Effects of probiotic Lactobacillus casei on streptozotocin diabetic rats via decreasing oxidative stress, inflammation and inhibiting Nrf-2/bcl-2/NF-κB/TLR-4 and caspase-3 signalling pathway.

IF 3.2 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Betul Apaydin Yildirim, Enes Tercanli, Kubra Asena Terim Kapakin, Tuba Karaarslan
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引用次数: 0

Abstract

This study aimed to investigate the beneficial effects of Lactobacillus casei (LC) against diabetes (DM). The levels of serum glucose, HbA1c, pancreatic tissue MDA, TNF-α, and IL-1β were increased in the diabetes group compared with the non-diabetic control group, while serum insulin levels, CAT, and SOD activities were lower in the diabetes group. LC reduced the levels of NF-κB, TLR-4, and caspase-3, whereas Bcl-2 and Nrf-2 were elevated. Based on biochemical parameters and histopathological findings, LC, as determined in preliminary studies, effectively lowered blood glucose, HbA1c levels in diabetic rats, reduced lipid peroxidation, enhanced antioxidant enzyme activity, and mitigated oxidative stress. Furthermore, since limited studies have investigated the impact of Lactobacillus casei on NF-κB, Tlr-4 and the Bcl-2, caspase-3, and Nrf-2 signalling pathways in STZ-induced diabetic pancreatic tissue, this study serves as a pioneering contribution to the literature.

益生菌干酪乳杆菌通过降低氧化应激、炎症和抑制Nrf-2/bcl-2/NF-κB/TLR-4和caspase-3信号通路对链脲佐菌素糖尿病大鼠的影响
本研究旨在探讨干酪乳杆菌(LC)对糖尿病(DM)的有益作用。与非糖尿病对照组相比,糖尿病组血清葡萄糖、HbA1c、胰腺组织MDA、TNF-α和IL-1β水平升高,而糖尿病组血清胰岛素水平、CAT和SOD活性降低。LC降低了NF-κB、TLR-4和caspase-3的水平,而Bcl-2和Nrf-2升高。根据生化参数和组织病理学结果,初步研究确定LC能有效降低糖尿病大鼠的血糖、HbA1c水平,减少脂质过氧化,增强抗氧化酶活性,减轻氧化应激。此外,由于研究干酪乳杆菌对stz诱导的糖尿病胰腺组织中NF-κB、Tlr-4以及Bcl-2、caspase-3和Nrf-2信号通路的影响的研究有限,因此本研究是对文献的开创性贡献。
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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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