Document Detail


Potential role of Borreria hispida in ameliorating cardiovascular risk factors.
MedLine Citation:
PMID:  19455054     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Borreria hispida (BHE), a weed of Rubiaceae family, is being used from time immemorial as an alternative therapy for diabetes. To evaluate the scientific background of using BHE as therapy to reduce cardiovascular risk, a group of rats were given BHE for a period of 30 days, whereas control animals were given the vehicle only. The animals were sacrificed, the hearts were isolated, and perfused with buffer. All the hearts were subjected to 30-minute ischemia followed by 2-hour reperfusion. Compared with vehicle-treated rats, BHE-treated rat hearts showed improved post-ischemic ventricular function and exhibited reduced myocardial infarct size and cardiomyocyte apoptosis. The level of cytochrome c expression and caspase 3 activation was also reduced. BHE elevated antiapoptotic proteins Bcl-2 and heme oxygenase-1 and stimulated the phosphorylation of survival protein Akt simultaneously decreasing the apoptotic proteins Bax and Src. In addition, BHE enhanced the protein expression of peroxisome proliferator-activated receptor-gamma, peroxisome proliferator-activated receptor-delta, and Glut-4, probably revealing the antiobese and antidiabetic potential of BHE. These results indicate that treatment with BHE improves cardiac function and ameliorates various risk factors associated with cardiac disease, suggesting that BHE can be considered as a potential plant-based nutraceutical and pharmaceutical agent for the management of cardiovascular diseases.
Authors:
Hannah R Vasanthi; Subhendu Mukherjee; Istvan Lekli; Diptarka Ray; Gayathri Veeraraghavan; Dipak K Das
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Publication Detail:
Type:  In Vitro; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of cardiovascular pharmacology     Volume:  53     ISSN:  1533-4023     ISO Abbreviation:  J. Cardiovasc. Pharmacol.     Publication Date:  2009 Jun 
Date Detail:
Created Date:  2009-06-22     Completed Date:  2009-10-08     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7902492     Medline TA:  J Cardiovasc Pharmacol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  499-506     Citation Subset:  IM    
Affiliation:
Herbal and Indian Medicine Research Laboratory, Department of Biochemistry, Sri Ramachandra University, Chennai, India.
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MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis / drug effects
Cell Survival / drug effects
Heart / drug effects*,  physiopathology
Heme Oxygenase-1 / metabolism
Male
Myocardial Reperfusion Injury / drug therapy*,  metabolism,  pathology,  physiopathology
Myocardium / metabolism,  pathology*
PPAR delta / metabolism
PPAR gamma / metabolism
Phosphorylation
Plant Components, Aerial / chemistry
Plant Extracts / chemistry,  pharmacology*,  therapeutic use
Rats
Rats, Sprague-Dawley
Risk Factors
Rubiaceae / chemistry*
Signal Transduction
bcl-2-Associated X Protein / metabolism
Grant Support
ID/Acronym/Agency:
HL 22559/HL/NHLBI NIH HHS; HL 33889/HL/NHLBI NIH HHS; HL 34360/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/PPAR delta; 0/PPAR gamma; 0/Plant Extracts; 0/bcl-2-Associated X Protein; EC 1.14.99.3/Heme Oxygenase-1

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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