TY - JOUR
T1 - Boldine prevents human liver microsomal lipid peroxidation and inactivation of cytochrome P4502E1
AU - Kringstein, Peter
AU - Cederbaum, Arthur I.
N1 - Funding Information:
Acknowledgements -- These studiesw ere supportedb y USPHS GrantA A-03312f romThe NationaIln stituteo n Alcohol Abusea nd AlcoholismW. e thankM r. Yan Dai for carryingo ut the Western Blot experimenDt,r . J. M. Lasker,f or providingth eanti-P4502E1 IgG, Dr. H. Speiskyf or the generougsi ft of boldinea, ndMs. Pilar Visco Cenizal for typing the manuscriptP.e terK ringsteinw as a Mount Sinai MedicalS tudenst ummevr olunteer.
PY - 1995/3
Y1 - 1995/3
N2 - Boldine, an alkaloid found in the leaves and bark of boldo, prevented the ferric-ATP catalyzed peroxidation of human liver microsomes. Lipid peroxidation, dependent upon electron transfer from NADPH or NADH, was comparably inhibited by boldine, with a KI value of about 5 μM. Inactivation and decreased content of human cytochrome P4502E1 as a consequence of incubating microsomes with ferric-ATP and reductant was completely prevented by boldine. However, inactivation of cytochrome P4502E1 by CC14 was not prevented by boldine, although the alkaloid prevented CC14-catalyzed lipid peroxidation. This suggests that the CC14 inactivation of P4502E1 may be independent of CC14-mediated lipid peroxidation. In view of its low toxicity, lack of effect on P450 activity, and strong inhibition of peroxidation of human liver microsomes, boldine may be valuable as an antioxidant and hepatoprotective agent.
AB - Boldine, an alkaloid found in the leaves and bark of boldo, prevented the ferric-ATP catalyzed peroxidation of human liver microsomes. Lipid peroxidation, dependent upon electron transfer from NADPH or NADH, was comparably inhibited by boldine, with a KI value of about 5 μM. Inactivation and decreased content of human cytochrome P4502E1 as a consequence of incubating microsomes with ferric-ATP and reductant was completely prevented by boldine. However, inactivation of cytochrome P4502E1 by CC14 was not prevented by boldine, although the alkaloid prevented CC14-catalyzed lipid peroxidation. This suggests that the CC14 inactivation of P4502E1 may be independent of CC14-mediated lipid peroxidation. In view of its low toxicity, lack of effect on P450 activity, and strong inhibition of peroxidation of human liver microsomes, boldine may be valuable as an antioxidant and hepatoprotective agent.
KW - Boldine
KW - CC1
KW - Cytochrome P4502E1
KW - Ferric-ATP
KW - Free radicals
KW - Human liver microsomes
KW - Lipid peroxidation
UR - http://www.scopus.com/inward/record.url?scp=0028968117&partnerID=8YFLogxK
U2 - 10.1016/0891-5849(94)E0138-9
DO - 10.1016/0891-5849(94)E0138-9
M3 - Article
C2 - 9101247
AN - SCOPUS:0028968117
SN - 0891-5849
VL - 18
SP - 559
EP - 563
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
IS - 3
ER -