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使用常见抗氧化剂保护血脑屏障内皮细胞免受香烟烟雾诱导的氧化应激:它们真的有益吗?

Protecting the BBB endothelium against cigarette smoke-induced oxidative stress using popular antioxidants: Are they really beneficial?

作者信息

Kaisar Mohammad Abul, Prasad Shikha, Cucullo Luca

机构信息

Department of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, Amarillo, TX 79106, United States.

Department of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, Amarillo, TX 79106, United States; Center for Blood-Brain Barrier Research, Texas Tech University Health Sciences Center, Amarillo, TX 79106, United States.

出版信息

Brain Res. 2015 Nov 19;1627:90-100. doi: 10.1016/j.brainres.2015.09.018. Epub 2015 Sep 26.

Abstract

Blood Brain Barrier (BBB) exposed to realistic concentrations (comparable to a chronic heavy smoker) of Cigarette Smoke Extract (CSE) triggers a strong endothelial inflammatory response which can lead to the onset of neurological disorders. The involvement of Reactive Oxygen Species (ROS) in this inflammatory cascade is evident from the up-regulation of nuclear factor erythroid 2 related factor 2 (Nrf-2), a transcription factor involved in anti-oxidant response signaling in CSE exposed endothelial cells. We have shown that pre-treatment with α-tocopherol and/or ascorbic acid is highly protective for the BBB, thus suggesting that, prophylactic administration of antioxidants can reduce CSE and/or inflammatory-dependent BBB damage. We have assessed and ranked the protective effects of 5 popular OTC antioxidants (Coenzyme Q10, melatonin, glutathione, lipoic acid and resveratrol) against CSE-induced BBB endothelial damage using hCMEC/D3 cells. The analysis of pro-inflammatory cytokines release by ELISA revealed that resveratrol, lipoic acid melatonin and Co-Q10 inhibited the BBB endothelial release of pro-inflammatory cytokines IL-6 and IL-8, reduced (not Co-Q10) CSE-induced up-regulation of Platelet Cell Adhesion Molecule-1 (PECAM-1), Vascular Cell Adhesion Molecule-1 (VCAM-1) & E-selectin and inhibited monocytes-endothelial cell adhesion. The anti-inflammatory effects correlated with the anti-oxidative protection endowed by these compounds as evidenced by upregulation of NADPH: Quinone Oxidoreductase 1 (NQO1) and reduced cellular oxidative stress. CSE-induced release of Vascular Endothelial Growth Factor (VEGF) was inhibited by all tested compounds although the effect was not strictly dose-dependent. Further in vivo studies are required to validate our results and expand our current study to include combinatorial treatments.

摘要

暴露于与慢性重度吸烟者相当的实际浓度香烟烟雾提取物(CSE)中的血脑屏障(BBB)会引发强烈的内皮炎症反应,这可能导致神经紊乱的发作。活性氧(ROS)参与这一炎症级联反应,这从核因子红细胞2相关因子2(Nrf-2)的上调中可以明显看出,Nrf-2是一种参与CSE暴露的内皮细胞抗氧化反应信号传导的转录因子。我们已经表明,用α-生育酚和/或抗坏血酸预处理对血脑屏障具有高度保护作用,因此表明预防性给予抗氧化剂可以减少CSE和/或炎症依赖性血脑屏障损伤。我们使用hCMEC/D3细胞评估并排名了5种常见的非处方抗氧化剂(辅酶Q10、褪黑素、谷胱甘肽、硫辛酸和白藜芦醇)对CSE诱导的血脑屏障内皮损伤的保护作用。通过酶联免疫吸附测定(ELISA)分析促炎细胞因子的释放发现,白藜芦醇、硫辛酸、褪黑素和辅酶Q10抑制了血脑屏障内皮细胞促炎细胞因子白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的释放,降低了(辅酶Q10除外)CSE诱导的血小板细胞黏附分子-1(PECAM-1)、血管细胞黏附分子-1(VCAM-1)和E-选择素的上调,并抑制了单核细胞与内皮细胞的黏附。这些抗炎作用与这些化合物赋予的抗氧化保护作用相关,烟酰胺腺嘌呤二核苷酸磷酸(NADPH)醌氧化还原酶1(NQO1)的上调和细胞氧化应激的降低证明了这一点。所有测试化合物均抑制了CSE诱导的血管内皮生长因子(VEGF)的释放,尽管这种作用并不严格依赖剂量。需要进一步的体内研究来验证我们的结果,并将我们目前的研究扩展到包括联合治疗。

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