Pharmacological interventions targeting the microcirculation following traumatic spinal cord injury

被引:7
作者
Wang, Rongrong [1 ,2 ]
Bai, Jinzhu [1 ,2 ]
机构
[1] Beijing Boai Hosp, Dept Spine & Spinal Cord Surg, China Rehabil Res Ctr, Beijing, Peoples R China
[2] Capital Med Univ, Sch Rehabil Med, Beijing, Peoples R China
关键词
blood-spinal cord barrier; drug therapy; microcirculation; microvascular blood flow; neuroprotection; pharmacological intervention; pharmacotherapy; spinal cord injury; trauma; LITHIUM-CHLORIDE CONTRIBUTES; FUNCTIONAL RECOVERY; HYDROGEN-SULFIDE; BSCB DISRUPTION; CONTUSION INJURY; CARBON-MONOXIDE; EDEMA FORMATION; VALPROIC ACID; UP-REGULATION; BLOOD-FLOW;
D O I
10.4103/1673-5374.375304
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Traumatic spinal cord injury is a devastating disorder characterized by sensory, motor, and autonomic dysfunction that severely compromises an individual's ability to perform activities of daily living. These adverse outcomes are closely related to the complex mechanism of spinal cord injury, the limited regenerative capacity of central neurons, and the inhibitory environment formed by traumatic injury. Disruption to the microcirculation is an important pathophysiological mechanism of spinal cord injury. A number of therapeutic agents have been shown to improve the injury environment, mitigate secondary damage, and/or promote regeneration and repair. Among them, the spinal cord microcirculation has become an important target for the treatment of spinal cord injury. Drug interventions targeting the microcirculation can improve the microenvironment and promote recovery following spinal cord injury. These drugs target the structure and function of the spinal cord microcirculation and are essential for maintaining the normal function of spinal neurons, axons, and glial cells. This review discusses the pathophysiological role of spinal cord microcirculation in spinal cord injury, including its structure and histopathological changes. Further, it summarizes the progress of drug therapies targeting the spinal cord microcirculation after spinal cord injury.
引用
收藏
页码:35 / 42
页数:8
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