Huang Jin-Lan, Wu Deng-Pan, Lu Lu, Li Fei, Zhong Zhen-Guo
Guangxi Medical University, Nanning 530021,China.
Zhong Yao Cai. 2012 Nov;35(11):1805-8.
To explore the effects of PNS on the content and activity of alpha-secretase in the brains of SAMP8 mice with Alzheimer's disease.
SAMP8 mice were randomly divided into four groups: PNS high-dosage group, PNS low-dosage group, huperzine A group and control group. The high-dosage group and low-dosage group were treated with 200 and 100 mg/kg PNS respectively per day and the huperzine A group was treated with 0.3 mg/kg huperzine A per day, all by intragastric administration for 8 consecutive weeks. The same volume of double distilled water was given to the control group. The activity of a-secretase was assayed by direct immunofluorescent method(DIF). Western blot was used to detect the content of alpha-secretase including ADAM9, ADAM10 and ADAM17 proteins.
The Relative Fluorescence Units (RFU) of PNS high-dosage and low-dosage groups were higher than that of control group (P < 0.01). The results of western blot showed that the level of ADAM9 protein expression in PNS high-dosage, low-dosage and huperzine A groups was significantly higher than that of control group (P < 0.05) while the levels of ADAM10 protein expression in PNS high-dosage, low-dosage and huperzine A groups was significantly lower than that of control group (P < 0.05), while level of ADAM17 of huperzine A group was higher than that of control group (P < 0.05).
PNS can increase activity of alpha-secretase in the brain of SAMP8 mouse via increasing the level of ADAM9 protein expression.
探讨三七总皂苷(PNS)对阿尔茨海默病SAMP8小鼠脑内α-分泌酶含量及活性的影响。
将SAMP8小鼠随机分为四组:PNS高剂量组、PNS低剂量组、石杉碱甲组和对照组。高剂量组和低剂量组分别每天按200和100mg/kg给予PNS,石杉碱甲组每天按0.3mg/kg给予石杉碱甲,均连续灌胃8周。对照组给予等体积双蒸水。采用直接免疫荧光法(DIF)检测α-分泌酶活性。采用蛋白质免疫印迹法检测α-分泌酶包括ADAM9、ADAM10和ADAM17蛋白的含量。
PNS高剂量组和低剂量组的相对荧光强度(RFU)高于对照组(P<0.01)。蛋白质免疫印迹结果显示,PNS高剂量组、低剂量组和石杉碱甲组ADAM9蛋白表达水平显著高于对照组(P<0.05),而PNS高剂量组、低剂量组和石杉碱甲组ADAM10蛋白表达水平显著低于对照组(P<0.05),石杉碱甲组ADAM17水平高于对照组(P<0.05)。
PNS可通过提高ADAM9蛋白表达水平增加SAMP8小鼠脑内α-分泌酶活性。