Investigating the effects of combined treatment of mesalazine with Lactobacillus casei in the experimental model of ulcerative colitis.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Frontiers in Molecular Biosciences Pub Date : 2024-10-03 eCollection Date: 2024-01-01 DOI:10.3389/fmolb.2024.1456053
Shabnam Bahrami, Nahid Babaei, Hadi Esmaeili Gouvarchin Ghaleh, Jaleh Mohajeri Borazjani, Mahdieh Farzanehpour
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Abstract

Introduction: Ulcerative colitis (UC), a common gastrointestinal disorder in affluent nations, involves chronic intestinal mucosal inflammation. This research investigated the effects of combined probiotic treatment of Lactobacillus casei (L. casei) and mesalazine on disease activity index and inflammatory factors in the UC model.

Methods: 20 male BALB/c mice were utilized and divided into four groups. To induce UC, all groups received 100 μL of 4% acetic acid (AA) intra-rectally. The first group received phosphate-buffered saline (PBS) (as a control group), the second group was treated with L. casei, the third group was treated with mesalazine and, the fourth group was treated with L. casei and mesalazine. Treatment with L. Casei and mesalazine commenced after the manifestation of symptoms resulting from UC induction. Finally, the mice were euthanized and the disease activity index, myeloperoxidase activity, nitric oxide rate, cytokines level (IL-1β, IL-6, TNF-α) and, gene expression (iNOS, COX-2, and cytokines) were evaluated.

Results: The combined treatment of L. casei and mesalazine led to a significant decrease in the levels of NO, MPO and inflammatory cytokines. In addition, the expression of cytokines, iNOS and COX-2 genes decreased in mice treated with the combination.

Discussion: This study shows that combined treatment of L. casei and mesalazine improves of experimental UC, which can be attributed to the anti-inflammatory properties of L. casei and mesalazine. In conclusion, this combination therapy can be considered a suitable option for the management of UC.

简介溃疡性结肠炎(UC)是富裕国家常见的胃肠道疾病,涉及慢性肠粘膜炎症。本研究探讨了酪酸乳杆菌(L. casei)和美沙拉嗪联合益生菌治疗对 UC 模型中疾病活动指数和炎症因子的影响。方法:20 只雄性 BALB/c 小鼠分为四组,每组直肠注射 100 μL 4% 乙酸(AA)诱导 UC。第一组接受磷酸盐缓冲盐水(PBS)(作为对照组),第二组接受干酪乳杆菌治疗,第三组接受美沙拉嗪治疗,第四组接受干酪乳杆菌和美沙拉嗪治疗。在诱导 UC 出现症状后,开始使用 L. Casei 和美沙拉嗪治疗。最后,小鼠被安乐死,并对疾病活动指数、髓过氧化物酶活性、一氧化氮率、细胞因子水平(IL-1β、IL-6、TNF-α)和基因表达(iNOS、COX-2 和细胞因子)进行评估:结果:L. casei 和美沙拉嗪联合治疗可显著降低 NO、MPO 和炎性细胞因子的水平。此外,接受联合治疗的小鼠细胞因子、iNOS 和 COX-2 基因的表达也有所下降:本研究表明,枸椽酸酪梨菌和美沙拉秦联合治疗可改善实验性 UC,这可归因于枸椽酸酪梨菌和美沙拉秦的抗炎特性。总之,这种联合疗法可被视为治疗 UC 的一种合适选择。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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