Titus Family Department of Clinical Pharmacy, School of Pharmacy, University of Southern California.
Homer Stryker M.D. School of Medicine, Western Michigan University.
J Vis Exp. 2022 Nov 11(189). doi: 10.3791/64567.
Anxiety disorders are one of the leading causes of disability in the United States (US). Current treatments are not always effective and less than 50% of patients achieve full remission. A critical step in developing a novel anxiolytic is to develop and utilize an animal model, such as mice, to study pathological changes and test drug target(s), efficacy, and safety. Current approaches include genetic manipulation, chronic administration of anxiety-inducing molecules, or the administration of environmental stress. These methods, however, may not realistically reflect anxiety induced throughout daily life. This protocol describes a novel anxiety model, which mimics the intentional or unintentional patterns of social isolation in modern life. The social isolation-induced anxiety model minimizes perceived distractions and invasiveness and utilizes wild type C57BL/6 mice. In this protocol, 6- to 8-week-old mice (male and female) are singly housed in opaque cages to visually block the external environment, such as neighboring mice, for 4 weeks. No environmental enrichments (such as toys) are provided, bedding material is reduced by 50%, any treatment of drug is administered as an agar form, and the exposure/handling of the mice is minimized. Socially isolated mice generated using this protocol exhibit greater anxiety-like behavior, aggression, as well as decreased cognition.
焦虑症是美国(US)导致残疾的主要原因之一。目前的治疗方法并不总是有效,只有不到 50%的患者达到完全缓解。开发新型抗焦虑药物的关键步骤是开发和利用动物模型,如小鼠,以研究病理变化和测试药物靶点、疗效和安全性。目前的方法包括遗传操作、焦虑诱导分子的慢性给药或环境应激的给药。然而,这些方法可能无法真实反映日常生活中引起的焦虑。本方案描述了一种新的焦虑模型,该模型模拟了现代生活中有意或无意的社交隔离模式。社交隔离诱导的焦虑模型最大限度地减少了感知干扰和侵入性,并利用野生型 C57BL/6 小鼠。在该方案中,6-8 周龄的雄性和雌性小鼠单独饲养在不透明的笼子中,以视觉方式阻挡外部环境,如相邻的小鼠,持续 4 周。不提供任何环境丰富物(如玩具),减少 50%的垫料材料,以琼脂形式给予任何药物治疗,尽量减少对小鼠的暴露/处理。使用该方案产生的社交隔离小鼠表现出更大的焦虑样行为、攻击性以及认知能力下降。