Zhu Hai-bo, Wang Zhen-hua, Tian Jing-wei, Fu Feng-hua, Liu Ke, Li Chang-ling
Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing l00050, China.
Yao Xue Xue Bao. 2005 Dec;40(12):1144-6.
To investigate the protective effect of hydroxysafflor yellow A (HSYA), a soluble element extracted from Carthamus tinctorius L., on focal cerebral ischemia in rats.
Focal cerebral ischemia in male Wistar-Kyoto (WKY) rats were induced by permanent middle cerebral artery occlusion (MCAO). Three doses of 1.5, 3.0 and 6.0 mg x kg(-1) of HSYA were administrated to three groups of rats, separately, via sublingular vein injection 30 min after the onset of ischemia. 24 h after ischemia in rats, neurological deficit scores were evaluated and the infarction area of brain was assessed by quantitative image analysis. The in vitro neuroprotective effect of HSYA was tested in cultured fetal cortical neurons exposed to glutamate and sodium cyanide (NaCN).
HSYA at doses of 3.0 and 6.0 mg x kg(-1) exerted significant neuroprotective effects on rats with focal cerebral ischemic injury as expressed by neurological deficit scores and reduced the infarct area as compared with saline group, and the potency of HSYA at dose of 6.0 mg x kg(-1) was similar to that of 0.2 mg x kg(-1) of nimodipine. In vitro studies, HSYA significantly inhibited neurons damage induced by exposure to glutamate and NaCN in cultured fetal cortical cells.
HSYA has potential neuroprotective action against focal cerebral ischemia in rats and cultured rat fetal cortical neurons as well.
研究从红花中提取的可溶性成分羟基红花黄色素A(HSYA)对大鼠局灶性脑缺血的保护作用。
采用永久性大脑中动脉闭塞(MCAO)法诱导雄性Wistar-Kyoto(WKY)大鼠发生局灶性脑缺血。在缺血发作30分钟后,通过舌下静脉注射将1.5、3.0和6.0mg·kg⁻¹三种剂量的HSYA分别给予三组大鼠。缺血24小时后,评估大鼠神经功能缺损评分,并通过定量图像分析评估脑梗死面积。在暴露于谷氨酸和氰化钠(NaCN)的培养胎鼠皮质神经元中测试HSYA的体外神经保护作用。
3.0和6.0mg·kg⁻¹剂量的HSYA对局灶性脑缺血损伤大鼠具有显著的神经保护作用,表现为神经功能缺损评分降低,与生理盐水组相比梗死面积减小,且6.0mg·kg⁻¹剂量的HSYA的效力与0.2mg·kg⁻¹的尼莫地平相似。体外研究中,HSYA显著抑制了培养的胎鼠皮质细胞中谷氨酸和NaCN诱导的神经元损伤。
HSYA对大鼠局灶性脑缺血以及培养的大鼠胎鼠皮质神经元具有潜在的神经保护作用。