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Silymarin Ameliorates Diabetes-Induced Proangiogenic Response in Brain Endothelial Cells through a GSK-3β Inhibition-Induced Reduction of VEGF Release
المؤلفون المشاركون
Alhusban, Ahmed
Alkhazaleh, Enaam
El-Elimat, Tamam
المصدر
العدد
المجلد 2017، العدد 2017 (31 ديسمبر/كانون الأول 2017)، ص ص. 1-9، 9ص.
الناشر
Hindawi Publishing Corporation
تاريخ النشر
2017-10-25
دولة النشر
مصر
عدد الصفحات
9
التخصصات الرئيسية
الملخص EN
Diabetes mellitus (DM) is a major risk factor for cardiovascular disease.
Additionally, it was found to induce a dysfunctional angiogenic response in the brain that was attributed to oxidative stress.
Milk thistle seed extract (silymarin) has potent antioxidant properties, though its potential use in ameliorating diabetes-induced aberrant brain angiogenesis is unknown.
Glycogen synthase kinase-3β is a regulator of angiogenesis that is upregulated by diabetes.
Its involvement in diabetes-induced angiogenesis is unknown.
To evaluate the potential of silymarin to ameliorate diabetes-induced aberrant angiogenesis, human brain endothelial cells (HBEC-5i) were treated with 50 μg/mL advanced glycation end (AGE) products in the presence or absence of silymarin (50, 100 μM).
The angiogenic potential of HBEC-5i was evaluated in terms of migration and in vitro tube formation capacities.
The involvement of GSK-3β was also evaluated.
AGE significantly increased the migration and tube formation rates of HBEC-5i by about onefold (p=0.0001).
Silymarin reduced AGE-induced migration in a dose-dependent manner where 50 μM reduced migration by about 50%, whereas the 100 μM completely inhibited AGE-induced migration.
Similarly, silymarin 50 μg/mL blunted AGE-induced tube formation (p=0.001).
This effect was mediated through a GSK-3β-dependent inhibition of VEGF release.
In conclusion, silymarin inhibits AGE-induced aberrant angiogenesis in a GSK-3β-mediated inhibition of VEGF release.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Alhusban, Ahmed& Alkhazaleh, Enaam& El-Elimat, Tamam. 2017. Silymarin Ameliorates Diabetes-Induced Proangiogenic Response in Brain Endothelial Cells through a GSK-3β Inhibition-Induced Reduction of VEGF Release. Journal of Diabetes Research،Vol. 2017, no. 2017, pp.1-9.
https://search.emarefa.net/detail/BIM-1173910
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Alhusban, Ahmed…[et al.]. Silymarin Ameliorates Diabetes-Induced Proangiogenic Response in Brain Endothelial Cells through a GSK-3β Inhibition-Induced Reduction of VEGF Release. Journal of Diabetes Research No. 2017 (2017), pp.1-9.
https://search.emarefa.net/detail/BIM-1173910
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Alhusban, Ahmed& Alkhazaleh, Enaam& El-Elimat, Tamam. Silymarin Ameliorates Diabetes-Induced Proangiogenic Response in Brain Endothelial Cells through a GSK-3β Inhibition-Induced Reduction of VEGF Release. Journal of Diabetes Research. 2017. Vol. 2017, no. 2017, pp.1-9.
https://search.emarefa.net/detail/BIM-1173910
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references
رقم السجل
BIM-1173910
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
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