天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2014年
1期
5-6
,共2页
马东东%曹波%路婷婷%周玉杰%葛善珍%陈虹%卢涛
馬東東%曹波%路婷婷%週玉傑%葛善珍%陳虹%盧濤
마동동%조파%로정정%주옥걸%갈선진%진홍%로도
五味子素%紫外线%皮肤%细胞,培养的%HaCat细胞
五味子素%紫外線%皮膚%細胞,培養的%HaCat細胞
오미자소%자외선%피부%세포,배양적%HaCat세포
SCHIZANDRIN%ultraviolet rays%skin%cells,cultured%HaCat cells
目的:探讨五味子乙素(SchB)对长波紫外线(UVA)诱导永生化人角质形成细胞(HaCat细胞)损伤后的保护作用及其可能的作用机制。方法用5 J/cm2的UVA照射HaCat细胞,给予不同浓度的SchB(0.1、0.01、0.001、0.0001μmol/L)处理UVA损伤后的HaCat细胞,检测细胞超氧化物歧化酶(SOD)及谷胱甘肽过氧化物酶(GSH-Px)的活性,乳酸脱氢酶(LDH)及NO含量。结果 UVA照射HaCat细胞后,SOD、GSH-Px活性降低,LDH及NO含量升高,给予不同浓度的SchB均能显著提高SOD、GSH-Px活性,降低LDH及NO含量,提高HaCat细胞的存活率,尤其以0.001μmol/L SchB的保护作用最强。结论0.001μmol/L SchB减轻UVA对HaCat细胞损伤的效果最佳。
目的:探討五味子乙素(SchB)對長波紫外線(UVA)誘導永生化人角質形成細胞(HaCat細胞)損傷後的保護作用及其可能的作用機製。方法用5 J/cm2的UVA照射HaCat細胞,給予不同濃度的SchB(0.1、0.01、0.001、0.0001μmol/L)處理UVA損傷後的HaCat細胞,檢測細胞超氧化物歧化酶(SOD)及穀胱甘肽過氧化物酶(GSH-Px)的活性,乳痠脫氫酶(LDH)及NO含量。結果 UVA照射HaCat細胞後,SOD、GSH-Px活性降低,LDH及NO含量升高,給予不同濃度的SchB均能顯著提高SOD、GSH-Px活性,降低LDH及NO含量,提高HaCat細胞的存活率,尤其以0.001μmol/L SchB的保護作用最彊。結論0.001μmol/L SchB減輕UVA對HaCat細胞損傷的效果最佳。
목적:탐토오미자을소(SchB)대장파자외선(UVA)유도영생화인각질형성세포(HaCat세포)손상후적보호작용급기가능적작용궤제。방법용5 J/cm2적UVA조사HaCat세포,급여불동농도적SchB(0.1、0.01、0.001、0.0001μmol/L)처리UVA손상후적HaCat세포,검측세포초양화물기화매(SOD)급곡광감태과양화물매(GSH-Px)적활성,유산탈경매(LDH)급NO함량。결과 UVA조사HaCat세포후,SOD、GSH-Px활성강저,LDH급NO함량승고,급여불동농도적SchB균능현저제고SOD、GSH-Px활성,강저LDH급NO함량,제고HaCat세포적존활솔,우기이0.001μmol/L SchB적보호작용최강。결론0.001μmol/L SchB감경UVA대HaCat세포손상적효과최가。
Objective To explore the protective effect of schisandrin B (SchB) on the permanent damage of human keratinocytes (HaCat) induced by long wave ultraviolet (UVA),and its possible mechanism thereof. Methods After HaCat was treated by 5 J/cm2 UVA, different concentrations of SchB (0.1, 0.01, 0.001 and 0.000 1μmol/L) were used to treat HaCat cells. The levels of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) activity, lactate dehydrogenase (LDH) and NO content were detected. Results The levels of SOD and GSH-Px activity were decreased, and he levels of LDH and NO content were increased in HaCat cells after being treated by UVA. The different concentrations of SchB showed significant ef-fects on the increased levels of SOD, GSH-Px activity and decreased levels of LDH and NO, and improved the survival rate of HaCat cells. The 0.001 μmol/L SchB showed the strongest protective effect. Conclusion The 0.001 μmol/L SchB showed the best effect on the damage of HaCat cells induce the UVA.