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Author(s): Tarani Prakash Shrivastava, Anand Shrivastava, Anup Chakraborty, Neeraj Upmanyu

Email(s): taranipshrivastava@gmail.com

Address: School of Pharmacy and Research, People's University, Bhanpur, Bhopal (M P.) India.

Published In:   Volume - 29,      Issue - 1,     Year - 2016


Cite this article:
Shrivastava, Shrivastava, Chakraborty and Upmanyu (2016).A Phenolic Fraction of Mulberry Fruit Extract Modulates Microvasculature Growth and Morphogenesis in Chick Aortic Ring Assay. Journal of Ravishankar University (Part-B: Science), 29(1), pp.104.



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A Phenolic Fraction of Mulberry Fruit Extract Modulates Microvasculature Growth and Morphogenesis in Chick Aortic Ring Assay

Tarani Prakash Shrivastava, Anand Shrivastava, Anup Chakraborty and Neeraj Upmanyu

School of Pharmacy and Research, People's University, Bhanpur, Bhopal (M P.) India

Corresponding author email:taranipshrivastava@gmail.com

[Received 13 January 2016, accepted 28 January 2016]

Abstract: To progress, cancers require a source of nutrition and oxygen. Tumour that lack angiogenesis remain doman rapid logarithmic growth follows the acquisition of a blood supply, tumour angiogenesis triggers this activation. Neoplain are able to synthesize or induce certain polypeptides, VEGF is one of the most critical factors that induce angiogenesis d being targeted for anti-angiogenesis treatment. However, most of current anti-VEGF agents cause side effects when given chronically, need of naturally ocurring VEGF inhibitors is highly evident. In present study a phenolic fraction of ethanolic extract of Mulberry fruit was subjected to study in- vitro anti-kinase activity and chick aortic ring assay. ELISA assay kit was used to determine the ability of MBE (mulberry extract) to inhibit VEGFR2 tyrosine kinase activity. A strong inhibition of VEGFR kinase activity, with an ICo of about 10ng/ml was exhibited. In aortic ring assay, chick aortic rings were embedded in the matrigel and fed with medium containing different concentrations of MBE, rings were then stimulated with VEGF or ECGS and sprout formation was observed microscopically, a dose dependent decrease in capillary sprouting was observed with MBE treatments, the growing sprouts were shorter and fewer cells migrated into the matrix indicating that MBE could inhibit VEGF and ECGS-induced micro vessel sprouting. This study warrants the potential usefulness of MBE as a safe, natural VEGF inhibitor.

Keywords: angiogenesis inhibitors, berbal medicine, VEGF, metastasis, microvasculature



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