Estres Oxidativo y Diferencia Sexual en el Higado de Ratas Expuestas a Ciclohexanona.
Cyclohexanone is an oily liquid that is mainly used in industrial chemical production for the organic synthesis of adipic acid, caprolactam, polyvinyl chloride and its copolymers, and methacrylate ester polymers (OECD, 1996). In 2014, 256,931 tons were manufactured in Korea, exposing 8,399 workers (KOSHA, 2014). Also, Europe manufactures or imports over 1,000,000 tons of it per year (ECHA, 2017). The current permissible exposure limit for Cyclohexanone established by the Occupational Safety and Health Administration is a concentration of 25 ppm over an eight hour time-weighted average (TWA) (OECD).
Inhalation exposure leads to central nervous system depression, the irritation to respiratory system, the eye and skin in human (New Jersey Department of Health, 2009). In addition, liver and kidney damage has been reported in humans as well as rabbits and monkeys (Cralley 1985; U. S. Department of Health and Human Services, 1988; IARC, 2018).
Oxidative stress results from an imbalance between the production of oxidizing species and antioxidants. Reactive oxygen species (ROS) may be harmful to cells, causing formation of radical products whose accumulation is associated with numerous diseases (Evans & Cooke, 2004). Oxidative stress may be mechanistically related to the toxicity some industrial chemicals. For example, trichloroethylene is used in industry as a general solvent, primarily for degreasing metal parts. It causes oxidative stress in the liver and kidney, which can increase the risk of cancer in laboratory animals and humans (Lock & Reed, 2006; Chen, 2000).
However, oxidative stress effect are rarely reported in cyclohexanone toxicity studies. In this study, we aimed to characterize the oxidative stress in the livers of rats exposed to cyclohexanone with immunohistochemistry.
MATERIAL AND METHOD
Forty specific-pathogen-free (SPF) F344 rats (20 males and 20 females) were divided into control group (0 ppm) and cyclohexanone exposed group (625 ppm) (10 per sex per group). The rats were purchased from Japan SLC Inc. (Shizuoka, Japan).They had free access to a commercial rodent diet (Teklad Global 18 % Protein Rodent Diet, Envigo Co., Huntingdon, UK) and filtered tap water. All rats were individually housed in stainless steel wire mesh cages (W 230 mm [yen] L 1200 mm [yen] H 200 mm). A whole-body exposure chamber (WITC-00-M, HCT Co., Icheon, Korea), with a gas generator (LVg-04-A, HCT Co., Icheon, Korea), was used to expose the rats to cyclohexanone at 0 and 625 ppm for 6 h/day, 5 days/week for 13 weeks. The chamber conditions, including temperature, relative humidity, pressure, and air ventilation, were controlled with an environmental controller (WITC-00-M, HCT Co., Icheon, Korea). The protocols used in the study were reviewed and approved by the Institutional Animal Care and Use Committee (IACUC-1710).
Tissue preparation for light microscopy. At 13 weeks of treatment, rats were euthanized. Livers were surgically removed from each animal during necropsy and fixed immediately in 10 % neutral buffered formalin. Livers were processed routinely, embedded in paraffin, sectioned to 3-4 mm, stained with hematoxylin and eosin, and examined microscopically under low- to high- power fields.
Immunohistochemical staining. Sections were deparaffinized and blocked for endogenous peroxidase activity with 3 % [H.sub.2][O.sub.2] for 10 min, boiled in 0.1 M citric acid buffer for 10 min, and treated with universal blocking reagent (Bio Genex, San Ramon, CA, USA) for 10 min at room temperature to eliminate nonspecific binding. Sections were incubated with 1:100 rabbit polyclonal anti-4-hydroxynonenal (4-HNE) antibody (Abcam, Cambridge, UK) overnight at 4 [degrees]C. Signals were developed with an avidin-biotin horseradish peroxidase complex and diaminobenzidine (DAB) chromogen using the RealTM EnvisonTM Detection system (Dako, Glostrup, Denmark). Sections were counterstained with Mayer's hematoxylin for 30s, dehydrated, covered with coverslip and examined by light microscopy. The intensity of staining was scored from 0 to 5 (0: No staining, 1: <10 %, 2: 10-30 %, 3: 30-50 %, 4: 50-70 %, 5: >70 %).
Statistical Analysis. Immunoreactivity scores were evaluated using SPSS (ver. 19.0, IBM, Chicago, IL, USA). The Mann-Whitney U test was used to assess statistical significance. P values below 0.05 indicated statistical significance.
Histopathology showed an increase of bile duct hyperplasia in the livers of the male was observed in cyclohexanone-exposed group compared to control group (Table I) (Fig. 1). However, abnormal lesions were not observed in the livers of the female control or cyclohexanone-exposed groups.
Immunohistochemistry showed that, in males, 4-HNE was strongly expressed in the cytoplasm of almost every hepatocyte of hepatic lobules of the cyclohexanone-exposed group, while it was expressed mainly in the cytoplasm of hepatocytes around the central vein of hepatic lobules in the control group. In particular, 4-HNE was strongly observed in hepatocytes around bile duct hyperplasia in the cyclohexanone-exposed group compared to the control group. In contrast to males, 4-HNE was weakly expressed in females in the cytoplasm of hepatocytes around central vein of hepatic lobules in the cyclohexanone-exposed group, while it was faintly expressed in the cytoplasm of hepatocytes around central vein of hepatic lobules in the control group (Fig. 2).
With semi-quantitative scoring, 4-HNE expression was significantly stronger in the cyclohexanone-exposed group compared to the control group in both sexes. However, it was significantly stronger in male groups compared to female groups (Fig. 3).
In this study, increased bile duct hyperplasia in the liver was only observed in males in the cyclohexanone-exposed group (Table I). These changes, known as background lesions, are usually found in older animals in rats and mice, but might be induced or exacerbated by the treatment in this study, as indicated by the incidence difference of the lesions between control and cyclohexanone-exposed groups (Thoolen et al., 2010).
Oxidative stress arises from an imbalance in the production neutralization and metabolism of ROS, resulting in the formation of free radicals (Evans & Cooke). Lipid peroxidation results from hydroxyl radical attack on fatty acyl chains of phospholipids and triglycerides (Brand, 2010; Sena & Chandel, 2012). 4-HNE is one of the major end products of lipid peroxidation, and it is associated with pathogenesis in a variety of diseases including Alzheimer's disease, cataract, and cancer (Esterbauer et al., 1991; Uchida, 2003). Several studies have revealed that the carbon-carbon double bond of 4-HNE can react with a variety of cellular components, including DNA and proteins (Uchida & Stadtman, 1992). Also, 4-HNE is a strong electrophile that can change cellular redox state significantly by decreasing cellular sulfhydryl compounds such as glutathione (GSH). Therefore, 4-HNE has been acknowledged as a mediator and inducer of oxidative stress (Awasthi et al., 2004). Also, 4-HNE has demonstrated induction of oxidative stress by immunohistochemistry in tissue obtained from animals treated with ethanol, iron combined with ethanol, or carbon tetrachloride (Tsukamoto et al., 1995; Hartley et al, 1997; Kono et al, 2001). Therefore, 4-HNE is an useful immunohistochemical marker for evaluating oxidative stress.
Immunohistochemistry showed that 4-HNE was more strongly expressed in the cytoplasm of hepatocytes in the cyclohexanone-exposed group than in control group in both sexes. Also, 4-HNE expression in the liver was stronger in the male groups compared to the female groups. This result indicates that the exposure to cyclohexanone caused oxidative stress in hepatocytes of liver and although bile ducts do not express positive signals, increased bile duct hyperplasia can also be caused by oxidative stress because hepatocytes around bile ducts express positive signals to a considerable degree. A previous study linked cyclohexanone treatment to acute liver damage. In rat induced with carbon tetrachloride, enhanced liver damage may have been caused by free radical oxygen that increased with cyclohexanone treatment (Kim et al., 2002), which supports our results. Differences between sexes in 4-HNE expression in the liver may be attributed to sexual dimorphism in cytochrome P450 that is associated with the metabolism of xenobiotics (Borras et al., 2003; Cederbaum, 2015).
In conclusion, the present study revealed oxidative stress in the livers of rats exposed to cyclohexanone, with different results observed based on sex. This provides useful information on the toxic mechanism of cyclohexanone.
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Dr. Yong-Hoon Lee
Inhalation Toxicity Research Center
Chemical Research Bureau
Occupational Safety and Health Research Institute
Korea Occupational Safety and Health Agency
339-30 Expo-ro, Yuseong-gu
REPUBLIC OF KOREA
Yong-Hoon Lee, Cheol-Hong Lim & Yong Hyun Chung
Inhalation Toxicity Research Center, Chemical Research Bureau, Occupational Safety and Health Research Institute, Korea Occupational Safety and Health Agency, Daejeon 305-380, Republic of Korea.
This work was supported by the Korea Occupational Safety and Health Agency, Ministry of Labor, Republic of Korea, and a Grant-in-Aid for chemical hazard assessment, 2017.
Caption: Fig. 1. Histological findings in livers of male rats exposed to cyclohexanone. A) No abnormal lesions were observed in control group livers, B) Bile duct hyperplasia at portal tract (arrow) was observed in the cyclohexanone-exposed group (625 ppm). Magnification x200.
Caption: Fig. 2. Immunohistochemical detection of 4-HNE expression in livers of control and cyclohexanone-exposed groups. In males, A) immunoreactivity of 4-HNE was observed mainly in the cytoplasm of hepatocytes around central vein of hepatic lobules in the control group (arrow), B) 4-HNE was strongly expressed in the cytoplasm of most hepatocyte of hepatic lobule in the cyclohexanone-exposed group (arrow). 4-HNE expression in hepatocytes near bile duct hyperplasia at the portal tract (arrow head). In females, C) 4-HNE was faintly expressed in the cytoplasm of hepatocytes around central vein of hepatic lobule in the control group (arrow). D) 4-HNE was weakly expressed in the cytoplasm of hepatocyte around central vein of hepatic lobule in the cyclohexanone-exposed group (arrow). Magnification x200.
Caption: Fig. 3. Semiquantitative Score of 4-HNE immunoreactivity in liver Significant differences compared with control group: ** p < 0.01. Significant differences compared with equivalent exposure male rat group : [dagger][dagger] p < 0.01
Table I. Incidence of bile duct hyperplasia in liver. Findings Grade Control Cyclohexanone (0 ppm) (625 ppm) Bile duct Minimal 1/10 2/10 hyperplasia Mild 1/10 2/10 Total 2/10 4/10
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|Author:||Lee, Yong-Hoon; Lim, Cheol-Hong; Hyun Chung, Yong|
|Publication:||International Journal of Morphology|
|Date:||Sep 1, 2018|
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