番茄红素补充地中海饮食改善小鼠实验性自身免疫性脑脊髓炎(EAE)并改变肠道微生物组

IF 6.2
Tutku Atuk Kahraman, Müge Yılmaz, Kübra Aslan, Halit Canatan, Ayca Kara, Ozkan Ufuk Nalbantoglu, Aycan Gundogdu, Ahmet Eken
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摘要

本研究旨在确定地中海饮食(MD)和番茄红素对EAE发展和炎症标志物的影响。在为期43天的研究中,将72只雌性C57BL/6小鼠按照EAE组和幼稚(对照)组、西式饮食组和MD饮食组以及是否给予番茄红素治疗组随机分为8组。研究期间,小鼠自由饲喂,番茄红素组每只小鼠每隔一天灌胃给予番茄红素10 mg/kg/d,共28 d。对小鼠进行EAE评分,处死,切除脾、淋巴结和脊髓。我们观察到MD-Lyc组EAE的发病时间比其他组稍晚,EAE临床评分也低于其他组。MD-Lyc组脾、淋巴结t细胞计数明显低于其他各组。IFN-γ和IL-22的产生明显高于其他各组。MD-Lyc组小鼠脾脏产生的il - 17a细胞因子明显低于其他各组。此外,MD-Lyc组的髓鞘形成评分最高。与其他组相比,MD-Lyc组也具有独特的微生物群特征。总之,MD和番茄红素给药对EAE评分和髓鞘形成有积极影响。然而,需要在体外和体内水平上进行更全面的研究来揭示这种干预对中枢神经系统细胞数量的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lycopene Supplemented Mediterranean Diet Ameliorates Experimental Autoimmune Encephalomyelitis (EAE) in Mice and Changes Intestinal Microbiome.

This study aimed to determine the effects of the Mediterranean diet (MD) and lycopene on the development of EAE and on inflammatory markers. In the 43-day study, 72 female C57BL/6 mice were randomly divided into eight groups according to whether they were EAE or naive (control) mice, fed a Western diet or a MD, and whether they received lycopene. During the study, mice were fed ad libitum, and lycopene groups were given 10 mg/kg/day lycopene per mouse every other day for 28 days in oral gavage. The mice were scored for EAE, sacrificed and their spleen, lymph nodes, and spinal cords were removed. We observed slightly delayed EAE onset in the MD-Lyc group compared to the others, and the EAE clinical scores were also lower than in the other groups. T-cell counts in the spleen and lymph nodes of the MD-Lyc group were significantly lower than in other groups. The production of IFN-γ and IL-22 was higher than in the other groups. IL-17 A cytokine produced in the spleen was lower in the MD-Lyc group than in the other groups. In addition, the highest myelination score was seen in the MD-Lyc group. MD-Lyc group also had a unique microbiome profile compared with the remaining groups. In summary, MD and lycopene administration positively impacted EAE scores and myelination. However, more comprehensive studies at the in vitro and in vivo levels are needed to reveal the effect of this intervention on cell numbers in the CNS.

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