AI Article Synopsis

  • Scorpion venom contains a variety of toxins that can be life-threatening and may increase levels of matrix metalloproteases (MMPs), leading to tissue damage.
  • The study examined the effects of scorpion envenomation on proteolysis in various organs, finding significant increases in activity, particularly in the heart and lungs.
  • Results indicate that metalloproteases play a critical role in the overall proteolytic activity, with increased MMPs and TIMP-1 levels suggesting potential for systemic damage across multiple organs due to uncontrolled protease activity.

Article Abstract

Background: Scorpion stings may be life-threatening since their venoms are comprised of a wide range of toxins and other bioactive molecules, such as enzymes. At the same time, scorpion envenomation may increase matrix metalloproteases (MMPs) levels, which enhance proteolytic tissue destruction by venom. However, investigations on the impact of many scorpions' venoms, such as those of , on tissue proteolytic activity and MMP levels have not yet been conducted.

Methods And Results: The present study aimed to examine the total proteolysis levels in various organs after envenomation and evaluate the metalloproteases and serine proteases' contributions to the total proteolytic activity. Changes in MMPs and TIMP-1 levels were tested as well. Envenomation led to a significant increase in proteolytic activity levels in all assessed organs, mostly in the heart (by 3.34 times) and lungs (by 2.25 times).

Conclusions: Since EDTA presence showed a noticeable decrease in total proteolytic activity level, metalloproteases appeared to play a prominent role in total proteolytic activity. At the same time, MMPs and TIMP-1 levels were increased in all assessed organs, suggesting that envenomation causes systemic envenomation, which may induce multiple organ abnormalities, mostly because of the uncontrolled metalloprotease activity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9970711PMC
http://dx.doi.org/10.1155/2023/5262729DOI Listing

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