, 2009, Nemoto et al., 2000, Campbell and Febbraio, 2001 and Foryst-Ludwig and Kintscher, Lumacaftor cost 2010). It has been observed that certain drugs can precipitate

or exacerbate steatosis and steatohepatitis by accentuating the predisposing factors, including those factors associated with estrogen deficiency (Farrel, 2002 and Mu et al., 2009). The steatotic phenotype of PPARα (peroxisome proliferator-activated receptor)-null mice, for example, is exacerbated by etomoxir, which abolishes lipid oxidation by inhibiting long-chain fatty acid transport into the mitochondria (Djouadi et al., 1998, Farrel, 2002 and Mu et al., 2009). Tamoxifen (TAM), the most well-known SERM, acts as an inhibitor of fatty acid β-oxidation and

oxidative phosphorylation (Berson et al., 1998 and Tuquet et al., 2000) and it has demonstrated to induce steatosis, steatohepatitis and cirrhosis in some women during the treatment of breast cancer (Oien et al., 1999 and Pratt et al., 1995). Raloxifen, on the other hand, is used in the menopausal period, in which there is an increased prevalence of lipid metabolism disturbances check details (Hewit et al., 2004 and Mu et al., 2009). Nevertheless, few studies have been conducted concerning the effects of RLX on lipid metabolism in female animals or humans, particularly during their menopausal period. The purpose of the present work was thus to examine the effects of RLX on fatty acid metabolism in an experimental model of estrogen deficiency in rats. The evaluation of the metabolism of a medium-chain and a long-chain fatty acid can help in the understanding of the mechanisms implicated in the possible metabolic alterations, since there are differences in the enzymatic systems responsible for

the entry of these fatty acids into the liver cells (Guo et al., 2006), the transformation to acyl-CoA (McGarry and Brown, 1997 and Eaton, 2002), the dependence from l-carnitine for the acyl-CoA entry into the mitochondria and in the enzymes that catalize the first steps of mitochondrial find more β-oxidation (McGarry and Brown, 1997). Moreover, both the medium- and long-chain fatty acids are also oxidized in the peroxisomes (Grum et al., 1994, Mannaerts et al., 1979, Piot et al., 1998 and Reddy and Mannaerts, 1994). For these reasons, in this work the oxidation of octanoate (medium-chain fatty acid) and palmitate (long-chain fatty acid) was assessed in the perfused livers and in isolated mitochondria and peroxisomes from ovariectomized (OVX) rats. The capacity of raloxifene in the induction of the peroxidase-dependent catalytic oxidation of H2O2 was also measured.