TY - JOUR
T1 - The Modulation of Phospho-Extracellular Signal-Regulated Kinase and Phospho-Protein Kinase B Signaling Pathways plus Activity of Macrophage-Stimulating Protein Contribute to the Protective Effect of Stachydrine on Acetaminophen-Induced Liver Injury
AU - Liu, Fu Chao
AU - Yu, Huang Ping
AU - Lee, Hung Chen
AU - Chen, Chun Yu
AU - Liao, Chia Chih
N1 - Publisher Copyright:
© 2024 by the authors.
PY - 2024/1/25
Y1 - 2024/1/25
N2 - Stachydrine, a prominent bioactive alkaloid derived from Leonurus heterophyllus, is a significant herb in traditional medicine. It has been noted for its anti-inflammatory and antioxidant characteristics. Consequently, we conducted a study of its hepatoprotective effect and the fundamental mechanisms involved in acetaminophen (APAP)-induced liver injury, utilizing a mouse model. Mice were intraperitoneally administered a hepatotoxic dose of APAP (300 mg/kg). Thirty minutes after APAP administration, mice were treated with different concentrations of stachydrine (0, 2.5, 5, and 10 mg/kg). Animals were sacrificed 16 h after APAP injection for serum and liver tissue assays. APAP overdose significantly elevated the serum alanine transferase levels, hepatic pro-inflammatory cytokines, malondialdehyde activity, phospho-extracellular signal-regulated kinase (ERK), phospho-protein kinase B (AKT), and macrophage-stimulating protein expression. Stachydrine treatment significantly decreased these parameters in mice with APAP-induced liver damage. Our results suggest that stachydrine may be a promising beneficial target in the prevention of APAP-induced liver damage through attenuation of the inflammatory response, inhibition of the ERK and AKT pathways, and expression of macrophage-stimulating proteins.
AB - Stachydrine, a prominent bioactive alkaloid derived from Leonurus heterophyllus, is a significant herb in traditional medicine. It has been noted for its anti-inflammatory and antioxidant characteristics. Consequently, we conducted a study of its hepatoprotective effect and the fundamental mechanisms involved in acetaminophen (APAP)-induced liver injury, utilizing a mouse model. Mice were intraperitoneally administered a hepatotoxic dose of APAP (300 mg/kg). Thirty minutes after APAP administration, mice were treated with different concentrations of stachydrine (0, 2.5, 5, and 10 mg/kg). Animals were sacrificed 16 h after APAP injection for serum and liver tissue assays. APAP overdose significantly elevated the serum alanine transferase levels, hepatic pro-inflammatory cytokines, malondialdehyde activity, phospho-extracellular signal-regulated kinase (ERK), phospho-protein kinase B (AKT), and macrophage-stimulating protein expression. Stachydrine treatment significantly decreased these parameters in mice with APAP-induced liver damage. Our results suggest that stachydrine may be a promising beneficial target in the prevention of APAP-induced liver damage through attenuation of the inflammatory response, inhibition of the ERK and AKT pathways, and expression of macrophage-stimulating proteins.
KW - acetaminophen
KW - AKT
KW - ERK
KW - inflammation
KW - liver injury
KW - macrophage-stimulating protein
KW - oxidative stress
KW - stachydrine
KW - Acetaminophen/toxicity
KW - Oxidative Stress
KW - Proto-Oncogene Proteins c-akt/drug effects
KW - Signal Transduction
KW - Chemical and Drug Induced Liver Injury/drug therapy
KW - Chemical and Drug Induced Liver Injury, Chronic/drug therapy
KW - Macrophages/metabolism
KW - Extracellular Signal-Regulated MAP Kinases/drug effects
KW - Macrophage Colony-Stimulating Factor/drug effects
KW - Animals
KW - Liver/metabolism
KW - Mice
KW - Proline/analogs & derivatives
UR - https://www.scopus.com/pages/publications/85184714291
U2 - 10.3390/ijms25031484
DO - 10.3390/ijms25031484
M3 - 文章
C2 - 38338766
AN - SCOPUS:85184714291
SN - 1661-6596
VL - 25
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 3
M1 - 1484
ER -