Arrigoni E, Averet N, Cohadon F
Laboratoire de Neurochirurgie Expérimentale et Neurobiologie, Université de Bordeaux II, C.N.R.S., France.
Biochem Pharmacol. 1987 Nov 1;36(21):3697-700. doi: 10.1016/0006-2952(87)90022-0.
Within the tissue surrounding the necrotic lesion, following a cryogenic injury of the brain, there is a definite activation of phospholipase A2 (at 2 and 4 hr post lesion) that accounts, at least in part, for the phospholipid breakdown. There is also an activation of cholinephosphotransferase (at 2 hr post lesion) that may correspond to an early process of phospholipid resynthesis. Oral CDP-choline in this model is able to completely inhibit the activation of phospholipase A2, but has no detectable effect on cholinephosphotransferase activity. The beneficial effect of CDP-choline might be explained by a prevention of destruction rather than by an enhancement of reconstruction of phospholipids.
在脑低温损伤后坏死灶周围的组织中,磷脂酶A2有明确的激活(损伤后2小时和4小时),这至少部分地导致了磷脂的分解。胆碱磷酸转移酶也有激活(损伤后2小时),这可能与磷脂重新合成的早期过程相对应。在该模型中,口服胞二磷胆碱能够完全抑制磷脂酶A2的激活,但对胆碱磷酸转移酶的活性没有可检测到的影响。胞二磷胆碱的有益作用可能是通过防止磷脂破坏而不是增强其重建来解释的。