Griffin William C, Middaugh Lawrence D, Cook Jennifer E, Tyor William R
Center for Drug and Alcohol Programs, and Department of Psychiatry and Behavioral Science, Medical University of South Carolina, Charleston, South Carolina, USA.
J Neurovirol. 2004 Apr;10(2):109-15. doi: 10.1080/13550280490428333.
The severe combined immunodeficient (SCID) mouse model of human immunodeficiency virus (HIV) encephalitis exhibits many of the histopathological and pathophysiological features of human HIV-associated dementia (HAD). Although deficits that may resemble HAD in humans have been reported for HIV-infected SCID mice, the cognitive deficit aspect of the model has very limited empirical support. Here, the authors report that HIV-infected SCID mice display cognitive deficits on a task requiring the animal to learn and remember the spatial relationship of cues in its environment in order to locate a submerged platform in a Morris water maze. The cognitive deficits manifest as longer latencies to locate the platform on the last day of the maze acquisition period and during a retention test 8 days later. Control experiments indicated that the poor performance by HIV-infected mice in comparison to controls was not due to impaired motor function or swimming ability, impaired visual acuity, or increased susceptibility to fatigue. Thus, the increased times required for HIV-infected mice to locate the submerged platform during the acquisition and memory tests likely reflect a cognitive deficit, rather than sensorimotor or emotional abnormalities. These behavioral deficits are associated with significant increases in astrogliosis and microgliosis in the HIV-infected mice. The results of this study strengthen the SCID mouse model of HIV encephalitis by definitively establishing cognitive deficits for the model in addition to its previously reported neuropathological features.
人类免疫缺陷病毒(HIV)脑炎的严重联合免疫缺陷(SCID)小鼠模型展现出许多人类HIV相关痴呆(HAD)的组织病理学和病理生理学特征。尽管已有报道称感染HIV的SCID小鼠存在可能类似于人类HAD的缺陷,但该模型的认知缺陷方面的实证支持非常有限。在此,作者报告称,感染HIV的SCID小鼠在一项任务中表现出认知缺陷,该任务要求动物学习并记住其环境中线索的空间关系,以便在莫里斯水迷宫中找到一个水下平台。认知缺陷表现为在迷宫获取期的最后一天以及8天后的记忆测试中找到平台的潜伏期更长。对照实验表明,与对照组相比,感染HIV的小鼠表现不佳并非由于运动功能或游泳能力受损、视力受损或疲劳易感性增加。因此,感染HIV的小鼠在获取和记忆测试中找到水下平台所需时间的增加可能反映了认知缺陷,而非感觉运动或情绪异常。这些行为缺陷与感染HIV的小鼠中星形胶质细胞增生和小胶质细胞增生的显著增加有关。这项研究的结果通过明确确立该模型除先前报道的神经病理学特征外的认知缺陷,加强了HIV脑炎的SCID小鼠模型。