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多酚通过 MAPK 信号通路调节奶牛 PPARγ 增加奶牛乳脂合成的计算机分析。

In silico analysis of polyphenols modulate bovine PPARγ to increase milk fat synthesis in dairy cattle via the MAPK signaling pathways.

机构信息

Faculty of Animal Production and Technology, Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan.

Department of Biology, Division of Molecular Biology and Genetics, Gaziantep University, Gaziantep, Turkey.

出版信息

J Anim Sci. 2024 Jan 3;102. doi: 10.1093/jas/skae248.

Abstract

This study investigates the potential phytochemicals that modulate bovine peroxisome proliferator-activated receptor gamma (PPARγ) and the mitogen-activated protein kinase (MAPK) pathways to enhance milk fat production in dairy animals. Bovine PPARγ, a key member of the nuclear hormone receptor superfamily, plays a vital role in regulating metabolic, cellular differentiation, apoptosis, and anti-inflammatory responses in livestock, while the MAPK pathway is contributory in cellular processes that impact milk fat synthesis. This approach involved an all-inclusive molecular docking analysis of 10,000 polyphenols to identify potential PPARγ ligands. From this extensive screening, top 10 compounds were selected that exhibited the highest binding affinities to bovine PPARγ. Particularly, curcumin sulfate, isoflavone, and quercetin emerged as the most promising candidates. These compounds demonstrated superior docking scores (-9.28 kcal/mol, -9.27 kcal/mol, and -7.31 kcal/mol, respectively) and lower RMSD values compared to the synthetic bovine PPARγ agonist, 2,4-thiazolidinedione (-4.12 kcal/mol), indicating a strong potential for modulating the receptor. Molecular dynamics simulations (MDS) further affirmed the stability of these polyphenols-bovine PPARγ complexes, suggesting their effective and sustained interactions. These polyphenols, known as fatty acid synthase inhibitors, are suggested to influence lipid metabolism pathways crucial to milk fat production, possibly through the downregulation of the MAPK pathway. The screened compounds showed favorable pharmacokinetic profiles, including nontoxicity, carcinogenicity, and high gastrointestinal absorption, positioning them as viable candidates for enhancing dairy cattle health and milk production. These findings may open new possibilities for the use of phytochemicals as feed additives in dairy animals, suggesting a novel approach to improve milk fat synthesis through the dual modulation of bovine PPARγ and MAPK pathways.

摘要

本研究旨在探讨潜在的植物化学物质,调节牛过氧化物酶体增殖物激活受体 γ(PPARγ)和丝裂原活化蛋白激酶(MAPK)通路,以提高奶牛的产奶量。牛过氧化物酶体增殖物激活受体 γ 是核激素受体超家族的关键成员,在调节家畜的代谢、细胞分化、凋亡和抗炎反应中起着至关重要的作用,而 MAPK 通路则有助于影响乳脂合成的细胞过程。本研究采用了一种全面的分子对接分析方法,对 10000 种多酚进行了分析,以确定潜在的 PPARγ 配体。通过广泛筛选,选择了前 10 种与牛过氧化物酶体增殖物激活受体 γ 结合能力最强的化合物。特别是硫酸姜黄素、异黄酮和槲皮素被认为是最有前途的候选化合物。这些化合物的对接评分(-9.28kcal/mol、-9.27kcal/mol 和-7.31kcal/mol)均优于合成的牛过氧化物酶体增殖物激活受体 γ 激动剂 2,4-噻唑烷二酮(-4.12kcal/mol),表明其具有较强的调节受体的潜力。分子动力学模拟(MDS)进一步证实了这些多酚-牛过氧化物酶体增殖物激活受体 γ 复合物的稳定性,表明它们具有有效的、持续的相互作用。这些多酚类化合物作为脂肪酸合酶抑制剂,可能通过下调 MAPK 通路,影响对乳脂生产至关重要的脂质代谢途径。筛选出的化合物具有良好的药代动力学特性,包括非毒性、致癌性和高胃肠道吸收,这使它们成为提高奶牛健康和产奶量的可行候选药物。这些发现为植物化学物质作为奶牛饲料添加剂的应用开辟了新的可能性,为通过双重调节牛过氧化物酶体增殖物激活受体 γ 和 MAPK 通路来提高乳脂合成提供了一种新的方法。

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