Selenium nanoparticles ameliorate methotrexate-induced gastric fundus injury in adult male albino rats via TLR4/NF-κB signaling, apoptosis, and intercellular junctions modulation: biochemical and histological study.

IF 4 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Sahar A Mokhemer, Esraa Mohammed Khairy, Rehab Ahmed Rifaai, Nashwa Fathy Gamal El-Tahawy, Randa Ahmed Ibrahim
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引用次数: 0

Abstract

Despite its widespread application in the treatment of cancer and autoimmune diseases, methotrexate (MTX) is associated with several adverse effects. Selenium nanoparticles (SeNPs) have antioxidant and anti-inflammatory effects. This study aimed to investigate the ameliorating effects of SeNPs against MTX-induced gastric fundus damage and the possible underlying mechanisms. Rats were randomly allocated into five groups: control group, SeNPs group, MTX group, and two SeNPs administered groups either prophylactic or concomitant. Physical and macroscopic evaluations were performed. Gastric fundus specimens were collected for biochemical and histological changes. The Methotrexate group showed a significant decrease in weight gain, food intake, and gastric total antioxidant capacity (TAC). Also, there was a disruption of the gastric epithelial barrier indicated by the significant decrease in occludin, E-cadherin gastric levels, and zonula occludens-1 (ZO-1) immune-expression, together with mucous barrier alteration indicated by a significant decrease in Periodic acid-Schiff (PAS) stain mean area fraction. While gastric malondialdehyde (MDA), toll-like receptors 4 (TLR4), and Myeloid differentiation primary response 88 (MYD88) levels, the nuclear factor kappa B (NF-κB) and cleaved caspase 3 immune-expression were significantly increased. Furthermore, histological assessment revealed mucosal ulceration, vascular congestion, and inflammatory cellular infiltration with a significant increase in mast cells. Surprisingly, SeNPs administration attenuated oxidative stress, apoptosis, and TLR4/NF-κB signaling. Moreover, a significant increase in occludin, E-cadherin, and ZO-1 and a significant decrease in mast cell number were noticed with SeNPs administration together with histological structure preservation. Notably, the prophylactic treatment with SeNPs caused more improvement than its concomitant administration.

纳米硒通过TLR4/NF-κB信号、细胞凋亡和细胞间连接调节改善甲氨蝶呤诱导的成年雄性白化大鼠胃底损伤:生化和组织学研究。
尽管甲氨蝶呤(MTX)广泛应用于癌症和自身免疫性疾病的治疗,但它也存在一些不良反应。硒纳米颗粒(SeNPs)具有抗氧化和抗炎作用。本研究旨在探讨SeNPs对mtx诱导的胃底损伤的改善作用及其可能的机制。将大鼠随机分为5组:对照组、SeNPs组、MTX组和SeNPs预防或同时给药组。进行了物理和宏观评价。取胃底标本进行生化和组织学检查。甲氨蝶呤组在体重增加、食物摄入量和胃总抗氧化能力(TAC)方面均有显著下降。此外,胃上皮屏障的破坏表现为occludin, E-cadherin胃水平和occluden -1 (ZO-1)免疫表达的显著降低,以及粘膜屏障的改变表现为周期性酸希夫(PAS)染色平均面积分数的显著降低。胃丙二醛(MDA)、toll样受体4 (TLR4)和髓样分化初级反应88 (MYD88)水平显著升高,核因子κB (NF-κB)和裂解型caspase 3免疫表达显著升高。此外,组织学检查显示粘膜溃疡、血管充血和炎性细胞浸润,肥大细胞显著增加。令人惊讶的是,SeNPs可以减弱氧化应激、细胞凋亡和TLR4/NF-κB信号。此外,给药SeNPs后,occludin、E-cadherin和ZO-1水平显著升高,肥大细胞数量显著减少,组织结构保持不变。值得注意的是,用SeNPs进行预防性治疗比同时给予治疗更有改善。
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来源期刊
Tissue Barriers
Tissue Barriers MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.60
自引率
6.50%
发文量
25
期刊介绍: Tissue Barriers is the first international interdisciplinary journal that focuses on the architecture, biological roles and regulation of tissue barriers and intercellular junctions. We publish high quality peer-reviewed articles that cover a wide range of topics including structure and functions of the diverse and complex tissue barriers that occur across tissue and cell types, including the molecular composition and dynamics of polarized cell junctions and cell-cell interactions during normal homeostasis, injury and disease state. Tissue barrier formation in regenerative medicine and restoration of tissue and organ function is also of interest. Tissue Barriers publishes several categories of articles including: Original Research Papers, Short Communications, Technical Papers, Reviews, Perspectives and Commentaries, Hypothesis and Meeting Reports. Reviews and Perspectives/Commentaries will typically be invited. We also anticipate to publish special issues that are devoted to rapidly developing or controversial areas of research. Suggestions for topics are welcome. Tissue Barriers objectives: Promote interdisciplinary awareness and collaboration between researchers working with epithelial, epidermal and endothelial barriers and to build a broad and cohesive worldwide community of scientists interesting in this exciting field. Comprehend the enormous complexity of tissue barriers and map cross-talks and interactions between their different cellular and non-cellular components. Highlight the roles of tissue barrier dysfunctions in human diseases. Promote understanding and strategies for restoration of tissue barrier formation and function in regenerative medicine. Accelerate a search for pharmacological enhancers of tissue barriers as potential therapeutic agents. Understand and optimize drug delivery across epithelial and endothelial barriers.
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