Department of Pharmacology, L. M. College of Pharmacy, Ahmedabad, Gujarat, India.
Department of Pharmacology, K. B. Institute of Pharmaceutical Education and Research, Gandhinagar, Gujarat, India.
Probiotics Antimicrob Proteins. 2021 Aug;13(4):1005-1017. doi: 10.1007/s12602-020-09738-4. Epub 2021 Feb 5.
Currently, there are no effective therapeutic agents to limit intestinal mucosal damage associated with inflammatory bowel disease (IBD). Based on several clinical studies, probiotics have emerged as a possible novel therapeutic strategy for IBD; however, their possible mechanisms are still poorly understood. Although probiotics in murine and human improve disease severity, very little is known about the specific contribution of cell wall contents of probiotics in IBD. Herein, we investigated the protective effects of cell wall contents of three Lactobacillus species in lipopolysaccharide (LPS)-induced colitis rats. LPS-sensitized rats were rendered colitic by colonic instillation of LPS (500 µg/rat) for 14 consecutive days. Concurrently, cell wall contents isolated from 10 CFU of L. casei (LC), L. acidophilus (LA), and L. rhamnosus (LA) was given subcutaneously for 21 days, considering sulfasalazine (100 mg/kg, p.o.) as standard. The severity of colitis was assessed by body weight loss, food intake, stool consistency, rectal bleeding, colon weight/length, spleen weight, and histological analysis. Colonic inflammatory markers (myeloperoxidase activity, C-reactive protein, and pro-inflammatory cytokines) and oxidative stress markers (malondialdehyde, reduced glutathione, and nitric oxide) were also assayed. Cell wall contents of LC, LA, and LR significantly ameliorated the severity of colitis by reducing body weight loss and diarrhea and bleeding incidence, improving food intake, colon weight/length, spleen weight, and microscopic damage to the colonic mucosa. The treatment also reduced levels of inflammatory and oxidative stress markers and boosted anti-oxidant molecule. In conclusion, cell wall contents of LC, LA, and LR attenuate LPS-induced colitis by modulating immuno-inflammation and oxidative stress.
目前,尚无有效药物可限制与炎症性肠病(IBD)相关的肠黏膜损伤。基于多项临床研究,益生菌已成为治疗 IBD 的一种新策略,但对其潜在机制仍知之甚少。尽管鼠类和人类的益生菌可改善疾病严重程度,但对于益生菌细胞壁成分在 IBD 中的具体作用知之甚少。在此,我们研究了三种乳杆菌(Lactobacillus species)细胞壁成分在脂多糖(LPS)诱导的结肠炎大鼠中的保护作用。LPS 致敏大鼠通过连续 14 天结肠内注入 LPS(500 µg/只)引发结肠炎。同时,将 10 CFU 的干酪乳杆菌(L. casei,LC)、嗜酸乳杆菌(L. acidophilus,LA)和鼠李糖乳杆菌(L. rhamnosus,LR)的细胞壁成分经皮下给予 21 天,以柳氮磺胺吡啶(100 mg/kg,po)为标准。通过体重减轻、食物摄入量、粪便稠度、直肠出血、结肠重量/长度、脾脏重量和组织学分析评估结肠炎的严重程度。还测定了结肠炎症标志物(髓过氧化物酶活性、C 反应蛋白和促炎细胞因子)和氧化应激标志物(丙二醛、还原型谷胱甘肽和一氧化氮)。LC、LA 和 LR 的细胞壁成分通过减少体重减轻和腹泻及出血发生率、改善食物摄入、结肠重量/长度、脾脏重量和结肠黏膜的微观损伤,显著改善了结肠炎的严重程度。该治疗还降低了炎症和氧化应激标志物的水平,并增强了抗氧化分子。综上所述,LC、LA 和 LR 的细胞壁成分通过调节免疫炎症和氧化应激来减轻 LPS 诱导的结肠炎。