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Diallyl disulfide ameliorates isoproterenol induced cardiac hypertrophy activating mitochondrial biogenesis via eNOS-Nrf2-Tfam pathway in rats.
Khatua, Tarak Nath; Dinda, Amit K; Putcha, Uday K; Banerjee, Sanjay K.
Affiliation
  • Khatua TN; Division of Medicinal Chemistry and Pharmacology, Indian Institute of Chemical Technology, Hyderabad 500607, India.
  • Dinda AK; Drug Discovery Research Center, Translational Health Science and Technology Institute, Faridabad 121001, India.
  • Putcha UK; Department of Pathology, All India Institute of Medical Sciences, New Delhi 110029, India.
  • Banerjee SK; Division of Pathology, National Institute of Nutrition, Hyderabad 500607, India.
Biochem Biophys Rep ; 5: 77-88, 2016 Mar.
Article in En | MEDLINE | ID: mdl-28955809
ABSTRACT
The beneficial effect of garlic on cardiovascular disease is well known. However, the use of raw garlic against cardiac hypertrophy is not established. In the present study we explored whether raw garlic and its compound, diallyl disulfide (DADS) could inhibit hypertrophy through H2S and/or mitochondrial biogenesis. Cardiac hypertrophy was induced in rat by giving isoproterenol at the dose of 5 mg/kg/day subcutaneously for 14 days through alzet minipump. Aqueous garlic homogenate, DADS and NaHS (liberate H2S) were fed to third, forth and fifth group of rats for 14 days at a dose of 250 mg/kg/day, 50 mg/kg/day, 14 µM/kg/day respectively. Garlic and DADS reduced cardiac hypertrophy markers and normalized mitochondrial ETC-complex activities, mitochondrial enzyme activites and mitochondrial biogenetic and apoptotic genes expression. Garlic and DADS enhanced eNOS and p-AKT level in rat heart along with increased NRF2 protein level and Tfam gene expression. However, normalization was not observed after administration of NaHS which generates H2S in-vivo. In conclusion, garlic and DADS induces mitochondrial biogenesis and ameliorates cardiac hypertrophy via activation of eNOS-Nrf2-Tfam pathway in rats.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biochem Biophys Rep Year: 2016 Document type: Article Affiliation country: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biochem Biophys Rep Year: 2016 Document type: Article Affiliation country: India
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