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TLR4-P38MAPK信号通路在LPS诱导BV2细胞中的表达及意义 被引量:3
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作者 吴非 罗涛 +1 位作者 郭远瑾 梅元武 《中国实用神经疾病杂志》 2013年第11期7-9,共3页
目的观察LPS诱导小胶质细胞后信号通路Toll样受体4(TLR4)-p38蛋白激酶(p38MAPK)的表达及意义。方法体外培养BV2小胶质细胞,分为对照组、LPS诱导组(LPS刺激12h及24h)及SB203580干预组(LPS+SB203580诱导12h及24h),应用ELISA法检测各组TNF... 目的观察LPS诱导小胶质细胞后信号通路Toll样受体4(TLR4)-p38蛋白激酶(p38MAPK)的表达及意义。方法体外培养BV2小胶质细胞,分为对照组、LPS诱导组(LPS刺激12h及24h)及SB203580干预组(LPS+SB203580诱导12h及24h),应用ELISA法检测各组TNF-α、IL-6水平,RT-PCR法检测各组TLR4mRNA和p38MAPK mRNA的表达变化。结果 LPS诱导组细胞分泌TNF-α、IL-6水平显著提高,诱导24h后细胞上清液含量分别为(513.67±14.05)pg/mg和(396.84±15.41)pg/mg。给予SB203580抑制剂后TLR4mRNA和p38MAPK mRNA表达明显减弱,细胞分泌TNF-α、IL-6含量表达与感染组比较也明显降低。结论 LPS刺激小胶质细胞可引起TLR4-p38MAPK信号通路的活化并释放炎性细胞因子,而SB203580则对其有明显的抑制作用,证明TLR4-p38MAPK信号通路与小胶质细胞的炎性活化密切相关。 展开更多
关键词 tlr4-p38MAPK信号通路 小胶质细胞 LPS SB203580
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黄芪甲苷介导TLR4-p38 MAPK信号通路在幼鼠急性肺损伤中的研究 被引量:6
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作者 王茜 万静 +3 位作者 谭扬茗 罗丹丹 熊海英 姜红 《中国比较医学杂志》 CAS 北大核心 2020年第6期106-112,共7页
目的探究黄芪甲苷介导TLR4-p38 MAPK信号通路在幼鼠急性肺损伤模型中的作用。方法以7日龄SD新生仔鼠为实验对象,利用脂多糖构建幼鼠急性肺损伤模型,以地塞米松为阳性药对照,每只幼鼠腹腔注射10 m L/kg黄芪甲苷,造模后12 h和24 h观察肺... 目的探究黄芪甲苷介导TLR4-p38 MAPK信号通路在幼鼠急性肺损伤模型中的作用。方法以7日龄SD新生仔鼠为实验对象,利用脂多糖构建幼鼠急性肺损伤模型,以地塞米松为阳性药对照,每只幼鼠腹腔注射10 m L/kg黄芪甲苷,造模后12 h和24 h观察肺组织病变,检测TLR4、p-p38蛋白和mRNA表达量,TNF-α、IL-6、IL-12炎症因子的mRNA表达量变化。结果模型组在建模后12 h呈现肺出血,大量肺泡萎陷,24 h呈现肺水肿,肺泡间隔明显增宽。和模型组相比,黄芪甲苷组肺组织的病变明显减轻。另外,蛋白检测结果表明,与模型组比较,黄芪甲苷组TLR4、p-p38蛋白表达量明显降低(P<0. 05,P<0. 001) q-PCR结果表明,与模型组比较,黄芪甲苷组TLR4 mRNA相对表达量均有明显的降低,并且和模型组有显著性差异(P<0. 05)。TNF-α、IL-6、IL-12各炎症因子均有下降的趋势,其中IL-12相对表达量和模型组有显著性差异(P<0. 05)。结论黄芪甲苷通过抑制TLR4-p38MAPK信号通路,在幼鼠急性肺损伤模型中起重要作用。 展开更多
关键词 黄芪甲苷 急性肺损伤模型 tlr4-p38 MAPKs信号通路 炎症因子
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Effect of Soothing Gan(Liver) and Invigorating Pi(Spleen) Recipes on TLR4-p38 MAPK Pathway in Kupffer Cells of Non-alcoholic Steatohepatitis Rats 被引量:17
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作者 GONG Xiang-wen XU Yong-jian +4 位作者 YANG Qin-he LIANG Yin-ji ZHANG Yu-pei WANG Guan-long LI Yuan-yuan 《Chinese Journal of Integrative Medicine》 SCIE CAS CSCD 2019年第3期216-224,共9页
Objective: To investigate the mechanism of inflammatory-mediated toll-like receptor 4(TLR4)-p38 mitogen-activated protein kinase(p38 MAPK) pathway in Kupffer cells(KCs) of non-alcoholic steatohepatitis(NASH) rats and ... Objective: To investigate the mechanism of inflammatory-mediated toll-like receptor 4(TLR4)-p38 mitogen-activated protein kinase(p38 MAPK) pathway in Kupffer cells(KCs) of non-alcoholic steatohepatitis(NASH) rats and the intervention effect of soothing Gan(Liver) and invigorating Pi(Spleen) recipes on this pathway. Methods: After 1 week of acclimatization, 120 Sprague-Dawley male rats were randomly divided into 8 groups using a random number table(n=15 per group): normal group, model group, low-dose Chaihu Shugan Powder(柴胡疏肝散, CHSG) group(3.2 g/kg), high-dose CHSG group(9.6 g/kg), low-dose Shenling Baizhu Powder(参苓白术散, SLBZ) group(10 g/kg), high-dose SLBZ(30 g/kg) group, and low-and highdose integrated recipe(L-IR, H-IR) groups. All rats in the model and treatment groups were fed with a high-fat diet(HFD). The treatments were administrated by gastrogavage once daily and lasted for 26 weeks. The liver tissues were detected with hematoxylin-eosin(HE) and oil red O staining. Levels of liver lipids, serum lipids and transaminases were measured. KCs were isolated from the livers of rats to evaluate the mRNA expressions of TLR4 and p38 MAPK by real-time fluorescence quantitative polymerase chain reaction, and proteins expressions of TLR4, p-p38 MAPK and p38 MAPK by Western blot. Levels of inflammatory cytokines including tumor necrosis factor α(TNF-α), interleukin(IL)-1 and IL-6 in KCs were measured by enzyme-linked immunosorbent assay. Results: After 26 weeks of HFD feeding, HE and oil red O staining showed that the NASH model rats successfully reproduced typical pathogenesis and histopathological features. Compared with the normal group, the model group exhibited significant increases in body weight, liver weight, liver index, serum levels of total cholesterol(TC), triglyceride(TG), low-density lipoprotein cholesterol, and aspartate aminotransferase as well as TC and TG levels in liver tissues, and significant decrease in serum level of high-density lipoprotein cholesterol(P<0.05 or P<0.01), while those indices were significantly ameliorated in the H-IR group(P<0.05 or P<0.01). Higher levels of TNF-α, IL-1 and IL-6 in KCs were observed in the model group compared with the normal group(P<0.01). Significant decreases in TNF-α, IL-1 and IL-6 were observed in the H-SLBZ, H-IR and L-IR groups compared with the model group(P<0.05 or P<0.01). The m RNA expressions of TLR4 and p38 MAPK and protein expressions of TLR4, p38 MAPK and p-p38 MAPK in KCs in the model group were significantly higher than the normal group(P<0.01), while those expression levels in the L-IR and H-IR groups were significantly lower than the model group(P<0.05 or P<0.01). Conclusions: Inflammation in KCs might play an important role in the pathogenesis of NASH in rats. The data demonstrated the importance of TLR4-p38 MAPK signaling pathway in KCs for the anti-inflammatory effect of soothing Gan and invigorating Pi recipes. 展开更多
关键词 non-alcoholic steatohepatitis soothing GAN (Liver)and invigorating PI (Spleen)recipes Kupffer cel toll-like receptor 4-p38 MITOGEN-ACTIVATED protein kinase signaling pathway inflammation Chinese medicine
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热休克蛋白在大鼠慢性吗啡镇痛耐受中的作用及机制 被引量:1
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作者 赵彦芬 赵峰 +1 位作者 刘鹏森 毛轲 《解放军医学杂志》 CAS CSCD 北大核心 2020年第12期1242-1247,共6页
目的探讨热休克蛋白60(HSP60)在慢性吗啡镇痛耐受中的作用及机制。方法50只雄性SD大鼠随机分为对照组(n=10)、吗啡组(n=10)、siRNA-阴性对照(siRNA-NC)+吗啡组(n=10)、siRNA-HSP60+吗啡组(n=10)与脂多糖(LPS)+siRNA-HSP60+吗啡组(n=10)... 目的探讨热休克蛋白60(HSP60)在慢性吗啡镇痛耐受中的作用及机制。方法50只雄性SD大鼠随机分为对照组(n=10)、吗啡组(n=10)、siRNA-阴性对照(siRNA-NC)+吗啡组(n=10)、siRNA-HSP60+吗啡组(n=10)与脂多糖(LPS)+siRNA-HSP60+吗啡组(n=10)。对照组和吗啡组分别于鞘内注射10μl生理盐水和吗啡;siRNA-NC+吗啡组和siRNA-HSP60+吗啡组分别给予10μl siRNA-NC和siRNA-HSP60,然后鞘内注射吗啡;LPS+siRNA-HSP60+吗啡组给予10μl siRNA-HSP60和LPS,然后鞘内注射吗啡。各组均连续处理7 d。采用RT-PCR和Western blotting检测大鼠脊髓组织中HSP60的mRNA和蛋白表达水平;采用水浴甩尾法观察沉默HSP60对疼痛耐受的影响;免疫荧光染色法检测脊髓小胶质细胞标志物OX-42的表达;RT-PCR法检测大鼠脊髓组织中白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)mRNA的表达;Western blotting检测大鼠脊髓组织中Toll样受体4(TLR4)和磷酸化p38丝裂原活化蛋白激酶(p-p38MAPK)的表达水平。结果鞘内注射siRNA-HSP60可显著下调吗啡诱导的HSP60的表达(P<0.05)。与对照组相比,吗啡组大鼠对疼痛的耐受度降低(P<0.05),HSP60缺失可增强大鼠对疼痛的耐受(P<0.05)。与siRNA-NC+吗啡组比较,siRNA-HSP60+吗啡组大鼠脊髓组织中OX-42阳性细胞数以及IL-1β、TNF-αmRNA的表达显著下调(P<0.05),TLR4和p-p38MAPK的表达水平降低(P<0.05),而LPS处理可上调TLR4和p-p38MAPK的表达(P<0.05),并能逆转HSP60缺失对吗啡耐受的作用(P<0.05)。结论HSP60缺失通过抑制小胶质细胞的活化及炎症反应改善吗啡耐受的形成,其机制可能与抑制TLR4-p38MAPK信号通路有关。 展开更多
关键词 热休克蛋白60 tlr4-p38MAPK 吗啡镇痛耐受
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小金丸治疗大鼠阴茎纤维化的作用及其机制研究
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作者 徐渊明 陈少峰 +3 位作者 赵丰 孙远 李重 耿强 《中国中西医结合外科杂志》 CAS 2024年第6期782-786,共5页
目的:研究小金丸对大鼠阴茎硬结症模型阴茎海绵体内Toll样受体4(TLR4)、p38丝裂原活化蛋白激酶(MAPK)、基质金属蛋白酶(MMP)1的表达调节及对大鼠阴茎纤维化作用的可能机制。方法:将雄性SD大鼠18只随机分为3组:对照组、模型组、小金丸治... 目的:研究小金丸对大鼠阴茎硬结症模型阴茎海绵体内Toll样受体4(TLR4)、p38丝裂原活化蛋白激酶(MAPK)、基质金属蛋白酶(MMP)1的表达调节及对大鼠阴茎纤维化作用的可能机制。方法:将雄性SD大鼠18只随机分为3组:对照组、模型组、小金丸治疗组;对照组阴茎海绵体白膜下注射生理盐水,饲养6周后双蒸水灌胃;模型组、小金丸治疗组阴茎海绵体白膜下注TGF-β1(转化生长因子-β1),饲养6周后用小金丸灌胃;模型组大鼠与小金丸治疗组等量双蒸水灌胃;3组灌胃处理4周后处死,留取大鼠阴茎组织。采用HE染色观察阴茎海绵体纤维化程度;PCR和Western Blot检测TLR4-p38MAPK-MMP1通路RNA和蛋白表达情况。结果:病理组织学HE染色发现,模型组比对照组纤维化明显增加;小金丸治疗组与模型组相比纤维化明显减少。对照组和小金丸治疗组的TLR4-p38MAPK-MMP1 RNA表达量及TLR4-p38MAPK-MMP1蛋白表达明显低于模型组,差异有统计学意义(P<0.01)。结论:阴茎硬结症大鼠模型阴茎海绵体内纤维化明显,TLR4-p38MAPK-MMP1表达增加;小金丸治疗后,纤维化明显改善,TLR4-p38MAPK-MMP1表达减少。小金丸治疗阴茎硬结症与TLR4-p38MAPK-MMP1介导的抗纤维化作用有关。 展开更多
关键词 阴茎硬结症 小金丸 tlr4-p38MAPK-MMP1信号通路 大鼠 抗纤维化
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