Hwang Eunmi, Kim Gye Won, Song Ki Duk, Lee Hak-Kyo, Kim Sung-Jo
Division of Cosmetics and Biotechnology, College of Life and Health Sciences, Hoseo University, Baebang, Asan 31499, Korea.
Brewing Research Center, Academic Industry Cooperation, Hankyong National University, Anseong 17579, Korea.
Asian-Australas J Anim Sci. 2019 Nov 1;32(11):1776-1788. doi: 10.5713/ajas.18.0874. Epub 2019 Mar 7.
The demand for measures to improve disease resistance and productivity of livestock are increasing, as most countries prohibit the addition of antibiotics to feed. This study therefore aimed to uncover functional feed additives to help enhance livestock immunity and disease resistance, using Acanthopanax sessiliflorus fruit extract (ASF).
ASF was extracted with 70% EtOH, and total polyphenolic and catechin contents were measured by the Folin-Ciocalteu and vanillin assay, respectively. The 3D4/31 porcine macrophage cells (MΦ) were activated by Phorbol 12-Myristate 13-Acetate (PMA), and cell survival and growth rate were measured with or without ASF treatment. Flow-cytometric analysis determined the lysosomal activity, reactive oxygen species levels (ROS), and cell cycle distribution. Nuclear factor kappa B (NF-κB) and superoxide dismutase (SOD) protein expression levels were quantified by western blotting and densitometry analysis. Quantitative PCR was applied to measure the lipid metabolism-related genes expression level. Lastly, the antibacterial activity of 3D4/31 MΦ cells was evaluated by the colony forming unit assay.
ASF upregulated the cell viability and growth rate of 3D4/31 MΦ, with or without PMA activation. Moreover, lysosomal activity and intracellular ROS levels were increased after ASF exposure. In addition, the antioxidant enzyme SOD2 expression levels were proportionately increased with ROS levels. Both ASF and PMA treatment resulted in upregulation of NF-κB protein, tumor necrosis factor (TNF) α mRNA expression levels, lipid synthesis, and fatty acid oxidation metabolism. Interestingly, co-treatment of ASF with PMA resulted in recovery of NF-κB, TNFα, and lipid metabolism levels. Finally, ASF pretreatment enhanced the in vitro bactericidal activity of 3D4/31 MΦ against Escherichia coli.
s: This study provides a novel insight into the regulation of NF-κB activity and lipid metabolism in MΦ, and we anticipate that ASF has the potential to be effective as a feed additive to enhance livestock immunity.
由于大多数国家禁止在饲料中添加抗生素,因此对提高牲畜抗病能力和生产力的措施的需求日益增加。因此,本研究旨在利用刺五加果实提取物(ASF),找出有助于增强牲畜免疫力和抗病能力的功能性饲料添加剂。
用70%乙醇提取ASF,分别采用福林-酚法和香草醛法测定总多酚和儿茶素含量。用佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)激活3D4/31猪巨噬细胞(MΦ),在有或无ASF处理的情况下测量细胞存活率和生长率。流式细胞术分析确定溶酶体活性、活性氧水平(ROS)和细胞周期分布。通过蛋白质免疫印迹和密度分析对核因子κB(NF-κB)和超氧化物歧化酶(SOD)蛋白表达水平进行定量。应用定量PCR检测脂质代谢相关基因的表达水平。最后,通过菌落形成单位试验评估3D4/31 MΦ细胞的抗菌活性。
无论是否经PMA激活,ASF均上调3D4/31 MΦ的细胞活力和生长率。此外,ASF处理后溶酶体活性和细胞内ROS水平升高。此外,抗氧化酶SOD2的表达水平与ROS水平成比例增加。ASF和PMA处理均导致NF-κB蛋白、肿瘤坏死因子(TNF)α mRNA表达水平、脂质合成和脂肪酸氧化代谢上调。有趣的是,ASF与PMA联合处理可使NF-κB、TNFα和脂质代谢水平恢复。最后,ASF预处理增强了3D4/31 MΦ对大肠杆菌的体外杀菌活性。
本研究为巨噬细胞中NF-κB活性和脂质代谢的调节提供了新的见解,我们预计ASF有潜力作为一种有效的饲料添加剂来增强牲畜免疫力。