Banner

Protective Effects of Alfa Lipoic Acid on Amiodarone Induced Hypothyroidism in Adult Male Albino Rats (A Biochemical, Histopathological and Immunohistochemical Study)

• 2022
العودة
معلومات البحث
المؤلفون Amal Mahmoud Elshazly1*,Bodour Baiomy1,Yasmeen Mohammed Ismail El Sayed2 , Asmaa Y.A. Hussein 3*, Neama Mahmoud Taha 4, and Ali Mohamed Ali 1
الكلمات المفتاحية Not Available
المجلة العلمية Not Available
الناشر Not Available
المجلد Not Available
العدد Not Available
الصفحات Not Available
publication.type Local
رابط البحث Not Available
المواد المرفقة Not Available
الملخص
Background: Amiodarone (AMD) is a highly effective antiarrhythmic agent. Its utilization is associated with toxic
effects on thyroid gland. The aim of this research to evaluate the AMD chronic administration potential toxic impact
on the thyroid gland and evaluate Alfa lipoic acid (α LA) possible protective impact.
Materials and methods: 40 adult male albino rats were equally separated into 4 groups, group I (control) given 1ml
distilled water for 12 wks., group II (AMD tested group) received a single dose of 40 mg/kg /day AMD for 12 wks.
Group III (AMD+ α-LA), where AMD was given as group II and a dose of 100 mg/kg of α-LA for 12 weeks, group
IV received AMD in doses similar to group II, then the drug was withdrawn and the rats took no treatment for
additional 4 weeks. All groups were sacrificed after 12 weeks except group IV after 16 weeks from the beginning of
the experiment. Results: In AMD treated group; the T3, T4 and catalase [CAT] serum levels were significantly
reduced along with significant elevation in TSH, IL6 and malondialdehyde [MDA] level, light microscopic
examination of AMD group showed cellular degeneration of follicles and colloid peripheral vacuolation along with
strong positive immune reaction for Ki-67 declared in AMD group as compared to those of other groups.
Additionally, electron microscopic studies supported these results. Conclusion: Chronic administration of AMD
induced thyroid damage which could be improved by Co-supplementation of α-LA.