Department of Pharmaceutical Toxicology, School of Pharmaceutical Science, China Medical University, Shenyang 110001, China.
Brain Res Bull. 2011 Jul 15;85(6):396-402. doi: 10.1016/j.brainresbull.2011.05.002. Epub 2011 May 11.
Baicalin is an important medicinal herb purified from the dry roots of Scutellaria baicalensis Georgi. The present study was undertaken to evaluate the neuroprotective effects of baicalin in gerbils subjected to transient global cerebral ischemic-reperfusion injury. Baicalin at doses of 50, 100 and 200mg/kg was intraperitoneally injected into the gerbils immediately after cerebral ischemia. Seven days after reperfusion, hematoxylin and eosin (HE) staining was performed to analyze hippocampal CA1 pyramidal damage histopathologically. In addition, in order to understand the potential protective mechanism of baicalin, we examined anti-oxidative enzymes, such superoxide dismutase (SOD), glutathione peroxidase (GSH-PX), non-enzymatic scavenger glutathione (GSH) and measured the content of malondialdehyde (MDA) in hippocampus. The mRNA and protein expressions of BDNF were determined in ischemic hippocampus by real-time RT-PCR and Western blot, respectively. Evidence for neuronal apoptosis was detected by real-time RT-PCR, Western blot and caspase-3 activity measurement. Histopathological examination showed that the administration of baicalin by the dose of 100 and 200mg/kg significantly attenuated ischemia-induced neuronal cell damage. Reduced level of MDA, obviously elevated activities of SOD and GSH as well as GSH-PX were also found in baicalin-treated groups. Further investigation demonstrated that treatment with baicalin remarkably promoted the expression of BDNF and inhibited the expression of caspase-3 at mRNA and protein levels by real-time RT-PCR and Western blot, respectively. Besides, caspase-3 activity assay also elucidated that the administration of baicalin could significantly suppress caspase-3 in ischemic gerbils hippocampus. Theses findings suggest that baicalin's neuroprotection appears to be associated with its anti-oxidative and anti-apoptotic properties in global cerebral ischemia in the gerbils.
黄芩苷是从黄芩干燥根中提取的一种重要药用植物。本研究旨在评价黄芩苷对局灶性脑缺血再灌注损伤沙鼠的神经保护作用。缺血后立即腹腔注射黄芩苷 50、100 和 200mg/kg。再灌注 7 天后,苏木精-伊红(HE)染色法对海马 CA1 锥体神经元损伤进行组织病理学分析。此外,为了了解黄芩苷的潜在保护机制,我们检测了超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-PX)、非酶性清除剂谷胱甘肽(GSH)等抗氧化酶,测量了海马丙二醛(MDA)的含量。通过实时 RT-PCR 和 Western blot 检测缺血海马中 BDNF 的 mRNA 和蛋白表达。通过实时 RT-PCR、Western blot 和 caspase-3 活性测定检测神经元凋亡的证据。组织病理学检查显示,100 和 200mg/kg 黄芩苷给药可显著减轻缺血诱导的神经元细胞损伤。黄芩苷处理组 MDA 水平降低,SOD 和 GSH-PX 活性明显升高。进一步研究表明,黄芩苷治疗可显著促进 BDNF 的表达,并通过实时 RT-PCR 和 Western blot 分别抑制 caspase-3 的表达。此外,caspase-3 活性测定也阐明了黄芩苷给药可显著抑制缺血沙鼠海马中的 caspase-3。这些发现表明,黄芩苷的神经保护作用可能与其在沙鼠全脑缺血中的抗氧化和抗凋亡特性有关。