Toshiaki Koizumi

Role of oxidative stress in single‐dose, cadmium‐induced testicular cancer

Treatment of rats with a single carcinogenic dose of CdCl2 (i.e., 30 mumol/kg) caused severe hemorrhagic damage in the testis within the first 12 h after the metal. Subsequently, atrophy with calcification developed in the next 2-3 mo. Atrophied tissues regenerated during the 1 yr after exposure. Twelve hours after exposure to the Cd treatment, lipid peroxidation levels, Fe content, and cellular production of H2O2 were remarkably elevated in testicular Leydig cells, the target cell population for Cd carcinogenesis. At the same time, glutathione peroxidase activity rose, glutathione reductase and catalase activities were reduced, and superoxide dismutase activity was unchanged. Xanthine oxidase activity in Leydig cells was also elevated at 6 and 9 h after the Cd treatment. Reduced glutathione in testes was decreased and oxidized glutathione was increased 12 h after exposure to the metal. These facts suggest that the carcinogenic doses of Cd induced oxidative stress while compromising cellular defense mechanisms against such stress. Therefore, active oxygen species such as H2O2 may have an important role in the initiation of carcinogenesis within the target cell population.

Mechanism of cadmium-induced cytotoxicity in rat hepatocytes: cadmium-induced active oxygen-related permeability changes of the plasma membrane.

The present study was performed to further elucidate the mechanism of cadmium (Cd)-induced cytotoxicity in rat hepatocytes focusing on the effects of Cd-induced acidification on cellular production of H2O2, and the integrity of the plasma membrane. Exposure of cells to Cd levels < 50 μm stimulated cellular production of H2O2 in a dose-dependent manner. In cells exposed to 50 μM Cd, generation of the toxic oxygen increased from 5 min after exposure, and reached a plateau at 15 min. The acidic medium at pH 6.5, a value which is corresponding to the cellular pH at maximal acidification induced by Cd, also enhanced production of the active oxygen at almost the same level as 25 μM Cd. These treatments affected permeability barrier of plasma membranes as assessed by nuclear staining with propidium iodide (PI, MW 668) and release of intracellular lactic dehydrogenase (LDH) into surrounding medium. Cd at 50 μM caused nuclear staining by the fluorescent probe, beginning from 15 min at exposure, reaching a peak at 60 min. LDH leakage likewise started from 60 min of Cd exposure onward. The acidic medium induced only a weak nuclear labeling with PI beginning at 30 min. Cd-induced nuclear staining was partially prevented by l-ascorbic acid pretreatment. H2O2-induced nuclear staining increased with the increasing pH values from 6.7 to 7.1 Cd at 50 μM lowered the cellular pH within 5 min, but the decreased cellular pH returned to a value near physiological levels 25 min later. Pretreatment with Amiloride, an inhibitor of the Na+H+ exchange, partially blocked this pH recovery after acidification. The results indicate that Cd caused H2O2 accumulation and H+, Cd and H2O2-related permeability changes of the plasma membrane. This may link to subsequent extensive membrane damage occurring at near physiological cellular pH.

Potential mechanism of cadmium-induced cytotoxicity in rat hepatocytes: inhibitory action of cadmium on mitochondrial respiratory activity

The present study was designed to clarify the mechanism of cadmium (Cd)-induced toxicity in rat hepatocytes. Cd and Mg-ATP induced cellular acidification at concentrations lower than 25 microM. In Mg-ATP-treated cells, maximal acidification occurred within 2.5 min, with a subsequent return to control levels. In Cd-treated cells, maximal acidification (pH 6.76) occurred 10 min after exposure to the metal, then the cytoplasmic pH began to rise but did not return to normal. Cd eliminated the membrane potential of isolated mitochondria in media at both pH 6.5 and 7.4. This effect of Cd on membrane potential was approximately equivalent in both media when the metal concentration was 5 microM, but was more intense in the medium at pH 6.5 than in the medium at pH 7.4 at the metal concentration > 5 microM. Acidic medium alone had no effect on membrane potential. Mitochondrial uptake of Cd increased in a dose-dependent manner in media at both pH 7.4 and 6.5. The uptake of 5 microM Cd was significantly increased by acidic medium, however at Cd concentrations > 5 microM, there were no pH-dependent differences in Cd uptake. The incubation of hepatocytes in the medium at pH 6.0 and 6.5 resulted in 5 and 7.5% inhibition of mitochondrial respiration in intact cells, respectively. The presence of 10 microM Cd in the medium at pH 6.0 enhanced this inhibition. Mitochondrial respiration was inhibited to 60% of the control mitochondria at pH 7.4 when exposed to the medium at pH 6.5 without Cd and this inhibition was extended to 70% by the presence of 5 microM Cd. Cd in the medium at pH 7.4 had no deleterious effect on mitochondrial respiration at all concentrations examined. The results indicate that the respiratory activity of mitochondria is sensitive to the low pH rather than to Cd although the metal strongly inhibits the activity when in the medium at low pH. Therefore, it appears Cd-induced acidification plays an important role in the initiation of deteriorative processes in mitochondria.

Protective effect of sodium molybdate against the acute toxicity of cadmium chloride

Pretreatment of rats with Na2MoO4 (1.24 mmol/kg, once a day for 3 days, i.p.) partially protected them against the acute toxicity of CdCl2 (0.075 mmol/kg, once, s.c., 24 h after pretreatment with Na2MoO4). The survival number of rats per total number of rats in the CdCl2-dosed group was 10/10, 8/10, 6/10, 2/10 and 0/10 on 0, 1, 2, 6 and 18 days after treatment with CdCl2 whereas in the group where CdCl2 is given after pretreatment with Na2MoO4 it is 10/10 and 6/10 on 0 and 18 days. The body weight of CdCl2-dosed rats consistently decreased until their death while that of Na2MoO4-CdCl2-dosed rats similarly decreased up to 4 days after exposure to CdCl2 but then increased almost normally. In order to elucidate the mechanism of protective action of Na2MoO4 against the acute toxicity of CdCl2, cellular components such as DNA, inorganic cations and metallothionein were measured in the liver after exposure to CdCl2. The treatment with CdCl2 alone reduced K content and increased Ca content but pretreatment with Na2MoO4 prevented such alterations in the levels of those cations caused by CdCl2. Metallothionein content in the liver was significantly elevated in the CdCl2-treated groups as compared to saline controls although the protein content was higher in the Na2MoO4-CdCl2-dosed group than in the CdCl2-dosed group. There was no difference in the protein content of the liver between saline controls and the Na2MoO4-dosed group. This suggests that Na2MoO4 alleviated the acute toxicity of CdCl2 in the rat and the protective mechanism by the metal is in part related to the enhancement of liver Cd-metallothionein induction.

Effects of zinc on the distribution and toxicity of cadmium in isolated interstitial cells of the rat testis

To investigate mechanisms by which zinc prevents cadmium carcinogenicity in the rat testis, the effect of in vivo zinc pretreatment on the distribution, influx, efflux and in vitro cytotoxicity of cadmium in isolated testicular interstitial cells was studied. Zinc pretreatment resulted in marked reduction of cadmium-induced cytotoxicity, as reflected by reduced loss of both intracellular K and glutamic-oxaloacetic transaminase (GOT) from interstitial cells. The subcellular distribution of cadmium was also altered in zinc pretreated cells, with a major shift of cadmium away from the nuclei to other subcellular components such as mitochondria, microsomes and cytosol. In vitro cadmium accumulation in isolated nuclei was also decreased by in vivo zinc pretreatment. In vivo zinc pretreatment also greatly enhanced both influx and efflux of cadmium. These results suggest that a major preventive effect of zinc against cadmium-induced testicular tumors may be due to its ability to reduce the cytotoxicity of cadmium in interstitial cells by enhancing efflux of cadmium and decreasing accumulation of cadmium in nuclei of this target cell population.

Protective effect of metallothionein on intracellular pH changes induced by cadmium

In order to gain further insight into the protective mechanism of metallothionein (MT) against Cd cytotoxicity, the effects of in vivo Zn- or Cd-pretreatment on the cytotoxicity and alteration in cellular pH induced by Cd were examined in isolated rat hepatocytes and testicular Leydig cells. These pretreatments both induced the synthesis of MT in the hepatocytes, but not in the Leydig cells. Both pretreatments alleviated Cd cytotoxicity in the hepatocytes. Cd- or Zn-pretreatment was also effective in preventing Cd-induced cellular acidification in hepatocytes but neither pretreatment was effective in Leydig cells. In fact, Cd-pretreatment stimulated acidification in Leydig cells. Exposure in vitro of hepatocytes from untreated rats to probenecid, an inhibitor of HCO3-/Cl- exchange, also ameliorated Cd-induced cellular acidification, suggesting an involvement of HCO3-/Cl- exchange in the preventive action of MT against Cd-induced acidification. These results suggest that Cd cytotoxicity in various cells may be initiated by alterations in plasma membrane ion transport systems such as the HCO3-/Cl- exchange and consequential cellular acidification. Induction of MT, therefore, may prevent Cd cytotoxicity, at least in rat hepatocytes, by preventing an alteration in ion transport at the plasma membrane as well as by intracytoplasmic binding of the metal molecules.

Mechanism of cadmium-induced cytotoxicity in rat hepatocytes. Cd-induced acidification causes alkalinization accompanied by membrane damage.

Exposure of rat hepatocytes to cadmium below 50 μM for a short period (10 min) resulted in cellular acidification. Conversely, exposure to Cd more than 50 μM for a long period (60 min) caused cellular alkalinization accompanied by membrane damage as reflected by decrease in cellular K content and loss of intracellular lactic dehydrogenase. In hepatocytes exposed to 5 μM Cd, a concentration sufficient to induce acidification without cytotoxicity, the metal was preferentially associated with the crude nuclei and cell debris fractions, suggesting an interaction between Cd and cell membranes to cause acidification. Omission of bicarbonate from the incubation medium induced cellular acidification. The presence of Cd in this medium did not potentiate the medium-induced acidification. Mg-ATP (25 μM) induced cellular acidification in relation to an increase in the concentration of cytosolic free Ca. The coexistence of Mg-ATP and Cd at the concentrations which had no effect on cellular pH in the presence of either agants induced cellular acidification.These observations suggest that Cd induced cellular acidification by modulating the process connected with the rise in cytosolic free Ca via interaction with plasma membranes. This acidification had no strong immediate cytotoxic actions but led to subsequent cellular alkalinization accompanied with severe cytotoxicity and membrane breakage.

Protective effect of sodium molybdate on the acute toxicity of mercuric chloride. V. Enhancement of renal regeneration after exposure to HgCl2

Pretreatment with Na2MoO4 protected rats from HgCl2-induced decreases in the renal concentration of amino acids, RNA, DNA, ATP and dry matter. It also reduced the mercury-induced increases in renal water, Ca and serum creatinine. Ma2MoO4 considerably elevated the RNA/DNA ratio in the renal cortex after treatment with HgCl2. In addition, subcellular distribution of mercury was markedly altered by pretreatment with Na2MoO4, specifically Na2MoO4 pretreatment decreased the mercury content in the particulate fractions such as the nuclei and mitochondria while increasing the mercury content of the cytosol. Sephadex G-75 gel filtration showed that the increase in mercury content in the cytosol of Na2MoO4-pretreated rats is due to an increase in the metal content of a metallothionein-like fraction. These results suggest that Na2MoO4-pretreatment protects against HgCl2 renal toxicity by stimulating mercury-mediated metallothionein induction in the renal cortex and renal regenerative processes.

Protective mechanism of sodium molybdate against the acute toxicity of cadmium in rats. II. Prevention of cytoplasmic acidification

In order to clarify the protective mechanism of sodium molybdate against the acute toxicity of cadmium chloride in rat, the effect of in vivo sodium molybdate pretreatment on the cytotoxic action of cadmium in isolated hepatocytes was studied. The cytosolic pH of hepatocytes isolated from untreated rats immediately decreased with incubation in either neutral Hanks balanced salt solution (HBS), pH 7.4, containing 5 µM cadmium chloride minimum or acidic HBS (pH 7.1, 6.8, 6.5, and 6.2). The presence of 5 µM cadmium in HBS adjusted to pH 7.1 aggravated cytosalic acidification induced by the acidic medium alone. Cell viability of hepatocytes incubated in HBS at pH 6.2 was significantly reduced as compared to that of control cells in HBS at pH 7.4, but the presence of cadmium in the acidic HBS had no aggravating action against such a toxic action of the acidic medium although cellular uptake of the metal in the medium increased, as compared to that in HBS at pH 7.4. Molybdenum pretreatment alleviated cytoplasmic acidification induced by the treatment with HBS at pH 7.4 or 7.1 containing cadmium or by extracellular acid load wothout cadmium. This pretreatment also prevented the loss of cell viability induced by the treatment with HBS at pH 6.2 but could not attenuate that when cadmium was present in the medium.These facts suggest that molybdenum pretreatment alleviated the acute toxicity of cadmium in rat by preventing cytoplasmic acidification caused by the harmful metal.

Effect of molybdenum on the acute toxicity of mercuric chloride. IV. Effect of molybdenum on mercury-mediated metallothionein mRNA induction

In order to elucidate the mechanism of the stimulative effect of molybdenum on mercury-mediated renal metallothionein induction, the levels of translatable metallothionein mRNA (MT mRNA) in the kidneys of rats treated with saline or Na2MoO4 or HgCl2 or Na2MoO4 and HgCl2 were measured by translation experiments in cell-free protein synthesizing systems. The time course of accumulation of mercury in renal nuclei of rats given HgCl2 with or without Na2MoO4-pretreatment was also investigated. Molybdenum, itself, did not elevate levels of MT mRNA compared to saline controls at all time points (0, 6 and 14 h after exposure to HgCl2) but rapidly elevated the levels of the mRNA more than Hg-dosed rats when HgCl2 was also administered. On the other hand, the time course study in renal nuclei showed that the mercury content of nuclei was consistently lower in Mo-Hg-dosed rats than in Hg-dosed rats at all time points (4, 8 and 24 h after exposure to HgCl2). These results suggest that the stimulative effect of molybdenum on mercury-mediated metallothionein induction is coupled with an increase of the mRNA coding for the low molecular weight protein and that such an increase in the levels of translatable MT mRNA is not due to the difference in uptake of mercury into renal nuclei.