Nürnberger Daniela, Wagner Lisa, Müller Simon F, Leiting Silke, Leidolf Regina, Alber Jörg, Hamann Melanie, Geyer Joachim
Faculty of Veterinary Medicine, Institute of Pharmacology and Toxicology, Justus Liebig University Giessen, Giessen, Germany.
Front Vet Sci. 2022 Feb 21;8:808392. doi: 10.3389/fvets.2021.808392. eCollection 2021.
The multidrug resistance gene MDR1 (syn. ABCB1) encodes for the multidrug efflux transporter P-glycoprotein (P-gp), which is highly expressed at the blood-brain barrier and protects the brain from potentially neurotoxic compounds, such as ivermectin. MDR1 mutation in dogs is known to be linked to dramatically increased brain accumulation of ivermectin and life-threatening neurological toxicity. The present report describes two suspected ivermectin-sensitive Maine Coon cats, which exhibited neurological toxicity following subcutaneous application of therapeutic doses of ivermectin. Both cats showed a homozygous 2-bp deletion in the MDR1/ABCB1 coding sequence (1930_1931del TC, syn. MDR1 nt1930(del2)) that had previously been associated with a drug-sensitive phenotype in cats. For cat MDR1 genotyping, a novel TaqMan allelic discrimination assay was established and validated. This assay was used for 1930_1931del TC genotyping of the drug-sensitive cats as well as of more than 50 relatives. About half of them had the heterozygous MDR1(+/-) genotype, while none of these related cats with former ivermectin treatment had a history of drug-sensitivity. In conclusion: The present study supports previous findings on drug-sensitivity in cats with homozygous 1930_1931del TC mutation. The newly established TaqMan allelic discrimination assay provides a useful and reliable method for routine MDR1 genotyping in cats in order to identify drug-sensitive cats prior to treatment with established P-gp substrates such as ivermectin and other macrocyclic lactones and thus to improve therapeutic safety.
多药耐药基因MDR1(同义词ABCB1)编码多药外排转运蛋白P-糖蛋白(P-gp),该蛋白在血脑屏障处高度表达,可保护大脑免受潜在神经毒性化合物(如伊维菌素)的侵害。已知犬类中的MDR1突变与伊维菌素在大脑中的蓄积显著增加以及危及生命的神经毒性有关。本报告描述了两只疑似对伊维菌素敏感的缅因库恩猫,它们在皮下注射治疗剂量的伊维菌素后出现了神经毒性。两只猫在MDR1/ABCB1编码序列中均表现出纯合的2个碱基缺失(1930_1931del TC,同义词MDR1 nt1930(del2)),该缺失先前已与猫的药物敏感表型相关。为了对猫进行MDR1基因分型,建立并验证了一种新型TaqMan等位基因鉴别分析方法。该分析方法用于对药物敏感猫以及50多只亲属进行1930_1931del TC基因分型。其中约一半具有杂合MDR1(+/-)基因型,而这些曾接受伊维菌素治疗的相关猫中,没有一只具有药物敏感史。总之:本研究支持了先前关于纯合1930_1931del TC突变猫药物敏感性的研究结果。新建立的TaqMan等位基因鉴别分析方法为猫的常规MDR1基因分型提供了一种有用且可靠的方法,以便在使用伊维菌素和其他大环内酯类等既定P-糖蛋白底物进行治疗之前识别药物敏感猫,从而提高治疗安全性。