Igwe Orisa J, Li Ning
Division of Pharmacology, School of Pharmacy, University of Missouri-Kansas City, Kansas City, MO 64108-2792 USA.
Pain. 1994 Jul;58(1):63-75. doi: 10.1016/0304-3959(94)90185-6.
Unilateral intraplantar injection of Freund's complete adjuvant (FCA) into 1 hind paw of rats was used as a model of peripheral inflammation and persistent pain in order to examine time course effects of a continuous barrage of nociceptive input on the second-messenger transducing systems in the spinal cord. cAMP, cGMP and inositol 1,4,5-trisphosphate (insP3) were extracted from the lumbosacral cord at days 1, 7, 14, 21 and 42 following FCA injection and quantified by either radioreceptor-assay (RRA) or radioimmunoassay (RIA). The lumbosacral contents of cAMP and cGMP when quantified in whole lumbosacral cord segment were not significantly changed by FCA treatment at all time points. InsP3 accumulation was significantly increased on days 14, 21 and 42 following FCA injection relative to sham-treated time-matched controls. However, cGMP and insP3 contents were significantly increased in the left longitudinal half of the lumbar enlargement ipsilateral to the injected paw on day 21 following FCA treatment, but not in the sham-treated time-matched controls. With [3H]insP3 as a ligand, Scatchard (Rosenthal) analyses of the concentration-dependent saturation curves showed that the densities (Bmax) of insP3 receptors (insP3R) were significantly increased throughout the time course of adjuvant-induced peripheral inflammation. The binding affinities (KD) for insP3R were significantly decreased on days 7, 14 and 21 following FCA injection corresponding to the times of most stable and peak inflammation. InsP3R from the cerebelli of the same rats as used in the lumbosacral insP3R characterization was used as a positive control in this study and did not show any change in both Bmax and KD as a result of FCA treatment, thus demonstrating that the changes in lumbosacral insP3R characteristics might be specific to the nociceptive sensory pathway such as the spinal cord. Thus it appears that sustained afferent nociceptive input induced by FCA injection increased the accumulation of cGMP, insP3 and insP3R density in the spinal cord through increased neuronal activities of functional receptors coupled to major classes of chemical mediators of nociception including neuropeptides and excitatory aminoacids. Changes in insP3 accumulation in the lumbosacral cord following FCA injection were significantly correlated with changes in insP3R density. Changes in the ratios of lumbosacral insP3 contents and insP3R density were also significantly correlated with changes in body weight and hind paw size induced by FCA injection.(ABSTRACT TRUNCATED AT 400 WORDS)
将弗氏完全佐剂(FCA)单侧足底注射到大鼠的一只后爪中,以此作为外周炎症和持续性疼痛的模型,以研究伤害性传入持续刺激对脊髓中第二信使转导系统的时程效应。在FCA注射后的第1、7、14、21和42天,从腰骶脊髓中提取环磷酸腺苷(cAMP)、环磷酸鸟苷(cGMP)和肌醇1,4,5-三磷酸(InsP3),并通过放射受体分析法(RRA)或放射免疫分析法(RIA)进行定量。在所有时间点,FCA处理对整个腰骶脊髓节段中cAMP和cGMP的腰骶含量进行定量时均无显著变化。与假手术处理的时间匹配对照组相比,FCA注射后第14、21和42天InsP3的积累显著增加。然而,FCA处理后第21天,注射爪同侧腰膨大左侧纵半部分的cGMP和InsP3含量显著增加,而假手术处理的时间匹配对照组则无此现象。以[3H]InsP3作为配体,对浓度依赖性饱和曲线进行Scatchard(罗森塔尔)分析表明,在佐剂诱导的外周炎症的整个时程中,InsP3受体(InsP3R)的密度(Bmax)显著增加。FCA注射后第7、14和21天,对应于炎症最稳定和峰值的时间,InsP3R的结合亲和力(KD)显著降低。本研究中,将与腰骶InsP3R特性研究中所用大鼠相同的大鼠小脑的InsP3R用作阳性对照,结果显示FCA处理后Bmax和KD均无变化,从而表明腰骶InsP3R特性的变化可能是脊髓等伤害性感觉通路所特有的。因此,似乎FCA注射诱导的持续传入伤害性刺激通过增加与包括神经肽和兴奋性氨基酸在内的主要伤害性化学介质偶联的功能性受体的神经元活动,增加了脊髓中cGMP、InsP3的积累和InsP3R密度。FCA注射后腰骶脊髓中InsP3积累的变化与InsP/R密度的变化显著相关。腰骶InsP3含量与InsP3R密度的比值变化也与FCA注射引起的体重和后爪大小变化显著相关。(摘要截短至400字)