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茶多酚对小鼠口腔癌的保护作用及机制

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目的 探究茶多酚(TP)对小鼠口腔癌的保护机制。方法 50只小鼠分为对照组、模型组、TP组、Selisistat组、TP+Selisistat组,每组10只。对照组灌胃生理盐水,模型组、TP组、Selisistat组、TP+Selisistat组灌胃300 mg/L 4-NQO建立小鼠口腔癌模型后分别灌胃生理盐水、200 mg/kg TP、0。01 mg/kg Selisistat、200 mg/kg TP+0。01 mg/kg Selisistat。比较各组小鼠体重变化情况;采用 HE 染色观察小鼠口腔组织病理形态学;酶联免疫吸附法检测血清中丙二醛(MDA)、超氧化物歧化酶(SOD)水平;免疫印迹、免疫组织化学法检测小鼠口腔组织中沉默信息调节因子(Sirt1)、核因子E2相关因子2(Nrf2)蛋白表达。结果 与对照组相比,模型组小鼠体重[(23。19±1。36)g]降低,血清SOD 水平[(91。64±8。75)U/ml]降低,MDA 水平[(5。18±0。46)nmol/ml]升高,口腔组织 Sirt1(0。38± 0。05)、Nrf2(0。36±0。05)蛋白表达降低,Nrf2乙酰化水平(0。84±0。11)升高(均P<0。05)。与模型组相比,TP组小鼠体重[(25。28±1。25)g]升高,血清SOD水平[(121。24±10。68)U/ml]升高,MDA水平[(3。89±0。42)nmol/ml]降低,口 腔组织 Sirt1(0。61±0。09)、Nrf2(0。58±0。06)蛋白表达升高,Nrf2乙酰化水平(0。39±0。05)降低;Selisistat组小鼠体重[(21。41±1。07)g]降低,血清SOD水平[(72。16±7。43)U/ml]降低,MDA 水平[(5。87±0。41)nmol/ml]升高,口腔组织 Sirt1(0。23±0。04)、Nrf2(0。24±0。03)蛋白表达降低,Nrf2 乙酰化水平(1。12±0。14)升高(P<0。05)。TP+Selisistat 组小鼠体重[(23。32±1。27)g]、血清 SOD 水平[(92。58±8。13)U/ml]、口腔组织 Sirt1(0。41±0。06)、Nrf2(0。38±0。05)蛋白表达高于 Selisistat 组,MDA[(5。11±0。38)nmol/ml]、Nrf2 乙酰化水平(0。82± 0。09)低于Selisistat组(均P<0。05)。结论 茶多酚可缓解口腔癌小鼠口腔组织损伤,减轻氧化应激反应,其机制可能与上调Sirt1/Nrf2通路有关。
The protective effect and mechanism of tea polyphenols on oral cancer in mice
Objective To explore the protective mechanism of tea polyphenols(TP)on mouse oral cancer.Methods A total of 50 mice were divided into control group,model group,TP group,Selisistat group,TP+Selisistat group,with 10 mice in each group.The control group was gavaged with physiological saline,while the model group,TP group,Selisistat group,and TP+Selisistat group were gavaged with 300 mg/L 4-NQO to establish a mouse oral cancer model.Physiological saline,200 mg/kg TP,0.01 mg/kg Selisistat,and 200 mg/kg TP+0.01 mg/kg Selisistat were gavaged respectively.The weight changes of each group of mice were compared;HE staining was used to observe the morphology of mouse oral tumor tissue;Enzyme linked immunosorbent assay was used to detect the levels of malondialdehyde(MDA)and superoxide dismutase(SOD)in serum;Immunoblotting and immunohistochemistry were used to detect the expression of silencing information regulatory factor(Sirt1)and nuclear factor E2 related factor 2(Nrf2)proteins in mouse oral tissues.Results Compared with the control group,the model group mice had a decrease in body weight[(23.19±1.36)g],a decrease in serum SOD level[(91.64±8.75)U/ml],an increase in MDA level[(5.18±0.46)nmol/ml],a decrease in Sirt1(0.38±0.05)and Nrf2(0.36±0.05)protein expression in oral tissue,and an increase in Nrf2 acetylation level(0.84±0.11)(all P<0.05).Compared with the model group,the TP group mice had an increase in body weight[(25.28±1.25)g],elevated serum SOD levels[(121.24±10.68)U/ml],decreased MDA levels[(3.89±0.42)nmol/ml],increased expression of Sirt1(0.61±0.09)and Nrf2(0.58±0.06)proteins in oral tissue,and decreased Nrf2 protein acetylation levels(0.39±0.05);The Selisistat group mice showed a decrease in body weight[(21.41±1.07)g],a decrease in serum SOD levels[(72.16±7.43)U/ml],an increase in MDA levels[(5.87±0.41)nmol/ml],a decrease in Sirt1(0.23±0.04)and Nrf2 protein(0.24±0.03)expression in oral tissue,and an increase in Nrf2 acetylation levels(1.12±0.14)(P<0.05).The body weight[(23.32±1.27)g],serum SOD levels[(92.58±8.13)U/ml],and oral Sirt1(0.41±0.06)and Nrf2(0.38±0.05)protein expression in the TP+Selisistat group mice were higher than those in the Selisistat group,while MDA[(5.11±0.38)nmol/ml]and Nrf2 acetylation levels(0.82±0.09)were lower than those in the Selisistat group(all P<0.05).Conclusions Tea polyphenols can alleviate oral tissue damage and alleviate oxidative stress in mice with oral cancer,and their mechanism may be related to the upregulation of the Sirt1/Nrf2 pathway.

Mouth neoplasmsTea polyphenolsSilence information regulator 2-related enzymes 1Nuclear erythrocyte-related factors 2

赵泽霖、孙科家、郑照杰、金晓明、吴懿

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宁波市鄞州区第二医院口腔科,宁波 315000

口腔肿瘤 茶多酚 沉默信息调节因子2相关酶1 核红细胞相关因子2

浙江省自然科学基金

LY19H160037

2024

中国医师杂志
中华医学会 湖南省医学会

中国医师杂志

CSTPCD
影响因子:0.876
ISSN:1008-1372
年,卷(期):2024.26(3)
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