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1.
Indian J Exp Biol ; 2007 Jun; 45(6): 515-23
Artigo em Inglês | IMSEAR | ID: sea-58981

RESUMO

Present investigation was planned to evaluate the therapeutic effectiveness of chelating agents against vanadium intoxication on blood and reproductive organs of rats. Male and female albino rats were injected vanadyl sulphate (7.5 mg/kg, po, for 21 days, 5 days in a week). Chelating agents tiron (T) alone and in combination with lipoic acid (LA), vitamin E (vit E) and selenium (Se) were given for 2 days/week. With the administration of vanadyl sulphate to rats fructose level in seminal vesicles was significantly (P< or =0.05) declined. The activities of alkaline phosphatase and adenosine triphosphatase were also decreased, whereas glycogen content and acid phosphatase activity increased in testis, seminal vesicles, ovaries and uterus after toxicant exposure. Significant changes in serum transaminases, serum alkaline phosphatase and lactate dehydrogenase were recouped by chelation therapy. Lipid peroxidation, reduced glutathione level and triglycerides levels altered significantly after exposure to vanadium in rats. The ultrastructural damage in spermatogenic stages in treated animals showed recovery pattern after therapy. Co-treatment with antioxidants restored these activities. The most effective combination was tiron + selenium followed by tiron + vitamin E, and tiron + lipoic acid.


Assuntos
Sal Dissódico do Ácido 1,2-Di-Hidroxibenzeno-3,5 Dissulfônico/administração & dosagem , Adenosina Trifosfatases/metabolismo , Fosfatase Alcalina/metabolismo , Animais , Biomarcadores/sangue , Quelantes/uso terapêutico , Terapia por Quelação , Combinação de Medicamentos , Feminino , Glicogênio/metabolismo , Gônadas/efeitos dos fármacos , Masculino , Ratos , Ratos Sprague-Dawley , Selênio/administração & dosagem , Ácido Tióctico/administração & dosagem , Vanádio/toxicidade , Vitamina E/administração & dosagem
2.
Indian J Exp Biol ; 2004 Oct; 42(10): 993-7
Artigo em Inglês | IMSEAR | ID: sea-55973

RESUMO

Ethanolic extract of propolis was administered to rats intoxicated by carbon tetrachloride. Administration of bolus dose of CCl4 (1.5 ml/kg, ip) resulted in elevation of serum transaminases and serum alkaline phosphatase activities. Levels of hepatic lipid peroxidation were significantly increased. On the contrary, there was significant decrease in hepatic reduced glutathione level. The propolis extract (100 and 200 mg/kg, po) exhibited recoupment in both pre- and post-treatment (prophylactic and curative studies) of biochemical changes induced by CCl4. The post treatment of 200 mg/kg, po extract showed most significant hepatoprotective effect. Histopathological studies showed damage in hepatocytes and disturbed chord arrangement after toxicant administration. Propolis extract (200 mg/kg, po) was found to be more effective in restoring CCl4 induced histopathological alterations.


Assuntos
Animais , Antioxidantes/metabolismo , Abelhas , Tetracloreto de Carbono/antagonistas & inibidores , Feminino , Glutationa/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/efeitos dos fármacos , Própole/farmacologia , Ratos , Ratos Sprague-Dawley
3.
Indian J Exp Biol ; 2002 Nov; 40(11): 1254-9
Artigo em Inglês | IMSEAR | ID: sea-58193

RESUMO

Efficacy of propriety herbal formulation (PHF) against carbon tetrachloride (CCl4) induced liver damage was investigated in adult rats. Administration of CCl4 (0.2 ml/kg; i.p.) twice a week for 12 weeks resulted in significant elevation in serum transaminases activity. Level of reduced glutathione was significantly decreased. On the contrary, significant elevation was found in the hepatic lipid peroxidation level. Proliferation of fibroblast replaced the hepatic parenchyma cells in focal areas. Cell organelles like mitochondria, endoplasmic reticulum and nucleus showed severe degeneration after CCl4 exposure. PHF was effective in restoring the CCl4 induced biochemical and histological ultrastructural changes.


Assuntos
Alanina Transaminase/metabolismo , Animais , Aspartato Aminotransferases/metabolismo , Tetracloreto de Carbono/toxicidade , Intoxicação por Tetracloreto de Carbono/tratamento farmacológico , Núcleo Celular/efeitos dos fármacos , Retículo Endoplasmático/efeitos dos fármacos , Fibroblastos/efeitos dos fármacos , Glutationa/metabolismo , Doença Hepática Induzida por Substâncias e Drogas/metabolismo , Peroxidação de Lipídeos/efeitos dos fármacos , Fígado/efeitos dos fármacos , Masculino , Mitocôndrias/efeitos dos fármacos , Fitoterapia , Preparações de Plantas/uso terapêutico , Ratos , Ratos Sprague-Dawley
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