Authors :
Satabdi Sinha
Volume/Issue :
Volume 9 - 2024, Issue 7 - July
Google Scholar :
https://tinyurl.com/j4ms37e6
Scribd :
https://tinyurl.com/4a4vr3mu
DOI :
https://doi.org/10.38124/ijisrt/IJISRT24JUL1170
Abstract :
From ancient time whenever we face any
problem, we came to nature for the solution. Our nature
is self renewable, she has solution for every problem, but
we have to find the right path to respond more quickly.
This review is regarding chemical nature of snake venom
and about different life saving drugs extracted from
snake venom. Venoms were originated from non
poisonous proteins, and with subsequent generations
under evolution these proteins become mutated and
modified multiple times to develop deadly poison. With
every modification venom becomes enriched with new
diverse group of compounds. Main constituents of
venom is hydrolyses, PLA2, phosphodiesterases, serine
proteases and metalloproteases. Snakes use their venom
to paralyzed their prey and to digest food, but these
components can be used to treat various life threatening
disease. Cobra, krait and rattle snakes are most
poisionous snakes and their venom contains different
enzymes, are classified as neurotoxic, haemotoxic and
cytotoxic in nature and these have different impact upon
exposure to animal. Neurotoxic venom destroy nervous
system, haemotoxic venom leads to the destruction of red
blood cells and also interfere with blood clotting factors,
whereas cytotoxic venom can cause necrosis and
apoptosis. With the discovary of modern techniques,
isolation of different proteins and peptides and analysis
of their nature are become easier. Most widely used
drugs extracted from snake venom are Tirofiban,
Eptifibatide, Captopril, enalapril, cobratide and
batroxobin ete. The source of tirofiban, captopril,
enalapril batroxobin is the venom of different viper
species. On the other hand, eptifibatide is extracted from
rattle snake and cobratide is from Chinese cobra .
References :
- Daltry, J. C., Wüster, W., & Thorpe, R. S. (1996). Diet and snake venom evolution. Nature, 379(6565), 537-540.
- Koh, D. C. I., Armugam, A., & Jeyaseelan, K. (2006). Snake venom components and their applications in biomedicine. Cellular and Molecular Life Sciences CMLS, 63, 3030-3041.
- Chippaux, J. P., Williams, V., & White, J. (1991). Snake venom variability: methods of study, results and interpretation. Toxicon, 29(11), 1279-1303.
- Osipov, A., & Utkin, Y. (2023). What are the neurotoxins in hemotoxic snake venoms? . International journal of molecular sciences, 24(3), 2919.
- Minton, S. A. (1990, March). Neurotoxic snake envenoming. In Seminars in Neurology (Vol. 10, No. 01, pp. 52-61). © 1990 by Thieme Medical Publishers, Inc..
- Loring, R. H., Aizenman, E., Lipton, S. A., & Zigmond, R. E. (1989). Characterization of nicotinic receptors in chick retina using a snake venom neurotoxin that blocks neuronal nicotinic receptor function. Journal of Neuroscience, 9(7), 2423-2431.
- Chan, Y. S., Cheung, R. C. F., Xia, L., Wong, J. H., Ng, T. B., & Chan, W. Y. (2016). Snake venom toxins: toxicity and medicinal applications. Applied microbiology and biotechnology, 100, 6165-6181.
- Escoubas, P., & King, G. F. (2009). Venomics as a drug discovery platform. Expert review of proteomics, 6(3), 221-224.
- Jimenez, R., Ikonomopoulou, M. P., Lopez, J. A., & Miles, J. J. (2018). Immune drug discovery from venoms. Toxicon, 141, 18-24.
- Peigneur, S., & Tytgat, J. (2018). Toxins in drug discovery and pharmacology. Toxins, 10(3), 126.
- Almeida, J. R., Resende, L. M., Watanabe, R. K., Carregari, V. C., Huancahuire-Vega, S., da S Caldeira, C. A., ... & Da Silva, S. L. (2017). Snake venom peptides and low mass proteins: molecular tools and therapeutic agents. Current medicinal chemistry, 24(30), 3254-3282.
- Diniz-Sousa, R., Caldeira, C. A. D. S., Pereira, S. S., Da Silva, S. L., Fernandes, P. A., Teixeira, L. M., ... & Soares, A. M. (2023). Therapeutic applications of snake venoms: An invaluable potential of new drug candidates. International Journal of Biological Macromolecules, 238, 124357.
From ancient time whenever we face any
problem, we came to nature for the solution. Our nature
is self renewable, she has solution for every problem, but
we have to find the right path to respond more quickly.
This review is regarding chemical nature of snake venom
and about different life saving drugs extracted from
snake venom. Venoms were originated from non
poisonous proteins, and with subsequent generations
under evolution these proteins become mutated and
modified multiple times to develop deadly poison. With
every modification venom becomes enriched with new
diverse group of compounds. Main constituents of
venom is hydrolyses, PLA2, phosphodiesterases, serine
proteases and metalloproteases. Snakes use their venom
to paralyzed their prey and to digest food, but these
components can be used to treat various life threatening
disease. Cobra, krait and rattle snakes are most
poisionous snakes and their venom contains different
enzymes, are classified as neurotoxic, haemotoxic and
cytotoxic in nature and these have different impact upon
exposure to animal. Neurotoxic venom destroy nervous
system, haemotoxic venom leads to the destruction of red
blood cells and also interfere with blood clotting factors,
whereas cytotoxic venom can cause necrosis and
apoptosis. With the discovary of modern techniques,
isolation of different proteins and peptides and analysis
of their nature are become easier. Most widely used
drugs extracted from snake venom are Tirofiban,
Eptifibatide, Captopril, enalapril, cobratide and
batroxobin ete. The source of tirofiban, captopril,
enalapril batroxobin is the venom of different viper
species. On the other hand, eptifibatide is extracted from
rattle snake and cobratide is from Chinese cobra .