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Molecular assessment of protective effect of Vitex negundo in ISO induced myocardial infarction in rats.
- Source :
-
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2017 Aug; Vol. 92, pp. 249-253. Date of Electronic Publication: 2017 May 24. - Publication Year :
- 2017
-
Abstract
- Myocardial infarction (MI) is the one of the major causes of death worldwide, however the molecular mechanisms hidden under this disease conditions remain unknown. This demands serious attention to unravel the molecular mechanisms to identify the therapeutic strategies either to prevent or to control MI. Ayurveda is becoming one of the best alternatives for the modern medicines. On the other hand, Vitex negundo is one of the medicinally important plants used for various diseases and to date, its cardioprotective role is not fully elucidated. In the present study, we made an attempt to understand the cardiac signaling cascade of Akt1 and NF-κB in isoproterenol (ISO)-induced MI, and targeting these signaling molecules by using V. negundo leaf ethanolic extract (VNE). Our findings demonstrate that VNE significantly protects the ISO-induced MI by regulating NF-κB and Akt1experssion in rats.<br /> (Copyright © 2017 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Animals
Cardiotonic Agents isolation & purification
Cardiotonic Agents pharmacology
Male
Myocardial Infarction metabolism
NF-kappa B antagonists & inhibitors
NF-kappa B metabolism
Proto-Oncogene Proteins c-akt antagonists & inhibitors
Proto-Oncogene Proteins c-akt metabolism
Rats
Rats, Wistar
Treatment Outcome
Cardiotonic Agents therapeutic use
Isoproterenol toxicity
Myocardial Infarction chemically induced
Myocardial Infarction prevention & control
Vitex
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 92
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 28551544
- Full Text :
- https://doi.org/10.1016/j.biopha.2017.05.078