Study on the anti-endotoxin effect of sinomenine using an Agilent genome array
Study on the anti-endotoxin effect of sinomenine using an Agilent genome array
复制标题
利用安捷伦基因组芯片研究青藤碱的抗内毒素作用
DOI:
10.1093/qjmed/hcx234
复制
发表时间:
2018-03
影响因子:
13.3
通讯作者:
He K.
中科院分区:
文献类型:
--
作者:
Hu Y.;Li B.;Wen L.;He K.
Background
Endotoxin is a significant contributing factor underlying the occurrence of fever, diarrhea, inflammation, edema, coagulation, shock and other syndromes associated with gram-negative bacterial infections. To date, there is no effective treatment for endotoxemia.
Aim
The aim of this study was to characterize differentially expressed genes in sinomenine-treated and lipopolysaccharide (LPS)-induced endothelial cells by microarray analysis and to determine the potential pharmacological activity of sinomenine.
Design
The cultured cells of five treatment groups (n = 3) were collected. Participants: total RNA was extracted and subjected to Agilent Porcine 4 × 44 K whole genome microarray.
Methods
Kyoto encyclopedia of genes and genomes and gene ontology software were applied to screen and analyze differentially regulated genes.
Results
The results showed that 723 differentially regulated genes were identified including 410 up-regulated genes and 313 down-regulated genes in therapy group vs. LPS group. Ten genes may be key controlled genes in the pathogenesis of LPS, including five up-regulated genes (ARG1, TLR2, IL1A, VCAM1, DKK3) and five down-regulated genes (HABP2, ID1, CHDH, GPX3, PTGFR), which primarily contribute to biological processes such as inflammatory response, vascular lesion, metabolic process and cell cycle. IL1A and FMO3 were considered as potent target genes.
Conclusion
Global gene expression profile analysis showed that sinomenine might effectively be useful to regulate inflammatory responses as part of future anti-endotoxin therapies.
登录
查看更多内容
影响因子:
3.7
作者:
Li J;Zhao L;He X;Zeng YJ;Dai SS
通讯作者:
Dai SS
影响因子:
3.6
作者:
E. Thorgersen;A. Macagno;C. Rossetti;T. Mollnes
通讯作者:
E. Thorgersen;A. Macagno;C. Rossetti;T. Mollnes
DOI:
10.1152/ajpendo.00220.2002
发表时间:
2002-11
期刊:
American journal of physiology. Endocrinology and metabolism
影响因子:
--
作者:
R. Orellana;P. M. O'Connor;Hanh V. Nguyen;Jill A. Bush;A. Suryawan;M. Thivierge;M. Fiorotto;T. Davis
通讯作者:
R. Orellana;P. M. O'Connor;Hanh V. Nguyen;Jill A. Bush;A. Suryawan;M. Thivierge;M. Fiorotto;T. Davis
DOI:
10.1124/jpet.102.035758
发表时间:
2002-11
影响因子:
3.5
作者:
Taiyo Suganuma;K. Irie;E. Fujii;T. Yoshioka;T. Muraki
通讯作者:
Taiyo Suganuma;K. Irie;E. Fujii;T. Yoshioka;T. Muraki
影响因子:
6.7
作者:
Gao, J.;Zhao, W. X.;Chen, Z. Q.
通讯作者:
Chen, Z. Q.