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1.
Appl Biochem Biotechnol ; 195(2): 905-918, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-36227501

RESUMO

Urolithiasis is a common urological disorder, which causes considerable morbidity in both genders at all age groups worldwide. Though treatment options such as diuretics and non-invasive techniques to disintegrate the deposits are available, but often they are found less effective in the clinics. In this work, we planned to investigate the ameliorative effects of daidzin against the ethylene glycol (EG)-induced urolithiasis in rats. The male albino rats were distributed into four groups (n = 6) as control (group I), urolithiasis induced by the administration of 0.75% EG (group II), urolithiasis induced rats treated with 50 mg/kg of daidzin (group III), and urolithiasis rats treated with standard drug 750 mg/kg of cystone (group IV). The urine volume, pH, and total protein in the urine were assessed. The activities of marker enzymes in both plasma and kidney tissues were analyzed using assay kits. The levels of kidney function markers such as calcium, oxalate, urea, creatinine, uric acid, magnesium, BUN, and phosphorous were estimated using assay kits. The status of antioxidants and inflammatory cytokines were also examined using kits. The renal tissues were examined by histopathological analysis. Our results revealed that the daidzin treatment effectively decreased the urine pH and protein level and increased the urine volume in the urolithiasis rats. Daidzin decreased the calcium, oxalate, uric acid, and urea, creatinine, and BUN levels and also improved the magnesium and phosphorus in the urolithiasis rats. The activities of AST, ALT, ALP, GGT, and LDH were effectively reduced by the daidzin in both serum and renal tissue. Daidzin also reduced the inflammatory marker and increased the antioxidant levels. Histopathology results also proved the therapeutic effects of daidzin. Together, our results displayed that daidzin is effective in the amelioration of EG-induced urolithiasis in rats.


Assuntos
Rim , Urolitíase , Feminino , Masculino , Ratos , Antioxidantes/metabolismo , Cálcio/metabolismo , Creatinina , Etilenoglicol/efeitos adversos , Etilenoglicol/metabolismo , Rim/metabolismo , Magnésio/metabolismo , Oxalatos/efeitos adversos , Oxalatos/metabolismo , Extratos Vegetais/farmacologia , Ureia , Ácido Úrico/metabolismo , Ácido Úrico/farmacologia , Urolitíase/induzido quimicamente , Urolitíase/tratamento farmacológico , Urolitíase/metabolismo , Animais
2.
Xenobiotica ; 46(3): 253-67, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26337830

RESUMO

1. The metabolism of the endothelin receptor antagonist macitentan has been characterized in bile duct-cannulated rats and dogs. 2. In both species, macitentan was metabolized along five primary pathways, i.e. conjugation with glucose (M9), oxidative depropylation (M6), aliphatic hydroxylation (M7), oxidative cleavage of the ethylene glycol linker (M4) and hydrolysis of the sulfamide moiety (M3). Most of the primary metabolites underwent subsequent biotransformation including conjugation with glucuronic acid or glucose, hydrolysis of the sulfamide group or secondary oxidation of the ethylene glycol moiety. 3. Though there were species differences in their relative importance, all metabolic pathways were present in rat and dog. The depropylated M6 was the only metabolite present in plasma of both species. 4. Metabolism was a prerequisite for macitentan excretion as relevant amounts of parent drug were neither detected in bile nor urine. Biliary excretion was the major elimination pathway, while renal elimination was of little importance.


Assuntos
Antagonistas dos Receptores de Endotelina/farmacocinética , Pirimidinas/farmacocinética , Sulfonamidas/farmacocinética , Animais , Ductos Biliares/metabolismo , Biotransformação , Cromatografia Líquida de Alta Pressão , Cães , Relação Dose-Resposta a Droga , Avaliação Pré-Clínica de Medicamentos , Antagonistas dos Receptores de Endotelina/urina , Etilenoglicol/metabolismo , Feminino , Glucose/metabolismo , Hepatócitos/metabolismo , Hidroxilação , Masculino , Redes e Vias Metabólicas , Microssomos Hepáticos/metabolismo , Pirimidinas/urina , Ratos , Ratos Wistar , Sulfonamidas/urina
3.
Artigo em Inglês | MEDLINE | ID: mdl-17393118

RESUMO

In order to compare the effects of several experimental renal calcium oxalate stones formation models in rats and to find a simple and convenient model with significant effect of calcium oxalate crystals deposition in the kidney, several rat models of renal calcium oxalate stones formation were induced by some crystal-inducing drugs (CID) including ethylene glycol (EG), ammonium chloride (AC), vitamin D(3)[1alpha(OH)VitD(3), alfacalcidol], calcium gluconate, ammonium oxalate, gentamicin sulfate, L-hydroxyproline. The rats were fed with drugs given singly or unitedly. At the end of experiment, 24-h urines were collected and the serum creatinine (Cr), blood urea nitrogen (BUN), the extents of calcium oxalate crystal deposition in the renal tissue, urinary calcium and oxalate excretion were measured. The serum Cr levels in the stone-forming groups were significantly higher than those in the control group except for the group EG+L-hydroxyproline, group calcium gluconate and group oxalate. Blood BUN concentration was significantly higher in rats fed with CID than that in control group except for group EG+L-hydroxyproline and group ammonium oxalate plus calcium gluconate. In the group of rats administered with EG plus Vitamin D(3), the deposition of calcium oxalate crystal in the renal tissue and urinary calcium excretion were significantly greater than other model groups. The effect of the model induced by EG plus AC was similar to that in the group induced by EG plus Vitamin D(3). EG plus Vitamin D(3) or EG plus AC could stably and significantly induced the rat model of renal calcium oxalate stones formation.


Assuntos
Oxalato de Cálcio/urina , Cálculos Renais/metabolismo , Rim/metabolismo , Cloreto de Amônio/efeitos adversos , Cloreto de Amônio/metabolismo , Cloreto de Amônio/urina , Animais , Nitrogênio da Ureia Sanguínea , Cálcio/sangue , Cálcio/metabolismo , Cálcio/urina , Gluconato de Cálcio/efeitos adversos , Gluconato de Cálcio/metabolismo , Gluconato de Cálcio/urina , Oxalato de Cálcio/metabolismo , Creatinina/sangue , Cristalização , Modelos Animais de Doenças , Etilenoglicol/efeitos adversos , Etilenoglicol/metabolismo , Etilenoglicol/urina , Gentamicinas/efeitos adversos , Gentamicinas/metabolismo , Gentamicinas/urina , Hidroxicolecalciferóis/efeitos adversos , Hidroxicolecalciferóis/metabolismo , Hidroxicolecalciferóis/urina , Hidroxiprolina/efeitos adversos , Hidroxiprolina/metabolismo , Hidroxiprolina/urina , Rim/patologia , Cálculos Renais/induzido quimicamente , Cálculos Renais/prevenção & controle , Magnésio/metabolismo , Magnésio/urina , Masculino , Microscopia de Polarização , Oxalatos/efeitos adversos , Oxalatos/metabolismo , Oxalatos/urina , Fósforo/sangue , Distribuição Aleatória , Ratos , Ratos Wistar
4.
Artigo em Inglês | MEDLINE | ID: mdl-12049128

RESUMO

This laboratory proof-of-concept research examined the feasibility of adding solid, slow-release macronutrients to a biofilm reactor system to achieve the effective biodegradation of a predominately organic polluted storm water. The target scenario was treating ethylene glycol in storm water, representing the runoff of airport deicing and anti-icing fluids. However, the results can also be generalized for any water polluted with a predominately carbonaceous material. The use of a solid, slow-release nutrient source, compared to amending with a soluble solution in proportion to influent flow, would be ideal for storm water applications and other specialized wastewater flows when maintenance requirements and operational support must be minimized. Several commercially available fertilizers were preliminarily examined to determine which had the best potential to provide the required amount of nutrients. A time-released, polymer-coated granular fertilizer was ultimately selected. Based on laboratory studies, it was found that this fertilizer could provide a controllable source of macronutrients that enabled treatment to a similar degree as if the macronutrients had been dissolved in the influent. The only major operational problem was reduced nutrient delivery from the fertilizer after it became coated with a thick biofilm. However, the inherent intermittent nature of storm water production resulting in wet/dry cycles may minimize the development of a thick biofilm.


Assuntos
Reatores Biológicos , Etilenoglicol/metabolismo , Poluentes Químicos da Água/metabolismo , Biodegradação Ambiental , Biofilmes , Fertilizantes , Nitrogênio/metabolismo , Fósforo/metabolismo , Polímeros , Chuva , Movimentos da Água
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