Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.toxicon.2009.12.023
Title: Venom neutralization by purified bioactive molecules: Synthetic peptide derivatives of the endogenous PLA2inhibitory protein PIP (a mini-review)
Authors: Thwin, M. 
Samy, R.P. 
Gopalakrishnakone, P. 
Satyanarayanajois, S.D.
Keywords: Antivenom
Metalloproteinase
Neutralization
Peptide inhibitor
Secretory phospholipase A2
Snake venom
Issue Date: 2010
Source: Thwin, M., Samy, R.P., Gopalakrishnakone, P., Satyanarayanajois, S.D. (2010). Venom neutralization by purified bioactive molecules: Synthetic peptide derivatives of the endogenous PLA2inhibitory protein PIP (a mini-review). Toxicon 56 (7) : 1275-1283. ScholarBank@NUS Repository. https://doi.org/10.1016/j.toxicon.2009.12.023
Abstract: Envenomation due to snakebite constitutes a significant public health problem in tropical and subtropical countries. Antivenom therapy is still the mainstay of treatment for snake envenomation, and yet despite recent research focused on the prospects of using antivenom adjuncts to aid in serotherapy, no new products have emerged so far for therapeutic use. Various methodologies including molecular biology, crystallography, functional and morphological approaches, etc., are employed in the search for such inhibitors with a view to generate molecules that can stop partially or completely the activities of toxic phospholipase A2 (PLA2) and snake venom metalloproteinase (SvMPs) enzymes at the molecular level. Herein, both natural and synthetic inhibitors derived from a variety of sources including medicinal plants, mammals, marine animals, fungi, bacteria, and from the venom and blood of snakes have been briefly reviewed. Attention has been focused on the snake serum-based phospholipase A2 inhibitors (PLIs), particularly on the PLI derived from python snake serum (PIP), highlighting the potential of the natural product, PIP, or possible derivatives of it, as a complementary treatment to serotherapy against the inflammation and/or muscle-damaging activity of snake venoms. The data indicate a more efficient pathway for inhibition and blocking the activity of PLA2s and matrix metalloproteinases (MMPs), thus representing a feasible complementary treatment for snakebites. Such information may be helpful for interfering on the biological processes that these molecules are involved in human inflammatory-related diseases, and also for the development of new drugs for treatment of snake envenomation. © 2010 Elsevier Ltd.
Source Title: Toxicon
URI: http://scholarbank.nus.edu.sg/handle/10635/23976
ISSN: 00410101
DOI: 10.1016/j.toxicon.2009.12.023
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