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Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom

Snake venom proteins, which are responsible for deadly snakebite envenomation, induce severe injuries including neurotoxicity, myotoxicity, cardiotoxicity, hemorrhage, and the disruption of blood homeostasis. Yet, many snake-venom proteins have been developed as potential drugs for treating human di...

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Autores principales: Abdelkafi-Koubaa, Zaineb, ELBini-Dhouib, Ines, Souid, Soumaya, Jebali, Jed, Doghri, Raoudha, Srairi-Abid, Najet, Essafi-Benkhadir, Khadija, Micheau, Olivier, Marrakchi, Naziha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704781/
https://www.ncbi.nlm.nih.gov/pubmed/34941741
http://dx.doi.org/10.3390/toxins13120904
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author Abdelkafi-Koubaa, Zaineb
ELBini-Dhouib, Ines
Souid, Soumaya
Jebali, Jed
Doghri, Raoudha
Srairi-Abid, Najet
Essafi-Benkhadir, Khadija
Micheau, Olivier
Marrakchi, Naziha
author_facet Abdelkafi-Koubaa, Zaineb
ELBini-Dhouib, Ines
Souid, Soumaya
Jebali, Jed
Doghri, Raoudha
Srairi-Abid, Najet
Essafi-Benkhadir, Khadija
Micheau, Olivier
Marrakchi, Naziha
author_sort Abdelkafi-Koubaa, Zaineb
collection PubMed
description Snake venom proteins, which are responsible for deadly snakebite envenomation, induce severe injuries including neurotoxicity, myotoxicity, cardiotoxicity, hemorrhage, and the disruption of blood homeostasis. Yet, many snake-venom proteins have been developed as potential drugs for treating human diseases due to their pharmacological effects. In this study, we evaluated the use of, an L-amino acid oxidase isolated from Cerastes cerastes snake venom CC-LAAO, as a potential anti-glioblastoma drug, by investigating its in vivo and in vitro pharmacological effects. Our results showed that acute exposure to CC-LAAO at 1 and 2.5 µg/mL does not induce significant toxicity on vital organs, as indicated by the murine blood parameters including aspartate transaminase (AST), alanine transaminase (ALT), lactate dehydrogenase (LDH) activities, and creatinine levels. The histopathological examination demonstrated that only at high concentrations did CC-LAAO induce inflammation and necrosis in several organs of the test subjects. Interestingly, when tested on human glioblastoma U87 cells, CC-LAAO induced a dose-dependent apoptotic effect through the H(2)O(2) generated during the enzymatic reaction. Taken altogether, our data indicated that low concentration of CC-LAAO may be safe and may have potential in the development of anti-glioblastoma agents.
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spelling pubmed-87047812021-12-25 Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom Abdelkafi-Koubaa, Zaineb ELBini-Dhouib, Ines Souid, Soumaya Jebali, Jed Doghri, Raoudha Srairi-Abid, Najet Essafi-Benkhadir, Khadija Micheau, Olivier Marrakchi, Naziha Toxins (Basel) Article Snake venom proteins, which are responsible for deadly snakebite envenomation, induce severe injuries including neurotoxicity, myotoxicity, cardiotoxicity, hemorrhage, and the disruption of blood homeostasis. Yet, many snake-venom proteins have been developed as potential drugs for treating human diseases due to their pharmacological effects. In this study, we evaluated the use of, an L-amino acid oxidase isolated from Cerastes cerastes snake venom CC-LAAO, as a potential anti-glioblastoma drug, by investigating its in vivo and in vitro pharmacological effects. Our results showed that acute exposure to CC-LAAO at 1 and 2.5 µg/mL does not induce significant toxicity on vital organs, as indicated by the murine blood parameters including aspartate transaminase (AST), alanine transaminase (ALT), lactate dehydrogenase (LDH) activities, and creatinine levels. The histopathological examination demonstrated that only at high concentrations did CC-LAAO induce inflammation and necrosis in several organs of the test subjects. Interestingly, when tested on human glioblastoma U87 cells, CC-LAAO induced a dose-dependent apoptotic effect through the H(2)O(2) generated during the enzymatic reaction. Taken altogether, our data indicated that low concentration of CC-LAAO may be safe and may have potential in the development of anti-glioblastoma agents. MDPI 2021-12-16 /pmc/articles/PMC8704781/ /pubmed/34941741 http://dx.doi.org/10.3390/toxins13120904 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abdelkafi-Koubaa, Zaineb
ELBini-Dhouib, Ines
Souid, Soumaya
Jebali, Jed
Doghri, Raoudha
Srairi-Abid, Najet
Essafi-Benkhadir, Khadija
Micheau, Olivier
Marrakchi, Naziha
Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom
title Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom
title_full Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom
title_fullStr Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom
title_full_unstemmed Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom
title_short Pharmacological Investigation of CC-LAAO, an L-Amino Acid Oxidase from Cerastes cerastes Snake Venom
title_sort pharmacological investigation of cc-laao, an l-amino acid oxidase from cerastes cerastes snake venom
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704781/
https://www.ncbi.nlm.nih.gov/pubmed/34941741
http://dx.doi.org/10.3390/toxins13120904
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