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Biological Research

versión impresa ISSN 0716-9760

Biol. Res. vol.46 no.2 Santiago  2013

http://dx.doi.org/10.4067/S0716-97602013000200011 

 

REVIEW ARTICLE

 

Protective effects of lycopene on oxidative stress, proliferation and autophagy in iron supplementation rats

 

Chongbin Liu *, Rui Wang, Bo Zhang, Chen Hu and Hong Zhang

Department of Physiology, Basic Medical Science Building, Huzhou Normal College, 313000, Huzhou, People's Republic of China


ABSTRACT

Lycopene is common in diet and known for its antioxidant activities. However, the impact of lycopene on iron metabolism is poorly investigated. In this study, we hypothesize that lycopene can prevent iron-mediated oxidative stress, proliferation and autophagy in liver and use a rat model of nutritional iron supplementation to confirm its intervention in these defence mechanisms. We found that iron supplementation induced cell proliferation predominantly in non parenchymal cells compared with hepatocytes, but not apoptosis. In addition, iron was accumulated within the hepatic lysosomes where it triggered autophagy as evidenced by the formation of autophagic vesicles detected by LC3-B staining. Iron supplementation also induced morphologic alterations of the mitochondrial membranes probably due to increased lipid peroxidation as indicated by elevated iron and malondialdehyde concentrations in serum and tissues. Lycopene reduced iron-catalyzed lipid peroxidation by decreasing the malondialdehyde level in the liver and colon and enhancing the total superoxide dismutase activities in serum and tissues. The result suggest that lycopene prevents iron-induced oxidative stress, proliferation and autophagy at both biochemical and histological levels due to its potent free radical scavenging and antioxidant properties.

Key Terms: Autophagy, iron supplementation, lycopene, oxidative stress, proliferation


 

INTRODUCTION

Iron is an essential element for microbes, plants and higher animals. It is a component of heme and iron-sulphur centers in many key redox enzymes, and is an essential component of oxygen storage and transporting proteins such as haemoglobin and myoglobin (Andrews, 1999). It is also an integral part of several classes of enzymes involved in the synthesis of steroid hormones, detoxification of foreign substances in the liver, synthesis of neurotransmitters and DNA synthesis and breakdown (Garrick, 2011). In all species, the concentration of iron in biological fluids is tightly regulated to provide iron as needed and to avoid toxicity, because iron excess can lead to the generation of reactive oxygen species (ROS) by catalyzing the Fenton reaction and highly generates reactive hydroxyl radicals, which can damage the lipid membranes, proteins and nucleic acids (Eaton and Qian, 2002; Gao et al, 2009). Iron overload caused by frequent blood transfusions, high red meat consumption, and intake of iron supplements or caused by the genetic disorder hereditary hemochromatosis can promote troubles in many organs, mainly in the liver, which is the major location for iron storage (Andrews and Schmidt, 2007; Nahdi et al., 2010). Hepatic iron deposits and changes induced by this metal could be detected by electron microscopy based on the electron-dense iron content (Iancu, 2011). Hepatocyte alterations are promoted by different mechanisms: apoptosis, autophagy and necrosis (Galluzzi et al., 2007). Some studies also argued that, in situation of iron overload when ferritin may be iron-saturated, lysosomal destabilization is thought to be an adaptive response to provide the supply of energy needed for cell survival and repair induced by environmental stress (Garner et al., 1997; Kurz et al., 2007). In these last decades, there was growing interest in the association of specific components of human nutrition and oxidative stress (Morihara et al., 2006; Dairam et al., 2008). Lycopene, a carotenoid compound, occurring naturally in tomato and other fruits like papaya, pink guava and watermelon has been shown to neutralize free radicals, especially those derived from oxygen, thereby conferring protection against cancer of the prostate, breast, lung, bladder, cervix and skin, atherosclerosis and associated coronary artery disease (Sharma and Goswami, 2011). Dietary intakes of cooked tomatoes and their by-products account for 90% of the lycopene in the average Southern and North American diet (Bose and Agrawal, 2007; Garciaalonso et al., 2007). However, the impact of lycopene, known for its anti-cell-proliferative, anticarcinogenic and antiatherogenic activities, on iron metabolism has been poorly understood.

In the present work, we hypothesized that lycopene could prevent iron-induced oxidative damage. We investigated the effects of chronic administration of different doses of lycopene on systemic iron status in rats fed with a normal or iron supplementation diet. Our aim was to determine whether iron supplementation associated with lycopene consumption promoted liver protection of rats. At the same time, our study was designed to evaluate the degree of damage induced by iron and determine the early defence mechanisms developed by hepatocytes with special attention to proliferation, apoptosis and autophagy, and to determine if the antioxidant effect of lycopene can be observed at the ultrastructure level and participate in these defence mechanisms.

METHODS

Chemicals

Serum iron, total iron-binding capacity (TIBC), malondialdehyde (MDA) contents and the total superoxide dismutase (T-SOD) activities in tissues were quantified using commercial kit (Jiancheng Biological Engineering Company, Nanjing, China). Lycopene was purchased from Sigma (St. Louis, USA). The mouse Ki-67 monoclonal antibody (a cellular marker for proliferation), the mouse caspase-3 monoclonal antibody (a member of the apoptosis) and rabbit microtubule-associated protein (LC3-B) polyclonal antibody were used (Biyuntian Biological Engineering Company, Shanghai, China). They were also processed for immunohistochemical analysis and electron microscopy. Other chemicals used in the present study were of analytical grade and were purchased from Sigma (St. Louis, USA).

Animals and diets

Thirty-six adult male Wistar rats (220 - 245 g) were procured from the Central Animal House of the College (Wenzhou, China). The animals were housed in stainless steel cages, and maintained in a controlled environment under hygienic conditions of temperature (25 ± 2 °C), relative humidity of 40%, and light (12-hour light/dark cycle, lights on 0700-1900). The rats were allowed to acclimatize in the animal facility for a period of 1 week before the beginning of the study. During that period of time, they had free access to standard animal diet and water ad libitum. All the procedures were performed in accordance with ethical guidelines on the care and use of animals in laboratory research which were approved by the Institutional Animal Ethics Committee (IAEC). The diet used during the experiment was prepared by thoroughly mixing the ingredients and chemical compounds (Table I) to obtain a homogeneous paste that was dried at 45 °C, sliced and stored at 4 °C for a short time. The basal diet contained 50 mg/kg diet as ferrous sulfate (FeSO4-7H2O). This iron supply corresponds to the recommended supply in growing rats and is slightly lower than the recommended supplies in humans (Nahdi et al., 2010). For the iron-treated group, this diet was supplemented with 1000 mg/kg diet. According to the rat's body weight, animals were intragastric administered lycopene dissolved in corn oil or 0.9% saline solution for 6 weeks (Kaur et al., 2011).

TABLE I

Ingredient composition of the basal diet fed to rats during the experimental period

a Vitamin mixture (unit/kg of mixture): synthetic vitamin A concentrate = 250,000 UI; cholecalciferol = 50,000 UI; -tocopherolacetate = 0.100 g; thiamin hydrochloride = 0.100 g; riboflavin sodium phosphate = 0.075 g; pyridoxine hydrochloride = 0.100 g; ascorbic acid = 2.500 g; nicotinamide = 0.500 g; dexpanthenol =0.200 g.

b Mineral mixture (g/100 g mineral salt): MgSO4-7H2O = 73.82; ZnSO4-7H2O = 19.66; MnSO4-H2O = 4.22; CuSO4-5H2O = 0.73; KIO3 = 0.06; Na2SeO3 = 0.9

Experimental protocol

Rats were weighed and randomly allocated into six groups of six individuals: control group (received the basal diet and was fed distilled water by gavage at nine every day), iron group (received the basal diet supplemented with ferrous sulfate 1000 mg/kg diet and was fed distilled water by gavage at nine every day), lycopene group (received the basal diet and was given lycopene dissolved in corn oil by gavage at nine every day, at a dose of 15 mg/kg body weight), iron + lycopene groups (received the basal diet supplemented with ferrous sulfate 1000 mg/kg diet and was given lycopene dissolved in corn oil by gavage at nine every day, at doses of 20, 15 and 10 mg/kg body weight respectively). The rats received a fixed amount of food every day, and the remaining food was weighed to calculated the daily food intake per group. Sacrifice of all the group's rats was done 6 weeks after the beginning of the treatments. The rats were weighed, anesthetized by 10% chloral hydrate (intraabdominally), and killed. Blood was immediately collected and centrifuged at 3000 χ g for 15 min. Serum was stored frozen at -20 °C until use. The liver, heart, spleen, colon and kidney were dissected out, weighed and sectioned, and then tissue fragments were kept at -80 °C. The liver fragments were fixed in 4% polyoxymethylene followed by routine paraffin embedding and stained with hematoxylin-eosin for routine evaluation. They were also processed for immunohistochemical analysis and electron microscopy.

Evaluation of iron status

Serum iron concentrations and total iron-binding capacity (TIBC) were quantified using commercial kit, according to manufacture's instructions. The tissue iron contents were determined by acid digestion of tissue samples as described previously (Lyoumi et al., 2007; Nahdi, 2010), followed by iron quantification using a commercial kit, according to manufacture's instructions.

Markers of oxidative stress

Tissue homogenate (10% W/V) was prepared in 50 mM phosphate-buffered saline (PBS) using potter-Elvehjemtype glass homogenizer. The homogenate was centrifuged at 2000 x g for 15 min at 4 °C. The content of malondialdehyde (MDA) was determined using a commercial kit. Briefly, the amount of MDA was measured by the reaction with thiobarbituric acid at 532 nm. The results were expressed as nmoles MDA/ mg protein using molar extinction coefficient of MDA-thiobarbituric acid chromophore. Protein concentration in supernatants was measured using Bradford method (Bradford, 1976; Nahdi et al., 2010). The total superoxide dismutase (T-SOD) activity in tissues was also quantified using a commercial kit according to the manufacture's instructions. Briefly, the reaction was initiated by the addition of hydroxylamine hydrochloride to the reaction mixture containing nitrobluetetrazolium (NBT) and post mitochondrial supernatant (PMS). The enzyme activity was measured at 560 nm and expressed as units/mg protein, where one unit of enzyme was defined as the amount of enzyme inhibiting the rate of a reaction by 50%.

Histology and immunohistochemistry

Paraffin sections at 4 μm were stained with Perls' Prussian Blue method for iron visualization. In the immunohistochemistry analysis, paraffin sections were incubated for 20 min in an autoclave at 95 °C in citric buffer (0.01 M, pH 6.0) and left to cool for 20 min at room temperature. The slices were washed with phosphate-buffered saline (PBS) (0.01 M, pH 7.4) before incubating in 0.6% H2O2 for 20 min to quench the endogenous peroxidase activity. Then, the slices were incubated overnight at 4 °C with the mouse anti-active caspase-3 monoclonal antibody (1:50), the mouse anti-Ki-67 monoclonal antibody (1:100) or the rabbit LC3-B polyclonal antibody (1:200) according to the manufacturer's recommendations. The slices were then washed three times with PBS for 10 min. Biotinylated goat anti-mouse secondary antibody was used at a dilution of 1:200 in 60 min incubation at 37 °C. The antigen-antibody complexes were stained with diaminobenzidine (DAB) as chromogen, which generated a brown colour. Sections were counterstained with hematoxylin for 5 min and mounted in a mounting medium (Dako). Negative controls were run in parallel by replacing the primary antibody with non-immune immunoglobulins. Sections were observed using an Olympus DP70 microscope with DP-controller set to the same parameters. The number of caspase-3 and Ki-67 positive cells was counted in 100 fields per group of rats, in order to detect apoptotic and proliferative cells respectively. The results were expressed as number of labelled cells/mm2. LC3-B immunostaining was performed for detection of autophagy in hepatocytes.

Electron microscopy

Liver sections were fixed in 2.5% glutaraldehyde in cacodylate buffer (0.1 M, pH 7.4), postfixed in a 1% osmium tetroxide solution, and embedded in Epon 812 resin. Ultra-thin sections were observed on a H-7500 transmission electron microscope (Hitachi in Japan) after lead citrate and uranyl acetate contrast. Some ultra-thin sections were not contrasted in order to visualize iron deposits in tissue.

Statistical analysis

Results were expressed as the mean ± SD of six animals per group. Statistical analysis were performed using SPSS 16.0 for Windows (SPSS, Chicago, USA). Statistical differences were calculated using a one-way analysis of variance (ANOVA), followed by LSD's post hoc test. Statistical significance was defined as a P value of less than 0.05.

RESULTS

Effect of lycopene and /or iron supplementation on body weight and food intake

At the end of the 6 weeks treatment, the body weights of all rats were increased. There was no significant difference in body weight in the iron supplementation, lycopene and iron supplementation + lycopene groups versus the control rats despite the elevated food intake (P < 0.05) of treated animals compared with the controls. However, in the last 2 weeks, the weight gain of the iron supplementation group increased but less (P < 0.05) than that of the combined group (iron supplementation + mean lycopene). Indeed, food intake was higher (P < 0.05) in the iron supplementation + mean lycopene treated rats than in the iron supplementation rats (Table II).

Effect of lycopene administration on serum and tissues iron concentrations

At the end of the 6 weeks treatment, iron supplementation induced a significant increase in iron concentrations in serum, heart, colon (P < 0.01), as well as in the liver, spleen in iron treated group (P < 0.05) compared with the control group. Iron supplementation had no effect on the kidney iron concentration (Table III). Iron supplementation also induced a significant decrease in serum TIBC (P < 0.01) compared with the control group. Lycopene alone did not modify the iron indices except in the liver where a significant decrease (P < 0.01) was noticed compared with the control group. Compared with the iron treatment, there was a significant decrease in iron concentration in serum in the iron + lycopene rats (P < 0.01), as well as in the spleen (P < 0.01) and colon (P < 0.05) in the iron + high lycopene rat. Accompanying this finding, a significant increase (P < 0.01) was noticed in serum TIBC in the iron + high lycopene and the iron + mean lycopene rats (Table U ). Compared with the lycopene alone group, there was a significant increase in iron concentration in serum in the iron + mean lycopene and the iron + low lycopene rats (P < 0.01), as well as in liver in the iron + high lycopene and the iron + mean lycopene rats and the colon in the iron + high lycopene rat (P < 0.05), but a significant decrease in serum TIBC in the iron + low lycopene rat (P < 0.01) and the iron + mean lycopene rat (P < 0.05) (Table III).

Effect of lycopene administration on markers of oxidative stress

In this study, MDA and T-SOD were used as markers of oxidative damage mediated by iron supplementation. We found that MDA concentration was enhanced by iron supplementation in the liver, heart (P < 0.05), as well as in the colon (P < 0.01). However, lycopene administration to the iron-treated animals for 6 weeks significantly decreased the MDA concentration in the liver, heart in the iron + high lycopene rat, colon in the iron + high lycopene and the iron + low lycopene rats (P < 0.05), as well as in kidney in the iron + high lycopene rat (P < 0.01) and moderately in the spleen when compared with iron supplementation animals. Compared with the lycopene alone group, there was a significant increase of the MDA concentration in the liver and colon (P < 0.05) in the iron + lycopene groups (Figure 1A-F). Along with this, there was a significant increase in T-SOD activity in the serum (P < 0.01) and the liver (P < 0.05) by iron supplementation compared with the control group. However, in the heart and colon, antioxidant T-SOD activity decreased (P < 0.01) in iron treatment group. Accompanying this finding, a significant decrease was noticed in T-SOD activities in serum in the iron + lycopene groups (P < 0.05), but a significant increase (P < 0.05) in heart in the iron + high lycopene group and in colon (P < 0.01) in the iron + lycopene groups compared with iron supplementation group. In the kidney, only the iron + high lycepone and the iron + mean lycopene groups enhanced the activity of T-SOD (P < 0.05). Lycopene alone increased the kidney and the spleen T-SOD activities moderately but not significantly compared with the control group (Figure 2A-F).

Effect of lycopene administration on hepatic structure, cell proliferation and apoptosis

Hematoxylin-eosin stained sections showed no morphological changes. However, Perls' reaction sections showed large amount of iron accumulated in the liver of iron supplementation rats (Figure 3B) compared with the control group (Figure 3A), whereas lycopene treatment reduced the iron staining to a comparable level as in the control or lycopene only groups (Figure 3C, D). Immunohistochemistry analysis showed the number of caspase-3 labelled cells were not changed by the different treatments (Figure 4). In contrast, iron supplementation significantly increased (P < 0.05) the number of proliferating hepatocytes and non parenchymal cells (P < 0.05) compared with the control group (Figure 5). Interestingly, positive cells were predominantly non parenchymal ones. Consumption of both lycopene and iron increased proliferation in hepatocytes (P < 0.05) and non parenchymal cells (P < 0.05) compared with the control group, but decreased it (P < 0.05) in the non parenchymal cells compared with iron intake alone. Lycopene alone had no effect on the number of Ki-67-positive cells (Figure 5).

Figure 3 The Perls' reaction and iron accumulation in animals

A. Control group; B. Iron group; C. Lycopene group; D. Iron + mean lycopene group

Ultrastructural alterations and autophagy in liver

The liver of the control (Figure 6A-B) and lycopene alone treated rats showed few distributed cytoplasmic electron-dense particles, typically corresponding to ferritin with more lipid droplets in the lycopene group (Figure 6C). The liver of iron supplementation rats showed large electron-dense bodies localized in the lumen and near the bile canaliculi (BC) forming membrane-encapsulated clusters (Figure 6D) similar to the lysosomes observed in severe conditions of iron overload (Figure 6E) (Gutierrez et al, 2009; Iancu, 1992). The liver of iron supplementation rats also showed the presence of autophagic vacuoles with different shapes and stages containing iron-rich ferritin molecules (Figure 6F). Ultrastructural changes were found in the liver of iron supplementation rats, including mitochondria (M) swelling (Figure 6G), rough endoplasmic reticulum (RER) expanding (Figure 6H). However, in the iron + mean lycopene group, there were more lipid droplets than in the iron supplementation group, and the integrity of the mitochondria membranes was preserved, but microvillus of bile canaliculus reduced (Figure 6I). In addition, iron was accumulated within the hepatic lysosomes where it triggered autophagy as evidenced by the formation of autophagic vesicles detected by LC3-B staining. In agreement with the above detection of autophagosomes by electron microscopy, we observed the characteristic punctuate vesicular staining of LC3-B following iron treatment localized mainly around the portal spaces (Figure 7B). The staining was attenuated in the iron supplementation + mean lycopene group (Figure 7D), and absent in the control and lycopene groups (Figure 7A, C).

Figure 7 Detection of autophagy in the liver of rats

A. Control group; B. Iron group; C. Lycopene group; D. Iron + mean lycopene group. Representative LC3-B immunohistochemistry for the detection of autophagy in the liver of the control and treated groups showed punctuated vesicular staining following iron treatment mainly localized around the portal spaces. (*portal vein branch). The staining was attenuated in the iron + mean lycopene group and absent in the control and lycopene group, but punctuated vesicular staining of LC3-B in the iron supplementation rats.

DISCUSSION

This study focused on the effect of lycopene on protection against oxidative damages mediated by nutritional iron supplementation. We also investigated the effect of iron supplementation on apoptosis, proliferation and autophagy in the liver and the capacity of lycopene to reduce these effects at histological and ultrastructural levels. We found that the presence of lycopene in diet offered a protection against lipid peroxidation mediated by iron supplementation. The iron-supplemented liver presented morphological changes associated with proliferation and autophagy but no apoptosis, damages prevented by lycopene pre-treatment.

Dietary intakes of tomatoes and tomato products containing lycopene have been shown to be associated with decreased risk of chronic diseases such as cancer and cardiovascular diseases in several recent studies (Huang and Hu, 2011; Sharma and Goswami, 2011). In this study, we noted the increase in food ingestion observed in rats with lycopene supplementation. The improvement of dietary intake may be due to the fact that lycopene gives the food a special flavour which can increase dietary consumption. Iron excess resulted in an increased oxidative damage in the liver and thus causing mitochondrial membrane alterations. Lipid peroxidation occurred as shown by MDA increase and could thereby change the fluidity of the inner mitochondrial membrane and subsequent mitochondrial swelling, in agreement with previous results (Reifen et al., 2004; Lafay et al., 2005). Such a damage affected especially the liver because it is the major recipient for excessive iron and might indicate a process of iron removal from the liver. Lipid peroxidation also affected the colon, heart, and spleen because these organs accumulated this metal and the colon participated in iron absorption. A recent study showed that the colon iron absorption represented approximately 14% of the duodenal absorption and that caecal and proximal colon mucosa accumulated iron to a much lower extent than the duodenal mucosa (Blachier et al., 2007). There was no accumulation of iron in kidney suggesting that the kidney might be an efficient way of eliminating excess iron. A recent study demonstrated that the ability to express transferrin receptor-1 (TfR1), divalent metal transporter-1 (DMT 1), ferroportin-1 (FPN 1), iron regulatory protein (IRP), hepcidin (Hepc) and other iron metabolism proteins (Veuthey et al., 2008). However, our study also showed that lycopene treatment diminished the electron-dense ferritin storage and protected the mitochondrial membranes. This was confirmed by decreased MDA in the liver and other organs.

An increased serum iron with decreased TIBC in iron group was shown here. When plasma iron concentration exceeds the iron-binding capacity of transferrin, iron accumulates in the body as non-transferrin bound iron and prone to the formation of reactive oxygen species (ROS) and causes cell damages (Papanikolaou and Pantopoulos, 2005; Ghorbel et al., 2011). However, lycopene treatment in the combined group prevented iron-damages by decreasing the level of serum iron and increasing the iron-binding capacity. A previous study showed that garlic alone diminished DMT1 mRNA expression, which decreased the intestinal iron absorption and therefore lowered the iron concentration in the tissues (Nahdi et al., 2010).

Compared with iron supplementation rats, we also found lycopene-treated groups T-SOD activities were enhanced in the heart, colon and kidney, giving evidence of the role of lycopene in scavenging hydroxyl radicals and activating an antioxidant defence enzyme. Interestingly, iron supplementation rats  increased hepatic T-SOD activity but decreased it in the colon kidney has the and heart may be T-SOD behaves towards oxidative stress  in two different manners. If stress is sustained and produces  massive toxic ROS as shown by the important elevation of the colonic iron concentration, the enzyme will be destroyed and  its concentration will decrese (Mena et al., 1991).

The potential of iron damage is particularly high in liver, the primary organ for storage of excess iron. In this  study, we found that hepatic iron deposits in rats with iron supplementation compared with the control rats.  Immunohistochemical study in the liver showed that iron supplementation did not induce apoptosis but induced proliferation in hepatocytes and non parenchymal cells with a predominance in non parenchymal cells, suggesting an imbalance between these two processes. Caspase-3 may function as the primary executioner in the initiation of apoptosis, and active caspase-3 may promote apoptosis by degrading key structural and regulatory proteins within the cell. In the combined group, the proliferation rate was intermediate between the control and iron groups suggesting that lycopene reduced the iron mediated proliferation by lowering the iron storage in the liver. Many studies in the liver have demonstrated that chronic iron overload was accompanied by cell proliferation and that it was due to the elevation of both cyclin D1 protein and mRNA levels (Brown et al., 2006; Furutani et al., 2006). Excessive ROS production can lead to oxidation of macromolecules and has been implicated in mtDNA mutations, ageing, and cell death. Mitochondria-generated ROS play an important role in the release of cytochrome c and other proapoptotic proteins, which can trigger caspase activation and apoptosis. Other studies reported that Fe-NTA could lead to oxidative stress and apoptosis in hepatocyte cultures (Walter et al., 2002; Rauen et al., 2004).

Our results showed that ferritin deposits in the liver of iron supplementation rats were dispersed in the cytoplasm of cells or localized in lysosomes mainly near the bile canaliculi, in agreement with previous results (Gutierrez et al., 2009). We also demonstrated that iron supplementation was accompanied by activation of autophagy, an adaptive mechanism to cell damages. However, iron + lycopene groups diminished the electron-dense ferritin storage, protected the mitochondrial membranes and reduced punctuated LC3-B staining compared with iron group. The autophagic vesicles were barely detectable in control, lycopene treated and iron + lycopene treated groups. Autophagy is a housekeeping process that ensures the turnover of damaged protein aggregates and organelles to maintain cell homeostasis (Xie and Klionsky, 2007). Lysosomes are central in autophagy as they fuse with autophagosomes to form autophagolysosomes where a variety of organelles and proteins are degraded via their acid hydrolases. Therefore, the lysosomal membrane peroxidation takes place and lysosomes become leaky after a delay that is dependent on the magnitude of oxidative stress.

This is followed by reparative autophagy which is an early defence mechanism of the cell (Antunes et al., 2001). Our study demonstrated an unexpected early upregulation of autophagy and proliferation in response to iron supplementation. Autophagy can provide an early adaptive mechanism avoiding apoptosis. Lycopene significantly prevented iron-mediated oxidative stress in the liver and colon and iron-induced mitochondrial alteration and autophagy in the liver due to its potent free radical scavenging and antioxidant properties.

ACKNOWLEDGMENT

The authors thank all reviewers and Prof. P.H. Backx (University of Toronto, Canada) and Prof. Z.M. Qian (The Hong Kong Polytechnic University, China) for critical reading. We are grateful to the Zhejiang Province Natural Sciences Foundation (Y2110388) and Zhejiang Province Technological Research (Y2011C37091) for financial support.

 

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List of abbreviations: BC, bile canaliculus; DAB, diaminobenzidine; DMT1, divalent metal transporter 1; LYS, lysosomes; M, mitochondria; MDA, malondialdehyde; NBT, nitrobluetetrazolium; PBS, phosphate-buffered saline; PMS, post mitochondrial supernatant; RER, rough endoplasmic reticulum; ROS, reactive oxygen species; TIBC, total iron-binding capacity; T-SOD, total superoxide dismutase.

*Correspondence: Chongbin Liu: liuchongbin1972@126.com. Tel: +86-572-2321201; Fax: +86-572-2321203. E-mail addresses for all authors: C.B. Liu, liuchongbin1972@126.com; R. Wang, wangrui1593@163.com; B. Zhang, zhangbo88@hutc.zj.cn; C. Hu, chenillehu@163.com; H. Zhang, zhanghong@hutc.zj.cn

Received: January 14, 2013. In Revised form: May 6, 2013. Accepted: May 7, 2013

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