Shi Jing, Tian Jin-zhou, Zhu Ai-hua, Yin Jun-xiang, Gao Yang, Lin Jia-you, Wang Yong-yan
Department of Care of Elderly, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.
Zhongguo Zhong Yao Za Zhi. 2004 Jun;29(6):570-5.
To observe inhibiting effect of CGE (compound ginseng extract) on increased expression of IL-1beta and c-fos protein following cerebral ischemia-reperfusion.
The vascular dementia model was made by middle cerebral artery occlusion for 2 hours. Expression of IL-1beta and c-fos were determined by immunohistochemistry in the hippocampus regions in brain tissue at the 0.5 h-7 d after reperfusion. CGE was diluted by CMC and poured into the stomach by 0.7 mL x (100 g)(-1) with a high dosage (19.34 x 10(3) g x L(-1) row herbs), a middle dosage (9.67 x 10(3) g x L(-1)), a low dosage (4.83 x 10(3) g x L(-1)). There were an IL-1ra (rhIL-1ra 20 microg injected into the left cerebral ventricle), a sham operation (NaCl 20 microL injected into the left cerebral ventricle) and a model as control.
Compared with control group, three dose groups (low, middle and high) in CGE showed significant inhibiting effects on the expression of c-fos protein at 2, 3, 4, 12 hours and 3 day following cerebral ischaemic-reperfusion. The level of the inhibiting effects in small and middle groups were lower at all time points than that in IL-1ra group (P < 0.05 to P < 0.01). CGE inhibited the expression of hippocampus IL-1beta protein, taking effect from the 2 h after reperfusion. Both HD group (531 +/- 151.1) and MD group (589.3 +/- 78.6) showed more obvious effect which lasted until the 72 h compared with the model group (687.6 +/- 116.7) (P < 0.01 and 0.05). Large dose group (81.3 +/- 16.1) showed the same level of the inhibiting effect on expression of c-fos protein as IL-1ra group (67.2 +/- 25.7) from 4 hour on following cerebral ischaemic reperfusion (P > 0.05).
CGE with function of Yiqi Bushen, Huoxue Huatan has effect of inhibiting up-regulated expression of IL-1beta and c-fos protein following cerebral ischemia-reperfusion. However, this effect of CGE starts relatively later than that of IL-1ra. The effect of CGE is associated with its dosage, i.e. a larger dosage has a better effect on expression of c-fos protein in post-stroke dementia.
观察复方人参提取物(CGE)对脑缺血再灌注后白细胞介素-1β(IL-1β)和c-fos蛋白表达上调的抑制作用。
采用大脑中动脉闭塞2小时制备血管性痴呆模型。于再灌注后0.5小时至7天,用免疫组织化学法检测脑组织海马区IL-1β和c-fos的表达。CGE用羧甲基纤维素钠(CMC)稀释,分别以高剂量(19.34×10³g/L生药)、中剂量(9.67×10³g/L)、低剂量(4.83×10³g/L)按0.7 mL/(100 g)灌胃。设白细胞介素-1受体拮抗剂(IL-1ra,20 μg重组人白细胞介素-1受体拮抗剂注入左侧脑室)、假手术组(20 μL氯化钠注入左侧脑室)及模型组作为对照。
与对照组相比,CGE的三个剂量组(低、中、高)在脑缺血再灌注后2、3、4、12小时及3天对c-fos蛋白表达均有显著抑制作用。小剂量组和中剂量组在各时间点的抑制作用水平均低于IL-1ra组(P<0.05至P<0.01)。CGE抑制海马区IL-1β蛋白表达,再灌注后2小时开始起效。高剂量组(531±151.1)和中剂量组(589.3±78.6)与模型组(687.6±116.7)相比,作用更明显,持续至72小时(P<0.01和0.05)。脑缺血再灌注后4小时起,高剂量组(81.3±16.1)对c-fos蛋白表达的抑制作用与IL-1ra组(67.2±25.7)相当(P>0.05)。
具有益气补肾、活血化瘀作用的CGE对脑缺血再灌注后IL-1β和c-fos蛋白的上调表达有抑制作用。然而,CGE的这种作用起效相对晚于IL-1ra。CGE的作用与其剂量有关,即较大剂量对中风后痴呆中c-fos蛋白表达的作用更好。