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Carvacrol, a Food-Additive, Provides Neuroprotection on Focal Cerebral Ischemia/Reperfusion Injury in Mice

机译:香芹酚,一种食品添加剂,对小鼠局灶性脑缺血/再灌注损伤具有神经保护作用

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摘要

Carvacrol (CAR), a naturally occurring monoterpenic phenol and food additive, has been shown to have antimicrobials, antitumor, and antidepressant-like activities. A previous study demonstrated that CAR has the ability to protect liver against ischemia/reperfusion injury in rats. In this study, we investigated the protective effects of CAR on cerebral ischemia/reperfusion injury in a middle cerebral artery occlusion mouse model. We found that CAR (50 mg/kg) significantly reduced infarct volume and improved neurological deficits after 75 min of ischemia and 24 h of reperfusion. This neuroprotection was in a dose-dependent manner. Post-treatment with CAR still provided protection on infarct volume when it was administered intraperitoneally at 2 h after reperfusion; however, intracerebroventricular post-treatment reduced infarct volume even when the mice were treated with CAR at 6 h after reperfusion. These findings indicated that CAR has an extended therapeutic window, but delivery strategies may affect the protective effects of CAR. Further, we found that CAR significantly decreased the level of cleaved caspase-3, a marker of apoptosis, suggesting the anti-apoptotic activity of CAR. Finally, our data indicated that CAR treatment increased the level of phosphorylated Akt and the neuroprotection of CAR was reversed by a PI3K inhibitor LY-294002, demonstrating the involvement of the PI3K/Akt pathway in the anti-apoptotic mechanisms of CAR. Due to its safety and wide use in the food industry, CAR is a promising agent to be translated into clinical trials.
机译:香芹酚(CAR)是一种天然的单萜酚和食品添加剂,已被证明具有抗微生物,抗肿瘤和抗抑郁的作用。先前的研究表明,CAR具有保护大鼠肝脏免受缺血/再灌注损伤的能力。在这项研究中,我们调查了CAR对大脑中动脉阻塞小鼠模型中脑缺血/再灌注损伤的保护作用。我们发现,局部缺血75分钟和再灌注24小时后,CAR(50 mg / kg)显着减少了梗塞体积并改善了神经功能缺损。这种神经保护作用是剂量依赖性的。当再灌注后2 h腹膜内注射CAR后,CAR的治疗仍可为梗塞体积提供保护。然而,即使再灌注后6小时用CAR治疗小鼠,脑室内后处理也可以减少梗塞体积。这些发现表明,CAR具有更长的治疗窗口,但给药策略可能会影响CAR的保护作用。此外,我们发现CAR显着降低了裂解的胱天蛋白酶3(一种凋亡的标志物)的水平,表明CAR的抗凋亡活性。最后,我们的数据表明,CAR治疗增加了磷酸化Akt的水平,并且PI3K抑制剂LY-294002逆转了CAR的神经保护作用,表明PI3K / Akt途径参与了CAR的抗凋亡机制。由于其安全性和在食品工业中的广泛应用,CAR是一种有前途的药物,可以转化为临床试验。

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