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Biomarkers ; 28(2): 177-189, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-36511112

RESUMO

IntroductionDiabetes mellitus is still a raging disease not fully subdued globally, especially in Africa. Our study aims to evaluate the anti-diabetic potentials of Justicia carnea extracts [crude (JCC), free (JFP) and bound phenol (JBP) fractions], in streptozotocin (STZ)-induced type-1 diabetes in male albino rats.Materials and MethodsAbout thirty (30) animals were induced for type 1 diabetes with STZ; thereafter, treatment began for 14 days, after which the animals were euthanized, blood/serum was collected, the liver was removed and divided into two portions, for biochemical and histopathological analyses. Standard procedures were used to evaluate the liver biomarkers, like alanine transaminase (ALT), fructose-1,6-bisphosphatase, glucose-6- phosphatase, hexokinase activities, albumin, bilirubin, hepatic glucose concentrations; antioxidant status and pro- and anti-inflammatory cytokines were similarly assessed.ResultsThese results revealed that the extracts ameliorated the harmful effects of STZ-induced diabetes in the liver by enhancing the activities of liver-based biomarkers, reducing the concentrations of pro-inflammatory cytokines and increasing the anti-inflammatory cytokine.DiscussionThe results agreed with previous research, and the free phenol fraction showed excellent results compared to othersConclusionThese suggested that J. carnea could serve as an alternative remedy in ameliorating liver complications linked to oxidative damage and inflammation in STZ-induced type-1 diabetes.


Assuntos
Carcinoma Hepatocelular , Diabetes Mellitus Experimental , Diabetes Mellitus Tipo 1 , Justicia , Neoplasias Hepáticas , Animais , Masculino , Antioxidantes/farmacologia , Antioxidantes/metabolismo , Biomarcadores/metabolismo , Glicemia/metabolismo , Carcinoma Hepatocelular/complicações , Citocinas/metabolismo , Diabetes Mellitus Experimental/complicações , Diabetes Mellitus Tipo 1/tratamento farmacológico , Diabetes Mellitus Tipo 1/complicações , Diabetes Mellitus Tipo 1/metabolismo , Glucose/metabolismo , Glucose/farmacologia , Inflamação/metabolismo , Justicia/metabolismo , Fígado/metabolismo , Neoplasias Hepáticas/patologia , Estresse Oxidativo , Fenóis , Estreptozocina/metabolismo , Estreptozocina/farmacologia , Ratos
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