Zhang X, Verge V, Wiesenfeld-Hallin Z, Ju G, Bredt D, Synder S H, Hökfelt T
Department of Histology and Neurobiology, Karolinska Institute, Stockholm, Sweden.
J Comp Neurol. 1993 Sep 22;335(4):563-75. doi: 10.1002/cne.903350408.
With the immunofluorescence technique, nitric oxide synthase (NOS)-like immunoreactivity (LI) was found in a few medium-sized and small sensory neurons in lumbar (L) 4 and L5 dorsal root ganglia (DRG) of normal rat, and in most of these neurons, NOS-LI coexisted with calcitonin gene-related peptide and sometimes with substance P and galanin. NOS-immunoreactive nerve fibers, terminals and small neurons were also located in the dorsal horn of the segments 4 and 5 of the rat lumbar spinal cord with the highest density in inner lamina II. Many NOS-positive neurons and fibers were seen in the area around the central canal. A sparse network of NOS-immunoreactive nerve fibers was found in the ventral horn. After unilateral sciatic nerve cut in the rat, the number of NOS-positive neurons increased in the ipsilateral L4 and L5 DRGs, mainly in medium and small neurons, but also in some large neurons and very small neurons. NOS-LI could now also be seen in the ipsilateral dorsal roots, and in an increased number of fibers and terminals in both outer and inner lamina II of the ipsilateral dorsal horn. The number of NOS-immunoreactive neurons in lamina II of the ipsilateral dorsal horn was reduced. In the monkey L4 and L5 DRGs, many small neurons were NOS-immunoreactive, but only a few weakly stained nerve fibers and terminals were found in laminae I-IV of the dorsal horn at L4 and L5 lumbar levels. A few NOS-positive neurons were present in lamina X. The number of NOS-immunoreactive neurons was somewhat reduced in DRGs 14 days after peripheral axotomy, but no certain effect was seen in the dorsal horn. These results, together with earlier in situ hybridization studies, demonstrate that axotomy in rat induces a marked upregulation of NOS synthesis in primary sensory neurons, thus suggesting a role for NO in lesioned sensory neurons. In contrast, no such effect was recorded in monkey, perhaps indicating distinct species differences.
应用免疫荧光技术,在正常大鼠腰4和腰5背根神经节(DRG)的一些中小型感觉神经元中发现了一氧化氮合酶(NOS)样免疫反应性(LI),并且在大多数这些神经元中,NOS-LI与降钙素基因相关肽共存,有时还与P物质和甘丙肽共存。NOS免疫反应性神经纤维、终末和小神经元也位于大鼠腰脊髓第4和第5节段的背角,在内侧II层密度最高。在中央管周围区域可见许多NOS阳性神经元和纤维。在腹角发现了稀疏的NOS免疫反应性神经纤维网络。大鼠单侧坐骨神经切断后,同侧腰4和腰5背根神经节中NOS阳性神经元数量增加,主要在中小型神经元中,但也在一些大型神经元和非常小的神经元中增加。现在在同侧背根中也可以看到NOS-LI,并且在同侧背角外侧和内侧II层的纤维和终末数量增加。同侧背角II层中NOS免疫反应性神经元数量减少。在猴的腰4和腰5背根神经节中,许多小神经元呈NOS免疫反应性,但在腰4和腰5水平的背角I-IV层中仅发现少数弱染色的神经纤维和终末。在X层中有一些NOS阳性神经元。外周轴突切断14天后,背根神经节中NOS免疫反应性神经元数量有所减少,但在背角未观察到确切影响。这些结果与早期的原位杂交研究一起表明,大鼠轴突切断诱导初级感觉神经元中NOS合成的显著上调,从而提示NO在损伤的感觉神经元中起作用。相比之下,在猴中未记录到这种效应,这可能表明存在明显的物种差异。