Department of Pharmacology, Physiology and Neuroscience, New Jersey Medical School, Rutgers University, Newark, New Jersey, USA.
Dev Neurosci. 2024;46(3):188-200. doi: 10.1159/000531650. Epub 2023 Jun 22.
Hypoxic-ischemic (HI) brain injury in neonatal encephalopathy triggers a wave of neuroinflammatory events attributed to causing the progressive degeneration and functional deficits seen weeks after the primary damage. The cellular processes mediating this prolonged neurodegeneration in HI injury are not sufficiently understood. Consequently, current therapies are not fully protective. In a recent study, we found significant improvements in neurologic outcomes when a small molecule antagonist for activin-like kinase 5 (ALK5), a transforming growth factor beta (TGF-β) receptor was used as a therapeutic in a rat model of moderate term HI. Here, we have extended those studies to a mouse preterm pup model of HI. For these studies, postnatal day 7 CD1 mice of both sexes were exposed to 35-40 min of HI. Beginning 3 days later, SB505124, the ALK5 receptor antagonist, was administered systemically through intraperitoneal injections performed every 12 h for 5 days. When evaluated 23 days later, SB505124-treated mice had ∼2.5-fold more hippocampal area and ∼2-fold more thalamic tissue. Approximately 90% of the ipsilateral hemisphere (ILH) was preserved in the SB505124-treated HI mice compared to the vehicle-treated HI mice, where the ILH was ∼60% of its normal size. SB505124 also preserved the subcortical white matter. SB505124 treatment preserved levels of aquaporin-4 and n-cadherin, key proteins associated with blood-brain barrier function. Importantly, SB505124 administration improved sensorimotor function as assessed by a battery of behavioral tests. Altogether, these data lend additional support to the conclusion that SB505124 is a candidate neuroprotective molecule that could be an effective treatment for HI-related encephalopathy in moderately injured preterm infants.
缺氧缺血(HI)脑损伤在新生儿脑病中引发了一波神经炎症事件,据认为这些事件导致了原发性损伤后数周内逐渐出现的退行性变和功能缺陷。介导 HI 损伤中这种长期神经退行性变的细胞过程尚未得到充分理解。因此,目前的治疗方法并非完全有效。在最近的一项研究中,我们发现,在中度 HI 大鼠模型中,使用激活素样激酶 5(ALK5)的小分子拮抗剂作为治疗药物时,神经功能结局有显著改善。在这项研究中,我们将这些研究扩展到了 HI 的早产幼鼠模型中。对于这些研究,雄性和雌性 CD1 幼鼠在出生后第 7 天经历 35-40 分钟的 HI。从第 3 天开始,ALK5 受体拮抗剂 SB505124 通过腹腔注射进行全身给药,每 12 小时给药一次,持续 5 天。在 23 天后评估时,SB505124 治疗组的海马区面积增加了约 2.5 倍,丘脑组织增加了约 2 倍。与载体处理的 HI 小鼠相比,SB505124 处理的 HI 小鼠的同侧半球(ILH)保留了约 90%,而载体处理的 HI 小鼠的 ILH 仅为其正常大小的 60%。SB505124 还保留了皮质下白质。SB505124 治疗组水通道蛋白-4 和 N-钙黏蛋白的水平也得到了保留,这些蛋白是血脑屏障功能的关键蛋白。重要的是,SB505124 给药改善了传感器运动功能,这通过一系列行为测试得到了评估。总的来说,这些数据为 SB505124 是一种候选神经保护分子的结论提供了额外的支持,它可能成为中度 HI 早产儿相关脑病的有效治疗方法。