Zinc Oxide Nanoparticles: The Hidden Danger
International Journal of Biochemistry, Biophysics & Molecular Biology • 2016
معلومات البحث
المؤلفون
Mona A. El Shemy1, Naglaa Ibrahim Azab2, *, Rabab Fawzy Salim
الكلمات المفتاحية
Keywords: Zinc Oxide Nanoparticles (ZnO-NPs), Vitamin E, Liver, Oxidative Stress,
Tumor Necrosis Factor Alpha (TNF- α)
المجلة العلمية
International Journal of Biochemistry, Biophysics & Molecular Biology
الناشر
science publishing group
المجلد
2
العدد
1
الصفحات
1-9
publication.type
International
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
Abstract: Zinc oxide nanoparticles (ZnO-NPs) are used in many industries and medications, increasing the exposure to
ZnO-NPs that may have harmful side effects. So, we studied the hepatotoxic effect of ZnO-NPs and explored the role of
vitamin E in the reduction of their toxic effects. Forty male albino rats, divided into four groups (10 rats per group) were
included in the study; control group, ZnO-NPs intoxicated group, vitamin E control group and vitamin E protected ZnO-NPs
intoxicated group. ZnO-NPs were given in a dose of 400 mg / kg body weight for seven days. Vitamin E was given in a dose of
100 mg / kg body weight for four weeks. Our results showed that ZnO-NPs induced liver damage indicated by significant
increase of serum ALT and AST and significant decrease of serum albumin and total protein levels. Moreover, ZnO-NPs
induced oxidative stress in the liver suggested by significant elevation of malondialdehyde level and significant reduction of
reduced glutathione level, glutathione peroxidase activity and glutathione peroxidase-1 expression in liver homogenate.
Furthermore, ZnO-NPs caused significant increase in the serum pro-inflammatory biomarker, tumor necrosis factor alpha
(TNF- α). On the other hand, vitamin E alleviated the liver damage, oxidative stress and the elevated serum TNF- α induced by
ZnO-NPs
ZnO-NPs that may have harmful side effects. So, we studied the hepatotoxic effect of ZnO-NPs and explored the role of
vitamin E in the reduction of their toxic effects. Forty male albino rats, divided into four groups (10 rats per group) were
included in the study; control group, ZnO-NPs intoxicated group, vitamin E control group and vitamin E protected ZnO-NPs
intoxicated group. ZnO-NPs were given in a dose of 400 mg / kg body weight for seven days. Vitamin E was given in a dose of
100 mg / kg body weight for four weeks. Our results showed that ZnO-NPs induced liver damage indicated by significant
increase of serum ALT and AST and significant decrease of serum albumin and total protein levels. Moreover, ZnO-NPs
induced oxidative stress in the liver suggested by significant elevation of malondialdehyde level and significant reduction of
reduced glutathione level, glutathione peroxidase activity and glutathione peroxidase-1 expression in liver homogenate.
Furthermore, ZnO-NPs caused significant increase in the serum pro-inflammatory biomarker, tumor necrosis factor alpha
(TNF- α). On the other hand, vitamin E alleviated the liver damage, oxidative stress and the elevated serum TNF- α induced by
ZnO-NPs
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