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Brazilian Journal of Medical and Biological Research

Print version ISSN 0100-879XOn-line version ISSN 1414-431X

Braz J Med Biol Res vol.39 no.6 Ribeirão Preto June 2006

http://dx.doi.org/10.1590/S0100-879X2006000600009 

Braz J Med Biol Res, June 2006, Volume 39(6) 767-772 (Short Communication)

Peripheral markers of oxidative stress in chronic mercuric chloride intoxication

L.L.P. Gutierrez1, N.G. Mazzotti1, A.S.R. Araújo1, R.B. Klipel1, T.R.G. Fernandes1, S.F. Llesuy2 and A. Belló-Klein1

1Laboratório de Fisiologia Cardiovascular, Departamento de Fisiologia, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brasil
2Cátedra de Química General e Inorgánica, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires, Argentina

Abstract
Text
References
Acknowledgments
Correspondence and Footnotes


Abstract

The present study was designed to evaluate the time course changes in peripheral markers of oxidative stress in a chronic HgCl2 intoxication model. Twenty male adult Wistar rats were treated subcutaneously daily for 30 days and divided into two groups of 10 animals each: Hg, which received HgCl2 (0.16 mg kg-1 day-1), and control, receiving the same volume of saline solution. Blood was collected at the first, second and fourth weeks of Hg administration to evaluate lipid peroxidation (LPO), total radical trapping antioxidant potential (TRAP), and superoxide dismutase (Cu,Zn-SOD), glutathione peroxidase (GPx), glutathione-S-transferase (GST), and catalase (CAT). HgCl2 administration induced a rise (by 26%) in LPO compared to control (143 ± 10 cps/mg hemoglobin) in the second week and no difference was found at the end of the treatment. At that time, GST and GPx were higher (14 and 24%, respectively) in the Hg group, and Cu,Zn-SOD was lower (54%) compared to control. At the end of the treatment, Cu,Zn-SOD and CAT were higher (43 and 10%, respectively) in the Hg group compared to control (4.6 ± 0.3 U/mg protein; 37 ± 0.9 pmol/mg protein, respectively). TRAP was lower (69%) in the first week compared to control (43.8 ± 1.9 mM Trolox). These data provide evidence that HgCl2 administration is accompanied by systemic oxidative damage in the initial phase of the process, which leads to adaptive changes in the antioxidant reserve, thus decreasing the oxidative injury at the end of 30 days of HgCl2 administration. These results suggest that a preventive treatment with antioxidants would help to avoid oxidative damage in subjects with chronic intoxication.

Key words: Heavy metals, Antioxidant enzymes, Lipid peroxidation, Total radical-trapping antioxidant potential, HgCl2


Mercury is a widespread environmental and industrial pollutant which induces severe alterations in the tissues of both animals and humans (1). According to the Brazilian Health Ministry, 974,069 cases of human intoxication were registered in Brazil from 1985-2003 with 6,228 deaths. Mortality due to Hg2+ intoxication observed in Brazil in the same period was about 2,500, with the agricultural use of pesticides promoting greater lethality (2). Various mechanisms have been proposed to explain the biological toxicity of mercuric chloride (HgCl2), including oxidative stress. Hg2+ reacts with thiol groups (-SH), thus depleting intracellular thiols, especially glutathione, and causing cellular oxidative stress or predisposing cells to it (3). Other antioxidants, including ascorbic acid and vitamin E, have been reported to be depleted in HgCl2-treated rats (4). If animals are pretreated with superoxide dismutase (Cu,Zn-SOD) before acute intoxication is induced, histological changes are prevented (5). Many experiments suggest that oxidative stress can be involved in cellular damage and that it can be implicated in the toxicity of many xenobiotics.

The evaluation of the extent of blood oxidative stress by standardized methods can be useful to define the role of oxidative stress in different pathologies and can be used for clinical diagnosis. Kinesiological and electrophysiological parameters, as well as biochemical determinations made in feces, saliva, sweat and urine, are usually considered to be noninvasive peripheral markers. Biochemical procedures carried out in plasma and blood cells are considered to be minimally invasive peripheral markers (6). Thus, the purpose of the present study was to monitor some peripheral markers of oxidative stress during chronic HgCl2 intoxication to examine how the antioxidant system of animals responds to HgCl2 with time.

Twenty male Wistar rats (250 g) were obtained from the Central Animal House of Universidade Federal do Rio Grande do Sul. The animals were housed in plastic cages (4 animals each) and received water and pelleted food ad libitum. They were maintained under standard laboratory conditions (controlled temperature of 21ºC, 12-h light/dark cycle). Animals were weighed weekly. The animals were divided into two groups of 10: Hg group, that received daily subcutaneous HgCl2 injections, 0.16 mg kg body weight-1 day-1 (7) dissolved in saline solution, and control, that received the same volume of saline subcutaneously daily. The animals were injected daily for 30 consecutive days, always at the same time, from 8:00 to 10:00 o'clock, to avoid circadian oscillations.

Blood samples were taken at the end of the 1st, 2nd and 4th weeks of treatment. Blood was collected always at the same time of day and on the same day of the week by retro-orbital venous plexus puncture under ether anesthesia to measure oxidative stress at these three time points. Heparinized venous blood samples were washed in a solution of 9 g/L sodium chloride and centrifuged three times at 3000 g for 10 min at room temperature. Plasma was separated and stored for total radical-trapping antioxidant potential (TRAP) determination. White cells were discarded by aspiration and the erythrocytes diluted 1/10 in 1 mM acetic acid and 4 mM magnesium sulfate, placed in an ice bath for 10 min and centrifuged at 4200 g for 20 min at 0ºC. The supernatant was used for enzyme and lipid peroxidation (LPO) assays (6).

At the end of treatment, animals were euthanized by cervical dislocation, and total blood was collected by cardiac puncture to measure Hg2+ concentration. This determination was done by atomic absorption spectrophotometry at the Toxilab Clinical Analysis Laboratory (Porto Alegre, RS, Brazil). The lower limit of sensitivity was 0.02 ppb. Chemiluminescence was used to evaluate LPO. Chemiluminescence was measured with a liquid scintillation counter in the out-of-coincidence mode (LKB Rack Beta Liquid Scintillation Spectrometer 1215, LKB - Produkter AB, Bromma, Sweden). Blood samples were placed in low-potassium vials at a protein concentration of 0.5-1.0 mg protein/mL in a reaction medium consisting of 120 mM KCl in 30 mM sodium phosphate buffer, pH 7.4. Measurements were started by the addition of 3 mM tert-butyl hydroperoxide and the data are reported as counts per second per milligram hemoglobin (cps/mg Hb) (8).

TRAP, which indicates plasma total antioxidant capacity, was measured by luminescence using 2,2'-azo-bis(2-amidinopropane; ABAP), a source of alkyl peroxyl free radicals, and luminol. A mixture consisting of 50 µM ABAP, 40 µM luminol, and 50 mM sodium phosphate buffer, pH 7.4, was incubated and a steady-state luminescence arose from the free radical-mediated luminol oxidation. This emission was almost completely quenched by the addition of Trolox (water-soluble vitamin E), yielding induction times linearly related to the free radical scavenger concentration added. A calibration curve was obtained by using 0.2 to 1 µM Trolox. The addition of plasma samples instead of Trolox elicits an induction time related to the initial amount of sample added (9). Luminescence was measured with a scintillation counter in the out-of-coincidence mode and the results are reported as mmol Trolox L-1 mg protein-1.

Catalase (CAT) activity was determined by following the decrease in 240-nm absorption in a reaction medium containing 50 mM sodium phosphate buffer, pH 7.2, and 10 mM hydrogen peroxide (10). CAT activity is reported as picomol hydrogen peroxide reduced per minute per milligram of protein.

Glutathione peroxidase (GPx) oxidizes reduced glutathione in the presence of peroxides. Its activity is reported as nmol peroxide/hydroperoxide reduced min-1 mg protein-1. Selenium-dependent and -independent GPx activities were measured by following NADPH oxidation at 340 nm in a reaction medium containing 0.17 mM reduced glutathione, 0.2 U/mL glutathione reductase, and 0.5 mM tert-butyl hydroperoxide (which reacts with both the Se-dependent and non-Se-dependent GPx), as described by Flohé and Gunzler (11).

Cu,Zn-SOD activity was determined based on the inhibition of superoxide radical reaction with pyrogallol and the results are reported as units per milligram of protein (12). Cu,Zn-SOD activity was determined by measuring the rate of pyrogallol oxidation. The reaction medium contained 50 mM Tris buffer, pH 8.20, 24 mM pyrogallol, and 30 mM CAT. Absorbance changes were measured at 420 nm for 2 min.

Glutathione-S-transferase (GST) activity, reported as pmol/mg protein, was measured by the rate of formation of dinitrophenyl-S-glutathione at 340 nm. The reaction medium consisted of 19 mM sodium phosphate buffer, pH 6.5, 1 mM GSH, 1 mM chloride dinitrobenzene, and erythrocytes (13).

The conversion of hemoglobin to cyanomethemoglobin by the Drabkin reagent was measured against a standard curve (14).

Protein was measured by the method of Lowry et al. (15) using bovine serum albumin as standard.

Tert-butyl hydroperoxide was from Aldrich (Milwaukee, WI, USA) and ABAP was from Polyscience (Warrington, PA, USA). All other chemicals were purchased from Sigma (St. Louis, MO, USA).

Data were analyzed by two-way analysis of variance and are reported as means ± SEM. Values of P < 0.05 were considered to be significant.

Blood Hg2+ concentration was higher in treated animals (reaching 73.5 µg/dL) compared to control (P < 0.01), which showed no detectable concentration of this metal in blood. The body weight curve constructed to follow the animals' growth demonstrated that the initial body weight of the control (249.0 ± 1.3 g) and Hg (248.1 ± 1.0 g) animals did not differ significantly. Body weight increased by 26% in control from the first and the last day of the experiment (day 30), and was reduced by 19% in the Hg group, during the same period of treatment. There was a significant body weight difference between groups after the first week of treatment (data not shown).

LPO measured by chemiluminescence in blood samples from the Hg group was increased by 26% compared to control during the second week of treatment (P < 0.01). No significant differences in LPO levels were observed between the first and last week of treatment in either group. Control animals showed no significant variations in LPO levels at the time points studied. These results are shown in Figure 1A.

In the Hg group, TRAP was decreased by 69% in the first week of treatment and increased progressively in the subsequent weeks, with no difference being observed in relation to control during the last week of treatment. Control animals showed no significant changes in TRAP at the three time points. These data can be observed in Figure 1B.

Table 1 shows the activities of CAT, Cu,Zn-SOD, GPx, and GST in erythrocytes from animals of both experimental groups. There was no difference in antioxidant enzyme activity between the two groups during the first week of treatment. During the second week, GST and GPx activities were significantly increased by 14 and 24%, respectively, in the treated group, while Cu,Zn-SOD activity was decreased by 54% compared to control. During the last week of treatment, Cu,Zn-SOD was increased by 43% and CAT by 10%, both significantly different from control animals at the same time point, while the activities of the other enzymes did not change significantly.

In the present study, chronic administration of HgCl2 to rats caused an imbalance in oxidative stress as monitored by means of some peripheral markers, providing a kinetic view of this complex phenomenon. Oxidative stress was measured through very sensitive methods that are detected by chemiluminescence allowing high precision determinations with small amounts of sample.

Chronic HgCl2 intoxication induced a significant decrease in the animal's body weight compared to control. Besides weight loss, the animals showed signs of intoxication like yellowish fur and a cachectic appearance.

When peripheral markers of oxidative stress were analyzed in the present study, important HgCl2-induced changes in TRAP (Figure 1B) and LPO (Figure 1A) were detected. The TRAP technique measures the antioxidant capacity of plasma, which is a combination of the effect of all of the chain-breaking antioxidants, including thiol groups (especially glutathione), uric acid and ascorbic acid (16). In the present study, antioxidant capacity was decreased in the first week of treatment, probably because of the binding of mercuric ions to thiols, leading to intracellular depletion of these groups, especially glutathione. Furthermore, other cellular antioxidants such as vitamins C and E may also have been depleted, as described previously (4), in an attempt to recover the antioxidant status before the occurrence of oxidative damage.

As a consequence, an imbalance in antioxidant protective mechanisms takes place, leading to oxidative stress in the cells. In fact, a drastic increase in reactive oxygen species production has been reported during acute treatment with HgCl2, inducing LPO in rat brain (7). In the present study, we also observed an increase in systemic LPO levels during the second week of treatment (Figure 1A), possibly as a consequence of the depletion of antioxidants. During week 2, some changes in antioxidant enzyme activity were observed. Cu,Zn-SOD activity was decreased by 54%, possibly indicating an increased superoxide radical production and a consequently higher hydroxyl radical formation. Enhanced levels of the latter may contribute to LPO initiation (8), as observed in the present study. Increased LPO levels are indicative of an oxidative stress situation that might lead to the induction of thioredoxin, a member of an evolutionarily conserved family of redox-active proteins containing a conserved active site dithiol motif. This enzyme could be induced in oxidative stress situations and may play a protective role against specific toxicologic conditions (17). Although thioredoxin activity and/or induction were not measured in this experimental model, increased thioredoxin activity may replace reduced glutathione levels, as reflected by the progressive increase in TRAP observed in the present study.

GST and GPx activities increased during the second week of treatment with HgCl2. The elevation in GST activity indicates that an oxidative stress condition is occurring, since GST is considered to be an oxidative stress marker (18). GST catalyzes the conjugation of electrophilic molecules with GSH, being part of the mechanism of detoxification of xenobiotics (13). GST is also involved in the detoxification of peroxidation products (18). Increased GPx activity indicates an increase in the amount of organic and non-organic peroxides, such as hydrogen peroxide, which are substrates for the enzyme (19).

At the end of the experimental protocol, CAT and Cu,Zn-SOD activities were increased. This may indicate that hydrogen peroxide and superoxide radical production is enhanced. It has been reported that HgCl2 may disturb mitochondrial inner membrane function, resulting in increased formation of hydrogen peroxide by the mitochondrial electron transport chain (1). The increased CAT activity observed in the present study can be understood as an adaptive response to increased hydrogen peroxide production.

Taken together, the present results suggest that animals treated with HgCl2 respond at the cellular level by mobilizing different substances to avoid or compensate for the metal's toxicity. This adaptive response is reflected on the peripheral markers of oxidative stress measured. The novelty of this study is the oxidative stress time course evaluation in the HgCl2 intoxication. This is a minimally invasive approach and these markers could be determined in patients exposed to Hg2+ to monitor the clinical evolution of antioxidant therapies against cellular oxidative damage.


Figure 1. Effect of HgCl2 administration on lipid peroxidation levels and total radical trapping antioxidant potential (TRAP) of rats. A, Lipid peroxidation levels, measured by chemiluminescence and reported as cps/mg hemoglobin. Data are reported as mean ± SEM for 10 animals per group. *P < 0.05 compared to control at the same time point (two-way ANOVA). B, TRAP, reported as mM Trolox in plasma. Data are reported as means ± SEM for 10 animals per group. *P < 0.01 compared to all other experimental groups (two-way ANOVA).

[View larger version of this image (46 K JPG file)]


Table 1. Antioxidant enzyme activities in erythrocytes of rats treated subcutaneously with HgCl2 daily for 30 days. 

[View larger version of this table (70 K JPG file)]


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Acknowledgments

We thank the TOXILAB Clinical Analysis Laboratory (Porto Alegre, RS, Brazil) for mercury determinations.


Correspondence and Footnotes

Address for correspondence: A. Belló-Klein, Rua Sarmento Leite, 500, 90050-170 Porto Alegre, RS, Brasil. Fax: +55-51-3316-3166. E-mail: belklein@ufrgs.br

Research supported by CAPES, FINEP, CNPq, and FAPERGS. Received September 29, 2004. Accepted March 2, 2006.

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