P-glycoproteins in anthelmintic safety, efficacy, and resistance

被引:1
|
作者
Lespine, Anne [1 ]
Blancfuney, Clara [1 ]
Prichard, Roger [2 ]
Alberich, Melanie [1 ]
机构
[1] Univ Toulouse, INTHERES, INRAE, ENVT, Toulouse, France
[2] McGill Univ, Inst Parasitol, Ste Anne De Bellevue, PQ, Canada
关键词
MACROCYCLIC LACTONE RESISTANCE; GATED CHLORIDE CHANNEL; IN-VITRO EXPOSURE; HAEMONCHUS-CONTORTUS; CAENORHABDITIS-ELEGANS; IVERMECTIN RESISTANCE; ABC TRANSPORTERS; PARASITIC NEMATODES; EXPRESSION ANALYSIS; DRUG-RESISTANT;
D O I
10.1016/j.pt.2024.07.008
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
P-glycoprotein (PGP) is a pivotal transmembrane transporter governing the cellular flux of diverse substances shielding mammals from toxics. It can thwart the effectiveness of medicines such as ivermectin (IVM) and other macrocyclic lactone (ML) anthelmintics, undermining therapeutic efforts. We analyze the role of PGPs in limiting the toxicity of these drugs in hosts, and their potential contribution to anthelmintic resistance in nematodes. Targeting nematode PGPs to increase drug sensitivity to MLs seems interesting, but is hampered by the lack of selective inhibitors. The nuclear hormone receptor (NHR)-8 should be seriously considered as a target because it upregulates multiple PGPs involved in anthelmintic resistance and it is specific to nematodes. This would advance our understanding of host- pathogen dynamics and foster innovative therapeutic strategies.
引用
收藏
页码:896 / 913
页数:18
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