Esvelt Marian A, Freeman Zachary T, Pearson Alexander T, Harkema Jack R, Clines Gregory T, Clines Katrina L, Dyson Melissa C, Hoenerhoff Mark J
1 Unit for Laboratory Animal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
2 Animal Resource Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Toxicol Pathol. 2019 Feb;47(2):150-164. doi: 10.1177/0192623318816295. Epub 2018 Dec 30.
Zibotentan, an endothelin-A receptor antagonist, has been used in the treatment of various cardiovascular disorders and neoplasia. Castrated athymic nude mice receiving zibotentan for a preclinical xenograft efficacy study experienced weight loss, gastrointestinal bloat, and the presence of an audible respiratory click. Human side effects have been reported in the nasal cavity, so we hypothesized that the nasal cavity is a target for toxicity in mice receiving zibotentan. Lesions in the nasal cavity predominantly targeted olfactory epithelium in treated mice and were more pronounced in castrated animals. Minimal lesions were present in vehicle control animals, which suggested possible gavage-related reflux injury. The incidence, distribution, and morphology of lesions suggested direct exposure to the nasal mucosa and a possible systemic effect targeting the olfactory epithelium, driven by a type 2 immune response, with group 2 innate lymphoid cell involvement. Severe nasal lesions may have resulted in recurrent upper airway obstruction, leading to aerophagia and associated clinical morbidity. These data show the nasal cavity is a target of zibotentan when given by gavage in athymic nude mice, and such unanticipated and off-target effects could impact interpretation of research results and animal health in preclinical studies.
齐考诺肽,一种内皮素-A受体拮抗剂,已被用于治疗各种心血管疾病和肿瘤。在一项临床前异种移植疗效研究中,接受齐考诺肽治疗的去势无胸腺裸鼠出现了体重减轻、胃肠道胀气和可闻及的呼吸喀哒声。在鼻腔已报告有人类副作用,因此我们推测鼻腔是接受齐考诺肽治疗的小鼠的毒性靶点。在接受治疗的小鼠中,鼻腔病变主要靶向嗅上皮,在去势动物中更为明显。在赋形剂对照动物中存在最小病变,这提示可能与灌胃相关的反流损伤。病变的发生率、分布和形态表明直接暴露于鼻黏膜以及由2型免疫反应驱动、伴有2型固有淋巴细胞参与的针对嗅上皮的可能全身效应。严重的鼻腔病变可能导致反复的上呼吸道阻塞,进而导致吞气症和相关的临床发病率。这些数据表明,在无胸腺裸鼠中通过灌胃给予齐考诺肽时,鼻腔是其靶点,而这种意外的脱靶效应可能会影响临床前研究中研究结果的解读和动物健康。