Cobb Rami, Boeckh Albert
Fort Dodge Animal Health, Pharmaceutical Research and Development, Princeton, NJ, USA.
Parasit Vectors. 2009 Sep 25;2 Suppl 2(Suppl 2):S5. doi: 10.1186/1756-3305-2-S2-S5.
This article reviews the current knowledge of the use of moxidectin (MOX) in horses, including its mode of action, pharmacokinetic and pharmacodynamic properties, efficacy, safety and resistance profile.Moxidectin is a second generation macrocyclic lactone (ML) with potent endectocide activity. It is used for parasite control in horses in an oral gel formulation. The principal mode of action of MOX and of other MLs is binding to gamma-aminobutyric (GABA) and glutamate-gated chloride channels. Moxidectin is different from other MLs in that it is a poor substrate for P-glycoproteins (P-gps) and therefore less susceptible to elimination from parasite cells through this mechanism. Due to its unique physicochemical and pharmacokinetic characteristics, MOX provides broad distribution into tissues, long half-life, significant residual antiparasitic activity, and high efficacy against encysted cyathostomin larvae. These characteristics allow for high efficacy and longer treatment interval against all important nematodes, when compared to other equine anthelmintics. A combination of MOX with praziquantel provides expanded spectrum of activity by adding activity against cestodes. Appropriate use of MOX allows for the development of strategic anthelmintic programmes that are different from those with conventional anthelmintics. Fewer treatments are required over a period of time, and therefore impose less frequent selection pressure for resistance.
本文综述了莫西菌素(MOX)在马匹中的应用现状,包括其作用方式、药代动力学和药效学特性、疗效、安全性及耐药情况。莫西菌素是一种具有高效驱虫活性的第二代大环内酯类药物。它以口服凝胶制剂的形式用于马匹的寄生虫控制。莫西菌素及其他大环内酯类药物的主要作用方式是与γ-氨基丁酸(GABA)和谷氨酸门控氯离子通道结合。莫西菌素与其他大环内酯类药物的不同之处在于,它是P-糖蛋白(P-gps)的不良底物,因此通过这种机制从寄生虫细胞中消除的可能性较小。由于其独特的理化和药代动力学特性,莫西菌素能广泛分布于组织中,半衰期长,具有显著的残留抗寄生虫活性,对包囊圆线虫幼虫具有高效。与其他马用驱虫药相比,这些特性使其对所有重要线虫具有高效和更长的治疗间隔。莫西菌素与吡喹酮联合使用可通过增加对绦虫的活性来扩大活性谱。合理使用莫西菌素有助于制定与传统驱虫药不同的战略驱虫方案。在一段时间内所需的治疗次数较少,因此施加的耐药性选择压力也较小。