Rex Tonia S, Boyd Kelli, Apple Troy, Bricker-Anthony Courtney, Vail Krystal, Wallace Jeanne
Vanderbilt Eye Institute, Vanderbilt University School of Medicine, Nashville, Tennessee, USA; Vanderbilt Brain Institute, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Department of Pathology, Microbiology, and Immunology, Comparative Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
J Am Assoc Lab Anim Sci. 2016;55(3):295-9.
Repeated injection of urethane (ethyl carbamate) is carcinogenic in susceptible strains of mice. Most recent cancer studies involving urethane-induced tumor formation use p53(+/-) mice, which lack one copy of the p53 tumor suppressor gene. In contrast, the same protocol elicits at most a single tumor in wildtype C57BL/6 mice. The effect of repeatedly injecting urethane as a component of a ketamine-xylazine anesthetic mixture in the highly prevalent mouse strain C57BL/6 is unknown. Male C57BL/6J mice (n = 30; age, 3 mo) were anesthetized once monthly for 4 mo by using 560 mg/kg urethane, 28 mg/kg ketamine, and 5.6 mg/kg xylazine. The physical health of the mice was evaluated according to 2 published scoring systems. The average body condition score (scale, 1 to 5; normal, 3) was 3.3, 3.3, and 3.4 after the 2nd, 3rd, and 4th injections, respectively. The visual assessment score was 0 (that is, normal) at all time points examined. Within 1 wk after the 4th injection, the mice were euthanized, necropsied, and evaluated histopathologically. No histopathologic findings were noteworthy. We conclude that repeated monthly injection with urethane as a component of an anesthetic cocktail does not cause clinically detectable abnormalities or induce neoplasia in C57BL/6J mice. These findings are important because urethane combined with low-dose ketamine, unlike other anesthetic regimens, allows for accurate recording of neuronal activity in both the brain and retina. Longitudinal neuronal recordings minimize the number of mice needed and improve the analysis of disease progression and potential therapeutic interventions.
重复注射氨基甲酸乙酯(尿烷)对易患癌症的小鼠品系具有致癌性。最近涉及氨基甲酸乙酯诱导肿瘤形成的癌症研究使用了p53(+/-)小鼠,这些小鼠缺少一份p53肿瘤抑制基因拷贝。相比之下,相同的方案在野生型C57BL/6小鼠中最多引发一个肿瘤。在高度常见的小鼠品系C57BL/6中,将氨基甲酸乙酯作为氯胺酮-赛拉嗪麻醉混合物的成分进行重复注射的效果尚不清楚。雄性C57BL/6J小鼠(n = 30;年龄,3个月)每月使用560 mg/kg氨基甲酸乙酯、28 mg/kg氯胺酮和5.6 mg/kg赛拉嗪麻醉一次,持续4个月。根据2种已发表的评分系统评估小鼠的身体健康状况。在第2次、第3次和第4次注射后,平均身体状况评分(范围为1至5;正常为3)分别为3.3、3.3和3.4。在所有检查时间点,视觉评估评分均为0(即正常)。在第4次注射后1周内,对小鼠实施安乐死、进行尸检并进行组织病理学评估。未发现值得注意的组织病理学结果。我们得出结论,每月重复注射氨基甲酸乙酯作为麻醉混合物的成分不会在C57BL/6J小鼠中引起临床可检测到的异常或诱发肿瘤形成。这些发现很重要,因为与其他麻醉方案不同,氨基甲酸乙酯与低剂量氯胺酮联合使用能够准确记录大脑和视网膜中的神经元活动。纵向神经元记录可减少所需小鼠的数量,并改善对疾病进展和潜在治疗干预措施的分析。