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High density lipoprotein 3 inhibits oxidized low density lipoproteininduced apoptosis via promoting cholesterol efflux in RAW264.7 cells

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成果类型:
期刊论文
作者:
Jiang, P;Yan, PK;Chen, JX;Zhu, BY;Lei, XY;...
通讯作者:
Liao, DF
作者机构:
[Liao, DF] Nanhua Univ, Inst Pharm & Pharmacol, Div Pharmacoproteom, Hengyang 421001, Peoples R China.
Nanhua Univ, Sch Life Sci & Technol, Hengyang 421001, Peoples R China.
Vanderbilt Univ, Med Ctr, Dept Pathol, Nashville, TN 37232 USA.
通讯机构:
[Liao, DF] N
Nanhua Univ, Inst Pharm & Pharmacol, Div Pharmacoproteom, Hengyang 421001, Peoples R China.
语种:
英文
关键词:
cholesterol efflux;high density lipoprotein-3;apoptosis;oxidized low density lipoprotein
关键词(中文):
高密度脂蛋白3;细胞凋亡;胆固醇;RAW264.7细胞
期刊:
中国药理学报
ISSN:
1671-4083
年:
2006
卷:
27
期:
2
页码:
151-157
基金类别:
Project supported by the National Natural Science Foundation of China (No 30171084, 30470719), the National Major Basic Research Program of Ministry of Science and Technology of China (973)(G2000056905) and the Natural Science Foundation of Hunan (01JJY2145).
机构署名:
本校为第一且通讯机构
院系归属:
药学与生物科学学院
摘要:
Aim: To investigate the protective effect of high density lipoprotein 3 (HDL3) on oxidized low density lipoprotein (ox-LDL)-induced apoptosis in RAW264.7 cells. Methods: RAW264.7 cells were exposed to 50 mg/L ox-LDL for various durations up to 48 h, and apoptosis was detected using Hoechst 33258 staining and flow cytometric analysis. Total cholesterol levels were detected by high performance liquid chromatography, cholesterol efflux was determined by Tritium labeling, and the cellular lipid droplets were assayed by oil red O staining. Results: ...
摘要(中文):
Aim:To investigate the protective effect of high density lipoprotein 3(HDL3)onoxidized low density lipoprotein(ox-LDL)-induced apoptosis in RAW264.7 cells,Methods:RAW264.7 cells were exposed to 50 mg/L ox-LDL for various durationsup to 48h,and apoptosis was detected using Hoechst 33258 staining and flowcytometric analysis.Total cholesterol levels were detected by high performanceliquid chromatography,cholesterol efflux was determined by Tritium labeling,andthe cellular lipid droplets were assayed by oil red O staining.Results:Treatmentwith...

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