中国血液流变学杂志
中國血液流變學雜誌
중국혈액류변학잡지
CHINESE JOURNAL OF HEMORHEOLOGY
2014年
1期
21-24
,共4页
依折麦布%辛伐他汀%动脉粥样硬化%肿瘤坏死因子α%单核细胞趋化因子1
依摺麥佈%辛伐他汀%動脈粥樣硬化%腫瘤壞死因子α%單覈細胞趨化因子1
의절맥포%신벌타정%동맥죽양경화%종류배사인자α%단핵세포추화인자1
Ezetimibe%Simvastatin%atherosclerosis%TNF-α%MCP-1
目的:探讨辛伐他汀联合依折麦布对动脉粥样硬化的ApoE-/-小鼠血清炎性因子的影响。方法高脂饲料喂养ApoE-/-小鼠,建立动脉粥样硬化模型。将动脉粥样硬化的ApoE-/-小鼠30只随机分为3组。模型组不给药;单药治疗组给予辛伐他汀片20 mg?kg-1?d-1;联合治疗组给予辛伐他汀20 mg?kg-1?d-1及依折麦布片5 mg?kg-1?d-1,野生的普通C57小鼠10只作为对照组。给药4周后,酶法检测血清HDL-C、LDL-C、总胆固醇及甘油三酯。ELISA法检测各组血清TNF-α及MCP-1含量。结果与单药治疗组比较,联合治疗组更有效降低总胆固醇、甘油三酯、LDL-C,更显著降低TNF-α及MCP-1,差异有统计学意义。结论依折麦布与辛伐他汀联用较单用辛伐他汀可强化降脂、减轻炎症反应,发挥抗动脉粥样硬化作用。
目的:探討辛伐他汀聯閤依摺麥佈對動脈粥樣硬化的ApoE-/-小鼠血清炎性因子的影響。方法高脂飼料餵養ApoE-/-小鼠,建立動脈粥樣硬化模型。將動脈粥樣硬化的ApoE-/-小鼠30隻隨機分為3組。模型組不給藥;單藥治療組給予辛伐他汀片20 mg?kg-1?d-1;聯閤治療組給予辛伐他汀20 mg?kg-1?d-1及依摺麥佈片5 mg?kg-1?d-1,野生的普通C57小鼠10隻作為對照組。給藥4週後,酶法檢測血清HDL-C、LDL-C、總膽固醇及甘油三酯。ELISA法檢測各組血清TNF-α及MCP-1含量。結果與單藥治療組比較,聯閤治療組更有效降低總膽固醇、甘油三酯、LDL-C,更顯著降低TNF-α及MCP-1,差異有統計學意義。結論依摺麥佈與辛伐他汀聯用較單用辛伐他汀可彊化降脂、減輕炎癥反應,髮揮抗動脈粥樣硬化作用。
목적:탐토신벌타정연합의절맥포대동맥죽양경화적ApoE-/-소서혈청염성인자적영향。방법고지사료위양ApoE-/-소서,건립동맥죽양경화모형。장동맥죽양경화적ApoE-/-소서30지수궤분위3조。모형조불급약;단약치료조급여신벌타정편20 mg?kg-1?d-1;연합치료조급여신벌타정20 mg?kg-1?d-1급의절맥포편5 mg?kg-1?d-1,야생적보통C57소서10지작위대조조。급약4주후,매법검측혈청HDL-C、LDL-C、총담고순급감유삼지。ELISA법검측각조혈청TNF-α급MCP-1함량。결과여단약치료조비교,연합치료조경유효강저총담고순、감유삼지、LDL-C,경현저강저TNF-α급MCP-1,차이유통계학의의。결론의절맥포여신벌타정련용교단용신벌타정가강화강지、감경염증반응,발휘항동맥죽양경화작용。
Objective To investigate the effects of coadministration of Atorvastatin with Ezetimibe on serum inflammatory factors in atherosclerosis ApoE-/-mice. Methods Thirty ApoE-/-mice were treated with high cholesterol diet 8 weeks to set up atherosclerosis model. Then, thirty ApoE-/-atherosclerotic mice were randomly divided into 3 groups:model group (n=10), Simvastatin treatment group (n=10), and coadministration group (n=10) and respectively treated with no drug, Simvastatin 20 mg?kg-1?d-1, and Simvastatin 20 mg?kg-1?d-1+Ezetimibe 5 mg?kg-1?d-1 for 4 weeks. 10 common wild C57 mice served as control group. Serum lipid level(TG, TC, HDL-C and LDL-C) was measured by enzymatic method. Serum TNF-αand MCP-1 level were measured by ELISA. Results Compared with simvastatin treatment group, the coadministration of Ezetimibe could better decrease the level of serum TC, TG, LDL-C, TNF-αand MCP-1. There was significant difference between Simvastatin group and coadministration group. Conclusion The coadministration of Simvastain and Ezetimibe may play a good role in anti-atherosclerosis by decreasing the level of serum TC, TG and LDL-C and reducing the inflammation reaction.