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1.
Heliyon ; 10(8): e29518, 2024 Apr 30.
Artigo em Inglês | MEDLINE | ID: mdl-38665563

RESUMO

The need to explore the abundance of natural products cannot be overemphasized particularly in the management of various disease conditions. In traditional medical practice, Vernonia amygdalina has been widely adopted in the management of various inflammatory disorders. The objective of this investigation was to isolate the bioactive principles from the stem-bark and root of V. amygdalina and assess the anti-inflammatory (in vitro) activity of both the crude extracts and the isolated compounds. Following extraction with the methanol, the extract was subjected to gravity column chromatography and the resultant fractions was further purified to obtained pure compounds. The structural elucidation of the compounds were based on data obtained from 1H to 13C nuclear magnetic resonance (NMR) spectroscopies as well as fourier transform infrared (FT-IR). Using diclofenac as a control drug, the albumin denaturation assay was used to determine the in vitro anti-inflammatory activity of the extracts and isolates. Three distinct compounds characterized are vernoamyoside D, luteolin-7-α-o-glucuronide, and vernotolaside, a new glycoside. When compared to diclofenac, which has an IC50 of 167.8 µg/mL, luteolin-7-α-o-glucuronide, vernoamyoside D, and vernotolaside all showed significant inhibitions with respective IC50 values 549.8, 379.5, and 201.7 µg/mL. Vernotolaside is reported for the first time from the root. The assertion that the plant is used in traditional medicine for the management of inflammatory disorder is somewhat validated by the confirmation of the existence of the compounds with the biochemical actions. Further validation of the isolated compounds would be required in animal studies.

2.
Artigo em Inglês | MEDLINE | ID: mdl-33656407

RESUMO

With the rapid increase in pharmaceutical wastewater treatment for diverse applications and to contribute to the understanding of suitability of nanoparticles (NPs) in pharmaceutical effluent treatment, this study was conceptualized. Here, we profiled the concentration of selected heavy metals (Cd, Cr, Pb, Cu and Ni) in pharmaceutical effluent samples over three sampling periods using atomic absorption spectroscopy and evaluated the effectiveness of B. sapida synthesized copper nanoparticles (Cu NPs) in pharmaceutical effluent treatment. The results showed that there was no significant (p > 0.05) difference in the heavy metals concentration of the pharmaceutical effluents across the three sampling periods. This observation could be attributed to the low environmental concentration of the metals that prevented significant leaching into the company's water source through rainfall or the highly effective water treatment pathways that successfully reduced the metals concentration. Despite the observed increase in Cu ions in the treated samples due to the synthesized NPs, its concentration still conforms to the internationally accepted admissible limit in drinkable water. Studies seeking to understand the suitability and toxicological implications of use of the NP-treated effluents are highly encouraged and efforts are underway in this direction.


Assuntos
Blighia/metabolismo , Cobre/química , Nanopartículas/química , Preparações Farmacêuticas , Purificação da Água/métodos , Cobre/metabolismo , Monitoramento Ambiental , Metais Pesados/análise , Metais Pesados/química , Metais Pesados/isolamento & purificação , Nanopartículas/metabolismo , Águas Residuárias/química , Água/química , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/química , Poluentes Químicos da Água/isolamento & purificação
3.
Rev. bras. farmacogn ; 25(1): 29-34, Jan-Feb/2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-746055

RESUMO

Oxidative insult by free radicals has been implicated in drug-induced hepatic damage and this has resulted in frequent episodes of liver disorders. Therapeutic efficacy of antioxidants may provide a possible solution to this menace. This study was carried out to investigate the effect of combined administration of silymarin and vitamin C in rescuing acetaminophen-induced hepatotoxicity in rats. Hepatotoxic rats were orally administered with silymarin and vitamin C at 100 and 200 mg/kg body weight, respectively. At the end of the experiment, liver function indices, antioxidant parameters and histological analysis were evaluated. We observed that the significantly increased (p < 0.05) activities of alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, as well as levels of thiobarbituric acid reactive substances and serum total bilirubin, were markedly reduced following co-administration of silymarin and vitamin C. The compounds also effectively reversed the reduced activities of superoxide dismutase, catalase, glutathione peroxidase, glutathione S-transferase and total protein concentration in the hepatotoxic rats. These findings are indicative of hepatoprotective and antioxidant attributes of the two compounds which are also supported by the histological analysis. The available evidences in this study suggest that the complementary effects of silymarin and vitamin C proved to be capable of ameliorating acetaminophen-mediated hepatic oxidative damage and the probable mechanism is via antioxidative action.

4.
J Trace Elem Med Biol ; 27(4): 370-4, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23726816

RESUMO

Effects of fluoride on the levels of Lipid peroxidation (LP) and antioxidant enzymes in the brain regions of protein undernourished (PU) and well-fed rats (WF) rats exposed to 100 ppm fluoride in drinking water were investigated. The results indicate that the mean body weights and the total brain weights of PU rats as well as those given fluoride (both WF and PU) were significantly (P < 0.05) lower than their respective controls. The weights of different brain regions were also significantly reduced (P < 0.05) in PU rats compared to WF rats except in the brain stem. Fluoride ingestion diminished the weights of WF and PU rats affecting the cerebrum only (in the case of PU rats) and the cerebellum of both WF and PU rats without an effect on the brain stem of both WF and PU. Additionally, increased LP was observed in the cerebrum and cerebellum of PU rats but after fluoride ingestion, 30% increase in LP was observed only in the cerebrum. In the brain stem however, protein undernutrition was accompanied with a significant reduction in LP but the region seems insensitive to fluoride. There were significant reductions (P < 0.05) in CAT, SOD and GSH in all the brain regions (except the GSH level in the brain stem only) of PU rats. Fluoride induced reduction in the activity of CAT in the three brain regions and on SOD activity in cerebrum only for WF rats but no effect of fluoride on all the antioxidants studied in the three brain regions for PU rats. It is concluded that WF and PU rats responded differently to fluoride toxicity. However, it seems that at the dosage used, fluoride toxicity may be a direct effect on the antioxidant enzymes.


Assuntos
Antioxidantes/análise , Encéfalo/efeitos dos fármacos , Caseínas/administração & dosagem , Dieta , Fluoretos/farmacologia , Peroxidação de Lipídeos/efeitos dos fármacos , Animais , Antioxidantes/metabolismo , Encéfalo/enzimologia , Encéfalo/metabolismo , Catalase/análise , Catalase/antagonistas & inibidores , Catalase/metabolismo , Água Potável/química , Fluoretos/administração & dosagem , Glutationa/análise , Glutationa/antagonistas & inibidores , Glutationa/metabolismo , Masculino , Ratos , Ratos Wistar , Superóxido Dismutase/análise , Superóxido Dismutase/antagonistas & inibidores , Superóxido Dismutase/metabolismo
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