1-丙醇,3,3'-氧双-和1,2,3 -三甲基二氮吡啶是41种化合物中最有效的ER-α配体。对应激大鼠组织的显微检查显示出轻微到严重的组织学改变。在慢性应激过程中,食用鼹鼠表现出轻度至中度的保护作用。结论:这些发现表明,1-丙醇,3,3'-氧双-和1,2,3 -三甲基二氮吡啶可以进一步研究开发新的治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Moringa oleifera Docking to Estrogen Receptor α Ameliorates Placental and Brain Damage in Stressed Rats.

Background: Stress during pregnancy significantly impacts offspring early physiological programming. Herbal remedies are frequently used by pregnant women to enhance their wellbeing. Moringa oleifera Leaf Extract (MoLE) is believed to have both anti-stress and antioxidant properties which can act as a Selective Estrogen Receptor Modulator (SERM) that regulate activities of estrogen, and can have different effects on different tissues. Goal of this study is to compile information on molecular docking analysis of phytochemicals found in MoLE targeting Estrogen Receptor-alpha (ER-α) and assess effects of MoLE administration on dam's and fetal brain tissues and placenta, during gestational stress.

Methods: Phytochemical study of MoLE was determined using Gas Chromatography-Mass Spectrometry. Molecular docking technique was employed to predict aspects of interaction and binding affinities energy of bioactive phytocompounds in protein site of ER-α using autodock tools. 30 apparently healthy pregnant Albino-Wistar rats were randomly placed into 6 groups of 5 rats per group and exposed to Chronic Unpredictable Stress (CUS) protocol for two weeks, as follows: Group I (water and normal rat chow ad libitum), Group II (CUS protocol only), Group III (5 mg/kg body weight/day of MoLE), Group IV (10 mg/kg body weight/day of MoLE), Group V (CUS protocol +5 mg/kg body weight/day of MoLE), Group VI (CUS protocol +10 mg/kg body weight/day of MoLE).

Results: This study found that 1-Propanol, 3,3'-oxy bis- and 1, 2, 3-Trimethyldiaziridine are most potent ligands for ER-α among all 41 compounds. Photomicrograph examination of tissues from stressed rats showed mild to severe alterations in histology. Consumption of MoLE during chronic stress showed mild to moderate protective effects.

Conclusion: These findings suggest that 1-Propanol, 3,3'-oxy bis- and 1, 2, 3-Trimethyldiaziridine can be further investigated for development of novel therapeutics.

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来源期刊
Avicenna journal of medical biotechnology
Avicenna journal of medical biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
2.90
自引率
0.00%
发文量
43
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