目的探讨溃疡性结肠炎(ulcerative colitis,UC)患者血清Ras相关的C3肉毒素底物1(Rac1)、血管紧张素转化酶2(ACE2)水平与肠道功能损害的相关性。方法选取2020年3月至2022年3月驻马店中心医院就诊的UC患者60例为病例组,依据Mayo评分将病...目的探讨溃疡性结肠炎(ulcerative colitis,UC)患者血清Ras相关的C3肉毒素底物1(Rac1)、血管紧张素转化酶2(ACE2)水平与肠道功能损害的相关性。方法选取2020年3月至2022年3月驻马店中心医院就诊的UC患者60例为病例组,依据Mayo评分将病例组分为活动期组(36例)、缓解期组(24例),同时以同期健康体检者40例为对照组。分别静脉抽取所有研究对象空腹血液,ELISA法检测血清ACE2水平;q RT-PCR检测血清中Rac1 m RNA水平;同时检测肠道屏障指标(血清二胺氧化酶、细菌内毒素、D-乳酸)水平;采用Pearson法分析UC患者血清中ACE2、Rac1 m RNA水平的相关性以及两者分别与血清二胺氧化酶、细菌内毒素、D-乳酸的相关性。结果与对照组相比,病例组血清中ACE2、Rac1 m RNA水平显著下降,二胺氧化酶、细菌内毒素、D-乳酸水平显著增加(P<0.05);与缓解期组相比,活动期组ACE2、Rac1 m RNA水平显著下降(P<0.05);Pearson法结果显示,UC患者血清中ACE2与Rac1水平呈明显正相关(r=0.390,P<0.05),且分别与二胺氧化酶、细菌内毒素、D-乳酸呈负相关(P<0.05)。结论UC患者血清中ACE2与Rac1水平呈正相关,且分别与肠道屏障指标呈负相关,检测两者水平对于评定肠道功能损害可能具有一定临床价值。展开更多
目的探索莓茶提取物对2型糖尿病(type 2 diabetes mellitus,T2DM)大鼠糖脂代谢及肝脏沉默信息调节因子1(silence information regulator 1,SIRT1)、AMP活化蛋白激酶(AMP activated protein kinase,AMPK)、过氧化物酶体增殖物激活受体γ...目的探索莓茶提取物对2型糖尿病(type 2 diabetes mellitus,T2DM)大鼠糖脂代谢及肝脏沉默信息调节因子1(silence information regulator 1,SIRT1)、AMP活化蛋白激酶(AMP activated protein kinase,AMPK)、过氧化物酶体增殖物激活受体γ辅助活化因子1α(peroxisome proliferator-activated receptor-γcoactivator-1α,PGC-1α)蛋白表达的影响。方法高脂高糖喂养联合链脲佐菌素(35 mg/kg)腹腔注射建立T2DM大鼠模型,建模成功后随机分为模型组、莓茶低剂量组(0.4 g/kg)、莓茶高剂量组(0.8 g/kg),另设普通饲料喂养大鼠为正常组,每组8只。各组灌胃给药6周后,行口服葡萄糖耐量试验计算血糖-时间曲线下面积(area under the curve,AUC),ELISA法检测空腹血胰岛素(fasting insulin,FINS)水平,计算稳态模型以评估胰岛素抵抗指数(homeostatic model assessment for insulin resistance,HOMA-IR),全自动生化分析仪测定血清总胆固醇(total cholesterol,TC)、甘油三酯(triglycerides,TG)、高密度脂蛋白胆固醇(high density lipoprotein cholesterol,HDL-C)、低密度脂蛋白胆固醇(low density lipoprotein cholesterol,LDL-C)、超氧化物歧化酶(superoxide dismutase,SOD)、丙二醇(malondialdehyde,MDA)水平,HE染色观察肝脏组织形态学变化,Western blot检测肝脏SIRT1、AMPK、PGC-1α蛋白表达。结果与正常组比较,模型组FBG、AUC、FINS、HOMA-IR、TC、TG、LDL-C、MDA均明显升高(P<0.01),HDL-C、SOD和SIRT1、AMPK、PGC-1α蛋白表达均明显降低(P<0.01),肝脏组织肝索排列紊乱,肝细胞间隙不清晰,呈脂肪变性改变。与模型组比较,莓茶低剂量组、莓茶高剂量组FBG、FINS、HOMA-IR、TG、MDA均明显降低(P<0.05,P<0.01),SOD和SIRT1、AMPK、PGC-1α蛋白表达均明显升高(P<0.05,P<0.01),肝脏组织肝索排列相对整齐,脂肪变性得到改善;莓茶高剂量组AUC、TC均明显降低(P<0.05),HDL-C明显升高(P<0.05)。与莓茶低剂量组比较,莓茶高剂量组FBG、AUC、FINS、TC、MDA均明显降低(P<0.05),SIRT1、AMPK、PGC-1α蛋白表达均明显升高(P<0.05)。结论莓茶提取物能在一定程度上改善T2DM大鼠糖脂代谢,减轻胰岛素抵抗,其机制可能与改善氧化应激,调节肝脏SIRT1、AMPK、PGC-1α蛋白表达有关。展开更多
目的:分析关节腔积液中沉默信息调节因子2相关酶1(silencing information regulator 2 related enzyme 1,SIRT1),肿瘤坏死因子样弱凋亡诱导因子(tumor necrosis factor-like weak inducer of apoptosis,TWEAK)表达与膝骨关节炎的相关性...目的:分析关节腔积液中沉默信息调节因子2相关酶1(silencing information regulator 2 related enzyme 1,SIRT1),肿瘤坏死因子样弱凋亡诱导因子(tumor necrosis factor-like weak inducer of apoptosis,TWEAK)表达与膝骨关节炎的相关性。方法:选择2019年2月至2021年8月收治的103例膝骨关节患者(膝骨关节炎组),男40例,女63例,年龄(62.02±6.09)岁。根据改良Mankin评分将患者分为轻度组(Mankin评分1~4分,31例)、中度组(Mankin评分5~8分,40例)和重度组(Mankin评分≥9分,32例),另选择105例体检志愿者为对照组,男46例,女59例,年龄(62.11±6.34)岁。膝骨关节炎组检测关节腔积液和血清中SIRT1、TWEAK水平,对照组仅检测血清SIRT1、TWEAK水平。分析SIRT1、TWEAK与膝骨关节炎发生和病情的关系。结果:膝骨关节炎组关节腔积液TWEAK,血清TWEAK、C反应蛋白(C-reactive protein,CRP)、白细胞介素-6(interleukin,IL-6)、IL-1β、白细胞计数、红细胞沉降率(erythrocyte sedimentation rate,ESR)高于对照组(P<0.05),关节腔积液SIRT1、血清SIRT1低于对照组(P<0.05)。重度组关节腔积液中TWEAK水平高于中度组和轻度组(P<0.05),SIRT1低于中度组和轻度组(P<0.05)。关节腔积液中SIRT1水平与血清SIRT1水平呈正相关(P<0.05),与CRP、IL-6、IL-1β、白细胞计数、改良Mankin评分、ESR呈负相关(P<0.05);关节腔积液中TWEAK水平与血清TWEAK水平呈正相关(P<0.05),与CRP、IL-6、IL-1β、白细胞计数、改良Mankin评分、ESR呈正相关(P<0.05)。身体质量指数、从事重体力工作、关节腔积液TWEAK是膝骨关节炎发生的危险因素(P<0.05),关节腔积液SIRT1是膝骨关节炎发生的保护因素(P<0.05)。关节腔积液SIRT1、TWEAK诊断膝骨关节炎的曲线下面积(area undre curve,AUC)为0.641、0.653,联合关节腔积液SIRT1、TWEAK诊断膝骨关节炎的AUC为0.879,高于单独SIRT1、TWEAK(z=6.105、6.225,P<0.05)。结论:膝骨关节炎患者关节腔积液中SIRT1水平降低,TWEAK水平增高,低SIRT1和高TWEAK与膝骨关节炎发病以及病情加重均有关。展开更多
AIM:To explore the effect of silent information regulator factor 2-related enzyme 1(SIRT1)on modulating apoptosis of human lens epithelial cells(HLECs)and alleviating lens opacification of rats through suppressing end...AIM:To explore the effect of silent information regulator factor 2-related enzyme 1(SIRT1)on modulating apoptosis of human lens epithelial cells(HLECs)and alleviating lens opacification of rats through suppressing endoplasmic reticulum(ER)stress.METHODS:HLECs(SRA01/04)were treated with varying concentrations of tunicamycin(TM)for 24h,and the expression of SIRT1 and C/EBP homologous protein(CHOP)was assessed using real-time quantitative polymerase chain reaction(RT-PCR),Western blotting,and immunofluorescence.Cell morphology and proliferation was evaluated using an inverted microscope and cell counting kit-8(CCK-8)assay,respectively.In the SRA01/04 cell apoptosis model,which underwent siRNA transfection for SIRT1 knockdown and SRT1720 treatment for its activation,the expression levels of SIRT1,CHOP,glucose regulated protein 78(GRP78),and activating transcription factor 4(ATF4)were examined.The potential reversal of SIRT1 knockdown effects by 4-phenyl butyric acid(4-PBA;an ER stress inhibitor)was investigated.In vivo,age-related cataract(ARC)rat models were induced by sodium selenite injection,and the protective role of SIRT1,activated by SRT1720 intraperitoneal injections,was evaluated through morphology observation,hematoxylin and eosin(H&E)staining,Western blotting,and RT-PCR.RESULTS:SIRT1 expression was downregulated in TMinduced SRA01/04 cells.Besides,in SRA01/04 cells,both cell apoptosis and CHOP expression increased with the rising doses of TM.ER stress was stimulated by TM,as evidenced by the increased GRP78 and ATF4 in the SRA01/04 cell apoptosis model.Inhibition of SIRT1 by siRNA knockdown increased ER stress activation,whereas SRT1720 treatment had opposite results.4-PBA partly reverse the adverse effect of SIRT1 knockdown on apoptosis.In vivo,SRT1720 attenuated the lens opacification and weakened the ER stress activation in ARC rat models.CONCLUSION:SIRT1 plays a protective role against TM-induced apoptosis in HLECs and slows the progression of cataract in rats by inhibiting ER stress.These findings suggest a novel strategy for cataract treatment focused on targeting ER stress,highlighting the therapeutic potential of SIRT1 modulation in ARC development.展开更多
文摘目的探讨溃疡性结肠炎(ulcerative colitis,UC)患者血清Ras相关的C3肉毒素底物1(Rac1)、血管紧张素转化酶2(ACE2)水平与肠道功能损害的相关性。方法选取2020年3月至2022年3月驻马店中心医院就诊的UC患者60例为病例组,依据Mayo评分将病例组分为活动期组(36例)、缓解期组(24例),同时以同期健康体检者40例为对照组。分别静脉抽取所有研究对象空腹血液,ELISA法检测血清ACE2水平;q RT-PCR检测血清中Rac1 m RNA水平;同时检测肠道屏障指标(血清二胺氧化酶、细菌内毒素、D-乳酸)水平;采用Pearson法分析UC患者血清中ACE2、Rac1 m RNA水平的相关性以及两者分别与血清二胺氧化酶、细菌内毒素、D-乳酸的相关性。结果与对照组相比,病例组血清中ACE2、Rac1 m RNA水平显著下降,二胺氧化酶、细菌内毒素、D-乳酸水平显著增加(P<0.05);与缓解期组相比,活动期组ACE2、Rac1 m RNA水平显著下降(P<0.05);Pearson法结果显示,UC患者血清中ACE2与Rac1水平呈明显正相关(r=0.390,P<0.05),且分别与二胺氧化酶、细菌内毒素、D-乳酸呈负相关(P<0.05)。结论UC患者血清中ACE2与Rac1水平呈正相关,且分别与肠道屏障指标呈负相关,检测两者水平对于评定肠道功能损害可能具有一定临床价值。
文摘目的探索莓茶提取物对2型糖尿病(type 2 diabetes mellitus,T2DM)大鼠糖脂代谢及肝脏沉默信息调节因子1(silence information regulator 1,SIRT1)、AMP活化蛋白激酶(AMP activated protein kinase,AMPK)、过氧化物酶体增殖物激活受体γ辅助活化因子1α(peroxisome proliferator-activated receptor-γcoactivator-1α,PGC-1α)蛋白表达的影响。方法高脂高糖喂养联合链脲佐菌素(35 mg/kg)腹腔注射建立T2DM大鼠模型,建模成功后随机分为模型组、莓茶低剂量组(0.4 g/kg)、莓茶高剂量组(0.8 g/kg),另设普通饲料喂养大鼠为正常组,每组8只。各组灌胃给药6周后,行口服葡萄糖耐量试验计算血糖-时间曲线下面积(area under the curve,AUC),ELISA法检测空腹血胰岛素(fasting insulin,FINS)水平,计算稳态模型以评估胰岛素抵抗指数(homeostatic model assessment for insulin resistance,HOMA-IR),全自动生化分析仪测定血清总胆固醇(total cholesterol,TC)、甘油三酯(triglycerides,TG)、高密度脂蛋白胆固醇(high density lipoprotein cholesterol,HDL-C)、低密度脂蛋白胆固醇(low density lipoprotein cholesterol,LDL-C)、超氧化物歧化酶(superoxide dismutase,SOD)、丙二醇(malondialdehyde,MDA)水平,HE染色观察肝脏组织形态学变化,Western blot检测肝脏SIRT1、AMPK、PGC-1α蛋白表达。结果与正常组比较,模型组FBG、AUC、FINS、HOMA-IR、TC、TG、LDL-C、MDA均明显升高(P<0.01),HDL-C、SOD和SIRT1、AMPK、PGC-1α蛋白表达均明显降低(P<0.01),肝脏组织肝索排列紊乱,肝细胞间隙不清晰,呈脂肪变性改变。与模型组比较,莓茶低剂量组、莓茶高剂量组FBG、FINS、HOMA-IR、TG、MDA均明显降低(P<0.05,P<0.01),SOD和SIRT1、AMPK、PGC-1α蛋白表达均明显升高(P<0.05,P<0.01),肝脏组织肝索排列相对整齐,脂肪变性得到改善;莓茶高剂量组AUC、TC均明显降低(P<0.05),HDL-C明显升高(P<0.05)。与莓茶低剂量组比较,莓茶高剂量组FBG、AUC、FINS、TC、MDA均明显降低(P<0.05),SIRT1、AMPK、PGC-1α蛋白表达均明显升高(P<0.05)。结论莓茶提取物能在一定程度上改善T2DM大鼠糖脂代谢,减轻胰岛素抵抗,其机制可能与改善氧化应激,调节肝脏SIRT1、AMPK、PGC-1α蛋白表达有关。
基金Supported by National Natural Science Foundation for Young Scientists of China(No.82101097)National Natural Science Foundation of China(No.82070937).
文摘AIM:To explore the effect of silent information regulator factor 2-related enzyme 1(SIRT1)on modulating apoptosis of human lens epithelial cells(HLECs)and alleviating lens opacification of rats through suppressing endoplasmic reticulum(ER)stress.METHODS:HLECs(SRA01/04)were treated with varying concentrations of tunicamycin(TM)for 24h,and the expression of SIRT1 and C/EBP homologous protein(CHOP)was assessed using real-time quantitative polymerase chain reaction(RT-PCR),Western blotting,and immunofluorescence.Cell morphology and proliferation was evaluated using an inverted microscope and cell counting kit-8(CCK-8)assay,respectively.In the SRA01/04 cell apoptosis model,which underwent siRNA transfection for SIRT1 knockdown and SRT1720 treatment for its activation,the expression levels of SIRT1,CHOP,glucose regulated protein 78(GRP78),and activating transcription factor 4(ATF4)were examined.The potential reversal of SIRT1 knockdown effects by 4-phenyl butyric acid(4-PBA;an ER stress inhibitor)was investigated.In vivo,age-related cataract(ARC)rat models were induced by sodium selenite injection,and the protective role of SIRT1,activated by SRT1720 intraperitoneal injections,was evaluated through morphology observation,hematoxylin and eosin(H&E)staining,Western blotting,and RT-PCR.RESULTS:SIRT1 expression was downregulated in TMinduced SRA01/04 cells.Besides,in SRA01/04 cells,both cell apoptosis and CHOP expression increased with the rising doses of TM.ER stress was stimulated by TM,as evidenced by the increased GRP78 and ATF4 in the SRA01/04 cell apoptosis model.Inhibition of SIRT1 by siRNA knockdown increased ER stress activation,whereas SRT1720 treatment had opposite results.4-PBA partly reverse the adverse effect of SIRT1 knockdown on apoptosis.In vivo,SRT1720 attenuated the lens opacification and weakened the ER stress activation in ARC rat models.CONCLUSION:SIRT1 plays a protective role against TM-induced apoptosis in HLECs and slows the progression of cataract in rats by inhibiting ER stress.These findings suggest a novel strategy for cataract treatment focused on targeting ER stress,highlighting the therapeutic potential of SIRT1 modulation in ARC development.
