Resistance to artemisinin in falciparum malaria parasites: A redox-mediated phenomenon.


Journal

Free radical biology & medicine
ISSN: 1873-4596
Titre abrégé: Free Radic Biol Med
Pays: United States
ID NLM: 8709159

Informations de publication

Date de publication:
01 02 2022
Historique:
received: 29 07 2021
accepted: 16 08 2021
pubmed: 21 8 2021
medline: 1 2 2022
entrez: 20 8 2021
Statut: ppublish

Résumé

Malaria remains a major public health disease due to its high yearly mortality and morbidity. Resistance to the gold standard drug, artemisinin, is worrisome and needs better understanding in order to be overcome. In this work, we sought to study whether redox processes are involved in artemisinin resistance. As artemisinin is known to act among others via production of reactive species, we first compared the production of reactive oxygen species and concomitant protein oxidation in artemisinin-sensitive and artemisinin-resistant parasites when treated with artemisinin. The results undoubtedly demonstrated, using different original methods, that the level of ROS, including superoxide production, and oxidized protein were lower in the resistant strain. Interestingly, the major in-between strain difference was reported at the earlier ring stages, which are the forms able to enter in a quiescence state according to the ART resistance phenomenon. Moreover, we demonstrated a better homeostasis regulation in relation with higher expression of antioxidants in the artemisinin-resistant parasites than their sensitive counterparts after artemisinin exposure, notably, superoxide dismutase and the glutathione (GSH) system. These findings enrich the body of knowledges about the multifaceted mechanism of artemisinin resistance and will help in the design and development of newer antimalarials strategies active against resistant parasites.

Identifiants

pubmed: 34416340
pii: S0891-5849(21)00476-7
doi: 10.1016/j.freeradbiomed.2021.08.016
pii:
doi:

Substances chimiques

Antimalarials 0
Artemisinins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

317-327

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Chinedu O Egwu (CO)

PharmaDev, UMR 152, Université de Toulouse, IRD, UPS, Toulouse, 31400, France; Medical Biochemistry, College of Medicine, Alex-Ekwueme Federal University, Ndufu-Alike Ikwo, Abakaliki, Ebonyi State, Nigeria; LCC-CNRS, Laboratoire de Chimie de Coordination, Université de Toulouse, CNRS, Toulouse, France; MAAP, Inserm ERL 1289, New Antimalarial Molecules and Pharmacological Approaches, Toulouse, France; Institut de Pharmacologie et de Biologie Structurale, IPBS, Université de Toulouse, CNRS, UPS, France.

Pierre Pério (P)

PharmaDev, UMR 152, Université de Toulouse, IRD, UPS, Toulouse, 31400, France.

Jean-Michel Augereau (JM)

LCC-CNRS, Laboratoire de Chimie de Coordination, Université de Toulouse, CNRS, Toulouse, France; MAAP, Inserm ERL 1289, New Antimalarial Molecules and Pharmacological Approaches, Toulouse, France; Institut de Pharmacologie et de Biologie Structurale, IPBS, Université de Toulouse, CNRS, UPS, France.

Ioannis Tsamesidis (I)

PharmaDev, UMR 152, Université de Toulouse, IRD, UPS, Toulouse, 31400, France.

Françoise Benoit-Vical (F)

LCC-CNRS, Laboratoire de Chimie de Coordination, Université de Toulouse, CNRS, Toulouse, France; MAAP, Inserm ERL 1289, New Antimalarial Molecules and Pharmacological Approaches, Toulouse, France; Institut de Pharmacologie et de Biologie Structurale, IPBS, Université de Toulouse, CNRS, UPS, France. Electronic address: Francoise.Vical@inserm.fr.

Karine Reybier (K)

PharmaDev, UMR 152, Université de Toulouse, IRD, UPS, Toulouse, 31400, France. Electronic address: karine.reybier-vuattoux@univ-tlse3.fr.

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Classifications MeSH