伊维菌素
生物
突变
基因
遗传学
P-糖蛋白
分子生物学
抗药性
多重耐药
动物
作者
Katrina L. Mealey,Steve A. Bentjen,John Gay,Glenn H. Cantor
出处
期刊:Pharmacogenetics
[Lippincott Williams & Wilkins]
日期:2001-11-01
卷期号:11 (8): 727-733
被引量:447
标识
DOI:10.1097/00008571-200111000-00012
摘要
A subpopulation of collie dogs is extremely sensitive to neurotoxicity induced by ivermectin. The aim of this study was to determine the mechanistic basis for this phenomenon. The multi-drug-resistance gene (mdr1) encodes a large transmembrane protein, P-glycoprotein (P-gp), that is an integral part of the blood-brain barrier. P-gp functions as a drug-transport pump at the blood-brain barrier, transporting a variety of drugs from the brain back into the blood. Since ivermectin is a substrate for P-gp, we hypothesized that ivermectin-sensitive collies had altered mdr1 expression compared with unaffected collies. We report a deletion mutation of the mdr1 gene that is associated with ivermectin sensitivity. The 4-bp deletion results in a frame shift, generating several stop codons that prematurely terminate P-gp synthesis. Dogs that are homozygous for the deletion mutation display the ivermectin-sensitive phenotype, while those that are homozygous normal or heterozygous do not display increased sensitivity to ivermectin.
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