首页|姜黄素通过下调HO-1/NQO1保护肝癌模型小鼠

姜黄素通过下调HO-1/NQO1保护肝癌模型小鼠

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目的:观察姜黄素对N-亚硝基二乙胺(DEN)联合四氯化碳(CCl4)诱导的C57BL/6J小鼠肝癌模型的作用并探索其机制.方法:取14日龄雄性C57BL/6J小鼠腹腔注射DEN(25 mg/kg),随机分成模型组和姜黄素(100、200和400 mg/kg)给药组,另取同龄雄性小鼠10只作为正常对照组.模型组和姜黄素给药组从第8周开始灌4(5 mL/kg),每周2次;同时,给药组开始灌胃姜黄素,正常对照组灌胃等体积的蒸馏水,每天1次,连续14周.给药结束后处死小鼠,检测小鼠血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)活性,观察肝组织病理学变化,检测血红素加氧酶1(HO-1)和NAD(P)H-醌氧化还原酶1(NQO1)的mRNA表达水平,以及HO-1、NQO1和Ki67蛋白表达水平.结果:与正常对照组比较,模型组小鼠体重显著降低(P<0.01),肝脏指数显著增加(P<0.01),血清ALT和AST活性显著升高(P<0.01),HO-1和NQO1的mRNA表达水平无显著差异(P>0.05),HO-1和NQO1蛋白表达水平显著升高(P<0.05),Ki67阳性表达率显著增加(P<0.05).姜黄素治疗后,小鼠体重显著升高(P<0.01),肝脏指数无明显变化(P>0.05),癌结节数量显著减少(P<0.05或P<0.01),血清AST活性显著降低(P<0.01),HO-1和NQO1的mRNA及蛋白表达水平显著降低(P<0.05),Ki67阳性表达率显著降低(P<0.05).结论:姜黄素对DEN联合CCl4诱导的肝癌模型C57BL/6J小鼠具有显著保护作用,其机制与抑制HO-1和NQO1表达有关.
Curcumin protects against liver cancer in a mouse model by down-regu-lating HO-1/NQO1
AIM:To observe the effect of curcumin on a C57BL/6J mouse liver cancer model induced by N-ni-trosodiethylamine(DEN)combined with carbon tetrachloride(CCl4),and to explore its mechanism.METHODS:Forty young male C57BL/6J mice were intraperitoneally injected with DEN(25 mg/kg)14 d after birth and randomly divided in-to the following 4 groups at the 4th week(10 in each group):model control group and curcumin(100,200 and 400 mg/kg)groups.Ten male mice of the same age were used as normal control group.The mice in model group and curcumin groups were gavaged with 10%CCl4(5 mL/kg)twice a week from the 8th week on.At the same time,the mice in curcumin groups were gavaged with curcumin,and the mice in normal control group were gavaged with the same volume of distilled water once a day for 14 weeks.After administration,the mice were sacrificed,the liver surface was observed,and the number of tumor nodules was compared.The activity of alanine aminotransferase(ALT)and aspartate aminotransferase(AST)in serum was detected by an automatic biochemical instrument.The pathological changes of liver tissues were ob-served by HE staining.The mRNA expression levels of heme oxygenase-1(HO-1)and NAD(P)H-quinone oxidoreductase 1(NQO1)were detected by RT-qPCR,and the protein expression levels of HO-1,NQO1 and Ki67 were detected by Western blot and immunohistochemistry.RESULTS:Compared with normal control group,the body weight of the mice in model group was decreased significantly(P<0.01),the liver index was increased significantly(P<0.01),and the se-rum levels of ALT and AST were increased obviously(P<0.01).There was no significant difference in the mRNA expres-sion levels of HO-1 and NQO1(P>0.05),the protein levels of HO-1 and NQO1 were increased distinctly(P<0.05),and the positive expression rate of Ki67 was increased significantly(P<0.05).After curcumin treatment,the body weight of the mice was significantly increased(P<0.01),the liver index was not changed(P>0.05),and the number of tumor nodules in the liver was decreased significantly(P<0.05 or P<0.01).The serum level of AST was decreased significantly(P<0.01),the mRNA and protein expression levels of HO-1 and NQO1 were decreased significantly(P<0.05),and the posi-tive expression rate of Ki67 was decreased significantly(P<0.05).CONCLUSION:Curcumin significantly protects against liver cancer in a C57BL/6J mouse model induced by DEN combined with CCl4,and its mechanism may be related to the inhibition of HO-1 and NQO1 expression.

curcuminhepatocellular carcinomaheme oxygenase-1NAD(P)H-quinone oxidoreductase 1

牟海军、陈幸幸、刘安安、张丽、朱加兴、金海

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遵义医科大学附属医院消化病医院,遵义医科大学附属医院消化内科,贵州 遵义 563000

姜黄素 肝细胞癌 血红素加氧酶1 NAD(P)H-醌氧化还原酶1

国家自然科学基金贵州省科技计划省部共建协同创新中心项目遵义医科大学附属医院硕士启动基金

81960507黔科合LH字[2017]7095号教科技厅函[2020]39号院字[2013]15号

2024

中国病理生理杂志
中国病理生理学会

中国病理生理杂志

CSTPCD北大核心
影响因子:1.065
ISSN:1000-4718
年,卷(期):2024.40(3)
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