Mu Jingjing, Xu Jingwen, Wang Linlin, Chen Caifa, Chen Ping
School of Life Science, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
College of Health Sciences, Jiangsu Normal University, Xuzhou 221116, Jiangsu, P. R. China.
Food Funct. 2021 Nov 15;12(22):11503-11514. doi: 10.1039/d1fo02454j.
Purple sweet potato anthocyanins have been acknowledged for their beneficial effects on human inflammatory bowel diseases (IBD). Although the ability of anthocyanins in modulating the gut microbiota has been reported, the relationship between the bacteria modulated by anthocyanins and intestinal inflammation has not been fully elucidated. We aimed to ascertain whether the purple sweet potato anthocyanin extract (PSPAE) modulation of gut microbiota in the dextran sodium sulphate (DSS) induced chronic colitis mouse model could result in the maintenance of intestinal homeostasis and protection against bacterial intestinal inflammation. Chronic colitis was induced by adding DSS in drinking water while administering the mice with PSPAE gavage (20 mg kg). Effects on colon tissue damage, gut microbiota composition, tight junction protein, and cytokines were evaluated. PSPAE prevented the loss of and and inhibited the increase of Gammaproteobacteria and upon DSS treatment. The non-pathogenic-dependent and pathogenic-dependent microenvironments were established upon treatment with broad-spectrum antibiotics. Both PSPAE treatment and non-pathogenic treatments modified the colonic expression of mouse tight junction proteins and maintained the architecture of the colon. However, the non-pathogenic treatment could not attenuate intestinal inflammation. Moreover, the pathogenic-dependent dysbiosis was exacerbated because of the increasing colonization of pathogens such as . The PSPAE exerted the modulation of gut microbiota to maintain the gut microbiome homeostasis in DSS-induced chronic colitis mice, which may help to propose a new treatment that combines efficacy and reduction of the possibility of bacterial intestinal infection.
紫甘薯花青素因其对人类炎症性肠病(IBD)的有益作用而受到认可。尽管已有报道花青素具有调节肠道微生物群的能力,但花青素调节的细菌与肠道炎症之间的关系尚未完全阐明。我们旨在确定在葡聚糖硫酸钠(DSS)诱导的慢性结肠炎小鼠模型中,紫甘薯花青素提取物(PSPAE)对肠道微生物群的调节是否能维持肠道稳态并预防细菌性肠道炎症。通过在饮用水中添加DSS诱导慢性结肠炎,同时对小鼠进行PSPAE灌胃(20 mg/kg)。评估其对结肠组织损伤、肠道微生物群组成、紧密连接蛋白和细胞因子的影响。PSPAE可防止DSS处理后 和 的丢失,并抑制γ-变形菌和 的增加。用广谱抗生素处理后建立了非致病性依赖和致病性依赖的微环境。PSPAE处理和非致病性处理均改变了小鼠紧密连接蛋白的结肠表达并维持了结肠结构。然而,非致病性处理并不能减轻肠道炎症。此外,由于诸如 等病原体的定殖增加,致病性依赖的生态失调加剧。PSPAE对肠道微生物群进行调节,以维持DSS诱导的慢性结肠炎小鼠的肠道微生物群稳态,这可能有助于提出一种结合疗效和降低细菌性肠道感染可能性的新治疗方法。