Mitochondrial toxicity and antioxidant activity of a prenylated flavonoid isolated from Dalea elegans

被引:35
作者
Elingold, Igal [1 ]
Isollabella, M. Paula [2 ]
Casanova, Marta B. [1 ]
Celentano, Ana M. [3 ]
Perez, Cristina [4 ]
Cabrera, Jose Luis [5 ]
Diez, Roberto A. [2 ]
Dubin, Marta [1 ]
机构
[1] UBA CONICET, Fac Med, CEFYBP, Buenos Aires, DF, Argentina
[2] UBA, Fac Med, Dept Farmacol, Buenos Aires, DF, Argentina
[3] UBA, Fac Med, Dept Microbiol, Buenos Aires, DF, Argentina
[4] UBA, Fac Odontol, Dept Farmacol, Buenos Aires, DF, Argentina
[5] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Farm, RA-5000 Cordoba, Argentina
关键词
flavonoids; mitochondria; liver; antioxidant; toxicity;
D O I
10.1016/j.cbi.2007.10.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prenylated flavanone 2'-4'-dihidroxy-5'-(1"'-dimethylallyl)-6-prenylpinocembrin) (6PP), isolated from the roots of Dalea elegans, shows antimicrobial activity. The aim of this study was to evaluate mitochondrial toxicity and antioxidant properties of 6PP. Addition of micromolar concentrations of 6PP to rat liver mitochondria, stimulated O-2 uptake in state 4 and inhibited it in state 3 when malate-glutamate was the respiratory substrate, and inhibited O-2 uptake in state 3 when succinate was the substrate. Highest concentration of 6PP also inhibited O-2 uptake in state 4 in the latter case; in both conditions, respiratory control index values were decreased. This flavanone collapsed the mitochondrial membrane potential in a concentration-dependent manner. 6PP also inhibited FOF1-ATPase activity in coupled mitochondria and in submitochondrial particles. In the latter, this compound also inhibited NADH oxidase and succinate dehydrogenase activities. HEp-2 cells were incubated for 24h with 6PP in presence or absence of 0.5% albumin. As measured by reduction of the mitochondrial-related probe MTT, in the albumin-free condition, 6PP was cytotoxic in a concentration-dependent manner; on the other hand, albumin decreased 6PP effect. In addition, in rat liver microsomes 6PP: (1) inhibited the enzymatic lipid peroxidation, (2) exhibited significant scavenging activity, measured by DPPH reduction assay and (3) demonstrated significant antioxidant activity by decreasing the reduction of Mo(VI) to Mo(V). We suggest that 6PP impairs the hepatic energy metabolism by acting as mitochondrial uncoupler and by inhibiting enzymatic activities linked to the respiratory chain. 6PP also exerts both antioxidant and antiradical activities. Due to its cytotoxicity, this molecule, and its future structure developments, can be considered as a potentially promising therapeutic agent, for instance in cancer chemotherapy. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:294 / 305
页数:12
相关论文
共 57 条
[31]  
LEE JJ, 2006, AM J KIDNEY DIS, V48, P81
[32]   Cytochrome P450 2E1 null mice provide novel protection against cisplatin-induced nephrotoxicity and apoptosis [J].
Liu, H ;
Baliga, R .
KIDNEY INTERNATIONAL, 2003, 63 (05) :1687-1696
[33]   Hydrogen bond formation as basis for radical scavenging activity: A structure-activity study of C-methylated dihydrochalcones from Myrica gale and structurally related acetophenones [J].
Mathiesen, L ;
Malterud, KE ;
Sund, RB .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (1-2) :307-311
[34]   Antioxidant and prooxidant actions of prenylated and nonprenylated chalcones and flavanones in vitro [J].
Miranda, CL ;
Stevens, JF ;
Ivanov, V ;
McCall, M ;
Frei, B ;
Deinzer, ML ;
Buhler, DR .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (09) :3876-3884
[36]   Antifolate activity of epigallocatechin gallate against Stenotrophomonas maltophilia [J].
Navarro-Martínez, MD ;
Navarro-Perán, E ;
Cabezas-Herrera, J ;
Ruiz-Gómez, J ;
García-Cánovas, F ;
Rodríguez-López, JN .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (07) :2914-2920
[37]   Requirement for, promotion, or inhibition by alpha-tocopherol of radical-induced initiation of plasma lipoprotein lipid peroxidation [J].
Neuzil, J ;
Thomas, SR ;
Stocker, R .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (1-2) :57-71
[38]   Cationic chalcone antibiotics. Design, synthesis, and mechanism of action [J].
Nielsen, SF ;
Larsen, M ;
Boesen, T ;
Schonning, K ;
Kromann, H .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (07) :2667-2677
[39]   Induction of apoptosis by ginger in HEp-2 cell line is mediated by reactive oxygen species [J].
Padma, Viswanadha Vijaya ;
Christie, Swamidurai Arul Diana ;
Ramkuma, Kunga Mohan .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2007, 100 (05) :302-307
[40]  
PEDERSON TC, 1973, J BIOL CHEM, V248, P7134