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Argatroban promotes recovery of spinal cord injury by inhibiting the PAR1/JAK2/STAT3 signaling pathway
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作者 Chenxi Zhao Tiangang Zhou +9 位作者 Ming Li Jie Liu Xiaoqing Zhao Yilin Pang Xinjie Liu Jiawei Zhang Lei Ma Wenxiang Li Xue Yao Shiqing Feng 《Neural Regeneration Research》 SCIE CAS CSCD 2024年第2期434-439,共6页
Argatroban is a synthetic thrombin inhibitor approved by U.S.Food and Drug Administration for the treatment of thrombosis.However,whether it plays a role in the repair of spinal cord injury is unknown.In this study,we... Argatroban is a synthetic thrombin inhibitor approved by U.S.Food and Drug Administration for the treatment of thrombosis.However,whether it plays a role in the repair of spinal cord injury is unknown.In this study,we established a rat model of T10 moderate spinal cord injury using an NYU Impactor ModerⅢand performed intraperitoneal injection of argatroban for 3 consecutive days.Our results showed that argatroban effectively promoted neurological function recovery after spinal cord injury and decreased thrombin expression and activity in the local injured spinal cord.RNA sequencing transcriptomic analysis revealed that the differentially expressed genes in the argatroban-treated group were enriched in the JAK2/STAT3 pathway,which is involved in astrogliosis and glial scar formation.Western blotting and immunofluorescence results showed that argatroban downregulated the expression of the thrombin receptor PAR1 in the injured spinal cord and the JAK2/STAT3 signal pathway.Argatroban also inhibited the activation and proliferation of astrocytes and reduced glial scar formation in the spinal cord.Taken together,these findings suggest that argatroban may inhibit astrogliosis by inhibiting the thrombin-mediated PAR1/JAK2/STAT3 signal pathway,thereby promoting the recovery of neurological function after spinal cord injury. 展开更多
关键词 ARGATROBAN ASTROGLIOSIS jak/stat signaling pathway protease-activated receptor-1 spinal cord injury THROMBIN vimentin
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Exploring the mechanism of electroacupuncture at different acupoints on acute colitis rats based on JAK2/STAT3/SOCS1 signaling pathway
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作者 ZHANG Chun-qing TANG Kun-peng +2 位作者 YAN Li-ping WEN Tan WANG Hai-jun 《Journal of Hainan Medical University》 CAS 2024年第3期1-7,共7页
Objective:To investigate the mechanism of JAK2/STAT3/SOCS1 signaling pathway in electroacupuncture of different acupoints on acute colitis rats.Methods:36 SPF SD rats were randomly divided into 6 groups,with 6 rats in... Objective:To investigate the mechanism of JAK2/STAT3/SOCS1 signaling pathway in electroacupuncture of different acupoints on acute colitis rats.Methods:36 SPF SD rats were randomly divided into 6 groups,with 6 rats in each group.The rat model of acute colitis was prepared by enema with glacial acetic acid solution.After the model was established,electroacupuncture was given to each acupoint group,with density wave,frequency 2Hz-50 Hz,intensity 2 mA,muscle tremor as the degree 20 min/time,1 time/day,for 3 consecutive days.Observe the general condition of rats;the pathological changes of colonic mucosa in rats were observed by HE method.The contents of serum interleukin-4(IL-4)and interleukin-8(IL-8)were detected by ELISA.Western blot and RT-PCR were used to detect the expression of JAK2,STAT3,SOCS1 protein and mRNA in rat colon tissue.Results:In contrast to the normal group,the overall condition of the model group was worse,the colonic mucosa was severely damaged,even necrotic,and the ulcer surface was obvious.The content of IL-4 in serum was obviously reduced,and the content of IL-8 was obviously go up(P<0.01).The protein content of JAK2,STAT3 and the expression of JAK2,STAT3 mRNA in colon tissue of rats were obviously go up,while the protein content of SOCS1 and the expression of SOCS1 mRNA were obviously reduced(P<0.01).In contrast to the model group,the general condition of rats in each acupoint group was significantly improved,the damage and necrosis of colonic mucosa and ulcer surface were obviously alleviated,the content of IL-4 in serum was obviously go up,and the content of IL-8 was significantly decreased(P<0.01).The protein content of JAK2,STAT3 and the expression of JAK2,STAT3 mRNA in colon tissue of rats were obviously reduced,while the protein content of SOCS1 and the expression of SOCS1 mRNA were obviously go up(P<0.05,P<0.01).Comparison of different acupoint groups,the colonic mucosal injury in the Zusanli group was significantly reduced,the content of serum IL-4 was significantly increased,and the content of IL-8 was significantly decreased(P<0.05,P<0.01).The protein content and mRNA expression of JAK2 and STAT3 in colon tissue were significantly down-regulated,while the protein content and mRNA expression of SOCS1 were significantly go up(P<0.05,P<0.01).Conclusion:Electroacupuncture at each acupoint can improve the damage of colonic mucosa and reduce the inflammatory response.The therapeutic effect of Zusanli(ST36)is better than that of Tianshu(ST25),Dachangshu(BL25)and Shangjuxu(ST37).The mechanism may be related to the regulation of JAK2/STAT3/SOCS1 signaling pathway related proteins and inflammatory cytokines IL-4 and IL-8. 展开更多
关键词 ELECTROACUPUNCTURE Different acupoints Acute colitis Inflammatory factors jak2/stat3/SOCS1 signaling pathway
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黄芪-莪术对C5a介导JAK2/STAT3通路调控Lewis肺癌小鼠Th17/Treg细胞平衡影响的实验研究
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作者 田培裕 于泓洋 +2 位作者 李潇 闫梓乔 窦永起 《世界中西医结合杂志》 2024年第3期425-432,共8页
目的探讨黄芪-莪术影响C5a介导JAK2/STAT3通路调控肿瘤微环境中Th17/Treg细胞平衡,从而阐明其在此途径抑制肿瘤进展的相关机制。方法40只雄性C57BL/6小鼠按随机数字表法分为空白对照组、模型对照组、中药干预组、阳性对照药(PMX53)组,... 目的探讨黄芪-莪术影响C5a介导JAK2/STAT3通路调控肿瘤微环境中Th17/Treg细胞平衡,从而阐明其在此途径抑制肿瘤进展的相关机制。方法40只雄性C57BL/6小鼠按随机数字表法分为空白对照组、模型对照组、中药干预组、阳性对照药(PMX53)组,每组各10只。腋下接种Lewis细胞建立肺癌小鼠模型,于接种后第3天开始,中药干预组按8.2 g/kg剂量给予中药浓煎液灌胃,模型对照组和PMX53组予等容积灭菌双蒸水灌胃,连续14 d;PMX53组分别于第3、6、9、12、15天按1mg/kg剂量给予腹腔注射PMX53,模型对照组和中药干预组同时腹腔注射等容PBS溶液。每2 d测算各组小鼠肿瘤体积、绘制肿瘤生长曲线;于第15天处死,剖取瘤块,ELISA法检测血清C5a、IL6、IL-10、IL-17、TGF-β等因子水平,流式细胞术检测并计算外周血和肿瘤组织中Th17/Treg细胞比例,Western Blot和Real-time PCR法检测肿瘤组织中JAK2/STAT3信号通路相关蛋白及mRNA表达。结果与模型对照组比较,中药干预组和PMX53组肿瘤生长较缓慢,补体C5a、JAK2和STAT3蛋白及mRNA水平、p-JAK2/JAK2、p-STAT3/STAT3比值、Treg占比均降低,SOCS3蛋白及mRNA水平、Th17/Treg比例增高,差异有统计学意义(P<0.05)。结论黄芪-莪术可降低补体C5a进而抑制JAK2/STAT3通路活化,并调节肿瘤微环境中Th17/Treg平衡达到抑制肿瘤生长的作用。 展开更多
关键词 肿瘤微环境 补体C5A jak2/stat3通路 TH17/TREG 黄芪-莪术
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Mechanism of Yanghe Pingchaun granules on airway remodeling in asthmatic rats based on IL-6/JAK2/STAT3 signaling axis
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作者 LV Chuan ZHU Hui-zhi +4 位作者 LIU Xiang-guo CAO Xiao-mei XIA Yong-qi ZHANG Qiu-ping YU Zi-qi 《Journal of Hainan Medical University》 CAS 2024年第1期15-21,共7页
Objective: To investigate the effects of Yanghe Pingchuan Granules on airway remodeling in asthmatic rats, and to explore the mechanism of Interleukin-6/Janus kinase 2/ Signal transducing activator of transcription 3(... Objective: To investigate the effects of Yanghe Pingchuan Granules on airway remodeling in asthmatic rats, and to explore the mechanism of Interleukin-6/Janus kinase 2/ Signal transducing activator of transcription 3(IL-6/JAK2/STAT3) signal axis. Methods: We separated 42 healthy male SD rats into two groups, a control group (7) and a model group (35).The model group was sensitized with a combination of ovalbumin (OVA) and aluminum hydroxide for 2 weeks, while the control group was given an equal amount of physiological saline.After 2 weeks, the modeling group was randomly divided into Model group, Yanghe Pingchuan Granules high, medium and low dose groups and Dexamethasone group, each group consisted of 7 animals. After 4 weeks, OVA atomization and gavage were used for stimulation and treatment. Yanghe Pingchuan Granules high, middle and low groups were given 15.48, 7.74, 3.87 g∙kg-1 Yanghe Pingchuan Granules daily, dexamethasone group was given 0.0625 mg∙kg-1 dexamethasone daily, and the other groups were given the same amount of normal saline. HE, PAS and Masson staining were used to observe the lung histopathological changes in rats. The levels of interleukin-6, IL-23 and IL-17A were detected by ELISA. The expression levels of JAK-2, P-JAK2, STAT3 and P-STAT3 in lung tissues were detected by Western blot. Real-time quantitative polymerase chain reaction (qRT-PCR) was used to detect the mRNA expression levels of IL-6, JAK2 and STAT3 in rat lung tissue. Results: The lung tissue structure of the model group was severely damaged compared to the control group, accompanied by a great many of inflammatory cell infiltration, goblet cell hyperplasia, subepithelial collagen fiber deposition and airway epithelial thickening were more obvious. The expressions of IL-6, IL- 23 and IL-17A in serum were significantly increased (P<0.01), the protein expression levels of JAK-2, P-JAK2, STAT3 and P-STAT3 and the mRNA expression levels of IL-6, JAK2 and STAT3 in lung tissue were significantly increased (P<0.01);Compared with the model group, inflammatory cell infiltration, goblet cell proliferation, subepithelial collagen fiber deposition and airway epithelial thickening were significantly reduced in each administration group, and the expressions of IL-6, IL-23 and IL-17A in serum were significantly decreased (P< 0.01). The protein expression levels of JAK-2, P-JAK2, STAT3 and P-STAT3 and mRNA expression levels of IL-6, JAK2 and STAT3 in lung tissue were significantly decreased (P<0.01). Conclusion: Yanghe Pingchuan Granules can significantly alleviate airway remodeling in asthmatic rats, and its mechanism may be through inhibiting the IL-6/JAK2/STAT3 signal axis. 展开更多
关键词 Yanghe Pingchuan Granules Interleukin-6/Janus kinase 2/signal transducing activator of transcription 3(IL-6/jak2/stat3)signal axis Asthma Airway remodeling Mechanism study
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Effects of plumbagin on migration and invasion of human hepatoma cell line via JAK2/STAT3 signaling pathway
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作者 CHENG Tao WEI Yan-fei +2 位作者 LIU Huan LIU Hong DENG Shu-ye 《Journal of Hainan Medical University》 2023年第1期33-41,共9页
Objective:To study the effect of plumbagin(PL)on the migration and invasion of human hepatocellular carcinoma(HCC)cells and its possible mechanism.Methods:The cell counting kit(CCK-8)was used to detect the effects of ... Objective:To study the effect of plumbagin(PL)on the migration and invasion of human hepatocellular carcinoma(HCC)cells and its possible mechanism.Methods:The cell counting kit(CCK-8)was used to detect the effects of different concentrations of plumbagin on the proliferation of human hepatocellular carcinoma Huh-7 and LM3 cells.The effect of plumbagin on the migration ability of Huh-7 and LM3 cells was detected by scratch test and Transwell migration test,and the effect of on the invasion ability of Huh-7 and LM3 cells was detected by Transwell invasion test.Western Blot was used to detect the expression of E-cadherin,N-cadherin,matrix metalloproteinase-2 and related proteins in JAK2/STAT3 signaling pathway in Huh-7 and LM3 cells.Results:Plumbagin could inhibit the proliferation of Huh-7 and LM3 cells in a time-and concentration-dependent manner.Plumbagin inhibited the migration and invasion of Huh-7 and LM3 cells in a concentration dependent manner,and it can down-regulate the expression of N-cadherin and MMP-2 protein,up-regulate the expression of E-cadherin protein,and inhibit the activation of JAK2/STAT3 signaling pathway.Conclusion:Plumbagin can inhibit the migration and invasion of human hepatocellular carcinoma Huh-7 and LM3 cells,and the molecular mechanism of this process may be related to the inhibition of JAK2/STAT3 signaling pathway activation. 展开更多
关键词 PLUMBAGIN Hepatic carcinoma jak2/stat3 signaling pathway MIGRATION INVASION
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Morroniside ameliorates lipopolysaccharide-induced inflammatory damage in iris pigment epithelial cells through inhibition of TLR4/JAK2/STAT3 pathway
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作者 Wen-Jie Li Lin Liu Hong Lu 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2023年第12期1928-1934,共7页
AIM:To investigate the effect of morroniside(Mor)on lipopolysaccharide(LPS)-treated iris pigment epithelial cells(IPE).METHODS:IPE cells were induced by LPS and treated with Mor.Cell proliferation was detected by cell... AIM:To investigate the effect of morroniside(Mor)on lipopolysaccharide(LPS)-treated iris pigment epithelial cells(IPE).METHODS:IPE cells were induced by LPS and treated with Mor.Cell proliferation was detected by cell counting kit(CCK)-8,apoptosis was detected by flow cytometry,the levels of tumor necrosis factor-α(TNF-α),interleukin(IL)-6,and IL-8 were measured by enzyme-linked immunosorbent assay(ELISA)kits,and the protein expression of TLR4,JAK2,p-JAK2,STAT3,and p-STAT3 was analyzed by Western blotting.In addition,overexpression of TLR4 and Mor treatment of LPS-stimulated IPE cells were also tested for the above indices.RESULTS:Mor effectively promoted the proliferation and inhibited the apoptosis of LPS-treated IPE cells.In addition,Mor significantly reduced the levels of TNF-α,IL-6,and IL-8 and significantly inhibited the expression of TLR4,p-JAK2,and p-STAT3 in LPS-treated IPE cells.The effect of Mor on LPS-treated IPE cells was markedly attenuated after overexpression of TLR4.CONCLUSION:These findings suggest that Mor may ameliorate LPS-induced inflammatory damage and apoptosis in IPE through inhibition of TLR4/JAK2/STAT3 pathway. 展开更多
关键词 MORRONISIDE iris pigment epithelial cells INFLAMMATORY TLR4/jak2/stat3 pathway
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To explore the mechanism of Dahuang Lingxian Formula in relieving inflammatory response of bile duct cells based on IL-6/JAK/STAT3 signaling pathway
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作者 PANG Jiao-an Yu Yuan +7 位作者 CHEN Wei-tang YANG Wen LIU Chun-li XIAO Li-jun TENGJin-hao YE Gui-yuan LI Chen-ji GAN Yi-rong 《Journal of Hainan Medical University》 CAS 2023年第10期8-16,共9页
Objective:To explore the mechanism of action of Dahuang Lingxian Formula in alleviating the inflammatory response of bile duct cells in LPS-induced intrahepatic bile duct inflammation model rats based on IL-6/JAK/STAT... Objective:To explore the mechanism of action of Dahuang Lingxian Formula in alleviating the inflammatory response of bile duct cells in LPS-induced intrahepatic bile duct inflammation model rats based on IL-6/JAK/STAT3 signaling pathway.Methods:Fifty SD rats were randomly divided into five groups,blank group,model group,choling tablets(0.5 g/kg),and low and high concentration groups(2.4 g/kg and 4.8 g/kg)of Dahuang Lingxian Formula,ten rats in each group.Except for the blank group,the rats in each group were injected with 1.25 mg/kg LPS at the common bile duct at one time to construct an animal model of intrahepatic bile duct infection.After gavage on day 8,liver tissues were taken from rats at the hepatic hilum,and the histopathological changes of the hepatic hilum and biliary tree were observed by HE staining.The expression levels of serum glutamic alanine transaminase(ALT),glutamic oxalacetic transaminase(AST),malondialdehyde(MDA)and superoxide dismutase(SOD)were measured by biochemical method.The expression levels of interleukin 6(IL-6),Janus protein tyrosine kinase 2(JAK2),signal transducer and activator of transcription 3(STAT3)in rat serum were measured by enzyme-linked immunosorbent assay(ELISA).Protein immunoblotting(WB)and real-time fluorescence quantitative PCR(RT-qPCR)were used to detect the expression levels of IL-6,JAK2,STAT3 protein and mRNA in biliary tree tissues.Results:①Compared with the blank group,the structures such as interlobular bile ducts in the hepatic sinusoids and portal duct area of the model rats were destroyed,and inflammatory cells infiltrated around them.The expression of ALT,AST,MDA,IL-6,JAK2 and STAT3 in the serum increased significantly,the expression level of SOD decreased,and the expression levels of IL-6,JAK2 and STAT3 proteins and mRNA increased.②Compared with the model group,the degree of liver pathological damage in rats in the Chiling Ning tablet group and the low and high concentration groups of Dahuang Lingxian Formula were improved,which could significantly reduce the expression levels of ALT,AST,MDA,IL-6,JAK2,STAT3 and up-regulate SOD in serum,and down-regulate the expression of IL-6,JAK2,STAT3 protein and mRNA,with the best effect in the high concentration group of Dahuang Lingxian Formula.③Compared with the choling tablet group,the rats in the low and high concentration groups of Dahuang Lingxian Formula tended to normalize the degree of liver pathological damage,without obvious inflammatory cell infiltration,and the expression levels of ALT,AST,MDA,IL-6,JAK2,STAT3 and the expression levels of IL-6,JAK2,STAT3 protein and mRNA in serum were reduced,and the expression levels of SOD were increased,with the best effect of Dahuang Lingxian Formula The treatment effect was best in the high concentration group.Conclusion:The mechanism may be related to the down-regulation of IL-6/JAK/STAT3 signaling pathway activation,and the best therapeutic effect was achieved by the high concentration group of Dahuang Lingxian Formula. 展开更多
关键词 Dahuang Lingxian formula Cholangiocyte inflammation HEPATOLITHIASIS IL-6/jak/stat3 signaling pathway
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补阳还五汤通过调控PI3K/Akt、JAK2/STAT3信号促进BMSC趋化迁移对外伤性脊髓损伤大鼠神经元活性及认知功能的影响 被引量:2
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作者 宋颖军 李旭 +1 位作者 刘小舟 张国福 《中国老年学杂志》 CAS 北大核心 2023年第17期4206-4213,共8页
目的研究补阳还五汤通过调控磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/Akt)、内源性酪氨酸激酶(JAK)2/信号传导和转录启动因子(STAT)3信号促进骨髓间充质干细胞(BMSCs)趋化迁移对外伤性脊髓损伤大鼠的神经元活性及认知功能的影响。方法选取健... 目的研究补阳还五汤通过调控磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/Akt)、内源性酪氨酸激酶(JAK)2/信号传导和转录启动因子(STAT)3信号促进骨髓间充质干细胞(BMSCs)趋化迁移对外伤性脊髓损伤大鼠的神经元活性及认知功能的影响。方法选取健康大鼠53只,随机分为健康组(健康大鼠常规饲养)、损伤组(建立脊髓损伤模型)、干预组(补阳还五汤治疗)、对照组(甲泼尼龙治疗),每组12只,剩余5只大鼠用于补阳还五汤含药血清制备。流式细胞术鉴定BMSCs细胞。Transwell小室法测大鼠BMSCs迁移。高架十字迷宫和Morris水迷宫实验检测大鼠认知功能。苏木素-伊红(HE)染色检测脊髓组织病理形态。TUNEL测脊髓组织神经细胞凋亡。免疫组化检测p-JAK2、p-STAT3。Western印迹测PI3K、p-PI3K、Akt、p-Akt。结果传代后的培养细胞呈旋窝状或放射状贴壁生长,细胞多呈星形、梭形或三角状,培养3代后,细胞贴壁加快、形态均一,呈旋窝状或单层放射状生长。培养细胞表面抗原CD29、CD90为阳性,CD31、CD45为阴性,提示其为BMSCs细胞。与健康组相比,损伤组总路程、进入开臂次数、穿越平台次数显著降低,不同时间的潜伏期显著升高(P<0.05)。与损伤组相比,干预组与对照组总路程、进入开臂次数、穿越平台次数显著升高,不同时间的潜伏期显著降低(P<0.05)。干预组与对照组各指标对比无统计学差异(P>0.05)。健康组脊髓组织结构完整。损伤组脊髓组织疏松水肿,有细胞空泡变性产生。相较于损伤组,干预组与对照组大鼠脊髓组织病理形态有所改善。与健康组相比,损伤组BMSCs、PI3K、Akt、p-PI3K、p-Akt显著降低,神经细胞凋亡率、p-JAK2、p-STAT3显著升高(P<0.05)。与损伤组相比,干预组BMSCs、PI3K、Akt、p-PI3K、p-Akt显著升高,神经细胞凋亡率、p-JAK2、p-STAT3显著降低(P<0.05)。干预组与对照组各指标水平无统计学差异(P>0.05)。结论补阳还五汤通过激活PI3K/Akt通路抑制JAK2/STAT3信号通路的激活,促进BMSCs的迁移,减轻神经细胞的凋亡,起到神经保护的作用,从而改善脊髓损伤大鼠的认知功能。 展开更多
关键词 补阳还五汤 磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/Akt) 内源性酪氨酸激酶(jak)2/信号传导和转录启动因子(stat)3 骨髓间充质干细胞(BMSCs)趋化迁移 神经元活性 认知功能
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Elevated retinol binding protein 4 levels are associated with atherosclerosis in diabetic rats via JAK2/STAT3 signaling pathway 被引量:10
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作者 Wan Zhou Shan-Dong Ye Wei Wang 《World Journal of Diabetes》 SCIE 2021年第4期466-479,共14页
BACKGROUND Atherosclerosis is a major cause of mortality worldwide and is driven by multiple risk factors,including diabetes,which results in an increased atherosclerotic burden,but the precise mechanisms for the occu... BACKGROUND Atherosclerosis is a major cause of mortality worldwide and is driven by multiple risk factors,including diabetes,which results in an increased atherosclerotic burden,but the precise mechanisms for the occurrence and development of diabetic atheroscerosis have not been fully elucidated.AIM To summarize the potential role of retinol binding protein 4(RBP4) in the pathogenesis of diabetic atheroscerosis,particularly in relation to the RBP4-Janus kinase 2/signal transducer and activator of transcription 3(JAK2/STAT3)signaling pathway.METHODS Male Wistar rats were randomly divided into three groups,including a control group(NC group),diabetic rat group(DM group),and diabetic atherosclerotic rat group(DA group).The contents of total cholesterol(TC), high-density lipoprotein cholesterol(HDL-c), triglycerides(TG), low-density lipoprotein cholesterol(LDLc), fasting insulin(FINS),fasting plasma glucose,and hemoglobin A1 c(HbA1 c)were measured.Moreover,the adipose and serum levels of RBP4,along with the expression levels of JAK2, phosphorylated JAK2(p-JAK2), STAT3,phosphorylated STAT3(p-STAT3), B-cell lymphoma-2(Bcl-2), and Cyclin D1 in aortic tissues were also measured.Besides,homeostasis model assessment of insulin resistance(HOMA-IR) and atherogenic indexes(AI) were calculated.RESULTS Compared with the NC and DM groups,the levels LDL-c,TG,TC,FINS,HOMAIR,RBP4,and AI were upregulated,whereas that of HDL-c was downregulated in the DA group(P <0.05);the mRNA levels of JAK2,STAT3,Cyclin D1,and Bcl-2 in the DA group were significantly increased compared with the NC group and the DM group;P-JAK2,p-JAK2/JAK2 ratio,p-STAT3,p-STAT3/STAT3 ratio,Cyclin D1,and Bcl-2 at protein levels were significantly upregulated in the DA group compared with the NC group and DM group.In addition,as shown by Pearson analysis,serum RBP4 had a positive correlation with TG,TC,LDL-c,FINS,HbA1 C,p-JAK2,p-STAT3,Bcl-2,Cyclin D1,AI,and HOMA-IR but a negative correlation with HDL-c.In addition,multivariable logistic regression analysis showed that serum RBP4,p-JAK2,p-STAT3,and LDL-c were predictors of the presence of diabetic atherosclerosis.CONCLUSION RBP4 could be involved in the initiation or progression of diabetic atherosclerosis by regulating the JAK2/STAT3 signaling pathway. 展开更多
关键词 Diabetes mellitus Petinol binding protein 4 ATHEROSCLEROSIS jak2/stat3 signaling pathway Cyclin D1
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5, 7, 3′-三乙酰橙皮素对AA大鼠成纤维样滑膜细胞Jak2/Stat3信号通路及凋亡相关蛋白的影响 被引量:9
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作者 任丹阳 徐涛 +5 位作者 黄成 李荣 王亚丽 于明哲 黄艳 李俊 《中国药理学通报》 CAS CSCD 北大核心 2012年第8期1063-1068,共6页
目的研究5,7,3'-三乙酰橙皮素(5,7,3'-triacetylhesperetin,TAHP)对佐剂性关节炎大鼠成纤维样滑膜细胞(FLS)Jak2/Stat3信号通路及凋亡相关蛋白的影响。方法用弗氏完全佐剂诱导大鼠AA模型;MTT法检测FLS的增殖反应;Hoechst 33258... 目的研究5,7,3'-三乙酰橙皮素(5,7,3'-triacetylhesperetin,TAHP)对佐剂性关节炎大鼠成纤维样滑膜细胞(FLS)Jak2/Stat3信号通路及凋亡相关蛋白的影响。方法用弗氏完全佐剂诱导大鼠AA模型;MTT法检测FLS的增殖反应;Hoechst 33258染色法检测FLS的凋亡;RT-PCR法检测FLS中Jak2、Stat3、Bcl-2、Bax及Caspase-3的基因表达;Western blot法检测FLS中p-Stat3及Caspase-3的蛋白表达情况。结果 TAHP呈剂量和时间依赖性抑制FLS的增殖(P<0.05);Hoechst 33258染色结果提示TAHP可以明显地促进FLS的凋亡;同时TAHP(50,250μmol·L-1)可以明显降低Jak2、Stat3及Bcl-2表达,而上调Bax及Caspase-3表达。Western blot结果显示,TAHP可降低p-Stat3的表达、上调Caspase-3表达。结论 TAHP可以抑制FLS增殖,其作用机制可能与抑制FLS Jak2/Stat3信号通路、促进Bax及Caspase-3表达、抑制Bcl-2的表达有关。 展开更多
关键词 5 7 3′三乙酰橙皮素 佐剂性关节炎 jak2/stat3 成纤维样滑膜细胞 细胞凋亡 Caspase3
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miR-153靶向PRDM2基因并通过JAK/STAT信号通路影响膀胱癌的侵袭和迁移 被引量:16
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作者 李冠军 亚国伟 +1 位作者 唐正严 苏开德 《中国病理生理杂志》 CAS CSCD 北大核心 2018年第1期58-63,共6页
目的:研究微小RNA(miR)-153是否靶向正性调控域锌指蛋白2(PRDM2)基因并通过调控JAK/STAT信号通路影响膀胱癌细胞的侵袭和迁移。方法:运用q PCR检测miR-153在膀胱癌组织中的表达;运用免疫组化检测PRDM2在正常组织和膀胱癌组织中的表达;We... 目的:研究微小RNA(miR)-153是否靶向正性调控域锌指蛋白2(PRDM2)基因并通过调控JAK/STAT信号通路影响膀胱癌细胞的侵袭和迁移。方法:运用q PCR检测miR-153在膀胱癌组织中的表达;运用免疫组化检测PRDM2在正常组织和膀胱癌组织中的表达;Western blot检测不同膀胱癌细胞株中PRDM2的表达情况;双萤光素酶报告基因系统检测miR-153对PRDM2转录活性的影响;Transwell侵袭实验检测miR-153过表达对膀胱癌细胞RT4侵袭能力的影响;划痕实验检测miR-153过表达对膀胱癌细胞RT4迁移能力的影响;Western blot实验检测过表达miR-153后JAK/STAT信号通路蛋白的水平。结果:和正常组织比较,PRDM2蛋白在膀胱癌中表达较高(P<0.05);miR-153的表达水平在膀胱癌组织中较低(P<0.05);双荧光素酶报告基因系统检测结果显示,miR-153可以调控PRDM2的表达水平;过表达miR-153后,膀胱癌细胞株RT4的侵袭和迁移能力明显降低,p-JAK2和p-STAT3的蛋白水平下调。结论:miR-153靶向PRDM2,并通过JAK/STAT信号通路调控膀胱癌细胞的侵袭和迁移能力。 展开更多
关键词 膀胱癌 微小RNA-153 正性调控域锌指蛋白2 jak/stat信号通路
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IL-2通过Jak3-Stat5通路促进巨噬细胞M1极化 被引量:6
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作者 亓文静 李岩 +1 位作者 王玉 于爱莲 《基础医学与临床》 CSCD 2015年第8期1055-1060,共6页
目的探究IL-2在调控巨噬细胞极化分型方面的作用及机制。方法重组小鼠白介素-2(IL-2)刺激处于M0期的小鼠单核巨噬细胞RAW 264.7,同时以IL-4作为对照。Real-time PCR和Western blot检测M1型和M2型标志分子的表达;流式细胞术检测M1型和M2... 目的探究IL-2在调控巨噬细胞极化分型方面的作用及机制。方法重组小鼠白介素-2(IL-2)刺激处于M0期的小鼠单核巨噬细胞RAW 264.7,同时以IL-4作为对照。Real-time PCR和Western blot检测M1型和M2型标志分子的表达;流式细胞术检测M1型和M2型巨噬细胞的百分比;Western blot检测Jak3和Stat5活化水平。结果经IL-2刺激后,处于M0的RAW 264.7细胞显著上调表达M1型标记分子,如IL-1β、IL-12、TNF-α和i NOS等;IL-2使巨噬细胞中M1型的比例由3.2%上升到24.6%,同时Jak3和Stat5分子的磷酸化水平显著提高。结论 IL-2具有促进巨噬细胞由M0向M1极化的作用,且该作用可能是通过Jak3-Stat5通路实现。 展开更多
关键词 IL-2 IL-4 巨噬细胞 极化 jak3.stat5通路
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MDS-RA骨髓造血细胞JAK2/STAT5通路活化及AG490干预研究 被引量:3
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作者 田胜利 周永明 +6 位作者 葛垒 周韶红 何玮 薛志忠 胡明辉 许毅 罗梅宏 《检验医学》 CAS 北大核心 2006年第3期278-280,共3页
目的探索一种非受体型酪氨酸激酶2/信号转导子和转录活化子5(JAK2/STAT5)通路特异性抑制剂———苯亚甲基丙二腈脂类衍生物AG490对骨髓增生异常综合征-难治性贫血(MDS-RA)骨髓造血细胞细胞因子及信号转导的影响。方法建立MDS-RA骨髓造... 目的探索一种非受体型酪氨酸激酶2/信号转导子和转录活化子5(JAK2/STAT5)通路特异性抑制剂———苯亚甲基丙二腈脂类衍生物AG490对骨髓增生异常综合征-难治性贫血(MDS-RA)骨髓造血细胞细胞因子及信号转导的影响。方法建立MDS-RA骨髓造血细胞培养体系JAK2、STAT5、Bc l-xL基因表达的荧光定量聚合酶链反应(FQ-PCR)检测方法;粒单集落刺激因子(GM-CSF)激活10例MDS-RA骨髓单个核细胞培养液JAK2、STAT5、Bc l-xL表达,通过酶联免疫吸附试验(ELISA)方法检测AG490组、空白对照组培养体系上清细胞因子白细胞介素(IL)-2、IL-3、γ干扰素(IFN-γ)、肿瘤坏死因子(TNF-α)水平,FQ-PCR检测上述两组培养体系单个核细胞JAK2、STAT5、Bc l-xL基因表达拷贝数。结果AG490组IL-3、IFN-γ水平明显低于空白对照组(P<0.01),IL-2、INF-α水平差异无显著性;AG490组JAK2、STAT5、Bc l-xL基因表达与空白对照组比较,差异有显著性(P<0.05,P<0.01)。结论AG490可以调整MDS-RA骨髓造血细胞培养体系上清细胞因子水平,进而影响JAK2/STAT5通路信号转导,下调Bc l-xL表达。 展开更多
关键词 骨髓增生异常综合征 AG490 信号转导 jak2/stat5 Bcl—xL
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补肾益髓生血法AA大鼠含药血清对大鼠造血干细胞红系分化JAK2/STAT5信号通路的影响 被引量:6
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作者 田晨 赵宗江 +5 位作者 张新雪 张丰丰 程明秀 王颖超 赵敬 吴志奎 《世界中医药》 CAS 2014年第6期713-716,721,共5页
目的:探讨补肾益髓生血法再生障碍性贫血(Aplastic Anemia,AA,简称再障)大鼠含药血清对大鼠骨髓造血干细胞红系分化JAK2/STAT5信号通路的影响。方法:在前期整体动物实验的基础上,体外培养正常大鼠造血干细胞,诱导其定向红系分化,分为空... 目的:探讨补肾益髓生血法再生障碍性贫血(Aplastic Anemia,AA,简称再障)大鼠含药血清对大鼠骨髓造血干细胞红系分化JAK2/STAT5信号通路的影响。方法:在前期整体动物实验的基础上,体外培养正常大鼠造血干细胞,诱导其定向红系分化,分为空白对照组、正常对照组、模型组、司坦唑醇组(康力龙组)、益髓生血组、温肾生血组和滋肾生血组,在培养体系中加入含药血清干预4d后,提取红系细胞总RNA及蛋白,分别采用RT-PCR和Western blot检测细胞JAK2、STAT5mRNA及蛋白表达情况。结果:与正常对照组相比,模型组细胞JAK2、STAT5mRNA及蛋白表达均明显降低(P<0.01);与模型组相比,各治疗组JAK2、STAT5mRNA及蛋白表达明显升高(P<0.01或P<0.05);滋肾生血组JAK2、STAT5mRNA及蛋白表达高于益髓生血组和温肾生血组(P<0.05)。结论:补肾益髓生血法能够增强JAK2、STAT5的表达,可能通过影响JAK2/STAT5信号通路来促进红系细胞的分化成熟,其中滋肾生血法优于益髓生血法和温肾生血法。 展开更多
关键词 补肾益髓生血法 再障 造血干细胞 红系分化 jak2stat5信号通路
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有氧运动干预非酒精性脂肪肝小鼠肝脏JAK2/STAT5信号通路的变化 被引量:6
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作者 张树玲 李军汉 +2 位作者 王佳倩 李亚龙 王纯 《中国组织工程研究》 CAS 北大核心 2022年第17期2690-2695,共6页
背景:酪氨酸激酶2/信号传导及转录激活因子5信号通路在脂质代谢中起重要作用,运动有效预防与治疗非酒精性脂肪肝与改善内脏脂质沉积和脂质代谢密切相关。目的:探讨有氧运动对非酒精性脂肪肝小鼠肝脏酪氨酸激酶2/信号传导及转录激活因子... 背景:酪氨酸激酶2/信号传导及转录激活因子5信号通路在脂质代谢中起重要作用,运动有效预防与治疗非酒精性脂肪肝与改善内脏脂质沉积和脂质代谢密切相关。目的:探讨有氧运动对非酒精性脂肪肝小鼠肝脏酪氨酸激酶2/信号传导及转录激活因子5信号通路的影响及可能作用机制。方法:6周龄C57BL/6雄性小鼠48只,分为普通膳食组及高脂膳食诱导组(n=24),第10周末2组各随机抽取4只进行油红O染色观察肝脏病理形态变化。确定造模成功后,普通膳食组随机分为普通膳食+安静组、普通膳食+运动组(n=10);高脂膳食诱导组随机分为非酒精性脂肪肝+安静组、非酒精性脂肪肝+运动组(n=10),连续干预8周,直至实验结束。观察小鼠肝脏病理形态变化,检测小鼠肝脏组织泌乳素受体、肝脏酪氨酸激酶2、信号传导及转录激活因子5a、肝脏酪氨酸激酶2磷酸化、信号传导及转录激活因子5磷酸化蛋白表达量。结果与结论:(1)与普通膳食+安静组相比,非酒精性脂肪肝+安静组肝细胞脂肪变性加重,肝脏内酪氨酸激酶2/信号传导及转录激活因子信号通路蛋白表达量降低;(2)与非酒精性脂肪肝+安静组相比,非酒精性脂肪肝+运动组的肝细胞脂肪变性减轻,肝脏内酪氨酸激酶2/信号传导及转录激活因子5信号通路蛋白表达量升高;(3)肝脏病理形态指标与催乳素受体、肝脏酪氨酸激酶2、肝脏酪氨酸激酶2磷酸化、信号传导及转录激活因子5磷酸化均呈显著负相关(P<0.05);(4)提示有氧运动干预可通过调节非酒精性脂肪肝小鼠肝脏酪氨酸激酶2/信号传导及转录激活因子5信号通路,改善肝内脂质沉积及肝脏脂肪变性程度。 展开更多
关键词 有氧运动 非酒精脂肪肝 酪氨酸激酶2/信号传导及转录激活因子5信号通路(jak2/stat5) 磷酸化
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糖皮质激素对高氧诱导的新生小鼠肺功能损伤、炎症反应和JAK2/STAT5通路的影响 被引量:4
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作者 刘露 冯伟 郭轶男 《实验动物科学》 2020年第1期42-49,共8页
目的探究糖皮质激素(Glucocorticoid,Gluc)对高氧诱导的新生小鼠肺功能损伤、炎症反应和JAK2/STAT5通路的影响,为治疗肺功能损伤提供理论依据。方法构建肺损伤小鼠模型,将小鼠随机分为:对照组、Hyperoxia组、低剂量Gluc组、中剂量Gluc... 目的探究糖皮质激素(Glucocorticoid,Gluc)对高氧诱导的新生小鼠肺功能损伤、炎症反应和JAK2/STAT5通路的影响,为治疗肺功能损伤提供理论依据。方法构建肺损伤小鼠模型,将小鼠随机分为:对照组、Hyperoxia组、低剂量Gluc组、中剂量Gluc组、高剂量Gluc组。通过动物肺功能分析系统检测静息通气量、气道阻力、气道压力、肺容积、最大吸气流量。HE染色和TUNEL染色观察小鼠肺脏组织形态和细胞凋亡情况;RT-PCR、Western Blot检测α-SMA、TGF-β表达量;Elisa检测IL-6、MCP-1、iNOS含量;Western Blot检测JAK2、STAT5的磷酸化情况。结果与对照组相比,Hyperoxia组小鼠静息通气量、气道阻力、气道压力、肺容积、最大吸气流量显著降低(P<0.05),细胞凋亡数、α-SMA与TGF-β表达量、EOS比值、IL-6、MCP-1、iNOS含量均显著增加(P<0.05),且JAK2、STAT5磷酸化水平显著升高(P<0.05)。而中、高剂量Gluc可显著逆转高氧对小鼠以上指标的影响。此外,Hyperoxia组小鼠出现肺实质结构紊乱、肺泡间隔增宽等组织形态的改变,在低、中、高剂量Gluc组中组织形态改变程度逐渐降低。结论糖皮质激素可缓解肺组织损伤并下调模型小鼠肺脏组织中炎症因子含量,同时抑制JAK2/STAT5通路活性,对高氧诱导的肺组织损伤具有较好的治疗作用。 展开更多
关键词 糖皮质激素 高氧 肺功能 炎症 jak2 stat5
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EPO通过JAK2/STAT5信号通路减轻大鼠血管平滑肌细胞钙化 被引量:2
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作者 常晋瑞 魏明 +4 位作者 赵玉峰 南瑛 曹健 朱娟霞 孙娜 《山西医科大学学报》 CAS 2022年第4期436-441,共6页
目的研究促红细胞生成素(EPO)减轻血管钙化的信号通路。方法为了分别探索JAK2/STAT5、PI3K/Akt和ERK三条信号通路在EPO减轻血管钙化中的作用,将大鼠血管平滑肌细胞(VSMCs)各分为4组:对照组、钙化组、钙化+EPO组和钙化+EPO+各信号通路阻... 目的研究促红细胞生成素(EPO)减轻血管钙化的信号通路。方法为了分别探索JAK2/STAT5、PI3K/Akt和ERK三条信号通路在EPO减轻血管钙化中的作用,将大鼠血管平滑肌细胞(VSMCs)各分为4组:对照组、钙化组、钙化+EPO组和钙化+EPO+各信号通路阻断剂组(AG490或LY294002或PD98059)。采用高磷诱导细胞钙化。Western blot法检测VSMCs收缩表型标志分子平滑肌蛋白(Smoothelin)和钙结合蛋白(Calponin)以及成骨表型标志分子骨桥蛋白(OPN)的蛋白表达;碱性磷酸酶(ALP)活性、钙含量检测和茜素红染色检测钙化水平。结果与对照组相比,钙化组Smoothelin和Calponin蛋白表达水平降低(P<0.01),而OPN蛋白表达水平上升(P<0.05)。与钙化组相比,钙化+EPO组Smoothelin和Calponin蛋白水平显著升高(均P<0.01),OPN蛋白表达降低(P<0.05);ALP活性、钙含量和钙盐沉积均减少(均P<0.01)。与钙化+EPO组相比,钙化+EPO+AG490组Smoothelin和Calponin蛋白水平降低(P<0.05),而OPN蛋白水平显著上升(P<0.01);ALP活性、钙含量和钙盐沉积均增加(P<0.01或0.05)。与钙化+EPO组相比,钙化+EPO+LY294002组和钙化+EPO+PD98059组的钙含量和ALP活性均无明显变化。结论JAK2/STAT5通路可能介导了EPO减轻VSMCs钙化的作用。 展开更多
关键词 血管平滑肌细胞 钙化 促红细胞生成素 jak2/stat5
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骨髓增生异常综合征患者JAK2和STAT5基因表达的变化 被引量:2
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作者 周永明 田胜利 +5 位作者 周韶虹 薛志忠 何玮 罗梅宏 胡明辉 许毅 《临床血液学杂志》 CAS 2007年第2期70-72,共3页
目的:比较骨髓增生异常综合征(MDS-RA)型与MDS-RAEB型患者外周血JAK2、STAT5基因表达水平,探索JAK2和STAT5信号转导在MDS发病中的作用。方法:建立JAK2、STAT5基因表达的荧光定量FQ-PCR检测方法,检测10例正常人、15例MDS-RA患者和10例MDS... 目的:比较骨髓增生异常综合征(MDS-RA)型与MDS-RAEB型患者外周血JAK2、STAT5基因表达水平,探索JAK2和STAT5信号转导在MDS发病中的作用。方法:建立JAK2、STAT5基因表达的荧光定量FQ-PCR检测方法,检测10例正常人、15例MDS-RA患者和10例MDS-RAEB患者外周血JAK2、STAT5基因表达水平及其自细胞介素(IL)-2、IL-3、γ干扰素(γ-INF)、肿瘤坏死因子α(TNF-α)细胞因子水平。结果:正常人IL-2、IL-3、γ-INF、TNF-α分别为50.28±14.19、29.15±5.47、26.17±5.36、31.12±8.73;MDS-RA患者分别为51.16±13.44、67.72±10.19、43.39±13.08、62.36±12.78;MDS-RAEB患者为19.55±21.86、28.74±15.52、64.34±27.35、82.13±17.79。正常人JAK2、STAT5基因不表达或低表达,拷贝数分别为480.07±609.17、116.05±173.87,MDS-RA患者分别为4 725.63±3 931.59、1 265.36±1 087.80,显著高于正常人(均P<0.01); MDS-RAEB患者分别为23006.11±11 311.10、13 144.55±8 493.36,显著高于MDS-RA患者(均P<0.01)。结论:细胞因子及其相关的JAK2和STAT5基因参与了MDS的发病及其恶性转变,JAK和STAT可能是MDS细胞由低危MDS-RA型向高危MDS-RAEB型恶性转化的信号通路之一。 展开更多
关键词 骨髓增生异常综合征 信号转导 jak2基因表达 stat5基因表达
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rhEPO通过调节JAK2/STAT5信号通路减少大鼠脑出血后神经细胞凋亡 被引量:2
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作者 梁俊君 王亚冰 +1 位作者 辛海滨 刘伟 《中国当代医药》 2017年第16期8-12,共5页
目的探讨重组人促红细胞生成素rhEPO是否通过JAK2/STAT5信号通路减少脑出血后神经细胞的凋亡。方法将8周龄的Wistar雄性大鼠30只随机分3组:假手术组、ICH模型组、rhEPO组,每组10只。ICH模型组大鼠进行ICH造模,假手术组除不注血外,其余... 目的探讨重组人促红细胞生成素rhEPO是否通过JAK2/STAT5信号通路减少脑出血后神经细胞的凋亡。方法将8周龄的Wistar雄性大鼠30只随机分3组:假手术组、ICH模型组、rhEPO组,每组10只。ICH模型组大鼠进行ICH造模,假手术组除不注血外,其余步骤同ICH模型组,rhEPO组术后5 min给予腹腔注射rhEPO,所有动物24 h后进行神经功能学评分,收集大鼠脑组织,利用原位缺口末端标记法检测神经细胞凋亡的变化;采用免疫组织化学SP法检测凋亡蛋白Caspase3表达;并采用Real-time PCR和Western blot检测磷酸化JAK2、磷酸化STAT5基因和蛋白表达情况。结果手术建立脑出血模型后24 h进行神经功能评分。按Longa5分制标准判定,ICH组4只评价为1分,3只评价为2分,2只评价为3分;rhEPO组治疗后,5只评价为1分,2只评价为2分,1只评价为3分,说明rhEPO可以改善大鼠脑出血后神经元损伤,恢复神经功能。与假手术组相比,ICH模型组和rhEPO组中神经元凋亡细胞及Caspase3的蛋白表达阳性细胞数明显增多(P<0.05),而rhEPO组中凋亡细胞与ICH模型组相比明显减少(P<0.05);与假手术组相比,ICH模型组和rhEPO组中JAK2和STAT5的蛋白表达和m RNA表达显著上升(P<0.05),与ICH模型组相比,rhEPO组中JAK2和STAT5的蛋白表达和m RNA表达显著降低,差异均有统计学意义(P<0.05)。结论外源性rhEPO可以通过调节JAK2/STAT5信号改善大鼠脑出血后神经元损伤,对于神经系统具有保护作用。 展开更多
关键词 RH EPO 脑出血 神经保护 jak2/stat5信号通路
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基于EPO介导的JAK2/STAT5信号通路研究百会、大椎刺络促缺血性脑卒中后血管新生的调控机制 被引量:1
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作者 王保国 曹奕 +5 位作者 陈倩倩 张静波 高纺 张璨 施婧婧 周文婷 《安徽中医药大学学报》 CAS 2022年第5期67-72,共6页
目的基于促红细胞生成素(erythropoietin,EPO)介导的JAK2/STAT5信号通路探讨百会、大椎刺络促缺血性脑卒中后血管新生的调控机制。方法选取健康SD雄性大鼠150只,随机分为正常对照组、假手术组、模型对照组、刺络治疗组、刺络+EPO拮抗组... 目的基于促红细胞生成素(erythropoietin,EPO)介导的JAK2/STAT5信号通路探讨百会、大椎刺络促缺血性脑卒中后血管新生的调控机制。方法选取健康SD雄性大鼠150只,随机分为正常对照组、假手术组、模型对照组、刺络治疗组、刺络+EPO拮抗组,每组30只;正常对照组不进行手术,假手术组仅分离血管而不插线栓,模型对照组、刺络治疗组、刺络+EPO拮抗组采用改良的Zea-Longa法制备大脑中动脉局灶性脑缺血再灌注模型(middle cerebral artery occlusion/reperfusion model,MCAO/R)大鼠。模型制备后刺络治疗组、刺络+EPO拮抗组采用“百会”“大椎”穴刺络进行干预,刺络+EPO拮抗组在针刺前将脂质体-siEPO2复合物按5 mg/kg剂量对大鼠进行腹腔注射,使之进入合成EPO的靶细胞,在细胞内引起针对EPO的RNA干扰效应。采用苏木精-伊红染色观察各组大鼠脑皮质病理形态,RT-PCR法检测各组大鼠脑皮质中EPO、血管内皮生长因子(vascular endothelial growth factor,VEGF)mRNA表达水平,Western Blot法检测各组大鼠脑皮质中P-JAK2、P-STAT5、VEGF蛋白表达水平。结果与正常对照组比较,模型对照组及刺络+EPO拮抗组大鼠脑皮质病理损伤严重;与模型对照组比较,刺络治疗组大鼠脑皮质病理损伤明显改善。与正常对照组比较,模型对照组大鼠脑皮质中EPO、VEGF mRNA表达水平显著升高(P<0.05),P-JAK2、P-STAT5、VEGF蛋白表达水平显著升高(P<0.05),刺络治疗会进一步增强这种趋势;与刺络治疗组比较,刺络+EPO拮抗组大鼠脑皮质中EPO、VEGF mRNA表达水平降低(P<0.05),P-JAK2、P-STAT5、VEGF蛋白表达水平降低(P<0.05)。结论通过百会、大椎刺络能上调MCAO/R模型大鼠EPO的表达水平,激活JAK2/STAT5信号通路,促进下游VEGF的表达而促进缺血性脑卒中后血管的新生。 展开更多
关键词 缺血性脑卒中 促红细胞生成素 jak2 stat5 百会 大椎 血管新生
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