Therapeutic effects of selenium nanoparticles versus selenium on experimentally induced diabetic retinopathy via modulation of TLR4 / NF-kB P65 / VEGF / connexin 43 signaling.

IF 4 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Nafesa Ashraf Mahmoud Khashaba, Sara Mohamed Naguib Abdel Hafez, Walaa Yehia Abdelzaher, Rehab Ahmed Rifaai, Nada Amgad Mohamed Abdel Majeed
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引用次数: 0

Abstract

Diabetic retinopathy is the most prevalent microvascular consequences of diabetes mellitus that can result in vision loss. Nanotechnology has been widely used in the treatment of ophthalmic diseases. Selenium is a naturally occurring compound that has antioxidant and anti-inflammatory effects. This study aimed at comparing the possible ameliorating effect of selenium versus Nano-selenium on streptozotocin-induced diabetic retinopathy in rats. Sixty adult male albino-Wister rats were divided randomly into six groups; control, Selenium+ve, Nanoselenium+ve, diabetic, DR-Se treated group, and DR-NS treated group. Animals were anesthetized and sacrificed at the end of study. Eyes were removed and prepared for biochemical, histological, and immunohistochemical studies. The results showed that the diabetic group had an apparent decrease in retinal thickness, loss of photoreceptors, dilated congested blood vessels in retinal layers. Additionally, a significant increase in malondialdehyde and significant decrease in Total Antioxidant Capacity were detected. Significant increase in surface area fraction of vascular endothelial growth factor, nuclear factor kappa B, Glial fibrillary acidic protein immune stained cells were noticed, and significant decrease in connexin 43 expression was also detected. Improvement in all mentioned parameters in DR-Se and DR-NS groups was noticed. Our study suggested that Selenium, whether in its regular or nano form, holds promise for alleviating diabetic retinopathy in rats on biochemical, histological, and immunohistochemical basis.

纳米硒与硒通过调节TLR4 / NF-kB P65 / VEGF / connexin 43信号通路对实验性糖尿病视网膜病变的治疗作用
糖尿病视网膜病变是糖尿病最常见的微血管病变,可导致视力丧失。纳米技术已广泛应用于眼科疾病的治疗。硒是一种天然化合物,具有抗氧化和抗炎作用。本研究旨在比较硒与纳米硒对链脲佐菌素诱导的大鼠糖尿病视网膜病变的可能改善作用。将60只成年雄性白化wister大鼠随机分为6组;对照组、硒+ve、纳米硒+ve、糖尿病组、DR-Se治疗组、DR-NS治疗组。动物在研究结束时被麻醉并处死。摘除眼睛,准备进行生化、组织学和免疫组织化学研究。结果显示,糖尿病组视网膜厚度明显减少,光感受器丧失,视网膜各层血管扩张充血。此外,丙二醛显著增加,总抗氧化能力显著降低。血管内皮生长因子、核因子κ B、胶质原纤维酸性蛋白免疫染色细胞的表面积分数显著升高,连接蛋白43表达显著降低。DR-Se组和DR-NS组上述参数均有改善。我们的研究表明,无论是常规形式还是纳米形式的硒,在生化、组织学和免疫组织化学基础上,都有望缓解大鼠糖尿病视网膜病变。
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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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