Zulfiqar Tayyaba, Tipu Muhammad Khalid, Khan Muhammad Tariq, Abouzied Amr S, Al Kazman Bassam S M, Alshammari Saud O, Alshammari Qamar A, Alshammari Abdulkarim, Malik Muhammad Nasir Hayat, Ali Amir, Mazhar Muhammad Usama, Jabeen Hafsa
Department of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Department of Pharmaceutical Chemistry, College of Pharmacy, University of Hail, Hail, Saudi Arabia.
PLoS One. 2025 May 22;20(5):e0324060. doi: 10.1371/journal.pone.0324060. eCollection 2025.
Dysbiosis of gut microbiota and loss of gut-barrier integrity contribute to the development and severity of rheumatoid arthritis (RA). The available treatments pose a burden of major adverse effects and new treatment strategies are therefore the need of time. In this study, Pediococcus acidilactici NMCC-B (Probiotic) was evaluated for its safety and efficacy in complete Freund's adjuvant (CFA)-induced mice model of RA. Mice were treated with either Escherichia coli (1 × 109 CFU/ml) or P. acidilactici NMCC-B (1 × 109 CFU/ml, 2 × 109 CFU/ml) to assess acute, sub-acute, and chronic toxicities. In RA model, mice were either pre-treated with daily dose of P. acidilactici NMCC-B or treated concurrently (day 1-day 27) or post-treated (day 28-day 42). P. acidilactici NMCC-B inhibited gut permeability, lessened joint inflammation, and ameliorated RA progression. No signs of toxicity, pathogenicity or bacterial translocation were observed in animals treated with probiotic. P. acidilactici NMCC-B also restored total body weight, attenuated inflammation, improved antioxidants, alleviated soft tissue swelling, bone damage, and the expression of IL-1β, NF-κB and TNF-α in paw tissue. Based on current findings, it is perceivable that P. acidilactici NMCC-B could be a promising candidate for the management of RA.
肠道微生物群失调和肠道屏障完整性丧失会促使类风湿性关节炎(RA)的发展并加重其严重程度。现有的治疗方法会带来重大不良反应负担,因此新的治疗策略是当务之急。在本研究中,对嗜酸乳杆菌NMCC - B(益生菌)在完全弗氏佐剂(CFA)诱导的RA小鼠模型中的安全性和有效性进行了评估。用大肠杆菌(1×10⁹ CFU/ml)或嗜酸乳杆菌NMCC - B(1×10⁹ CFU/ml、2×10⁹ CFU/ml)处理小鼠,以评估急性、亚急性和慢性毒性。在RA模型中,小鼠要么每天预先给予嗜酸乳杆菌NMCC - B,要么同时处理(第1天至第27天)或事后处理(第28天至第42天)。嗜酸乳杆菌NMCC - B抑制肠道通透性,减轻关节炎症,并改善RA进展。在用益生菌处理的动物中未观察到毒性、致病性或细菌易位的迹象。嗜酸乳杆菌NMCC - B还恢复了总体重,减轻了炎症,改善了抗氧化剂水平,减轻了软组织肿胀、骨损伤以及爪组织中IL - 1β、NF - κB和TNF - α的表达。基于目前的研究结果,可以认为嗜酸乳杆菌NMCC - B可能是治疗RA的一个有前景的候选者。