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1.
Journal of the Egyptian Society of Toxicology. 2007; 37: 27-37
em Inglês | IMEMR | ID: emr-83721

RESUMO

The present study aimed to investigate the toxic effects of three trade names of chlorpyrifos [CPF] pesticide from different local manufactures; i.e. chlorozan [K], pestpan [W] and pyriban [H] on haematological indices, hepatic oxidative stress, in addition to lipid profile and thyroid hormone status in plasma of male albino rats. Also, to assess the therapeutic role of selenium [Se] under these conditions. Three compounds [K, W, and H] were administrated orally to rats at 23.43, 21.40 and 17.43 mg/kg b.w., respectively. [which represent the 1/4 LD50] with 5 doses per week for 28 days, and then these rats supplemented with Se at 50 micro g/day [RDA-US] as a therapeutic agent for 15 days. Additional group received Se [50 micro g/day] alone for the same time interval to assay whether Se has any biphasic effect. The results showed that CPF treatment [H], caused erythropenia, associated with decreasing of haemoglobin [Hb] concentration and packed cell volume [PCV] in rats. In contrast, the same treatment induced the leukocytosis and lymphocytosis. Also, Se-supplemented rats had leukocytosis and neutrophilia. However, supplemented rat with Se following treatment with CPF [H] improved the erythrogram, whereas leukopenia and lymphopenia occurred in rats received Se following treatment with CPF [K]. Chlorpyrifos treatments [K, W and H groups] did not alter markedly the hepatic lipid peroxidation [LPO] levels, while, the induction in the hepatic total glutathione [GSH] was occurred, compared with control group. The similar results were recorded in Se-supplemented rats. However, the fluctuation in the activity of alanine aminotransferase [ALT] was detected in chlorpyrifos-treated rats [W and H], whereas the aspartate aminotransferase [AST] activity did not change markedly. Supplementation rats with Se following treatment with CPF [K, W and H] reduced the levels of LPO, compared with CPF-treated rats [K, W and H]. This trend was more pronounced in Se- supplemented rats. In contrast, a significant enhancement in the activity of aminotransferases, i.e. ALT and AST was observed in rats supplemented with Se, after treatment with CPF [K and W]. Meanwhile, a marked inhibition in the activities of ALT and AST was detected in Se-supplemented rats. Overall, hypertriglyceridemia and hypercholesterolemia were observed in rats whether treated with CPF alone or pre-supplementation with Se and also in Se-supplemented rats. However, an elevation markedly in the thyroxine [T4] and triiodothyronine [T3] levels was found in CPF-treated rats [W and K, respectively]. While a marked decrease in the level of T3 was detected in rat supplemented with Se post-treatment with CPF [K and H] or alone. Moreover, the concentration of Se in hepatic tissues of rats received the Se following treatment with CPF was in order of W>H>K groups, whereas the Se element did not detected in liver tissues of Se-supplemented rats. Conclusion: Selenium supplementation to CPF-treated animals improved the haematological findings and hepatic lipid peroxidation level, in addition to lipidogram [i.e. HDL-C]


Assuntos
Animais de Laboratório , Masculino , Ratos , Selênio , Estresse Oxidativo , Lipídeos/sangue , Hormônios Tireóideos/sangue
2.
Journal of the Egyptian Society of Toxicology. 2006; 35: 69-78
em Inglês | IMEMR | ID: emr-78266

RESUMO

Toxicity data with single pesticides to test animals are far more abundant than with mixtures [Flipo et al., 1992]. Consequently, these data cannot be used directly to predict the effect of pesticide combinations. Three pesticides; imidacloprid, profenofos and carbosulfan, administered to rats per OS at low level dose equal 1/30 LD50 for each insecticide, which represent 111, 70 and 43 ppm, respectively on homeostasis status and haematological indices [El-Kashory and El-Said, 2001], were selected to explore their combined action of subchronic exposure studies for 90 days in adult male albino rats. Homeostasis-related parameters such as; aldosterone [Ald.], sodium ions [Na+], potassium ions [K+], total chloride ions [T.Cl-] levels, pH value and haematological indices were examined in rats after an administration with different insecticide combinations. Moreover, after withdrawal the pesticide combinations for 30 days, as a recovery period, the above mentioned parameters were evaluated, in comparison with the control group. Results showed that, pesticide combination imidacloprid/profenofos [I + P] induced significant decrease in Na+ and T.Cl- ions levels and significant increase in pH value. While, it did not alter both Ald. and K+ ions levels. Combination imidacloprid/carbosulfan [I + C] increased significantly Ald., T.Cl- ions levels and pH values. On the contrary, it reduced Na+ and K+ ions levels significantly. Combination of profenofos/carbosulfan [P + C] decreased Ald. and Na+ significantly, while, K+ and T.Cl- level and pH value did not alter. In addition, tri-combination imidacloprid/ profenofos/carbosulfan [I + P + C] increased Na+ and T.Cl- ions level and pH value; while, a marked decline in Na+ ions level was occurred, as well as, no appreciable changes in K+ ion levels were observed. The combinations of I + P and I + C caused erythropenia [reduced RBC mass] associated with a significant decrease in PCV in I + C-treated rats. While, di-combinations P + C, I + P and I + P + C tri-combinations increased markedly of PCV and MCV. However, leukocytosis [elevated WBCS count] was observed in I + P + C-treated rats. After the pesticides combination withdrawal, changes in some parameters returned to the normal values, in comparison with the control group; while, the others still altered. Moreover, some parameters did not exhibit any changes unless after the stop of the treatment. In conclusion, this study supports the notion that; an interactions effects of pesticide combinations may be consider as contributor factor enhance their side effects


Assuntos
Animais de Laboratório , Masculino , Organotiofosfatos/farmacologia , Carbamatos/farmacologia , Interações Medicamentosas , Homeostase/efeitos dos fármacos , Ratos , Praguicidas , Aldosterona/análise , Eletrólitos/análise
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