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1.
Cell Mol Biol (Noisy-le-grand) ; 67(1): 171-176, 2021 Jan 31.
Artigo em Inglês | MEDLINE | ID: mdl-34817350

RESUMO

Datura metel has been recommended in several human disorders including a remedy for liver toxicity. The current study was designed to evaluate the hepatoprotective effect of methanolic extract of D. metel in animal model. Acute toxicity of methanolic crude extract of Datura metel (MEDM) was studied in animals in various doses 500-2000 mg/kg. Mice of either sex were divided into groups (n=6). One group received normal saline intraperitonially as negative control, while other gentamicin 100mg/kg for 8 days as positive control. 3rd group received 50mg/kg silymarin as standard, 4th group received 100mg/kg of MEDM, 5th group received 200mg/kg MEDM while 6th group received 300mg/kg MEDM and gentamicin 100mg/kg for 8 days. The blood samples were collected on 9th day and the animals were then dissected and the liver of all the animals were isolated. MEDM was found safe in acute toxicity test at various doses up to 2000 mg/kg. The levels of serum glutamic pyruvic transaminase and alkaline phosphatase were elevated significantly with gentamicin treatment which significantly down-regulated by MEDM (100, 200 and 300 mg/kg) in a dose dependent manner.. The histological examination showed that the MEDM has markedly treated the inflammatory infiltrate, fatty changes and congested blood vessels which were induced by gentamicin.  The findings of our study thus proved the absolute of MEDM in acute toxicity test; followed by significant hepatoprotective effect in gentamicin induced hepatotoxic mice.


Assuntos
Doença Hepática Induzida por Substâncias e Drogas/prevenção & controle , Datura metel/química , Fígado/efeitos dos fármacos , Extratos Vegetais/farmacologia , Alanina Transaminase/sangue , Alanina Transaminase/metabolismo , Fosfatase Alcalina/sangue , Fosfatase Alcalina/metabolismo , Animais , Doença Hepática Induzida por Substâncias e Drogas/etiologia , Avaliação Pré-Clínica de Medicamentos , Feminino , Gentamicinas , Fígado/metabolismo , Fígado/patologia , Masculino , Metanol/química , Camundongos , Fitoterapia/métodos , Extratos Vegetais/química , Substâncias Protetoras/química , Substâncias Protetoras/farmacologia , Testes de Toxicidade Aguda/métodos
2.
Cell Mol Biol (Noisy-le-grand) ; 66(4): 208-213, 2020 06 25.
Artigo em Inglês | MEDLINE | ID: mdl-32583780

RESUMO

Datura metel is traditionally used as a remedy for renal toxicity. However, the nephroprotection has not been scientifically validated yet. To evaluate the nephroprotective like effect of methanolic extract of D. metel in gentamicin induced mice model, mice of either sex were divided into groups. One group received normal saline as negative control. The 2nd group received gentamicin 100mg/kg for 8 days as positive control, 3rd group received 50mg/kg silymarin as standard, while the reaming groups received 100, 200 and 300 mg/kg of MEDM and gentamicin 100mg/kg, for 8 days. The blood and urine samples were collected on 9th day, animals were then dissected and whole kidneys were removed and preserved in formalin for later histological examinations. The level of serum creatinine, blood urea nitrogen, urine creatinine and urine urea were significantly (P<0.05) elevated and the renal MDA level was also elevated significantly (P<0.05) by gentamicin in mice. After the treatment of test animals with MEDM, the elevated level of serum and urine biomarkers by gentamicin were reversed by MEDM. The nephroprotective effect was found in dose dependent manner. As the MEDM significantly protected the nephrotoxicity via its antioxidant effect. The findings of our study thus proved the scientific background for the nephroprotective effect of MEDM.


Assuntos
Datura metel/química , Gentamicinas/efeitos adversos , Nefropatias/induzido quimicamente , Nefropatias/patologia , Extratos Vegetais/uso terapêutico , Substâncias Protetoras/uso terapêutico , Animais , Nitrogênio da Ureia Sanguínea , Creatinina/sangue , Creatinina/urina , Modelos Animais de Doenças , Feminino , Rim/efeitos dos fármacos , Rim/patologia , Nefropatias/sangue , Nefropatias/urina , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Camundongos , Compostos Fitoquímicos/análise , Compostos Fitoquímicos/farmacologia , Compostos Fitoquímicos/uso terapêutico , Extratos Vegetais/farmacologia , Substâncias Protetoras/farmacologia , Ureia/urina
4.
Saudi Med J ; 37(9): 963-7, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-27570851

RESUMO

OBJECTIVES: To assess the association of adenomyotic foci with co-existing benign ovarian cysts.  METHODS: This prospective cross-sectional study consisted of 100 consecutive hysterectomy specimens referred to Histopathology Section of Pathology Department, Peshawar Medical College, Peshawar, Pakistan by its attached teaching hospitals from January 2011 to December 2012. Hematoxylin and eosin stained sections were examined for adenomyotic foci and the presence of co-existent ovarian cysts. For evaluation of estrogen receptor (ER) status immunohistochemical stains were applied and H-scoring system was used with a score greater than 50 as positive.  RESULTS: Out of the 100 hysterectomy specimens, 25 cases had both adenomyosis and ovarian cysts. The ER status of adenomyotic foci was positive in 20% cases and negative in 80% cases. The commonest type of ovarian cyst was hemorrhagic luteal cyst (28%), followed by serous and mucinous cystadenoma (20%) each. Out of the 28% cases of functional cysts, 71.5% were ER positive and 28.5% were ER negative. The p-value for association of ER status of adenomyotic foci with functional cysts was 0.0004; however, p-value was not significant in comparing cases with controls. All 72% cases of nonfunctional cysts were ER negative. However, 44% of functional cysts were not associated with adenomyotic foci.   CONCLUSION: This study concludes that besides functional ovarian cysts, other local factors may be responsible for the development of adenomyosis.


Assuntos
Adenomiose/complicações , Cistos Ovarianos/complicações , Adulto , Estudos Transversais , Feminino , Humanos , Imuno-Histoquímica , Pessoa de Meia-Idade , Estudos Prospectivos , Receptores de Estrogênio/análise
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