EFFECT OF FLUOXETINE ON RAT-LIVER MITOCHONDRIA

被引:80
作者
SOUZA, HEJ [1 ]
POLIZELLO, ACM [1 ]
UYEMURA, SA [1 ]
CASTROSILVA, O [1 ]
CURTI, C [1 ]
机构
[1] UNIV SAO PAULO,FAC CIENCIAS FARMACEUT,DEPT QUIM & FIS,BR-14040 RIBEIRAO PRET,SP,BRAZIL
关键词
ANTIDEPRESSANTS; FLUOXETINE; NORFLUOXETINE; MITOCHONDRIA; F0F1-ATPASE; RAT LIVER;
D O I
10.1016/0006-2952(94)90283-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The in vitro and in vivo effects of fluoxetine (and its active metabolite norfluoxetine) on mitochondrial respiration and F0F1-ATPase were studied, respectively, in mitochondria and submitochondrial particles isolated from rat liver. Fluoxetine in vitro inhibited state 3 mitochondrial respiration for alpha-ketoglutarate and succinate oxidations (50% of effect at 0.25 and 0.35 mM drug concentrations, respectively); stimulated state 4 for succinate; and induced a decrease in the respiratory control ratio (RCR) for both oxidizable substrates. The F0F1-ATPase activity was determined at various pH levels in the absence and presence of Triton X-100. The solubilized form was not affected markedly, but an inhibition, apparently non-competitive, was observed for the membrane-bound enzyme, with 50% of the effect at a 0.06 mM drug concentration in pH 7.4. These results suggest that fluoxetine in vitro acts on F0F1-ATPase through direct interaction with the membrane F-0 component (similar to oligomycin), or first with mitochondrial membrane and then affecting F-0. A very similar behavior concerning the respiratory parameters and F0F1-ATPase properties was observed with norfluoxetine. The in vivo studies with fluoxetine showed stimulation of mitochondrial respiration in state 4 for alpha-ketoglutarate or succinate oxidations in acute or prolonged treatments (1 hr after a single i.p. dose of 20 mg of drug/kg of body weight, and 22 hr after 12 days of treatment with a daily dose of 10 mg/kg of body weight, respectively), indicating uncoupling of oxidative phosphorylation. Pronounced changes were not observed in the K-0.5 values of F0F1-ATPase catalytic sites, but the V-max decreased during the prolonged treatment. The results show that fluoxetine (as well as norfluoxetine) has multiple effects on the energy metabolism of rat liver mitochondria, being potentially toxic in high doses. The drug effects seem to be a consequence of the drug and/or metabolite solubilization in the inner membrane of the mitochondria.
引用
收藏
页码:535 / 541
页数:7
相关论文
共 31 条
[1]  
[Anonymous], 2018, GOODMAN GILLMAN PHAR
[2]   EFFECT OF ANTI-DEPRESSANT AND NEUROLEPTIC DRUGS ON RESPIRATORY-FUNCTION OF RAT-HEART MITOCHONDRIA [J].
BACHMANN, E ;
ZBINDEN, G .
BIOCHEMICAL PHARMACOLOGY, 1979, 28 (24) :3519-3524
[3]   THE KINETIC AND STRUCTURAL-CHANGES OF THE MITOCHONDRIAL F1 -ATPASE WITH TEMPERATURE [J].
BARACCA, A ;
CURATOLA, G ;
CASTELLI, GP ;
SOLAINI, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 136 (03) :891-898
[4]   FLUOXETINE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES, AND THERAPEUTIC EFFICACY IN DEPRESSIVE-ILLNESS [J].
BENFIELD, P ;
HEEL, RC ;
LEWIS, SP .
DRUGS, 1986, 32 (06) :481-508
[5]  
BERTOLI E, 1973, BIOENERGETICS, V4, P591
[6]   A POSSIBLE ASSOCIATION BETWEEN FLUOXETINE USE AND SUICIDE [J].
BOST, RO ;
KEMP, PM .
JOURNAL OF ANALYTICAL TOXICOLOGY, 1992, 16 (02) :142-145
[7]   ACTION OF CHLORPROMAZINE AND IMIPRAMINE ON RAT-BRAIN MITOCHONDRIA [J].
BYCZKOWSKI, JZ ;
BORYSEWICZ, R .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1979, 10 (05) :369-372
[8]   INFLUENCE OF DOSE AND ROUTE OF ADMINISTRATION ON THE KINETICS OF FLUOXETINE AND ITS METABOLITE NORFLUOXETINE IN THE RAT [J].
CACCIA, S ;
CAPPI, M ;
FRACASSO, C ;
GARATTINI, S .
PSYCHOPHARMACOLOGY, 1990, 100 (04) :509-514
[9]   ANORECTIC ACTIVITY OF FLUOXETINE AND NORFLUOXETINE IN RATS - RELATIONSHIP BETWEEN BRAIN CONCENTRATIONS AND INVITRO POTENCIES ON MONOAMINERGIC MECHANISMS [J].
CACCIA, S ;
BIZZI, A ;
COLTRO, G ;
FRACASSO, C ;
FRITTOLI, E ;
MENNINI, T ;
GARATTINI, S .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1992, 44 (03) :250-254
[10]  
CHANCE B, 1955, J BIOL CHEM, V217, P409