Whitaker Christopher M, Beaumont Eric, Wells Michael J, Magnuson David S K, Hetman Michal, Onifer Stephen M
Kentucky Spinal Cord Injury Research Center, School of Medicine, University of Louisville, Louisville, KY 40292, USA.
Neurosci Lett. 2008 Jun 20;438(2):200-4. doi: 10.1016/j.neulet.2008.03.087. Epub 2008 Apr 8.
Rolipram, an inhibitor of phosphodiesterase 4 (PDE4) proteins that hydrolyze cAMP, increases axonal regeneration following spinal cord injury (SCI). Recent evidence indicate that rolipram also protects against a multitude of apoptotic signals, many of which are implicated in secondary cell death post-SCI. In the present study, we used immunohistochemistry and morphometry to determine potential spinal cord targets of rolipram and to test its protective potential in rats undergoing cervical spinal cord contusive injury. We found that 3 PDE4 subtypes (PDE4A, B, D) were expressed by spinal cord oligodendrocytes. OX-42 immunopositive microglia only expressed the PDE4B subtype. Oligodendrocyte somata were quantified within the cervical ventrolateral funiculus, a white matter region critical for locomotion, at varying time points after SCI in rats receiving rolipram or vehicle treatments. We show that rolipram significantly attenuated oligodendrocyte death at 24 h post-SCI continuing through 72 h, the longest time point examined. These results demonstrate for the first time that spinal cord glial cells express PDE4 subtypes and that the PDE4 inhibitor rolipram protects oligodendrocytes from secondary cell death following contusive SCI. They also indicate that further investigations into neuroprotection and axonal regeneration with rolipram are warranted for treating SCI.
咯利普兰是一种水解环磷酸腺苷(cAMP)的磷酸二酯酶4(PDE4)蛋白抑制剂,可促进脊髓损伤(SCI)后的轴突再生。最近的证据表明,咯利普兰还能抵御多种凋亡信号,其中许多信号与SCI后的继发性细胞死亡有关。在本研究中,我们使用免疫组织化学和形态测量法来确定咯利普兰在脊髓中的潜在靶点,并测试其对遭受颈脊髓挫伤性损伤大鼠的保护潜力。我们发现脊髓少突胶质细胞表达3种PDE4亚型(PDE4A、B、D)。OX - 42免疫阳性的小胶质细胞仅表达PDE4B亚型。在接受咯利普兰或赋形剂治疗的大鼠SCI后的不同时间点,对颈外侧索(对运动至关重要的白质区域)内的少突胶质细胞胞体进行了定量分析。我们发现,咯利普兰在SCI后24小时显著减轻了少突胶质细胞死亡,并持续至72小时(所检测的最长时间点)。这些结果首次证明脊髓胶质细胞表达PDE4亚型,且PDE4抑制剂咯利普兰可保护少突胶质细胞免受挫伤性SCI后的继发性细胞死亡。它们还表明,有必要进一步研究咯利普兰在治疗SCI方面的神经保护和轴突再生作用。