Cargando…

Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice

Diabetes mellitus is one of the major health problems. This study was designed to investigate the effect of biotin to regulate blood glucose level, reduced toxicity and oxidative stress in liver of diabetic mice STZ-induced type 1. Male mice were divided into three groups, the first one served as th...

Descripción completa

Detalles Bibliográficos
Autores principales: Aldahmash, Badr Abdullah, El-Nagar, Doaa Mohamed, Ibrahim, Khalid Elfakki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778583/
https://www.ncbi.nlm.nih.gov/pubmed/26981014
http://dx.doi.org/10.1016/j.sjbs.2015.09.027
_version_ 1782419489479983104
author Aldahmash, Badr Abdullah
El-Nagar, Doaa Mohamed
Ibrahim, Khalid Elfakki
author_facet Aldahmash, Badr Abdullah
El-Nagar, Doaa Mohamed
Ibrahim, Khalid Elfakki
author_sort Aldahmash, Badr Abdullah
collection PubMed
description Diabetes mellitus is one of the major health problems. This study was designed to investigate the effect of biotin to regulate blood glucose level, reduced toxicity and oxidative stress in liver of diabetic mice STZ-induced type 1. Male mice were divided into three groups, the first one served as the control group, the second and the third groups received single ip dose of 150 mg/kg of STZ, the second group served as the untreated diabetic group, the third group received daily oral dose of 15 mg/kg of biotin, livers and liver index showed insignificant difference among groups. Blood glucose level showed a significant decrease in treated diabetic mice compared to untreated diabetic mice. Biochemical analysis showed a significant decrease in liver enzymes AST and ALT compared to the control group. Histopathological examination showed severe changes in untreated diabetic liver tissue manifested by dilated portal vein, leukocytic infiltration, fatty degeneration and moderate to severe histopathological score, whereas, treated diabetic mice with biotin showed reduction in hepatotoxicity represented by appearance of relative healthy hepatocytes and normal histopathological score. Immunohistochemistry of acrolein showed intense immunoreactions in liver section of untreated diabetic mice and faint immunoreactions in treated diabetic mice with biotin as evidence to oxidative stress reduction.
format Online
Article
Text
id pubmed-4778583
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-47785832016-03-15 Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice Aldahmash, Badr Abdullah El-Nagar, Doaa Mohamed Ibrahim, Khalid Elfakki Saudi J Biol Sci Original Article Diabetes mellitus is one of the major health problems. This study was designed to investigate the effect of biotin to regulate blood glucose level, reduced toxicity and oxidative stress in liver of diabetic mice STZ-induced type 1. Male mice were divided into three groups, the first one served as the control group, the second and the third groups received single ip dose of 150 mg/kg of STZ, the second group served as the untreated diabetic group, the third group received daily oral dose of 15 mg/kg of biotin, livers and liver index showed insignificant difference among groups. Blood glucose level showed a significant decrease in treated diabetic mice compared to untreated diabetic mice. Biochemical analysis showed a significant decrease in liver enzymes AST and ALT compared to the control group. Histopathological examination showed severe changes in untreated diabetic liver tissue manifested by dilated portal vein, leukocytic infiltration, fatty degeneration and moderate to severe histopathological score, whereas, treated diabetic mice with biotin showed reduction in hepatotoxicity represented by appearance of relative healthy hepatocytes and normal histopathological score. Immunohistochemistry of acrolein showed intense immunoreactions in liver section of untreated diabetic mice and faint immunoreactions in treated diabetic mice with biotin as evidence to oxidative stress reduction. Elsevier 2016-03 2015-10-09 /pmc/articles/PMC4778583/ /pubmed/26981014 http://dx.doi.org/10.1016/j.sjbs.2015.09.027 Text en © 2015 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Aldahmash, Badr Abdullah
El-Nagar, Doaa Mohamed
Ibrahim, Khalid Elfakki
Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice
title Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice
title_full Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice
title_fullStr Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice
title_full_unstemmed Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice
title_short Attenuation of hepatotoxicity and oxidative stress in diabetes STZ-induced type 1 by biotin in Swiss albino mice
title_sort attenuation of hepatotoxicity and oxidative stress in diabetes stz-induced type 1 by biotin in swiss albino mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778583/
https://www.ncbi.nlm.nih.gov/pubmed/26981014
http://dx.doi.org/10.1016/j.sjbs.2015.09.027
work_keys_str_mv AT aldahmashbadrabdullah attenuationofhepatotoxicityandoxidativestressindiabetesstzinducedtype1bybiotininswissalbinomice
AT elnagardoaamohamed attenuationofhepatotoxicityandoxidativestressindiabetesstzinducedtype1bybiotininswissalbinomice
AT ibrahimkhalidelfakki attenuationofhepatotoxicityandoxidativestressindiabetesstzinducedtype1bybiotininswissalbinomice