Hongo T, Kudo N, Sasaki S, Yamashita M, Yoshida K, Ishizuka N, Mannen H
J Comp Neurol. 1987 Aug 8;262(2):159-94. doi: 10.1002/cne.902620202.
Nineteen physiologically identified group Ia and five group Ib fibers at the L3 and L4 levels of the spinal cord originating from various hind-limb muscles were intraaxonally injected with horseradish peroxidase (HRP). The trajectories of the stained axons were reconstructed. They extended for distances of 8.6 mm-18.0 mm rostrocaudally. Ascending axons ran in various regions of the dorsal funiculus: The ascending axon from a toe muscle (3 microns in diameter) ran in the ventral most part of the paramedian region; those from shank muscles (3.0-5.0 microns) in both dorsal and ventral paramedian regions; those from thigh muscles (5.0-7.0 microns) in both the paramedian and the more lateral regions; and those from hip muscles (6.0-7.0 microns) in the lateral region. Main collaterals arising from the parent fiber were given off at intervals of 0.5-6.2 mm (mean 2.4 mm). Collaterals of a fiber from a toe muscle (1.0 micron in diameter) entered Clarke's column from the dorsomedial side and ramified mostly in the dorsomedial one-third of the column. Collaterals of fibers from shank muscles (1.0-2.0 microns) entered Clarke's column from the dorsal side and terminated in its middle parts as well as in laminae V-VII. Collaterals of fibers from thigh muscles (1.0-2.5 microns) passed lateral to or through the lateral part of Clarke's column and terminated in its ventrolateral part and in laminae V-VIII. Collaterals of fibers from hip muscles (1.5-2.5 microns) passed lateral to Clarke's column and ramified mostly in laminae VII-IX. As the muscle of origin became more proximal, the proportion of termination outside of Clarke's column progressively increased. Thus, the trajectory of group I fibers was somatotopically organized both in the dorsal funiculus and in the gray matter. The long axis of boutons ranged from 0.5 to 17 microns in Ia fibers and from 0.5 to 8 microns in Ib fibers. "Giant" Ia boutons (above 7 microns) were found both in and outside Clarke's column.
在脊髓L3和L4水平,对来自各种后肢肌肉的19条经生理学鉴定的Ia类神经纤维和5条Ib类神经纤维进行轴突内辣根过氧化物酶(HRP)注射。对染色轴突的轨迹进行了重建。它们在前后方向上延伸的距离为8.6毫米至18.0毫米。上行轴突在背侧索的不同区域走行:来自趾肌(直径3微米)的上行轴突在旁正中区域的最腹侧走行;来自小腿肌肉(3.0 - 5.0微米)的轴突在背侧和腹侧旁正中区域走行;来自大腿肌肉(5.0 - 7.0微米)的轴突在旁正中区域和更外侧区域走行;来自髋部肌肉(6.0 - 7.0微米)的轴突在外侧区域走行。母纤维发出的主要侧支间隔为0.5 - 6.2毫米(平均2.4毫米)。来自趾肌(直径1.0微米)的纤维的侧支从背内侧进入克拉克柱,并主要在柱的背内侧三分之一处分支。来自小腿肌肉(1.0 - 2.0微米)的纤维的侧支从背侧进入克拉克柱,并在其中部以及V - VII层终止。来自大腿肌肉(1.0 - 2.5微米)的纤维的侧支从克拉克柱的外侧或穿过其外侧部分,并在其腹外侧部分以及V - VIII层终止。来自髋部肌肉(1.5 - 2.5微米)的纤维的侧支从克拉克柱外侧经过,并主要在VII - IX层分支。随着起始肌肉变得更靠近近端,在克拉克柱外终止的比例逐渐增加。因此,I类纤维的轨迹在背侧索和灰质中都呈躯体定位组织。Ia类纤维中终扣的长轴范围为0.5至17微米,Ib类纤维中为0.5至8微米。在克拉克柱内外均发现了“巨型”Ia类终扣(大于7微米)。