The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus

Verapamil is a calcium channel blocker that has been widely used in the treatment of cardiovascular abnormalities, hypertension and angina pectoris. The present study investigates the effect of bee venom against verapamil embryotoxicity, bee venom (BV) is characterized with anticancer, anti-inflamma...

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Main Author: Amin A. Seleem
Format: Article
Language:English
Published: SpringerOpen 2016-05-01
Series:Journal of Basic and Applied Zoology
Subjects:
BAK
Online Access:http://www.sciencedirect.com/science/article/pii/S2090989616300030
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spelling doaj-961a893cf1014582ae17019fa085d8512020-11-25T01:06:42ZengSpringerOpenJournal of Basic and Applied Zoology2090-98962016-05-0175C132710.1016/j.jobaz.2016.03.001The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculusAmin A. SeleemVerapamil is a calcium channel blocker that has been widely used in the treatment of cardiovascular abnormalities, hypertension and angina pectoris. The present study investigates the effect of bee venom against verapamil embryotoxicity, bee venom (BV) is characterized with anticancer, anti-inflammatory, anti-rheumatoid, pain-relieving and neuroprotective agents. The current study was carried out on 70 pregnant female mice which were divided into two main groups, the first main group divided into three subgroups, control, treated with single and twice dose daily of verapamil (40 mg/kg) that was treated from zero day of gestation to scarification of females at E10. The second main group that was treated from the seventh day of gestation was divided into four subgroups, control, treated with single dose daily of verapamil (40 mg/kg), injected with bee venom (150 μg/kg/BW) and treated with verapamil combined with bee venom, the females were sacrificed at E14 and E17. The results of this study showed that verapamil treated groups once or twice daily in the first main experiment showed abortion and resorption of uteri embryos. In the second main experiment, developing liver and kidney at E14 and E17 in verapamil treated group showed abnormal architecture of histological picture and alterations of immunohistochemical expression of heat shock protein and BAK that were associated with ultrastructure abnormalities at E17. Bee venom treated group showed the similar structure as control, verapamil combined with bee venom treated group exhibited amelioration against verapamil embryotoxicity. In conclusion, bee venom could be considered as a therapeutic agent and it has a curative effect against the toxicity of verapamil during development of liver and kidney.http://www.sciencedirect.com/science/article/pii/S2090989616300030VerapamilBee venomHeat shock proteinsBAKEmbryotoxicity
collection DOAJ
language English
format Article
sources DOAJ
author Amin A. Seleem
spellingShingle Amin A. Seleem
The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus
Journal of Basic and Applied Zoology
Verapamil
Bee venom
Heat shock proteins
BAK
Embryotoxicity
author_facet Amin A. Seleem
author_sort Amin A. Seleem
title The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus
title_short The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus
title_full The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus
title_fullStr The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus
title_full_unstemmed The protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice Mus musculus
title_sort protective effect of bee venom against verapamil embryotoxicity during prenatal liver and kidney development of mice mus musculus
publisher SpringerOpen
series Journal of Basic and Applied Zoology
issn 2090-9896
publishDate 2016-05-01
description Verapamil is a calcium channel blocker that has been widely used in the treatment of cardiovascular abnormalities, hypertension and angina pectoris. The present study investigates the effect of bee venom against verapamil embryotoxicity, bee venom (BV) is characterized with anticancer, anti-inflammatory, anti-rheumatoid, pain-relieving and neuroprotective agents. The current study was carried out on 70 pregnant female mice which were divided into two main groups, the first main group divided into three subgroups, control, treated with single and twice dose daily of verapamil (40 mg/kg) that was treated from zero day of gestation to scarification of females at E10. The second main group that was treated from the seventh day of gestation was divided into four subgroups, control, treated with single dose daily of verapamil (40 mg/kg), injected with bee venom (150 μg/kg/BW) and treated with verapamil combined with bee venom, the females were sacrificed at E14 and E17. The results of this study showed that verapamil treated groups once or twice daily in the first main experiment showed abortion and resorption of uteri embryos. In the second main experiment, developing liver and kidney at E14 and E17 in verapamil treated group showed abnormal architecture of histological picture and alterations of immunohistochemical expression of heat shock protein and BAK that were associated with ultrastructure abnormalities at E17. Bee venom treated group showed the similar structure as control, verapamil combined with bee venom treated group exhibited amelioration against verapamil embryotoxicity. In conclusion, bee venom could be considered as a therapeutic agent and it has a curative effect against the toxicity of verapamil during development of liver and kidney.
topic Verapamil
Bee venom
Heat shock proteins
BAK
Embryotoxicity
url http://www.sciencedirect.com/science/article/pii/S2090989616300030
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