Vizzard M A
Department of Neurology and Anatomy and Neurobiology, University of Vermont College of Medicine, Burlington 05405, USA.
Somatosens Mot Res. 1999;16(4):369-81. doi: 10.1080/08990229970429.
Alterations in the expression of growth-associated protein 43 (GAP-43) were examined in lower urinary tract micturition reflex pathways 6 or 8 weeks following complete spinal cord transection (approximately T9). In control animals, expression of GAP-43 was present in specific regions of the gray matter in the rostral lumbar and caudal lumbosacral spinal cord, including: (1) the dorsal commissure; (2) the corticospinal tract; (3) the dorsal horn; and (4) the regions of the intermediolateral cell column (L1-L2) and the sacral parasympathetic nucleus (L6-S1); and (5) in the lateral collateral pathway of Lissauer in L6-S1 spinal segments. Densitometry analysis has demonstrated significant increases (p < or =0.001; 1.3-6.4-fold increase) in GAP-43-immunoreactivity (IR) in these regions of the rostral lumbar (L1-L2) and caudal lumbosacral (L6-S1) spinal cord 6 weeks following spinal cord injury. Changes in GAP-43-IR were restricted to the L1-L2 and L6-S1 segments that are involved in lower urinary tract reflexes. Changes in GAP-43-IR were not observed at the L5 segmental level except for an increase in GAP-43-IR in the superficial, dorsal horn at 6 weeks post-injury. In all segments examined, GAP-43-IR was decreased (2-5-fold) in the corticospinal tract (dorsal division) 6 and 8 weeks following spinal cord injury. Eight weeks following spinal cord injury, changes in GAP-43-IR had returned to control levels except for the persistence of increased GAP-43-IR in the region of the sacral parasympathetic nucleus and the lateral collateral pathway in the S1 spinal segment. Alterations in GAP-43-IR following chronic spinal cord injury may suggest a reorganization of bladder afferent projections and spinal elements involved in urinary bladder reflexes consistent with alterations in urinary bladder function (hyperreflexia) observed in animals following spinal cord injury above the lumbosacral spinal cord.
在脊髓完全横断(约T9)后6周或8周,检测下尿路排尿反射通路中生长相关蛋白43(GAP - 43)表达的变化。在对照动物中,GAP - 43表达存在于腰髓上段和腰骶髓下段灰质的特定区域,包括:(1)背侧连合;(2)皮质脊髓束;(3)背角;(4)中间外侧细胞柱(L1 - L2)和骶副交感核(L6 - S1)区域;以及(5)L6 - S1脊髓节段的利骚厄外侧副通路。密度测定分析表明,脊髓损伤后6周,腰髓上段(L1 - L2)和腰骶髓下段(L6 - S1)脊髓的这些区域中GAP - 43免疫反应性(IR)显著增加(p≤0.001;增加1.3 - 6.4倍)。GAP - 43 - IR的变化局限于参与下尿路反射的L1 - L2和L6 - S1节段。除了损伤后6周浅表背角的GAP - 43 - IR增加外,在L5节段水平未观察到GAP - 43 - IR的变化。在所有检测节段中,脊髓损伤后6周和8周,皮质脊髓束(背侧部分)的GAP - 43 - IR降低(2 - 5倍)。脊髓损伤8周后,除了骶副交感核区域和S1脊髓节段外侧副通路中GAP - 43 - IR持续增加外,GAP - 43 - IR的变化已恢复到对照水平。慢性脊髓损伤后GAP - 43 - IR的改变可能提示膀胱传入投射和参与膀胱反射的脊髓成分发生了重组,这与腰骶脊髓以上脊髓损伤动物中观察到膀胱功能改变(反射亢进)一致。