Stevens Craig W, Kajander Keith C, Bennett Gary J, Seybold Virginia S
Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis, MN 55455 USA Neurobiology and Anesthesiology Branch, National Institute of Dental Research, National Institutes of Health, Bethesda, MD 20892 USA.
Pain. 1991 Sep;46(3):315-326. doi: 10.1016/0304-3959(91)90114-D.
Quantitative receptor autoradiography was used to assess mu, delta and kappa opioid binding sites in the lumbar spinal cord of rats with neuropathic pain due to a unilateral chronic constriction injury (CCI) of the sciatic nerve. Sections from spinal segment L4 were obtained from animals of treatment groups (left side CCI, right side sham-operated) at 2, 5 and 10 days post surgery and from control animals (left side sham-operated, right side untreated) 10 days post surgery. Autoradiograms were made of the equilibrium binding of the highly selective opioid radioligands, 3H-sufentanil (mu ligand), 3H-[D-Pen2,5]-enkephalin (DPDPE, delta ligand) and 3H-U69593 (Upjohn compound, kappa ligand). Computerized grain counting was performed on discrete regions of the autoradiograms corresponding to areas within laminae I-II, V and X on both sides of the spinal cord; the sciatic nerve's small diameter axons terminate in these areas. With a single exception, there were no changes in binding for any of the ligands in any of the areas at 10 days post surgery in the control animals. The exception was a small increase in kappa binding in laminae I-II on the sham-operated side. After nerve injury, however, there were marked changes (compared to the sham-operated side of the control animals) in the amount of binding for all ligands, and most of these changes were bilateral. Mu binding was significantly increased 2-5 days post injury, bilateral to the injury in laminae V and X but only ipsilateral in laminae I-II. Mu binding in all laminae gradually declined towards control values. By day 10 significant differences remained only in lamina X. Delta binding displayed little change at 2 days post injury but declined gradually thereafter. By day 10 post injury, delta binding was significantly decreased in all three areas; these decreases were bilateral in all areas and approximately equal in laminae V and X but were significantly greater on the nerve-injured side in laminae I-II. Kappa binding displayed a complex pattern of changes at day 2 post injury: a significant increase in ipsilateral laminae I-II and a significant increase in contralateral lamina X but no change on either side in lamina V. There was a rapid decrease in kappa binding in all three areas on both sides of the spinal cord by day 5 post injury, and these decreases were little changed by day 10.(ABSTRACT TRUNCATED AT 400 WORDS)
采用定量受体放射自显影术,评估坐骨神经单侧慢性缩窄性损伤(CCI)所致神经性疼痛大鼠腰段脊髓中的μ、δ和κ阿片样物质结合位点。术后2天、5天和10天从治疗组动物(左侧CCI,右侧假手术)以及术后10天从对照动物(左侧假手术,右侧未处理)获取L4脊髓节段的切片。利用高选择性阿片样物质放射性配体3H-舒芬太尼(μ配体)、3H-[D- Pen2,5]-脑啡肽(DPDPE,δ配体)和3H-U69593(Upjohn化合物,κ配体)进行平衡结合放射自显影。对放射自显影片上对应于脊髓两侧I-II层、V层和X层内区域的离散区域进行计算机化颗粒计数;坐骨神经的小直径轴突终止于这些区域。除一个例外,对照动物术后10天时,任何区域中任何配体的结合均无变化。例外情况是假手术侧I-II层中κ结合略有增加。然而,神经损伤后,所有配体的结合量均有显著变化(与对照动物的假手术侧相比),且大多数变化是双侧性的。损伤后2 - 5天,μ结合显著增加,在V层和X层中双侧损伤部位增加,而在I-II层中仅同侧增加。所有层中的μ结合逐渐降至对照值。到第10天时,仅在X层仍存在显著差异。δ结合在损伤后2天变化不大,但此后逐渐下降。到损伤后10天时,所有三个区域中的δ结合均显著降低;这些降低在所有区域均为双侧性,在V层和X层中大致相等,但在I-II层中神经损伤侧的降低显著更大。κ结合在损伤后第2天呈现复杂的变化模式:同侧I-II层显著增加,对侧X层显著增加,但V层两侧均无变化。损伤后第5天,脊髓两侧所有三个区域中的κ结合迅速下降,到第10天时这些下降变化不大。(摘要截短于400字)