Title : GTS-21 ameliorates polymicrobial sepsis-induced hepatic injury by modulating autophagy through α7nAchRs in mice.

Pub. Date : 2020 Apr

PMID : 32018068






4 Functional Relationships(s)
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1 BACKGROUND: Previous studies showed that GTS-21, a selective alpha 7 nAchR agonist, can trigger anti-inflammatory effects and improve the survival of septic animals. 3-(2,4-dimethoxybenzylidene)anabaseine cholinergic receptor, nicotinic, alpha polypeptide 7 Mus musculus
2 The administration of GTS-21 inhibited pro-inflammatory cytokine production and hepatic enzymatic marker expression, promoted the expression of LC3-II, Atg7, Atg5, and decreased the expression of p62, which could be reversed by alpha-BGT treatment. 3-(2,4-dimethoxybenzylidene)anabaseine autophagy related 7 Mus musculus
3 The administration of GTS-21 inhibited pro-inflammatory cytokine production and hepatic enzymatic marker expression, promoted the expression of LC3-II, Atg7, Atg5, and decreased the expression of p62, which could be reversed by alpha-BGT treatment. 3-(2,4-dimethoxybenzylidene)anabaseine autophagy related 5 Mus musculus
4 The administration of GTS-21 inhibited pro-inflammatory cytokine production and hepatic enzymatic marker expression, promoted the expression of LC3-II, Atg7, Atg5, and decreased the expression of p62, which could be reversed by alpha-BGT treatment. 3-(2,4-dimethoxybenzylidene)anabaseine nucleoporin 62 Mus musculus