Mazarati A M, Halászi E, Telegdy G, Tóth G, Varga J
Institute of Pathophysiology, A. Szent-Gyorgyi Medical University, Szeged, Hungary.
Life Sci. 1993;52(3):PL19-24. doi: 10.1016/0024-3205(93)90227-t.
The administration of rANP(1-28) in doses of 1.0 and 2.0 nmol (but not 0.2 nmol) into the lateral cerebral ventricle (i.c.v) of rats preliminarily kindled with picrotoxin resulted in an increase of the severity of picrotoxin-kindled convulsions 24 hrs after injection of the peptide. I.c.v. injection of pBNP(1-32) also resulted in a proepileptic effect when it was applied in the same doses with a similar time course; the increased seizure severity was observed 48 hrs after injection of pBNP in a dose of 2 nmol. I.c.v. administration of CNP(1-22) in a dose of 2 nmol induced an increase in the severity of picrotoxin-kindled convulsions 24 and 48 hrs after application of the peptide. None of the peptides influenced the seizure syndrome immediately after the injections. It is presumed that the delayed proepileptic properties of the three natriuretic peptides could be caused by some of their stable fragments which accumulate during their metabolism.
向预先用印防己毒素点燃惊厥的大鼠侧脑室注射剂量为1.0和2.0纳摩尔(而非0.2纳摩尔)的大鼠心房钠尿肽(1 - 28),在注射该肽24小时后导致印防己毒素引发的惊厥严重程度增加。侧脑室注射脑钠肽(1 - 32),当以相同剂量并在相似时间进程应用时也产生致癫痫作用;在注射2纳摩尔脑钠肽48小时后观察到惊厥严重程度增加。侧脑室注射剂量为2纳摩尔的C型钠尿肽(1 - 22)在应用该肽24小时和48小时后导致印防己毒素引发的惊厥严重程度增加。注射后,这些肽均未立即影响癫痫发作综合征。据推测,这三种利钠肽的延迟致癫痫特性可能由其代谢过程中积累的一些稳定片段所致。