DNA damage by ochratoxin A in rat kidney assessed by the alkaline comet assay

Braz J Med Biol Res, December 2006, Volume 39(12) 1563-1568

DNA damage by ochratoxin A in rat kidney assessed by the alkaline comet assay

D. Želježić, A.-M. Domijan and M. Peraica

Institute for Medical Research and Occupational Health, Zagreb, Croatia

References

^{Correspondence and Footnotes}

Abstract

There are few studies of ochratoxin A (OTA) genotoxicity in experimental animals and the results obtained with cell cultures are inconsistent, although the carcinogenic potential of OTA for the kidney of experimental animals has been well established. We studied the genotoxic potential of OTA in the kidney of adult female Wistar rats (5 in each group) treated intraperitoneally with OTA (0.5 mg kg body weight^-1 day^-1 for 7, 14, and 21 days) measuring DNA mobility on agarose gel stained with ethidium-bromide using standard alkaline single-cell gel electrophoresis (comet assay). Negative control animals were treated with solvent (Tris buffer, 1.0 mg/kg) and positive control animals were treated with methyl methanesulfonate (40 mg/kg) according to the same schedule. OTA concentrations in plasma and kidney homogenates in 7-, 14-, and 21-day treated animals were 4.86 ± 0.53, 7.52 ± 3.32, 7.85 ± 2.24 µg/mL, and 0.87 ± 0.09, 0.99 ± 0.06, 1.09 ± 0.15 µg/g, respectively. In all OTA-treated groups, the tail length, tail intensity, and tail moment in kidney tissue were significantly higher than in controls (P < 0.05). The tail length and tail moment were higher after 14 days than after 7 days of treatment (P < 0.05), and still higher after 21 days (P < 0.05). The highest tail intensity was observed in animals treated for 21 days, and it differed significantly from animals treated for 7 and 14 days (P < 0.05). OTA concentrations in plasma and kidney tissue increased steadily and OTA concentration in kidney tissue strongly correlated with tail intensity and tail moment values. These results confirm the genotoxic potential of OTA, and show that the severity of DNA lesions in kidney correlates with OTA concentration.

Key words: Comet assay, DNA adducts, Experimental animals, Mycotoxin

Introduction

Ochratoxin A (OTA) is a mycotoxin produced by some strains of Penicillium and Aspergillus molds that naturally contaminate food and feed under all climatic conditions (1). Humans are exposed to OTA by ingestion of contaminated food of vegetable or animal origin. OTA has been shown to be nephrotoxic, hepatotoxic, immunotoxic, and teratogenic in laboratory animals. Exposure to OTA is believed to cause endemic nephropathy, a fatal human disease affecting some regions of Bosnia and Herzegovina, Bulgaria, Croatia, Romania, and Serbia (2). In endemic regions, a high incidence of otherwise rare urothelial tumors has also been attributed to exposure to OTA. It was proven that OTA increases the incidence of uncommon tubular cell adenomas and of tubular cell carcinomas in rats of both sexes in a dose-dependent manner and the incidence and multiplicity of fibroadenomas of the mammary gland in female rats (3). The International Agency for Research on Cancer classified OTA as a 2B group compound (possibly carcinogenic to humans and with sufficient evidence for carcinogenicity in laboratory animals), although the mechanism of its carcinogenicity is not understood (4). It is believed that this assumed OTA carcinogenicity should reflect in DNA changes. The genotoxicity of OTA was tested in various cell lines, but the results were inconclusive (4), probably because routine genotoxicity tests were contrasting, equivocal or negative in compounds whose genotoxic activity depended on tissue-specific mechanisms. Furthermore, the genotoxic activity is organ and tissue specific for compounds with distinct targets for carcinogenicity (5). The genotoxicity of OTA in laboratory animals has been postulated mainly on the basis of the results of ³²P-postlabeling experiments, which showed OTA-dependent formation of DNA adduct spots (6,7). The single available report on genotoxicity tested by the comet assay in rat kidneys revealed DNA fragmentation, but animals were treated with a single, very high oral OTA dose (10 mg/kg body weight) (8).

The alkaline single-cell gel electrophoresis (comet) assay is a sensitive and powerful method for determining DNA strand breaks and alkali labile sites (oxidative DNA base damage, and DNA-DNA/DNA-protein cross-linking, DNA adducts) at the cell level and has been widely used for genotoxicity studies. Since the comet assay does not require cell cultivation, the genotoxic potential of a substance of interest can be assessed in the cells of specific target tissue. The aim of the present study was to determine the time course of OTA-produced DNA damage by assessing alkali-labile sites using the comet assay in rat kidney tissue.

Material and Methods

Chemicals

OTA (99% purity), Na₂EDTA, methyl methanesulfonate, and the chemicals needed for the comet assay were purchased from Sigma (St. Louis, MO, USA). Tris (hydroxymethyl) aminomethane and NaCl were from Kemika (Zagreb, Croatia). Water (Merck, Darmstadt, Germany) and methanol (Kemika, Zagreb, Croatia) used for the high-performance liquid chromatography (HPLC) mobile phase were of HPLC grade.

Animal treatment schedule

Adult female Wistar rats weighing 190 g maintained on a 12-h light/dark cycle and at a constant temperature of 24ºC were kept in macrolone cages. Animals were fed a standard diet for laboratory rodents (Pliva, Zagreb, Croatia) and had free access to water. The study was approved by the Ethics Committee of the Institute for Medical Research and Occupational Health, Zagreb, according to current laws of the Republic of Croatia.

The rats were randomly assigned to nine groups of 5 animals each receiving either OTA (0.5 mg/kg body weight) dissolved in Tris buffer or solvent only (1.0 mL/kg, negative control animals) intraperitoneally (ip) every day for up to three weeks. The ip treatment was chosen because it is considered to be a valuable tool for clarifying the mechanism of action of mycotoxins (9). Positive control animals were treated with methyl methanesulfonate (40 mg/kg body weight) according to the same schedule.

Twenty-four hours after the 7th, 14th, and 21st doses, 5 OTA-treated, 5 negative and 5 positive control animals were killed with coal gas. Kidneys were collected, washed in saline, and kept on ice until the comet assay and OTA analysis.

OTA analysis

OTA concentrations in plasma and 10% kidney homogenate (0.9% sterile solution of NaCl) were determined by HPLC according to methods described by Peraica et al. (10) and Bauer et al. (11), respectively.

OTA was determined by HPLC (Varian, Walnut-Creek, CA, USA) with fluorescence detection. The guard column and analytical column were LiChrospher RP-18 (Merck, Darmstadt, Germany) 4.0 x 4.0 and 125.0 x 4.0 mm, respectively, with 5-µm particles. Chromatography results were processed using Star Chromatography Workstation software (version 5.0; Varian).

For OTA detection, the mobile phase consisted of methanol, water and acetic acid (70:30:2) with a flow rate of 0.5 mL/min. Detector wavelengths were set at l_ex 336 and l_em 464. OTA was identified by constant retention time and quantified by comparison with peak areas of spiked samples. For the calibration curve, OTA-free plasma and kidney homogenates were spiked with a known amount of OTA and were cleaned up as samples. OTA-positive samples were confirmed by adding a known amount of standard OTA solution.

Preparation of kidney tissue homogenate for the comet assay

Tissue samples were homogenized in chilled homogenization buffer, pH 7.5, containing 75 mM NaCl and 24 mM Na₂EDTA to obtain a 10% tissue solution. A Potter-type homogenizer was used, and kidney samples were kept on ice during and after homogenization (12).

Alkaline comet assay

We used a modified alkaline comet assay protocol according to Sasaki et al. (12). Six microliters of kidney homogenate was suspended on 0.5% low-melting agarose and sandwiched between a layer of 0.6% normal-melting agarose and a top layer of 0.5% low melting agarose on fully frosted slides. The slides were kept on ice during the polymerization of each gel layer. After the solidification of the 0.6% agarose layer, the slides were immersed in a lysis solution (1% sodium sarcosinate, 2.5 M NaCl, 100 mM Na₂EDTA, 10 mM Tris-HCl, 1% Triton X-100, and 10% DMSO) at 4^oC. After 1 h, the slides were placed in electrophoresis buffer (0.3 M NaOH, 1 mM Na₂EDTA, pH 13) for 10 min at 0ºC to allow DNA to unwind. Electrophoresis was performed for 10 min at 300 mA and 1 V/cm. The slides were neutralized with Tris-HCl buffer, pH 7.5, and stained with 20 µg/mL ethidium-bromide for 10 min. Each slide was analyzed using the Leitz Orthoplan (Wetzlar, Germany) epifluorescence microscope. One hundred cells were analyzed on each slide using the comet assay II automatic digital analysis system (Perceptive Instruments Ltd., Halstead, Suffolk, UK) to determine tail length and tail intensity. Tail length (µm) is the distance of DNA migration from the center of the body of the nuclear core and is used to evaluate the extent of DNa damage. Tail intensity (%) is the percentage of the genomic DNA that migrates during electrophoresis from the nuclear core to the tail. Both tail length and tail intensity are measured automatically by image analysis software. Tail moment was calculated according to the following formula: tail moment = tail length x tail intensity/100 (12). According to Robbiano et al. (8), data are shown as DNA-damaging potency (comet assay endpoint treated - comet assay endpoint control)/OTA concentration µM).

Statistical analysis

Possible differences in the comet assay endpoints between the kidney samples from control and treated rats were determined by the non-parametric Kruskal-Wallis test. The same statistical method was used to estimate the significance of differences between different treatment durations. Probability values of P < 0.05 were considered to be statistically significant.

The correlation between doses of OTA in kidney homogenates and comet assay endpoints was tested using the linear regression analysis.

Results

During the experiment there were no changes in body or kidney weight of OTA-treated rats compared to negative control animals.

The OTA concentrations in plasma (µg/mL) and kidney homogenate (µg/g tissue) of treated animals are reported as means ± SD (Table 1). During the experiment, OTA concentrations in plasma and kidney tissue increased steadily.

We assessed the time course of OTA genotoxicity in the kidney of treated animals using the comet assay as a highly effective tool for the biomonitoring of DNA integrity. In all OTA-treated groups (0.5 mg kg body weight^-1 day^-1 for 7, 14, and 21 days), the tail length in kidney tissue was significantly higher than in controls (P < 0.05; Table 2). Tail length in animals treated for 7, 14, and 21 days increased with the length of treatment, and the difference between all groups was significant (P < 0.05). Tail intensity in kidney cells of all treated groups was higher than in controls (P < 0.05; Table 2). The highest tail intensity was observed in animals treated for 21 days, and the difference was significant in respect to animals treated for 7 and 14 days (P < 0.05). Tail moment also increased with the length of treatment, with significant differences between all groups (P < 0.05; Table 2).

Table 1.
Concentrations of ochratoxin A in plasma and kidney of rats receiving ochratoxin A (ip, 0.5 mg kg body weight^-1 day^-1) for 7, 14 and 21 days.

Table 2.
Tail length, tail intensity (% of total genomic DNA found in the tail of the comets), and tail moment (tail length x tail intensity/100) measured with comet assay in kidney cells of animals treated with ochratoxin A.

Discussion

The genotoxic properties of OTA have been previously tested using the comet assay on Madin-Darby canine kidney (MDCK) cells, human fibroblasts, and human-derived hepatoma (HepG2) cells (13-15). OTA induced single-strand breaks in MDCK and HepG2 cells in a concentration-dependent manner, while in human fibroblasts it caused DNA breaks in a time- and dose-dependent manner. The increase in all comet assay endpoints observed in the present study agrees with DNA strand breaks detected with the comet assay in the above mentioned in vitro studies.

OTA is undoubtedly a carcinogenic compound that causes tumors in rat kidneys (3). Until now, evidence of OTA genotoxicity in vivo was obtained mostly by measuring DNA adducts in the kidneys of mice and rats using the ³²P-post-labeling method (6,7). While some investigators claim that OTA binds covalently to DNA, forming OTA-DNA adducts (16), others used a very sensitive method (liquid chromatography/mass spectrometry/mass spectrometry) to show that DNA binding of OTA in exposed rats cannot be detected and is unlikely to reveal the mechanism of OTA toxicity (17).

Robbiano et al. (8) were the first to report OTA genotoxicity based on tests using alkaline single-cell gel electrophoresis in the rat kidney. The statistically significant increase in the average frequency of DNA breaks and/or alkali labile sites was obtained with a very high single OTA dose (10 mg/kg body weight, that is ½ LD50). In the present study, 0.5 mg OTA kg body weight^-1 day^-1 for 7 days was sufficient to significantly increase the tail length and intensity in the kidney of experimental animals. Significant differences in tail length, tail intensity and tail moment between 7 and 21 days of treatment indicate that these lesions are time dependent.

When tested using linear regression analysis, OTA concentration in kidney tissue showed a high positive correlation with tail length, tail intensity and tail moment. OTA concentration was found to correlate more strongly with tail intensity (r² = 0.9936, P = 0.02) and tail moment (r² = 0.9874, P = 0.02) than with tail length (r² = 0.8679, P = 0.24). These results are expected because, during electrophoresis, DNA does not migrate as fragments. The tail of the comet is the result of the migration of relaxed DNA loops that are pulled by the electric field to a limited distance from the core. The length of these loops determines the length of the comet tail. Since tail intensity indicates the number of DNA breaks, it is assumed that beyond some critical amount of damage, what increases is tail intensity rather than tail length (18).

The present study confirms the genotoxicity of OTA reported in earlier studies on cell cultures and on experimental animals. The genotoxicity of OTA found in our study is consistent with its carcinogenic potential in the kidney of experimental animals.

Acknowledgments

We wish to thank Mrs. Jasna Mileković, Mrs. Marija Kramarić, and Mrs. Mirjana Matašin for technical assistance.

Address for correspondence: A.-M. Domijan, Institute for Medical Research and Occupational Health, Ksaverska c. 2, 10001 Zagreb, Croatia. Fax: [phone]. E-mail: [e-mail]

Research supported by the Mutagenesis Unit, Institute for Medical Research and Occupational Health and by the Ministry of Science, Education and Sports of the Republic of Croatia. Received September 12, 2005. Accepted August 29, 2006.

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Correspondence and Footnotes

Publication Dates

• Publication in this collection
  25 Oct 2006
• Date of issue
  Dec 2006

History

• Received
  12 Sept 2005
• Accepted
  29 Aug 2006