Tang Hao, Tang Yuping, Li Nianguang, Shi Qianping, Guo Jianming, Shang Erxin, Duan Jin-ao
Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Nanjing University of Chinese Medicine, Nanjing 210023, China; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Nanjing University of Chinese Medicine, Nanjing 210023, China; National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Pharmacol Biochem Behav. 2014 Mar;118:51-9. doi: 10.1016/j.pbb.2014.01.003. Epub 2014 Jan 11.
Scutellarin had protective effects against neuronal injury, however, there are few studies on the protective effect of scutellarein, which is the main metabolite of scutellarin in vivo. This study investigated whether the neural injury by ischemia/reperfusion would be influenced by different doses of scutellarin and scutellarein. Male Wistar rats were orally administered with scutellarin and scutellarein at the doses of 0.09, 0.17, 0.35, 0.70, 1.40 mmol/kg, respectively; then after six consecutive days, they were subjected to global ischemia by occlusion of the bilateral common carotid arteries (BCCAO). After reperfusion for about 21 h, neurological and histological examinations were performed. The present results showed that scutellarein attenuated neuronal cell damage, reduced cerebral water content, regulated the expression of glutamic acid (Glu), aspartic acid (Asp), glycine (Gly), γ-aminobutyric acid (GABA) and taurine (Tau), and improved the Ca(2+)-ATPase and Na(+),K(+)-ATPase activity. Meanwhile, significant difference was found among various doses of scutellarin and scutellarein. Our studies indicated that scutellarin and scutellarein could improve neuronal injury, and scutellarein had better protective effect than scutellarin in rat cerebral ischemia.
灯盏花素对神经元损伤具有保护作用,然而,关于灯盏乙素(灯盏花素在体内的主要代谢产物)的保护作用的研究却很少。本研究调查了不同剂量的灯盏花素和灯盏乙素是否会影响缺血/再灌注引起的神经损伤。雄性Wistar大鼠分别以0.09、0.17、0.35、0.70、1.40 mmol/kg的剂量口服灯盏花素和灯盏乙素;连续六天后,通过结扎双侧颈总动脉(BCCAO)使其遭受全脑缺血。再灌注约21小时后,进行神经学和组织学检查。目前的结果表明,灯盏乙素减轻了神经元细胞损伤,降低了脑含水量,调节了谷氨酸(Glu)、天冬氨酸(Asp)、甘氨酸(Gly)、γ-氨基丁酸(GABA)和牛磺酸(Tau)的表达,并提高了Ca(2+)-ATP酶和Na(+)、K(+)-ATP酶的活性。同时,不同剂量的灯盏花素和灯盏乙素之间存在显著差异。我们的研究表明,灯盏花素和灯盏乙素可以改善神经元损伤,并且在大鼠脑缺血中灯盏乙素的保护作用优于灯盏花素。