Feirabend H K P, Choufoer H, Ploeger S, Holsheimer J, van Gool J D
Neuroregulation Group, Department of Neurosurgery, Leiden University Medical Centre, LUMC, The Netherlands.
Brain. 2002 May;125(Pt 5):1137-49. doi: 10.1093/brain/awf111.
In spinal cord stimulation (SCS) large diameter cutaneous (Abeta) fibres in the dorsal columns (DCs) are activated and have an inhibiting effect on the transmission of pain signals by Adelta and C fibres from the corresponding dermatome(s). The largest Abeta fibres can be activated up to a maximum depth of about 0.25 mm in the DCs. No data are available on the distribution of the large fibres in this superficial human DC layer at the common SCS levels Th(10-11). Such data are indispensable to improve the predictive capability of a computer model of SCS. The whole myelinated fibre population in the superficial 300 microm of the dorsal column (DC(0-300)) at Th(10-11 )of two human subjects was morphometrically analysed. Some data was obtained from a third subject. The superficial dorsolateral column (DLC(0-300)) was included in this analysis because it was hypothesized that large dorsal spinocerebellar tract fibres could also be activated by SCS. Only very few fibres larger than 10.7 microm were found: a mean of 68 (0.5%) in DC(0-300) and 114 (2%) in DLC(0-300). Considering that the effect of SCS is primarily attributed to activation of these largest fibres, it is concluded that a surprisingly small average amount of 2.4 fibres per running 0.1 mm width and 6 fibres per segmental division of the DC is involved. Distinct mediolateral heterogeneity in fibre composition was found in both DC(0-300) and DLC(0-300). In the DC(0-300), the mean diameter of fibres > or =7.1 microm increases significantly by 5% from medial to lateral. Density (i.e. number of fibres per 1000 microm(2)) and frequency (i.e. percentage of a fibre size group compared to its parent population) of the large fibres increase significantly from medial to lateral in the DC(0-300). For fibres > or =10.7 microm, these parameters increase by 200 and 269%, respectively. It is concluded that the difference in stimulation threshold of large Abeta fibres in the median and lateral DC can be mainly attributed to the absence and presence, respectively, of collaterals at the stimulation site. Marked differences were found between DC(0-300) and DLC(0-300). The largest DLC(0-300) fibres (> or =10.7 microm) have a 320% higher frequency and a 473% higher density. Their mean diameter is, however, only 2% larger. The largest DLC(0-300) fibres are not likely to be recruited by SCS, since they are not larger than their DC(0-300) counterparts, they lack collaterals (which would reduce the threshold stimulus substantially) and they are more remote from the stimulation electrode.
在脊髓刺激(SCS)中,背柱(DCs)中的大直径皮肤(Aβ)纤维被激活,对来自相应皮节的Aδ和C纤维传递疼痛信号具有抑制作用。最大的Aβ纤维在背柱中可被激活至约0.25毫米的最大深度。在常见的SCS水平Th(10 - 11)下,关于该浅表人类背柱层中大纤维的分布尚无数据。此类数据对于提高SCS计算机模型的预测能力必不可少。对两名人类受试者Th(10 - 11)水平下背柱浅表300微米(DC(0 - 300))中的整个有髓纤维群体进行了形态计量分析。部分数据取自第三名受试者。浅表背外侧柱(DLC(0 - 300))也纳入了该分析,因为据推测,大的背脊髓小脑束纤维也可能被SCS激活。仅发现极少数直径大于10.7微米的纤维:DC(0 - 300)中平均有68根(0.5%),DLC(0 - 300)中平均有114根(2%)。考虑到SCS的效果主要归因于这些最大纤维的激活,得出的结论是,每运行0.1毫米宽度平均仅有2.4根纤维,每节段背柱仅有6根纤维参与其中,数量惊人地少。在DC(0 - 300)和DLC(0 - 300)中均发现纤维组成存在明显的中外侧异质性。在DC(0 - 300)中,直径≥7.1微米的纤维平均直径从中部到外侧显著增加5%。大纤维的密度(即每1000微米²中的纤维数量)和频率(即纤维尺寸组与其母体群体相比的百分比)在DC(0 - 300)中从中部到外侧显著增加。对于直径≥10.7微米的纤维,这些参数分别增加200%和269%。得出的结论是,中部和外侧背柱中大Aβ纤维刺激阈值的差异主要可分别归因于刺激部位有无侧支。在DC(0 - 300)和DLC(0 - 300)之间发现了显著差异。最大的DLC(0 - 300)纤维(≥10.7微米)频率高320%,密度高473%。然而,它们的平均直径仅大2%。最大的DLC(0 - 300)纤维不太可能被SCS募集,因为它们并不比DC(0 - 300)中的对应纤维大,它们缺乏侧支(这会大幅降低阈值刺激),并且它们离刺激电极更远。