{"title":"Evaluation of the Pharmacological Properties of Piscine Venoms from both Lionfish (Pterois) and Stonefish (Synanceja)","authors":"K. Ramalingam","doi":"10.2174/1573408016999201231204746","DOIUrl":null,"url":null,"abstract":"\n\n For the past 70 years, the focus of research is on the search for poisons and toxins\nfound in venomous and poisonous organisms, purely directed towards the pharmacological properties\nof the toxins. In the research of finding novel compounds in pharmaceutical research, the identified\nsource was the piscine venom.\n\n\n\nThe Scorpaenidae family was considered the most venomous of all. The toxins isolated from\nstonefish and lionfish are responsible for the effects caused in cardiovascular and neuromuscular systems\nand also for causing cytolytic activities. The main objective of the review is to study the mechanism of\nthe stonefish venom and portray its benefits in the field of drug discovery.\n\n\n\nA study on the mechanism of stonefish venom was carried out by inducing cardiovascular endothelium.\nThe release of neurotransmitter signals thus leads to the depolarisation of cell membrane by\nthe formation of pores in the cell membrane in the neuromuscular system of rabbits, porcine artery, mice\nand rats. Lionfish venom in cross-reactivity with the results evolved from a stonefish venom activity. The\npresence of enzymatic hyaluronidases in the primary structures of lionfish has evolved from stonefish and\ntheir anticancer potential has also been demonstrated for the benefits of drug discovery as they possess\nbiological and chemical activity.\n\n\n\nThis review depicts an overview of the pharmacological activities of lionfish venom in comparison\nwith the stonefish venom and their purpose of applications for future research in drug discovery.\n","PeriodicalId":35405,"journal":{"name":"Current Enzyme Inhibition","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Enzyme Inhibition","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1573408016999201231204746","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
For the past 70 years, the focus of research is on the search for poisons and toxins
found in venomous and poisonous organisms, purely directed towards the pharmacological properties
of the toxins. In the research of finding novel compounds in pharmaceutical research, the identified
source was the piscine venom.
The Scorpaenidae family was considered the most venomous of all. The toxins isolated from
stonefish and lionfish are responsible for the effects caused in cardiovascular and neuromuscular systems
and also for causing cytolytic activities. The main objective of the review is to study the mechanism of
the stonefish venom and portray its benefits in the field of drug discovery.
A study on the mechanism of stonefish venom was carried out by inducing cardiovascular endothelium.
The release of neurotransmitter signals thus leads to the depolarisation of cell membrane by
the formation of pores in the cell membrane in the neuromuscular system of rabbits, porcine artery, mice
and rats. Lionfish venom in cross-reactivity with the results evolved from a stonefish venom activity. The
presence of enzymatic hyaluronidases in the primary structures of lionfish has evolved from stonefish and
their anticancer potential has also been demonstrated for the benefits of drug discovery as they possess
biological and chemical activity.
This review depicts an overview of the pharmacological activities of lionfish venom in comparison
with the stonefish venom and their purpose of applications for future research in drug discovery.
期刊介绍:
Current Enzyme Inhibition aims to publish all the latest and outstanding developments in enzyme inhibition studies with regards to the mechanisms of inhibitory processes of enzymes, recognition of active sites, and the discovery of agonists and antagonists, leading to the design and development of new drugs of significant therapeutic value. Each issue contains a series of timely, in-depth reviews written by leaders in the field, covering a range of enzymes that can be exploited for drug development. Current Enzyme Inhibition is an essential journal for every pharmaceutical and medicinal chemist who wishes to have up-to-date knowledge about each and every development in the study of enzyme inhibition.