Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA 19129, USA.
Brain Res. 2011 Oct 18;1418:23-31. doi: 10.1016/j.brainres.2011.08.023. Epub 2011 Aug 22.
To evaluate bladder function recovery after spinal cord injury (SCI) in response to a combination treatment of an acutely administered AMPA/kainate receptor antagonist and delayed transplantation of neuronal precursors. Female rats received a contusion injury at T8/9. The AMPA/kainate receptor antagonist NBQX was directly administered into the lesion site immediately after injury. Nine days post-injury, NRP/GRP were delivered into the lesion site. Controls received NRP/GRP grafts only or no treatment (OP-Controls). Animals underwent bladder function testing during the course of the experiment and at the endpoint. Motor function was evaluated as well. After sacrifice, histological analysis of lesion site and lumbosacral spinal cord regions was performed. Rats receiving the combined treatment (NBQX&NRP/GRP) had voided volumes/micturition resembling that of normal animals and showed greater improvement of urodynamic parameters, compared to NRP/GRP alone or OP-Controls. Similarly, NBQX&NRP/GRP induced more spouting, regeneration or sparing of descending projections to the lumbosacral cord. The density of primary afferent projections at the lumbosacral spinal cord in rats with combined treatments was similar to that of NRP/GRP alone with decreased sprouting of primary afferents in lumbosacral cord, compared to OP-Control. Immunohistochemical evaluation revealed that the combined treatment reduced the size of the lesion to a greater extent than NRP/GRP alone or OP-Controls. NRP/GRP with and without NBQX produced a significant recovery of hindlimb compared to OP-Controls. In conclusion, transplants of NRP/GRP combined with NBQX promote recovery of micturition function following spinal cord injury, likely through increased neuroprotection.
为了评估急性给予 AMPA/海人藻酸受体拮抗剂和延迟移植神经前体细胞对脊髓损伤(SCI)后膀胱功能恢复的影响。雌性大鼠在 T8/9 处接受挫伤性损伤。损伤后立即将 AMPA/海人藻酸受体拮抗剂 NBQX 直接施用于损伤部位。损伤后 9 天,将 NRP/GRP 递送至损伤部位。对照组仅接受 NRP/GRP 移植物或不接受治疗(OP-对照)。动物在实验过程中和终点进行膀胱功能测试。运动功能也进行了评估。处死动物后,对损伤部位和腰骶脊髓区域进行组织学分析。接受联合治疗(NBQX&NRP/GRP)的大鼠排空量/排尿量类似于正常动物,并且与 NRP/GRP 单独或 OP-对照相比,尿动力学参数的改善更大。同样,NBQX&NRP/GRP 诱导更多的喷溅、再生或对腰骶脊髓下行投射的保留。与 NRP/GRP 单独或 OP-对照相比,联合治疗大鼠腰骶脊髓初级传入投射的密度相似,腰骶脊髓初级传入的发芽减少。免疫组织化学评估显示,与 NRP/GRP 单独或 OP-对照相比,联合治疗更能显著减小损伤体积。NRP/GRP 联合和不联合 NBQX 比 OP-对照更能显著恢复后肢功能。总之,NRP/GRP 移植联合 NBQX 可促进脊髓损伤后排尿功能的恢复,可能通过增加神经保护作用。