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六味补气方通过调控NLRP3/Caspase-1/GSDMD焦亡通路延缓大鼠慢性阻塞性肺疾病的发展
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作者 梅莉 张璐 +6 位作者 吴迪 丁焕章 王新汝 张西安 卫宇航 李泽庚 童佳兵 《南方医科大学学报》 CAS CSCD 北大核心 2024年第11期2156-2162,共7页
目的基于NLRP3/Caspase-1/GSDMD的细胞焦亡通路,探讨六味补气方治疗慢性阻塞性肺疾病(COPD)模型大鼠的作用机制。方法将40只SD大鼠随机分为对照组、模型组、六味补气方组、六味补气方+MCC950组(n=10),除对照组外,其余各组大鼠采用烟熏... 目的基于NLRP3/Caspase-1/GSDMD的细胞焦亡通路,探讨六味补气方治疗慢性阻塞性肺疾病(COPD)模型大鼠的作用机制。方法将40只SD大鼠随机分为对照组、模型组、六味补气方组、六味补气方+MCC950组(n=10),除对照组外,其余各组大鼠采用烟熏联合脂多糖气管滴注以及激素注射法造模,建立COPD模型大鼠,并分别给予六味补气方药物灌胃及合并MCC950腹腔注射。观察各组大鼠的一般情况变化,分析大鼠肺组织病理改变、肺功能、肺泡灌洗液(BALF)吉姆萨染色总细胞及白细胞分类计数、血清中炎症因子IL-6、TNF-α、IL-18及NO水平;qRT-PCR检测大鼠肺组织中焦亡相关蛋白NLRP3、ASC、Caspase-1、GSDMD-N、IL-1β、IL-18的mRNA表达。结果与对照组相比,模型组大鼠的肺组织病理损伤较重,肺功能下降(P<0.01),BALF中总细胞数增多,白细胞分类计数均上调(P<0.01),IL-6、TNF-α、IL-18及NO表达增多(P<0.01),肺组织相关蛋白含量增多(P<0.01);与模型组相比,六味补气方组大鼠的肺组织病理、肺功能均有改善(P<0.05),BALF中总细胞数及白细胞分类计数减少(P<0.01),IL-6、TNF-α、IL-18及NO表达下降(P<0.01),肺组织相关焦亡蛋白含量减少(P<0.01);与六味补气方组大鼠相比,使用MCC950后的大鼠肺组织病理、肺功能有改善,但差异无统计学意义(P>0.05);BALF中总细胞数及白细胞分类计数减少(P<0.05),IL-6、TNF-α、IL-18及NO表达下降(P<0.05),肺组织相关焦亡蛋白含量较少(P<0.05)。结论六味补气方可能通过调节NLRP3/Caspase-1/GSDMD通路抑制COPD模型大鼠的肺组织焦亡,从而降低炎症反应,减轻肺部损伤,延缓疾病的发生发展。 展开更多
关键词 六味补气方 慢性阻塞性肺疾病 NLRP3/Caspase-1/GSDMD 细胞焦亡 MCC950
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The dynamic metabolic profile of Qi-Yu-San-Long decoction in rat urine using UPLC-QTOF-MS^(E) coupled with a post-targeted screening strategy 被引量:1
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作者 Ting Zheng Yue Zhao +4 位作者 Ruijuan li Mengwen Huang An Zhou zegeng li Huan Wu 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2022年第5期755-765,共11页
Qi-Yu-San-Long decoction(QYSLD)is a traditional Chinese medicine that has been clinically used in the treatment of non-small-cell lung cancer(NSCLC)for more than 20 years.However,to date,metabolicrelated studies on QY... Qi-Yu-San-Long decoction(QYSLD)is a traditional Chinese medicine that has been clinically used in the treatment of non-small-cell lung cancer(NSCLC)for more than 20 years.However,to date,metabolicrelated studies on QYSLD have not been performed.In this study,a post-targeted screening strategy based on ultra-performance liquid chromatography coupled with quadrupole time-of-flight full information tandem mass spectrometry(UPLC-QTOF-MS^(E))was developed to identify QYSLD-related xenobiotics in rat urine.The chemical compound database of QYSLD constituents was established from previous research,and metabolites related to these compounds were predicted in combination with their possible metabolic pathways.The metabolites were identified by extracted ion chromatograms using predicted m/z values as well as retention time,excimer ions,and fragmentation behavior.Overall,85 QYSLD-related xenobiotics(20 prototype compounds and 65 metabolites)were characterized from rat urine.The main metabolic reactions and elimination features of QYSLD included oxidation,reduction,decarboxylation,hydrolysis,demethylation,glucuronidation,sulfation,methylation,deglycosylation,acetylation,and associated combination reactions.Of the identified molecules,14 prototype compounds and 58 metabolites were slowly eliminated,thus accumulating in vivo over an extended period,while five prototypes and two metabolites were present in vivo for a short duration.Furthermore,one prototype and five metabolites underwent the process of“appearing-disappearing-reappearing”in vivo.Overall,the metabolic profile and characteristics of QYSLD in rat urine were determined,which is useful in elucidating the active components of the decoction in vivo,thus providing the basis for studying its mechanism of action. 展开更多
关键词 Qi-Yu-San-Long decoction Post-targeted screening strategy Dynamic metabolic profile UPLC-QTOF-MS^(E)
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