TY - JOUR
T1 - Nrf2 counteracts cholestatic liver injury via stimulation of hepatic defense systems
AU - Okada, Kosuke
AU - Shoda, Junichi
AU - Taguchi, Keiko
AU - Maher, Jonathan M.
AU - Ishizaki, Kaoru
AU - Inoue, Yoshimi
AU - Ohtsuki, Makio
AU - Goto, Nobuharu
AU - Sugimoto, Hirokazu
AU - Utsunomiy, Hirotoshi
AU - Oda, Koji
AU - Warabi, Eiji
AU - Ishii, Tetsuro
AU - Yamamoto, Masayuki
PY - 2009/11
Y1 - 2009/11
N2 - The transcription factor Nrf2 is a key regulator for hepatic induction of detoxifying enzymes, antioxidative stress genes and Mrp efflux transporters. We aimed to investigate whether Nrf2 activation counteracts liver injury associated with cholestasis. The role of Nrf2 activation in counteracting cholestatic liver injury was studied using a bile duct-ligation (BDL) model of Keap1 gene-knockdown (Keap1-kd) mice that represent the sustained activation of Nrf2 in the liver. Upon Nrf2 activation, Keap1-kd mice showed large increases in Mrp efflux transporters, detoxifying enzymes and antioxidative stress genes in the livers. After BDL, the number of hepatic parenchymal necrosis and the reactive oxygen species content were significantly smaller in the livers of the Keap1-kd mice than in those of the WT mice. Moreover, the increase in serum bilirubin levels was attenuated in the Keap1-kd mice. In conclusion, the results suggest a hepatoprotective role of sustained Nrf2 activation against liver injury associated with cholestasis.
AB - The transcription factor Nrf2 is a key regulator for hepatic induction of detoxifying enzymes, antioxidative stress genes and Mrp efflux transporters. We aimed to investigate whether Nrf2 activation counteracts liver injury associated with cholestasis. The role of Nrf2 activation in counteracting cholestatic liver injury was studied using a bile duct-ligation (BDL) model of Keap1 gene-knockdown (Keap1-kd) mice that represent the sustained activation of Nrf2 in the liver. Upon Nrf2 activation, Keap1-kd mice showed large increases in Mrp efflux transporters, detoxifying enzymes and antioxidative stress genes in the livers. After BDL, the number of hepatic parenchymal necrosis and the reactive oxygen species content were significantly smaller in the livers of the Keap1-kd mice than in those of the WT mice. Moreover, the increase in serum bilirubin levels was attenuated in the Keap1-kd mice. In conclusion, the results suggest a hepatoprotective role of sustained Nrf2 activation against liver injury associated with cholestasis.
KW - Cytoprotection
KW - Keap1 gene-knockdown mouse
KW - Nrf2
KW - Obstructive cholestasis
KW - Oxidative stress
KW - Transcription factor
UR - http://www.scopus.com/inward/record.url?scp=70449713440&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=70449713440&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2009.08.156
DO - 10.1016/j.bbrc.2009.08.156
M3 - Article
C2 - 19732748
AN - SCOPUS:70449713440
SN - 0006-291X
VL - 389
SP - 431
EP - 436
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -