Search In this Thesis
   Search In this Thesis  
العنوان
Possible protective effect of dimethyl fumarate against isoproterenol-induced cardiac hypertrophy in rats /
المؤلف
Ahmed, Asmaa Ali.
هيئة الاعداد
باحث / Asmaa Ali Ahmed
مشرف / Amany Ali Eissa
مشرف / Engy Mohamed El Morsy
مشرف / Engy Mohamed El Morsy
مشرف / Engy Mohamed El Morsy
الموضوع
Pharmacy. Pharmatical science.
تاريخ النشر
2018.
عدد الصفحات
VIII, 176 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الصيدلة
الناشر
تاريخ الإجازة
1/1/2018
مكان الإجازة
جامعة حلوان - كلية الصيدلة - Pharmacology and Toxicology
الفهرس
Only 14 pages are availabe for public view

from 217

from 217

Abstract

Objectives: To investigate the effect of dimethyl fumarate (DMF) on Toll-like receptor (TLR) signalling pathway in isoproterenol (ISO)-induced cardiac
hypertrophy in rats.
Methods: Sixty adult male Sprague-Dawley rats were randomly allocated into three groups, group I: rats received the vehicles only; group 1I: rats were treated with ISO (5 mg/kg per day S.c.) to induce cardiac hypertrophy for 7 days; and group Ill: rats were given DMF (25 mg/kg per 12 h P.O.) for 28 days, and at the last 7 days, they were treated with ISO (5 mg/kg per day S.c.).
Key findings: Pretreatment with DMF decreased heart-to-body weight ratio,
heart rate and blood pressure and improved the electrocardiographic patterns when compared with ISO group. DMF exhibited cardioprotective effect as evidenced by the reduction in cardiac troponin I, creatine kinase-MS and atrial natriuretic peptide levels. Moreover, DMF alleviated the changed oxidative stress and inflammatory biochemical markers through its anti-inflammatory and antioxidant effects. DMF interfered with TLR signalling pathway, evidenced by decreased levels of the TLR adaptor protein MyD88 and p-ERK1I2 and increased p-Akt level.
Conclusions: Dimethyl fumarate exerted cardioprotective effect against ISO-
induced cardiac hypertrophy. This effect is suggested to be through interfering with TLR signalling pathway.
Key words: cardiac hypertrophy; dimethyl fumarate; isoproterenol; MyD88 ; TLR signaling pathway