Exposure to Nickel-Cadmium Contamination of Drinking Water Culminates in Liver Cirrhosis, Renal Azotemia, and Metabolic Stress in Rats.

Drinking water polluted by heavy metals has the potential to expose delicate biological systems to a range of health issues. This study embraced the health risks that may arise from subchronic exposure of thirty-four male Wistar rats to nickel (Ni)-cadmium (Cd)-contaminated water. It was done by using the Box-Behnken design (BBD) with three treatment factors (Ni and Cd doses at 50-150 mg/L and exposure at 14-21-28 days) at a single alpha level, resulting in seventeen experimental combinations. Responses such as serum creatinine (CREA) level, blood urea nitrogen (BUN) level, BUN/CREA ratio (BCR), aspartate and alanine aminotransferases (AST and ALT) activities, and the De Ritis ratio (DRR), as well as malondialdehyde (MDA) level, catalase (CAT), and superoxide dismutase (SOD) activities, were evaluated. The results revealed that these pollutants jointly caused hepatocellular damage by raising AST and ALT activities and renal dysfunction by increasing CREA and BUN levels in Wistar rats' sera (p < 0.05). These outcomes were further supported by BCR and DRR values beyond 1. In rats' hepatocytes and renal tissues, synergistic interactions of these metals resulted in higher MDA levels and significant impairments of CAT and SOD activities (p < 0.05). In order to accurately forecast the effects on the responses, the study generated seven acceptable regression models (p < 0.05) with r-squared values of > 80% at no discernible lack of fit (p > 0.05). The findings hereby demonstrated that Wistar rats exposed to these pollutants at varied doses had increased risks of developing liver cirrhosis and azotemia marked by metabolic stress.

Exposure of African Catfish (Clarias gariepinus) to Lead and Zinc Modulates Membrane-Bound Transport Protein: A Plausible Effect on Na+/K+-ATPase Activity.

The contamination of the aquatic ecosystem beyond tolerable limits may pose serious health challenges to its components. This study evaluated the toxic effects of a binary mixture of lead (Pb) and zinc (Zn) compounds on the activity of Na+/K+-ATPase in tissues of Clarias gariepinus in a controlled aquatic system. The study employed Box-Behnken Design (BBD) with 17 runs in which Pb and Zn concentrations were considered process variables in a time-dependent fashion. Metal exposure levels consisted of 0, 10 and 20% of 96 h-LC50 of Pb (55.12 mg/L) and Zn (32.15 mg/L) for three weeks. Thereafter, membrane-bound Na+/K+-ATPase activity was assessed in gill, hepatic and renal tissues, and data generated from the BBD were used for the development of models. Three regression models were obtained, for gill, hepatic and renal Na+/K+-ATPase activities with exposure to metals differ significantly (p < 0.05) at R2 > 90%, and no significant lack of fit (p > 0.05) was observed in each case. Congruent to the synergistic interactions observed between Pb and Zn in the study, the gill and hepatic Na+/K+-ATPase activities were significantly inhibited, whereas renal Na+/K+-ATPase activity was significantly stimulated (p < 0.05). The optimized models were considered reliable, as they were confirmed in the laboratory through accurate prediction of hepatic, renal and gill Na+/K+-ATPase activities with equivalences of 1.22 ± 0.17, 1.66 ± 0.07 and 3.50 ± 0.33 µmol pi/min/mg protein (p < 0.05) respectively. It is hereby concluded that the synergistic interaction between Pb and Zn truncated the physiological function of Na+/K+-ATPase activity in the respective tissues except for renal tissue of exposed C. gariepinus.

Effect of a controlled food-chain mediated exposure to cadmium and arsenic on oxidative enzymes in the tissues of rats.

OBJECTIVE: The present study aims to investigate the effect of cadmium and arsenic through a controlled food chain on the activities of some oxidative enzymes (Sulphite oxidase SO, Aldehyde oxidase AO, Monoamine oxidase MO and Xanthine oxidase, XO) in the liver, kidney, testes, heart and brain of rats. MATERIALS AND METHODS: Fish (the first trophic level) were exposed to both metals (singly and in mixture) using cadmium chloride (CdCl2) as the source of cadmium and arsenic trioxide (AS2O3) as the source of arsenic at a concentration of 0.4 mg of metals/100 ml of water for 1 month and then sacrificed. The contaminated fish were then used as a source of protein in compounding the experimental diet to which the rats (the second trophic level) were exposed to for a period of 1 and 3 months. The Cd- and As-load in the feed and tissues of rats as well as the activities of the oxidative enzymes were subsequently analyzed in the various tissues after both period of exposure. RESULTS: Metal analysis on the tissues of rats showed that the metals accumulated more in the liver than in other organs after the 1 month exposure but accumulated more in the kidney after the 3 months exposure. The activities of the oxidative enzymes in the liver were significantly (P < 0.05) decreased in all test groups after the 1 and 3 months exposure. However, after the 1 month exposure, the kidney, testes and heart showed an initial increase in the activities of these enzymes which were decreased after the 3 months exposure. In the brain, the activities of these enzymes were increased in both duration of study. CONCLUSION: From the results obtained in the current study, it could be concluded that exposure to cadmium and arsenic through the food chain leads to accumulation of these metals in the tissues of experimental rats leading to the inhibition of oxidative enzymes, thus affecting several normal metabolic processes.

Alteration in the activity of oxidative enzymes in the tissues of male Wistar albino rats exposed to cadmium.

OBJECTIVE: The objective of the present study was to investigate the effect of cadmium (Cd) on the activities of some oxidative enzymes [viz Aldehyde oxidase, AO (E.C. 1.2.3.1); Xanthine oxidase, XO (E.C. 1.2.3.2); Sulphite oxidase, SO (E.C.1.8.3.1.); and Monoamine oxidase, MO (E.C. 1.4.3.4)] in the liver and kidney. MATERIALS AND METHODS: Male Wistar albino rats were administered 1, 2 and 4 mg Cd(2+)/kg body weight for one and three months. The activities of the oxidative enzymes were subsequently analyzed in the liver and kidney after both periods of exposure. RESULTS: There was a dose dependent increase in liver and kidney Cd concentration in the test rats as compared to control after both periods of treatment with the liver retaining higher concentration of Cd than the kidney for each of the exposure dose. The oxidative enzymes were decreased in a dose dependent manner in the liver and kidney after both periods of treatment. The percentage inhibition of these enzymes was less in the liver of rats treated with Cd for three months relative to the one month treated rats for each of the exposure dose. Conversely, the inhibition of the activities of these enzymes in the kidney of rats in all the treatment groups was more pronounced after three months relative to the trend in the one month treated rats. However, the activities of the oxidative enzymes were higher in the liver as compared to the kidney in all the treatment groups after both durations of Cd treatment. CONCLUSION: Based on the results obtained, it can be concluded that the inhibition of the oxidative enzymes by Cd may disturb metabolism of bioactive endogenous substances, exogenous components of food and some xenobiotics.

Bioaccumulation of cadmium and its biochemical effect on selected tissues of the catfish (Clarias gariepinus).

The present study examines the pattern of accumulation of cadmium (Cd) and its biochemical effects on selected tissues of a variety of African catfish (Clarias gariepinus), after exposure to various doses of Cd. The results obtained indicate that at the end of 21 days of exposure, the total tissue organ cadmium concentration followed the pattern kidney > gill > liver > muscle for each of the exposure concentrations. The levels of Cd in these organs were higher than those in ambient water. Moreover, while the rate of uptake of Cd increased with time in the kidney, liver and muscle, it decreased in the gill. Superoxide dismutase (SOD) was significantly elevated only in the kidney of catfish treated with 0.2 and 0.4 ppm of Cd for 7 days compared with the control. Conversely, gill SOD was significantly decreased in the same concentrations of Cd-treated catfish relative to the control. Statistically similar levels of SOD were observed in the liver, brain and muscle with all the treatments after the same duration of treatment. In the fish exposed for 21 days, SOD activity was significantly decreased in the kidney with a corresponding increase in lipid peroxidation (LPO), but it manifested only with the 0.2- and 0.4-ppm Cd treatment relative to the control. In the liver, however, Cd exposure significantly increased SOD in the 0.2- and 0.4-ppm treatments of the same duration. In conclusion, the present study indicates that the accumulation of Cd and its effect on SOD and LPO in C. gariepinus is dependent on concentration, tissue and time.

A comparative study on the archives of xanthine oxidase and aldehyde oxidase in different fish species from two rivers in the Western Niger-Delta.

Glycaemia, a classical indicator of stress, xanthine oxidase and aldehyde oxidase which are involved in phase I detoxication were investigated in two different fish species from two rivers with different pollution levels in the Western Niger-Delta. Four sampling zones covering the entire lengths of Warri and Ethiope Rivers respectively were used in this study. For each species of fish five were obtained from a sampling zone in a river. Blood glucose was significantly higher (P < 0.001) in M. electricus from Warri River (82.13 +/- 5.50 mg cm(-3)) compared to the same species from Ethiope River (36.47 +/- 1.49 mg cm(-3)). With the same parameter a similar profile was observed for C. gariepinus; Warri River (56.92 +/- 10.31 mg cm(-3)); Ethiope River (37.65 +/- 0.90 mg cm(-3)) which was also significant (P < 0.01). The activity of xanthine oxidase in M. electricus from Warri River (255.80 +/- 41 it mol cm(-3)) was significantly higher (P < 0.001) compared to the value obtained for the same species (108 +/- 22.36 micro mol cm(-3)) from Ethiope River. Also the activity of xanthine oxidase in C. gariepinus from Warri River (197 +/- 34.65 micro mol cm(-3)) was significantly higher (P < 0.001) when matched with the value obtained for the same species (78.40 +/- 26.84 micro mol cm(-3)) from Ethiope River. That blood glucose level was related to xanthine oxidase activity in the two fish species from Warri River was supported by the high positive correlation between these two parameters (M. electricus. r = 1: C. gariepinus, r = 0.71). The activity of aldehyde oxidase in C. gariepinus from Warri River (143.80 +/- 28.45 micro mol cm(-3)) was significantly higher (P < 0.001) compared to the value obtained for the same species (61.20 +/- 15.21 micro mol cm(-3)) from Ethiope River. A similar profile in aldehyde oxidase activity observed for M. electricus; Warri River (130 +/- 28.39 micro mol cm(-3)); Ethiope River (89 +/- 19.70 micro mol cm(-3)) but an inferior statistical variation (P < 0.05) was obtained. The results obtained in this study indicate that the level of xanthine oxidase in M. electricus is a more specific marker and to a lesser extent its activity in C. gariepinus in monitoring environmental stress due to pollution.

Increased superoxide dismutase and Na+, K+-ATPase activities in aortic strips from potassium-adapted rats: implication for altered vascular reactivity.

The contributions of superoxide dismutase (SOD) and Na(+), K(+)-ATPase to the altered vascular reactivity in potassium-adapted rats were investigated to test the hypothesis that smooth muscle hyperpolarisation may be involved. Isometric contractions to noradrenaline (NA), 5-hydroxytryptamine (5-HT), and relaxations to acetylcholine (ACh), levcromakalim (LEV) and sodium nitroprusside (SNP), were measured in aortic rings from potassium-adapted rats. Pieces of the aortae were also excised from the animals and assayed for SOD and Na(+), K(+)-ATPase. Maximum contractile responses were significantly attenuated (P<0.05) in aortic rings from the potassium-adapted rats to NA and 5-HT, while relaxations were also significantly augmented (P<0.05) in the same rings to LEV and SNP, but not to ACh. Both SOD and Na(+), K(+)-ATPase activities were significantly higher (P<0.05) in the aortae from the potassium-adapted rats compared to controls. It is concluded that the alteration in vascular smooth muscle reactivity may be due to hyperpolarisation caused by the activities of SOD and Na(+), K(+)-ATPase.