Shamir Alon, Shaltiel Galit, Agam Galila
Stanley Foundation Research Center and Department of Clinical Biochemistry, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Prog Neuropsychopharmacol Biol Psychiatry. 2002 Jan;26(1):103-6. doi: 10.1016/s0278-5846(01)00226-3.
Inositol monophosphatase (IMPase) inhibition is a hypothesized mechanism of action of lithium (Li). To test this hypothesis, the authors used the approach of antisense administration. Three days of an intracerebroventricular (icv) administration of 5 microg/20 microl 3'-phosphorothioated IMPA-1 antisense oligonucleotide sequence resulted in 20% reduction of rat periventricular IMPase activity. Li potentiates pilocarpine-induced seizures, because inhibition of IMPase leads to reduction in brain inositol levels. However, antisense-induced reduction in IMPase activity was not followed by seizures induced by subconvulsive pilocarpine doses.
肌醇单磷酸酶(IMPase)抑制是锂(Li)作用的一种假设机制。为了验证这一假设,作者采用了反义给药的方法。连续三天脑室内(icv)注射5微克/20微升的3'-硫代磷酸化IMPA-1反义寡核苷酸序列,导致大鼠脑室周围IMPase活性降低20%。锂可增强毛果芸香碱诱发的癫痫发作,因为IMPase的抑制会导致脑内肌醇水平降低。然而,反义诱导的IMPase活性降低并未引发亚惊厥剂量毛果芸香碱诱发的癫痫发作。