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螺旋藻提取物通过抗细胞凋亡和抗 ROS 产生增强 1 型糖尿病的保护作用。

Spirulina Extract Enhanced a Protective Effect in Type 1 Diabetes by Anti-Apoptosis and Anti-ROS Production.

机构信息

Department of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam 13135, Korea.

Department of Senior Healthcare, BK21 Plus Program, Graduate School, Eulji University, Seongnam 13135, Korea.

出版信息

Nutrients. 2017 Dec 15;9(12):1363. doi: 10.3390/nu9121363.

Abstract

Interest in the nutritional value and pharmacological activities of blue-green algae has gradually increased. extracts show protective effects against apoptosis and inflammatory damage in various cell types. Here, we investigated the protective effects of extracts from in a cytokine-mediated type 1 diabetes model in vitro and in streptozotocin-induced diabetic Wistar rats in vivo. Interleukin-1β and interferon-gamma induced substantial cytotoxicity to RINm5F rat insulinoma cells, increasing nitric oxide (NO) production, nuclear factor-kappa B (NF-κB) activity, the expression of endoplasmic reticulum (ER) stress genes, and activation of mitogen-activated protein kinases and key genes related apoptosis. However, the cytotoxicity of cytokines was significantly attenuated by extract, which effectively prevented NO production by inhibiting the synthesis of cytokine-activated NO synthase (iNOS), and apoptosis was suppressed. These results suggest that extract might be effective to preserve the viability and function of pancreatic β-cells against cytotoxic conditions. Moreover, diabetic mice orally administered extract showed decreased glucose levels, increased insulin, and improvement in liver enzyme markers. The antioxidant effect of extract may be helpful in treating type 1 diabetes by enhancing the survival, and reducing or delaying cytokine-mediated β-cells destruction.

摘要

人们对蓝绿藻的营养价值和药理活性的兴趣逐渐增加。研究表明, 提取物对各种细胞类型的细胞凋亡和炎症损伤具有保护作用。在这里,我们研究了 提取物在体外细胞因子介导的 1 型糖尿病模型和体内链脲佐菌素诱导的糖尿病 Wistar 大鼠中的保护作用。白细胞介素-1β和干扰素-γ对 RINm5F 大鼠胰岛素瘤细胞具有显著的细胞毒性,增加了一氧化氮(NO)的产生、核因子-κB(NF-κB)活性、内质网(ER)应激基因的表达以及丝裂原活化蛋白激酶和与细胞凋亡相关的关键基因的激活。然而, 提取物显著减弱了细胞因子的细胞毒性,通过抑制细胞因子激活的一氧化氮合酶(iNOS)的合成有效阻止了 NO 的产生,并抑制了细胞凋亡。这些结果表明, 提取物可能有效保护胰腺β细胞的活力和功能免受细胞毒性条件的影响。此外,糖尿病小鼠口服 提取物后血糖水平降低,胰岛素水平升高,肝脏酶标志物改善。 提取物的抗氧化作用可能有助于通过增强生存能力、减少或延迟细胞因子介导的β细胞破坏来治疗 1 型糖尿病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2caa/5748813/76334c4d999b/nutrients-09-01363-g0A1.jpg

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