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These studies evaluated FDA-approved branded medications under controlled clinical trial conditions
IL-22 pretreatment significantly upregulates hepatic LC3-II(the PE-conjugated form of light chain 3) and phosphorylation of AMP-activated kinase (p-AMPK) in APAP-treated mice, and IL-22-mediated LC3-II conversion and protection against APAP-induced cytotoxicity are impaired when p-AMPK is blocked by compound C (an AMPK inhibitor) [203]
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