OU Neuroscience, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73117, USA.
Program in Aging and Metabolism, Oklahoma Medical Research Foundation, Oklahoma City, OK, 73104, USA.
Geroscience. 2022 Feb;44(1):67-81. doi: 10.1007/s11357-021-00506-y. Epub 2022 Jan 4.
Aging is associated with molecular and functional declines in multiple physiologic systems. We have previously reported age-related changes in spinal cord that included a decline in α-motor neuron numbers, axonal loss, and demyelination associated with increased inflammation and blood-spinal cord barrier (BSCB) permeability. These changes may influence other pathologies associated with aging, in particular loss of muscle mass and function (sarcopenia), which we and others have shown is accompanied by neuromuscular junction disruption and loss of innervation. Interventions to protect and maintain motor neuron viability and function in aging are currently lacking and could have a significant impact on improving healthspan. Here we tested a promising compound, OKN-007, that has known antioxidant, anti-inflammatory and neuroprotective properties, as a potential intervention in age-related changes in the spinal cord. OKN-007 is a low molecular weight disulfonyl derivative of (N-tert Butyl-α-phenylnitrone) (PBN) that can easily cross the blood-brain barrier. We treated middle age (16 month) wild-type male mice with OKN-007 in drinking water at a dose of 150 mg/kg/day until 25 months of age. OKN-007 treatment exerted a number of beneficial effects in the aging spinal cord, including a 35% increase in the number of lumbar α-motor neurons in OKN-treated old mice compared to age-matched controls. Brain spinal cord barrier permeability, which is increased in aging spinal cord, was also blunted by OKN-007 treatment. Age-related changes in microglia proliferation and activation are blunted by OKN-007, while we found no effect on astrocyte proliferation. Transcriptome analysis identified expression changes in a number of genes that are involved in neuronal structure and function and revealed a subset of genes whose changes in response to aging are reversed by OKN-007 treatment. Overall, our findings suggest that OKN-007 exerts neuroprotective and anti-inflammatory effects on the aging spinal cord and support OKN-007 as a potential therapeutic to improve α-motor neuron health.
衰老是与多个生理系统的分子和功能下降相关的。我们之前已经报道了与年龄相关的脊髓变化,包括α运动神经元数量的减少、轴突丢失和脱髓鞘,这些变化与炎症和血脊髓屏障(BSCB)通透性增加有关。这些变化可能会影响与衰老相关的其他病理,特别是肌肉质量和功能的丧失(肌肉减少症),我们和其他人已经表明,这伴随着神经肌肉接头的破坏和失去支配。目前缺乏保护和维持运动神经元活力和功能的干预措施,这可能会对提高健康寿命产生重大影响。在这里,我们测试了一种有前途的化合物 OKN-007,它具有已知的抗氧化、抗炎和神经保护特性,作为一种潜在的干预与年龄相关的脊髓变化。OKN-007 是(N-叔丁基-α-苯硝酮)(PBN)的低分子量二磺酰衍生物,可轻松穿过血脑屏障。我们用 OKN-007 处理中年(16 个月)野生型雄性小鼠的饮用水,剂量为 150mg/kg/天,直到 25 个月大。OKN-007 治疗在衰老的脊髓中产生了许多有益的效果,包括在 OKN 治疗的老年小鼠的腰段α运动神经元数量增加了 35%,与年龄匹配的对照组相比。在衰老的脊髓中增加的血脑脊髓屏障通透性也被 OKN-007 治疗所减弱。OKN-007 减弱了与年龄相关的小胶质细胞增殖和激活的变化,而我们没有发现对星形胶质细胞增殖的影响。转录组分析确定了许多参与神经元结构和功能的基因的表达变化,并揭示了一组基因,其对衰老的反应变化被 OKN-007 治疗所逆转。总的来说,我们的研究结果表明,OKN-007 对衰老的脊髓具有神经保护和抗炎作用,并支持 OKN-007 作为一种潜在的治疗方法来改善α运动神经元的健康。