湖南中医药大学学报
湖南中醫藥大學學報
호남중의약대학학보
Journal of Traditional Chinese Medicine University of Hunan
2015年
9期
20-22
,共3页
张运辉%伍大华%袁春云%张秀丽%彭文杰%姚婷
張運輝%伍大華%袁春雲%張秀麗%彭文傑%姚婷
장운휘%오대화%원춘운%장수려%팽문걸%요정
阿尔茨海默病%二苯乙烯苷%三七总皂苷%PC12细胞%配伍
阿爾茨海默病%二苯乙烯苷%三七總皂苷%PC12細胞%配伍
아이자해묵병%이분을희감%삼칠총조감%PC12세포%배오
Alzheimer's disease%stilbene glycoside%panax notoginseng saponins%PC12 cell%compatibility of medicines
目的 探讨二苯乙烯苷(TSG)和三七总皂苷(PNS)配伍对Aβ25-35诱导的PC12细胞损伤的影响. 方法 PC12细胞采用Aβ25-35诱导建立阿尔茨海默病的损伤模型,被随机分成空白组、模型组、多奈哌齐组(10 μmol/L)、TSG(100 mmol/L)组、PNS组(50 mg/L)、TSG-PNS配伍组(TSG100 mmol/L+PNS50 mg/L). 取细胞上清液测各组的乙酰胆碱酯酶(AchE)及超氧化物歧化酶(SOD)活力、丙二醛(MDA)含量. 结果 与模型组比较,TSG组、PNS组、TSG-PNS配伍组可降低AchE活力、MDA含量及提高SOD活力(P<0.05). 且TSG-PNS配伍组的效应比TSG或PNS单用组效应更好(P<0.01). 结论 TSG和PNS配伍对Aβ25-35诱导的PC12细胞损伤具有明显的保护作用,其作用机制可能与胆碱能系统及氧化应激有关.
目的 探討二苯乙烯苷(TSG)和三七總皂苷(PNS)配伍對Aβ25-35誘導的PC12細胞損傷的影響. 方法 PC12細胞採用Aβ25-35誘導建立阿爾茨海默病的損傷模型,被隨機分成空白組、模型組、多奈哌齊組(10 μmol/L)、TSG(100 mmol/L)組、PNS組(50 mg/L)、TSG-PNS配伍組(TSG100 mmol/L+PNS50 mg/L). 取細胞上清液測各組的乙酰膽堿酯酶(AchE)及超氧化物歧化酶(SOD)活力、丙二醛(MDA)含量. 結果 與模型組比較,TSG組、PNS組、TSG-PNS配伍組可降低AchE活力、MDA含量及提高SOD活力(P<0.05). 且TSG-PNS配伍組的效應比TSG或PNS單用組效應更好(P<0.01). 結論 TSG和PNS配伍對Aβ25-35誘導的PC12細胞損傷具有明顯的保護作用,其作用機製可能與膽堿能繫統及氧化應激有關.
목적 탐토이분을희감(TSG)화삼칠총조감(PNS)배오대Aβ25-35유도적PC12세포손상적영향. 방법 PC12세포채용Aβ25-35유도건립아이자해묵병적손상모형,피수궤분성공백조、모형조、다내고제조(10 μmol/L)、TSG(100 mmol/L)조、PNS조(50 mg/L)、TSG-PNS배오조(TSG100 mmol/L+PNS50 mg/L). 취세포상청액측각조적을선담감지매(AchE)급초양화물기화매(SOD)활력、병이철(MDA)함량. 결과 여모형조비교,TSG조、PNS조、TSG-PNS배오조가강저AchE활력、MDA함량급제고SOD활력(P<0.05). 차TSG-PNS배오조적효응비TSG혹PNS단용조효응경호(P<0.01). 결론 TSG화PNS배오대Aβ25-35유도적PC12세포손상구유명현적보호작용,기작용궤제가능여담감능계통급양화응격유관.
Objective To investigate the effect of compatibility of TSG and PNS on PC12 cell injury induced by Aβ25-35. Methods PC12 cell induced by Aβ25-35 was established Alzheimer's disease damage models, and PC12 cells were randomly divided into blank group, model group, Donay Patsy group (10 μmol/L), TSG group (100 mmol/L), PNS group (50 mg/L), TSG-PNS group (TSG 100 mmol/L + PNS 50 mg/L).The acetylcholinesterase (AchE), catalase (SOD) activity and malondialdehyde (MDA) content in supernatant were measured. Results Compared with the model group, the TSG group, PNS group and TSG-PNS group can reduce the vigor of AchE and the content of MDA, and increase the activity of SOD(P<0.05). Moreover, the effect of TSG-PNS group was better than only using TSG or PNS (P<0.01). Conclusion The compatibility of TSG and PNS exhibited a significant protective effect on PC12 cell injury induced by Aβ25-35 and its mechanism may be related to the cholinergic system and oxidative stress.