McMurray Matthew S, Oguz Ipek, Rumple Ashley M, Paniagua Beatriz, Styner Martin A, Johns Josephine M
Department of Psychology, University of Illinois at Chicago, Chicago, IL 60647, USA.
Department of Electrical and Computer Engineering, University of Iowa, Iowa, IA 52242, USA.
Neurotoxicol Teratol. 2015 Jan-Feb;47:80-8. doi: 10.1016/j.ntt.2014.11.007. Epub 2014 Nov 22.
Prenatal cocaine exposure has been associated with numerous behavioral phenotypes in clinical populations, including impulsivity, reduced attention, alterations in social behaviors, and delayed language and sensory-motor development. Detecting associated changes in brain structure in these populations has proven difficult, and results have been inconclusive and inconsistent. Due to their more controlled designs, animal models may shed light on the neuroanatomical changes caused by prenatal cocaine; however, to maximize clinical relevance, data must be carefully collected using translational methods. The goal of this study was two-fold: (1) to determine if prenatal cocaine alters developmental neuroanatomy using methods that are available to human researchers, specifically structural MRI and diffusion tensor imaging, and (2) to determine the feasibility of rodent in vivo neuroimaging for usage in longitudinal studies of developmental disorders. Cocaine-exposed (prenatal days 1-20, 30mg/kg/day) rat pups were sedated and imaged live using diffusion tensor imaging and postmortem (fixed) using magnetic resonance histology on postnatal day 14. Volume and diffusion properties in whole brain as well as specific regions of interest were then assessed from the resulting images. Whole brain analyses revealed that cocaine-exposed animals showed no change in whole brain volume. Additionally, we found alterations in fractional anisotropy across regions associated with reward processing and emotional regulation, especially in the thalamus and globus pallidus, as well as sex-dependent effects of cocaine in the right cortex. Reductions in fractional anisotropy were paired with reductions only in axial diffusivity, which preliminarily suggests that the changes observed here may be due to axonal damage, as opposed to reductions in myelination of the affected regions/pathways. Our data indicate that prenatal cocaine may target a number of developing brain structures but does not result in overt changes to brain volumes. These results highlight not only the brain alterations that result from prenatal cocaine but also the advancements in live imaging that allow longitudinal study designs in other models.
产前接触可卡因与临床人群中的多种行为表型有关,包括冲动、注意力下降、社交行为改变以及语言和感觉运动发育延迟。在这些人群中检测大脑结构的相关变化已被证明很困难,结果尚无定论且不一致。由于动物模型的设计更具可控性,它们可能有助于揭示产前接触可卡因所引起的神经解剖学变化;然而,为了最大限度地提高临床相关性,必须使用转化方法仔细收集数据。本研究的目标有两个:(1)使用人类研究人员可用的方法,特别是结构磁共振成像和扩散张量成像,确定产前接触可卡因是否会改变发育中的神经解剖结构;(2)确定啮齿动物体内神经成像在发育障碍纵向研究中的可行性。在出生后第14天,对产前接触可卡因(产前第1 - 20天,30mg/kg/天)的幼鼠进行镇静,并使用扩散张量成像进行活体成像,死后(固定)使用磁共振组织学成像。然后从所得图像中评估全脑以及特定感兴趣区域的体积和扩散特性。全脑分析显示,产前接触可卡因的动物全脑体积没有变化。此外,我们发现与奖励处理和情绪调节相关区域的分数各向异性发生了改变,特别是在丘脑和苍白球,以及可卡因对右侧皮质的性别依赖性影响。分数各向异性的降低仅与轴向扩散率的降低相关,这初步表明此处观察到的变化可能是由于轴突损伤,而不是受影响区域/通路髓鞘形成的减少。我们的数据表明,产前接触可卡因可能针对许多发育中的脑结构,但不会导致脑体积的明显变化。这些结果不仅突出了产前接触可卡因所导致的大脑改变,还突出了活体成像技术的进步,这些技术使得在其他模型中进行纵向研究设计成为可能。