Effect of glutamine on the acute liver injury by Galn/LPS
Lei Yin
Abstract
Lei Yin
Abstract
Objective To investigate the effect of glutamine on acute liver injury by Galn/LPS. Methods The acute liver injury model was established by Galn/LPS.Pretreatment with 3.5% glutamine solution by intraperitoneal at the dose of 1 g/kg weight.Male mice were treated with LPS plus D-galactosamine. Then blood removed from the vena was analyzed for ALT,and liver tissue was analyzed for the density of MDA,GSH and TNF-α. Results Pretreatment with glutamine could abrogate the high levels of plasma ALT activity,the density of TNF-α and MDA in liver by Galn/LPS,and maintain the density of GSH. Conclusion Glutamine can maintain the level of GSH in liver tissue,regulate the redox state,and prevent liver injury induced by Galn/LPS.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To investigate the effect of glutamine on acute liver injury by Galn/LPS. Methods The acute liver injury model was established by Galn/LPS.Pretreatment with 3.5% glutamine solution by intraperitoneal at the dose of 1 g/kg weight.Male mice were treated with LPS plus D-galactosamine. Then blood removed from the vena was analyzed for ALT,and liver tissue was analyzed for the density of MDA,GSH and TNF-α. Results Pretreatment with glutamine could abrogate the high levels of plasma ALT activity,the density of TNF-α and MDA in liver by Galn/LPS,and maintain the density of GSH. Conclusion Glutamine can maintain the level of GSH in liver tissue,regulate the redox state,and prevent liver injury induced by Galn/LPS.
Key concepts: Glutamine, Liver injury, Glutathione, Liver tissue, Intraperitoneal injection, Galactosamine, Pharmacology, Tumor necrosis factor alpha