Feuerstein G, Yue T L, Lysko P G
Division of Pharmacology, SmithKline Beecham, Philadelphia, Pa.
Stroke. 1990 Nov;21(11 Suppl):III90-4.
Platelet-activating factor (1-O-hexadecyl-2-acetyl-sn-glycero-3-phosphorylcholine) is a potent lipid autacoid produced by many cell types. Platelet-activating factor is produced by cerebellar granule cells in culture and has been extracted from brain tissue. Multiple platelet-activating factor receptors have been demonstrated in brain tissue. Activation of platelet-activating factor receptors in transformed neuronal cell lines involved increases in intracellular calcium. Platelet-activating factor has potent actions on cerebral vessels and cerebral metabolism when administered in vivo, but may not have direct effects on brain microvessels. Excessive platelet-activating factor production in pathological states of the nervous system such as neurotrauma and stroke has been shown in only a few models (e.g., spinal cord ischemia and reperfusion or focal repercussion brain injury). In multiple studies using highly specific and potent platelet-activating factor antagonists, reversal or prevention of key consequences of brain injury such as hypoperfusion following ischemia, reperfusion and edema, inflammatory cell accumulation, neurologic/motor deficits, and neuronal salvage were demonstrated. This review provides and analyzes evidence in support of the role that platelet-activating factor might have in modulation of brain function and pathophysiological processes in brain ischemia and trauma.
血小板活化因子(1-O-十六烷基-2-乙酰基-sn-甘油-3-磷酸胆碱)是一种由多种细胞类型产生的强效脂质自分泌调节因子。血小板活化因子由培养的小脑颗粒细胞产生,并已从脑组织中提取出来。在脑组织中已证实存在多种血小板活化因子受体。在转化的神经元细胞系中,血小板活化因子受体的激活会导致细胞内钙含量增加。血小板活化因子在体内给药时对脑血管和脑代谢有强效作用,但可能对脑微血管没有直接影响。仅在少数模型(如脊髓缺血再灌注或局灶性撞击性脑损伤)中显示,在神经创伤和中风等神经系统病理状态下会产生过量的血小板活化因子。在多项使用高度特异性和强效血小板活化因子拮抗剂的研究中,证实了脑损伤的关键后果如缺血、再灌注和水肿后的灌注不足、炎症细胞聚集、神经/运动功能缺损以及神经元挽救的逆转或预防。这篇综述提供并分析了证据,以支持血小板活化因子在调节脑功能以及脑缺血和创伤中的病理生理过程中可能发挥的作用。