Departments of Surgery and Pharmacology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA.
J Clin Biochem Nutr. 2010 Sep;47(2):121-9. doi: 10.3164/jcbn.10-29. Epub 2010 Jul 6.
Astaxanthin (ATX), a naturally occurring carotenoid pigment, is a powerful biological antioxidant. In the present study, we investigated whether ATX pharmacologically offers neuroprotection against oxidative stress by cerebral ischemia. We found that the neuroprotective efficacy of ATX at the dose of 30 mg/kg (n = 8) was 59.5% compared with the control group (n = 3). In order to make clear the mechanism of ATX neuroprotection, the up-regulation inducible nitric oxide synthase (iNOS) and heat shock proteins (HSPs) together with the oxygen glucose deprivation (OGD) in SH-SY5Y cells were also investigated. The induction of various factors involved in oxidative stress processes such as iNOS was suppressed by the treatment of ATX at 25 and 50 µM after OGD-induced oxidative stress. In addition, Western blots showed that ATX elevated of heme oxygenase-1 (HO-1; Hsp32) and Hsp70 protein levels in in vitro. These results suggest that the neuroprotective effects of ATX were related to anti-oxidant activities in global ischemia.
虾青素(ATX)是一种天然存在的类胡萝卜素色素,是一种强大的生物抗氧化剂。在本研究中,我们研究了 ATX 是否通过脑缺血对氧化应激具有药理保护作用。我们发现,与对照组(n=3)相比,ATX 剂量为 30mg/kg(n=8)时的神经保护效果为 59.5%。为了阐明 ATX 神经保护的机制,还研究了 SH-SY5Y 细胞中诱导型一氧化氮合酶(iNOS)和热休克蛋白(HSPs)的上调以及氧葡萄糖剥夺(OGD)。在用 ATX 处理后,可抑制各种与氧化应激过程相关的因素的诱导,如 iNOS,这些因素在 OGD 诱导的氧化应激后用 25 和 50µM 的 ATX 处理。此外,Western 印迹显示 ATX 可提高体外血红素加氧酶-1(HO-1;Hsp32)和 Hsp70 蛋白水平。这些结果表明,ATX 的神经保护作用与全脑缺血中的抗氧化活性有关。