Dehydroandrographolide Improvement of Acetaminophen-Induced Acute Liver Failure

Revista Brasileira de Farmacognosia - Tập 33 - Trang 523-533 - 2023
Lu Ding1, Wenxi Tan1, Yunfei Wei1, Hao Yu1, Lilei Zhao1, Jiaqi Cheng1, Haihua Feng1
1Key Laboratory of Zoonosis, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun, People’s Republic of China

Tóm tắt

Acetaminophen-induced drug-induced acute liver injury is a liver disease which is one of the most serious human health diseases. Dehydroandrographolide is a natural product found in Andrographis paniculata (Burm.f.) Wall., Acanthaceae, with therapeutical uses such as analgesic and hepatoprotective. The present study was designed to analyze the effect of dehydroandrographolide on acetaminophen-induced acute liver failure. The results showed that dehydroandrographolide attenuated the damage caused by acetaminophen-induced acute liver failure in C57BL/6 mice through a decreased level of serum aspartate aminotransferase and glutamic-pyruvic transaminase. In addition, dehydroandrographolide increased the levels of glutathione and significantly increased serum superoxide dismutase. In vitro, dehydroandrographolide significantly activating nuclear-related factor 2, glutamate-cysteine ligase, glutamate-cysteine ligase modifier, heme oxygenase-1, and NAD(P)H quinone dehydrogenase 1 proteins promoted the phosphorylation of acetyl-CoA carboxylase, and 5′ adenosine monophosphate–activated protein kinase (α and β), inhibited the phosphorylation of phosphoinositide 3-kinase, serine/threonine kinase, and mammalian target of rapamycin. These results suggest that dehydroandrographolide can improve acetaminophen-induced drug-induced acute liver failure in mice.

Tài liệu tham khảo

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