Chen S, Aston-Jones G
Department of Mental Health Sciences, Hahnemann University, Philadelphia, Pennsylvania 19102.
Exp Neurol. 1994 Apr;126(2):270-6. doi: 10.1006/exnr.1994.1064.
NADPH diaphorase (NADPH-D) histochemistry was examined following cerebellar lesions induced by stab or knife cuts. A population of Purkinje cells adjacent to the injury became NADPH-D positive after either type of lesion. These cells appeared by 3 days postlesion and were still seen after 6 weeks. Somata of reactive cells shrank gradually and were reduced about 38% in size by 6 weeks after lesion. In the inferior olive of animals subjected to cerebellar knife cut, NADPH-D-positive cells were found in the beta nucleus, dorsal cap, and subnucleus C. These cells became NADPH-D positive 5 days postlesion, were shrunken at 4 weeks postlesion, and were reduced about 26% in somata size by 6 weeks after lesion. Other cerebellar afferents did not exhibit obvious NADPH-D induction following these lesions. In unlesioned animals, no Purkinje cells or inferior olivary neurons were NADPH-D positive. The present study demonstrates that cerebellar damage induces NADPH-D, a marker for nitric oxide (NO) synthase, in Purkinje cells and inferior olivary neurons. In addition, these reactive neurons exhibit long-term degenerative changes. Taken together with previous studies, these findings indicate that NO, produced by the lesion-induced nitric oxide synthase (NOS), may contribute to the degeneration of brain neurons after injury. The lack of NADPH-D-positive neurons in either Purkinje or the inferior olivary neurons in nonlesioned animals indicates that this may provide a useful model system to study injury-induced NOS in brain.
在刺伤或刀切诱导的小脑损伤后,检测了NADPH黄递酶(NADPH-D)组织化学。两种损伤类型后,损伤附近的一群浦肯野细胞均变为NADPH-D阳性。这些细胞在损伤后3天出现,6周后仍可见。反应性细胞的胞体逐渐缩小,损伤后6周时大小减少约38%。在接受小脑刀切的动物的下橄榄核中,在β核、背帽和C亚核中发现了NADPH-D阳性细胞。这些细胞在损伤后5天变为NADPH-D阳性,在损伤后4周时萎缩,损伤后6周时胞体大小减少约26%。这些损伤后,其他小脑传入纤维未表现出明显的NADPH-D诱导。在未损伤的动物中,没有浦肯野细胞或下橄榄核神经元是NADPH-D阳性的。本研究表明,小脑损伤可诱导浦肯野细胞和下橄榄核神经元中的NADPH-D,这是一氧化氮(NO)合酶的标志物。此外,这些反应性神经元表现出长期的退行性变化。与先前的研究一起,这些发现表明,损伤诱导的一氧化氮合酶(NOS)产生的NO可能导致损伤后脑神经元的变性。未损伤动物的浦肯野细胞或下橄榄核神经元中缺乏NADPH-D阳性神经元,表明这可能为研究脑损伤诱导的NOS提供一个有用的模型系统。