Titus David J, Oliva Anthony A, Wilson Nicole M, Atkins Coleen M
Department of Neurological Surgery, The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, Florida, 33136, USA.
Curr Pharm Des. 2015;21(3):332-42. doi: 10.2174/1381612820666140826113731.
Developing therapeutics for traumatic brain injury remains a challenge for all stages of recovery. The pathological features of traumatic brain injury are diverse, and it remains an obstacle to be able to target the wide range of pathologies that vary between traumatic brain injured patients and that evolve during recovery. One promising therapeutic avenue is to target the second messengers cAMP and cGMP with phosphodiesterase inhibitors due to their broad effects within the nervous system. Phosphodiesterase inhibitors have the capability to target different injury mechanisms throughout the time course of recovery after brain injury. Inflammation and neuronal death are early targets of phosphodiesterase inhibitors, and synaptic dysfunction and circuitry remodeling are late potential targets of phosphodiesterase inhibitors. This review will discuss how signaling through cyclic nucleotides contributes to the pathology of traumatic brain injury in the acute and chronic stages of recovery. We will review our current knowledge of the successes and challenges of using phosphodiesterase inhibitors for the treatment of traumatic brain injury and conclude with important considerations in developing phosphodiesterase inhibitors as therapeutics for brain trauma.
开发针对创伤性脑损伤的治疗方法在恢复的各个阶段仍然是一项挑战。创伤性脑损伤的病理特征多种多样,能够针对创伤性脑损伤患者之间不同且在恢复过程中演变的广泛病理情况仍然是一个障碍。一个有前景的治疗途径是使用磷酸二酯酶抑制剂靶向第二信使环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP),因为它们在神经系统中具有广泛作用。磷酸二酯酶抑制剂有能力在脑损伤后的恢复全过程中针对不同的损伤机制。炎症和神经元死亡是磷酸二酯酶抑制剂的早期作用靶点,而突触功能障碍和神经回路重塑是磷酸二酯酶抑制剂后期可能的作用靶点。本综述将讨论通过环核苷酸的信号传导如何在恢复的急性和慢性阶段促成创伤性脑损伤的病理过程。我们将回顾目前关于使用磷酸二酯酶抑制剂治疗创伤性脑损伤的成功经验和挑战的知识,并以开发磷酸二酯酶抑制剂作为脑创伤治疗方法的重要考虑因素作为总结。