磷脂酶A2-重活化剂复合物治疗有机磷中枢中毒的研究OACSTPCD
Treatment ot central nervous system organophosphorus poisoning with a phospholipase A2-reactivator complex
目的 利用磷脂酶A2(PLA2)开放血脑屏障(BBB)的特性,促使抗毒药物酰胺磷定(HI-6)进入中枢起效,为治疗中枢神经系统中毒提供新的研究思路.方法 通过体外释放和体外稳定性实验等方法,对复合物(PLA2+HI-6)的组分进行物理性质表征.利用荧光素钠模拟水溶性药物进行荧光染色,通过评价脑组织荧光病理,定性考察复合物的中枢递送能力.通过激光共聚焦显微镜下碘化丙啶染色,定性观察PLA2对细胞膜通透性的影响.通过建立梭曼染毒小鼠模型,评价复合物对抗有机磷中枢中毒效果:(1)测定小鼠脑乙酰胆碱酯酶重活化率;(2)观察小鼠脑组织病理切片;(3)统计不同处理组小鼠生存时间.分别从细胞水平和动物水平评价PLA2的安全性.结果 体外释放和体外稳定性实验结果表明,加入PLA2并不影响HI-6的释放和降解.在动物水平,PLA2有助于荧光素钠进入脑组织被细胞摄取,表现出良好的中枢递送能力.PLA2与HI-6药物组合将染毒小鼠脑内乙酰胆碱酯酶的重活化率提升至50%,相比于单独给药HI-6,提高约12倍.小鼠脑组织病理结果显示,复合物能有效对抗神经毒剂中毒引起的中枢神经系统损伤,并在3倍染毒致死剂量下显著延长小鼠存活时间,同时明显缓解中枢中毒症状.递送机制研究发现,复合物通过增加细胞膜通透性,经跨细胞途径实现中枢递送.细胞水平和动物水平的安全性实验表明,PLA2在该研究中的使用剂量安全可靠,未造成不良反应.结论 该研究以PLA2为开放材料和小分子药物HI-6组合,成功构建一种能够有效穿透BBB的复合物PLA2-HI-6.该复合物具备一定中枢靶向性,能显著提高神经毒剂中毒后脑中乙酰胆碱酯酶重活化率,为解决有机磷中枢中毒救治难题提供了参考.
Objective To study the use of phospholipase A2(PLA2)to open blood brain barrier(BBB)by affecting the physiological barrier function and promote the antidote drug asoxime(HI-6)to take effect in brain,providing a new research idea for the treatment of central nervous system organophosphorus poisoning.Methods The stability of the complex of PLA2-HI-6 was characterized through methods such as release and stability experiments.The cerebral delivery ability of the complex was evaluated through brain tissue FLU fluorescence pathology.The effect of PLA2 on cell membrane permeability was evaluated by observation with propidium iodide(PI)staining.The mouse model of soman poisoning was established to evaluate cerebral effects of the complex against soman central poisoning:(1)measuring the reactivation rate of mouse brain acetylcholinesterase(AChE);(2)observing pathological sections of mouse brain tissues;(3)calculating the survival time of mice in different groups.The safety of PLA2 was evaluated at both cellular and animal levels.Results Releasing and stability test results showed that the addition of PLA2 didn't affect the release and degradation of HI-6.PLA2 helped FLU transport into brain tissues,demonstrating excellent central delivery capability.The complex of PLA2-H1-6 significantly increased the reactivation rate of AChE in the brain of poisoned mice to 50%,about 12 times higher than that treated by HI-6 alone.Pathological results of mouse brain tissue showed that the complex effectively counteracted the cerebral nervous system damage caused by organophosphorus poisoning,significantly prolonged the survival time of mice at three times the lethal dose,and significantly alleviated symptoms of central toxicity.Research on delivery mechanisms found that complex achieved central delivery by increasing the permeability of the cell membrane to crossing the cell.Safety tests at the cellular and animal levels showed that the dosage of PLA2 used in this study was safe and reliable,and did not cause any adverse reactions.Conclusion By using PLA2 as an open material,combined with the therapeutic drug of HI-6,a complexcapable of effectively penetrating the BBB was successfully constructed.This complex has a certain central targeting ability and significantly improves the reactivation rate of AChE in the brain after organophosphorus poisoning,whichprovides a referencefor solving the difficult problem of enzyme reactivation incentral nervous system organophosphorus poisoning.
曹文缤;王淋;隋昕;骆媛;杨军;王永安
军事科学院军事医学研究院,北京 100850
特种医学
神经性毒剂有机磷化合物磷脂酶A2乙酰胆碱酯酶重活化
nerve agentorganophosphorusphospholipase A2acetylcholinesterasereactivate
《军事医学》 2024 (006)
414-420 / 7
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