Rao M S, Sun Y, Vaidyanathan U, Landis S C, Zigmond R E
Department of Neurosciences, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4975.
J Neurobiol. 1993 May;24(5):571-80. doi: 10.1002/neu.480240504.
The regulation of the expression of substance P (SP) in the rat superior cervical ganglion was compared to that of vasoactive intestinal peptide (VIP) in vivo after axotomy and in vitro after explantation. Previous studies have demonstrated that both neuropeptides increase after explantation, depolarization, and decentralization; however, whereas VIP expression increases after postganglionic axotomy, SP expression reportedly does not. To compare the effect of axotomy on these two peptides directly, the content of both was determined in individual ganglia at various times after surgery. The level of VIP-like immunoreactivity (IR) is increased at 2 days, reaches a peak at 6 days, and then declines by 14 days to approximately half its peak value. The level of SP-IR also increases 2 days after axotomy, but returns to control values by day 6. The increase in SP-IR is accompanied by an increase in beta-preprotachykinin mRNA, suggesting that the elevation in SP content is due, at least in part, to enhanced peptide synthesis. Immunocytochemical localization of SP-IR revealed the presence of immunoreactive principal neurons in axotomized, but not in sham-operated ganglia. Similarities in the regulation of these two neuropeptides were also investigated in organ culture by examining the effects of dexamethasone and interleukin-1 beta on VIP content, since the former has been shown to prevent the increase in SP in culture, while the latter has been found to enhance this increase (Kessler, Adler, Bell, et al., 1983, Neuroscience 9:309-321; Freidin and Kessler, 1991, Proc. Natl. Acad. Sci. USA 88:3200-3203; Hart, Shadiack, and Jonakait, 1991, J. Neurosci. Res. 29:282-291). As with SP expression, dexamethasone reduces the increase in VIP expression, while interleukin-1 beta increases it. Thus, both in vivo and in vitro, similar changes in VIP and SP expression are observed following a number of experimental manipulations, suggesting that expression of the two peptides is regulated by qualitatively similar mechanisms in sympathetic neurons.
将大鼠颈上神经节中P物质(SP)的表达调控与血管活性肠肽(VIP)在体内轴突切断后及体外植入后的表达调控进行了比较。先前的研究表明,两种神经肽在植入、去极化和去传入后均会增加;然而,虽然节后轴突切断后VIP表达增加,但据报道SP表达并未增加。为了直接比较轴突切断对这两种肽的影响,在手术后不同时间测定了单个神经节中两种肽的含量。VIP样免疫反应性(IR)水平在2天时升高,在6天时达到峰值,然后在14天时降至峰值的约一半。轴突切断后2天SP-IR水平也升高,但在第6天恢复到对照值。SP-IR的增加伴随着β-前速激肽原mRNA的增加,表明SP含量的升高至少部分归因于肽合成的增强。SP-IR的免疫细胞化学定位显示,在轴突切断的神经节中存在免疫反应性的主神经元,而在假手术的神经节中则不存在。还通过研究地塞米松和白细胞介素-1β对VIP含量的影响,在器官培养中研究了这两种神经肽调控的相似性,因为前者已被证明可防止培养中SP的增加,而后者已被发现可增强这种增加(凯斯勒、阿德勒、贝尔等人,1983年,《神经科学》9:309 - 321;弗里丁和凯斯勒,1991年,《美国国家科学院院刊》88:3200 - 3203;哈特、沙迪亚克和乔纳凯特,1991年,《神经科学研究杂志》29:282 - 291)。与SP表达一样,地塞米松减少VIP表达的增加,而白细胞介素-1β则增加其表达。因此,在体内和体外,在多种实验操作后均观察到VIP和SP表达的相似变化,表明这两种肽在交感神经元中的表达受定性相似的机制调控。