Dekker A J, Tonnaer J A
CNS Pharmacology Department, Organon International, Oss, The Netherlands.
Brain Res. 1989 Jan 16;477(1-2):327-31. doi: 10.1016/0006-8993(89)91422-4.
The binding of the neurotrophic peptide, [3H]Org 2766 (55 nM), to rat spinal cord sections was studied, employing quantitative autoradiography. The binding was unevenly distributed over spinal cord structures and was displaceable by non-labelled Org 2766 to a limited extent (35%). Binding could not be displaced by the opiate antagonist, naloxone, indicating that [3H]Org 2766 binding sites are distinct from opiate receptors. However, the exact nature of the binding sites remains to be elucidated. A marked left-right difference in [3H]Org 2766 binding in the dorsal horns of the spinal cord at level L2 was observed, 6 days after unilateral crush lesioning of the sciatic nerve. No such effect was found at level T10. After 28 days, when sensorimotor functioning had completely recovered, the [3H]Org 2766 binding pattern was comparable to that in sham-operated rats again. It is suggested that Org 2766 binds to axonal sprouts or glia in the dorsal horn of the spinal cord.
利用定量放射自显影技术,研究了神经营养肽[3H]Org 2766(55 nM)与大鼠脊髓切片的结合情况。该结合在脊髓结构上分布不均,且可被未标记的Org 2766有限程度地取代(35%)。阿片拮抗剂纳洛酮不能取代这种结合,这表明[3H]Org 2766结合位点与阿片受体不同。然而,结合位点的确切性质仍有待阐明。在坐骨神经单侧挤压损伤6天后,观察到L2水平脊髓背角[3H]Org 2766结合存在明显的左右差异。在T10水平未发现这种效应。28天后,当感觉运动功能完全恢复时,[3H]Org 2766结合模式再次与假手术大鼠相当。提示Org 2766与脊髓背角的轴突芽或胶质细胞结合。