Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne and Melbourne Health, Australia.
Addict Biol. 2012 Jan;17(1):141-8. doi: 10.1111/j.1369-1600.2010.00266.x. Epub 2010 Nov 11.
Heroin addiction has been associated with impaired neuronal connectivity and cognitive deficits. One mechanism that potentially explains these findings is alterations in white matter connectivity secondary to chronic opiate use. However, few studies have quantitavely examined white matter deficits in opiate addiction (OA). Here, we investigated white matter microstructure in OA using diffusion tensor imaging (DTI). We performed voxel-wise analysis of fractional anisotropy (FA) in 24 participants with OA and 29 healthy controls. The OA group showed reduced FA in multiple pathways including the corpus callosum, thalamic radiation and inferior longitudinal fasciculus. This FA reduction was mainly the result of increased radial diffusivity (λ(⊥)), indicative of myelin pathology. Longer duration of OA was also associated with axonal diffusivity (λ(1)), most robustly in superior longitudinal fasciculi and right frontal white matter suggesting axonal injury in long-term users. Together, the findings indicate that chronic OA use has widespread and diverse effects on neuronal connectivity and function.
海洛因成瘾与神经元连接受损和认知缺陷有关。一种可能解释这些发现的机制是,由于慢性阿片类药物使用,白质连接发生改变。然而,很少有研究定量检查阿片类药物成瘾(OA)中的白质缺陷。在这里,我们使用弥散张量成像(DTI)研究 OA 中的白质微观结构。我们对 24 名 OA 患者和 29 名健康对照者进行了体素分析各向异性分数(FA)。OA 组在包括胼胝体、丘脑辐射和下纵束在内的多个通路上显示出 FA 降低。这种 FA 降低主要是由于径向弥散度(λ(⊥))增加所致,提示存在髓鞘病变。OA 持续时间较长也与轴突弥散度(λ(1))相关,在胼胝体上束和右侧额白质最为明显,提示长期使用者的轴突损伤。总之,这些发现表明慢性 OA 使用对神经元连接和功能有广泛而多样的影响。