Karlsten R, Gordh T, Svensson B A
Department of Anesthesiology, University Hospital, Uppsala, Sweden.
Anesth Analg. 1993 Oct;77(4):731-6. doi: 10.1213/00000539-199310000-00013.
Studies in animals have shown that the adenosine receptor agonist R-phenylisopropyl adenosine (R-PIA) induces antinociceptive effects after intrathecal administration. Before such a potentially antinociceptive drug could be considered for intrathecal injection in humans, a neurotoxicologic examination of the spinal cord must be performed in animal models. Rats were injected once every day for 14 consecutive days with R-PIA or saline (controls). The number and density of neuronal cells were calculated by using light microscopy, and further examined with electron microscopy. The "disector method," which is an unbiased stereologic estimator of cell number and mean cell volume, was used for quantitative morphometric analyses. With this technique no significant changes could be seen in rats that had received R-PIA as compared to control rats. We conclude that no significant histologic changes could be detected after chronic intrathecal administration of R-PIA.
动物研究表明,腺苷受体激动剂R-苯异丙基腺苷(R-PIA)鞘内给药后可产生抗伤害感受作用。在考虑将这种具有潜在抗伤害感受作用的药物用于人体鞘内注射之前,必须在动物模型中对脊髓进行神经毒理学检查。将大鼠连续14天每天注射一次R-PIA或生理盐水(对照组)。使用光学显微镜计算神经元细胞的数量和密度,并进一步用电子显微镜检查。“分割器法”是一种用于细胞数量和平均细胞体积的无偏立体测量估计方法,用于定量形态计量分析。与对照大鼠相比,接受R-PIA的大鼠未观察到明显变化。我们得出结论,慢性鞘内注射R-PIA后未检测到明显的组织学变化。