Department of Psychology, Program in Behavioral Neuroscience, University of South Carolina, 1512 Pendleton Street, Columbia, SC, 29208, USA.
J Neurovirol. 2018 Apr;24(2):229-245. doi: 10.1007/s13365-017-0544-x. Epub 2017 Jul 20.
Understanding the progression of HIV-1-associated neurocognitive disorders (HAND) is a critical need as the prevalence of HIV-1 in older individuals (>50 years) is markedly increasing due to the great success of combination antiretroviral therapy (cART). Longitudinal experimental designs, in comparison to cross-sectional studies, provide an opportunity to establish age-related disease progression in HAND. The HIV-1 transgenic (Tg) rat, which has been promoted for investigating the effect of long-term HIV-1 viral protein exposure, was used to examine two interrelated goals. First, to establish the integrity of sensory and motor systems through the majority of the animal's functional lifespan. Strong evidence for intact sensory and motor system function through advancing age in HIV-1 Tg and control animals was observed in cross-modal prepulse inhibition (PPI) and locomotor activity. The integrity of sensory and motor system function suggested the utility of the HIV-1 Tg rat in investigating the progression of HAND. Second, to assess the progression of neurocognitive impairment, including temporal processing and long-term episodic memory, in the HIV-1 Tg rat; the factor of biological sex was integral to the experimental design. Cross-modal PPI revealed significant alterations in the development of temporal processing in HIV-1 Tg animals relative to controls; alterations which were more pronounced in female HIV-1 Tg rats relative to male HIV-1 Tg rats. Locomotor activity revealed deficits in intrasession habituation, suggestive of a disruption in long-term episodic memory, in HIV-1 Tg animals. Understanding the progression of HAND heralds an opportunity for the development of an advantageous model of progressive neurocognitive deficits in HIV-1 and establishes fundamental groundwork for the development of neurorestorative treatments.
了解 HIV-1 相关神经认知障碍 (HAND) 的进展是非常必要的,因为随着联合抗逆转录病毒疗法 (cART) 的巨大成功,HIV-1 在老年人群(>50 岁)中的流行率显著增加。与横断面研究相比,纵向实验设计为 HAND 中与年龄相关的疾病进展提供了机会。HIV-1 转基因 (Tg) 大鼠被推广用于研究长期 HIV-1 病毒蛋白暴露的影响,用于检查两个相互关联的目标。首先,通过动物的大部分功能寿命来建立感觉和运动系统的完整性。通过对 HIV-1 Tg 和对照动物进行的跨模态 prepulse 抑制 (PPI) 和运动活动的研究,观察到了随着年龄的增长,感觉和运动系统功能完整的有力证据。感觉和运动系统功能的完整性表明 HIV-1 Tg 大鼠在研究 HAND 进展方面具有实用性。其次,评估 HIV-1 Tg 大鼠神经认知障碍的进展,包括时间处理和长时程情景记忆;生物性别是实验设计的一个重要因素。跨模态 PPI 显示,与对照组相比,HIV-1 Tg 动物的时间处理发展出现显著改变;与雄性 HIV-1 Tg 大鼠相比,雌性 HIV-1 Tg 大鼠的改变更为明显。运动活动显示出在 session 内习惯形成中的缺陷,提示 HIV-1 Tg 动物存在长时程情景记忆中断。了解 HAND 的进展为开发 HIV-1 中进行性神经认知缺陷的有利模型提供了机会,并为神经修复治疗的发展奠定了基础。