نمایش مختصر رکورد

dc.contributor.authorLi, Benkeen_US
dc.contributor.authorZeng, Mengnanen_US
dc.contributor.authorZhang, Beibeien_US
dc.contributor.authorKan, Yuxuanen_US
dc.contributor.authorWang, Shengchaoen_US
dc.contributor.authorWang, Yangyangen_US
dc.contributor.authorWu, Yuanyuanen_US
dc.contributor.authorXu, Ruiqien_US
dc.contributor.authorFeng, Weishengen_US
dc.contributor.authorZheng, Xiaokeen_US
dc.date.accessioned1399-07-09T08:25:51Zfa_IR
dc.date.accessioned2020-09-30T08:25:51Z
dc.date.available1399-07-09T08:25:51Zfa_IR
dc.date.available2020-09-30T08:25:51Z
dc.date.issued2020-11-01en_US
dc.date.issued1399-08-11fa_IR
dc.date.submitted2019-12-30en_US
dc.date.submitted1398-10-09fa_IR
dc.identifier.citationLi, Benke, Zeng, Mengnan, Zhang, Beibei, Kan, Yuxuan, Wang, Shengchao, Wang, Yangyang, Wu, Yuanyuan, Xu, Ruiqi, Feng, Weisheng, Zheng, Xiaoke. (2020). <i>Corallodiscus flabellata</i> B. L. Burtt extract alleviates lipopolysaccharide/D-galactosamine-induced acute liver failure and brain injury by inhibiting oxidative stress, apoptosis, and inflammation. Iranian Journal of Basic Medical Sciences, 23(11), 1445-1452. doi: 10.22038/ijbms.2020.45437.10567en_US
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.urihttps://dx.doi.org/10.22038/ijbms.2020.45437.10567
dc.identifier.urihttp://ijbms.mums.ac.ir/article_16487.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/341252
dc.description.abstract<em><strong>Objective(s):</strong></em> Corallodiscus flabellata B. L. Burtt (CF) is distributed along liver meridian, with a possible beneficial effect in the progression of acute liver failure. Therefore, the present study investigates the effect of CF extract on rats with acute liver failure.<br /><em><strong>Materials and Methods:</strong></em> Rats were divided into four experimental groups: Control, Lipopolysaccharide (LPS)/D-Galactosamine (D-GalN) (L/D), Wu Ling Powder + L/D (WLP+L/D) and CF + L/D. Animals were gavage for 7 days, after which all animals except the control group were injected intraperitoneally with LPS and D-GalN to induce acute liver failure. Subsequently, the urine was collected for the next 8 hr, and the liver pathological changes were observed. The levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), inflammatory factor and oxidative stress-related indicators were measured. The levels of reactive oxygen species (ROS), apoptosis marker in the liver, water content and aquaporin (AQPs) in the brain were detected. The concentration of ions and osmolality of urine and serum were determined.<br /><em><strong>Results:</strong></em> The results show that CF significantly improved the damage of liver and brain tissue, and reversed the changes of serum ALT, AST, inflammatory factor and Cl-. It modulated oxidative stress-related indicators, reduced the content of ROS, apoptosis markers, water content, the level of Cl- ions and osmolality in the urine and the expression of AQP1, and AQP4 in the brain, and increased the urine output. <br /><em><strong>Conclusion:</strong></em> It was found that the CF extract could alleviate the L/D induced acute liver failure by regulating the hepatocyte apoptosis and AQPs expression in the brain.en_US
dc.format.extent986
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Basic Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijbms.2020.45437.10567
dc.subjectAcute Liver Failureen_US
dc.subjectApoptosisen_US
dc.subjectAquaporinen_US
dc.subjectBrainen_US
dc.subjectCorallodiscus flabellata B. L. Burtten_US
dc.subjectInflammationen_US
dc.subjectOxidative stressen_US
dc.title<i>Corallodiscus flabellata</i> B. L. Burtt extract alleviates lipopolysaccharide/D-galactosamine-induced acute liver failure and brain injury by inhibiting oxidative stress, apoptosis, and inflammationen_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.contributor.departmentCollege of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, Chinaen_US
dc.citation.volume23
dc.citation.issue11
dc.citation.spage1445
dc.citation.epage1452
nlai.contributor.orcid0000-0002-9307-6682


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