Steulet A F, Stöcklin K, Wicki P, Waldmeier P
Research Department, Pharmaceuticals Division, CIBA-GEIGY Ltd., Basel, Switzerland.
Neurochem Res. 1993 Nov;18(11):1131-6. doi: 10.1007/BF00978363.
The effects on rat striatal dopamine (DA) metabolism of systemic and local administration of CGP 28014, an inhibitor of catechol-O-methyl-transferase (COMT), were studied by in vivo microdialysis. CGP 28014 (30 mg/kg i.p.) significantly reduced the levels of homovanillic acid (HVA), but did not modify DA and 3,4-dihydroxyphenylacetic acid (DOPAC). The intrastriatal administration (via the microdialysis probe) of 5, 7.5, 10, and 20 mM of CGP 28014 elicited a concentration-dependent, several-fold increase in extracellular DA but did not alter the levels of HVA and DOPAC. Thus, the effects of CGP 28014 observed after i.p. injection (decrease in HVA levels) are different from those measured after intrastriatal administration (increase in DA release). Therefore, the inhibition of COMT is likely to be due to the action of a metabolite of CGP 28014 formed in the periphery and not in the brain.
通过体内微透析研究了儿茶酚-O-甲基转移酶(COMT)抑制剂CGP 28014全身给药和局部给药对大鼠纹状体多巴胺(DA)代谢的影响。CGP 28014(腹腔注射30 mg/kg)显著降低了高香草酸(HVA)水平,但未改变多巴胺(DA)和3,4-二羟基苯乙酸(DOPAC)水平。向纹状体内注射(通过微透析探针)5、7.5、10和20 mM的CGP 28014可引起细胞外DA浓度依赖性的数倍增加,但未改变HVA和DOPAC水平。因此,腹腔注射后观察到的CGP 28014的作用(HVA水平降低)与纹状体内给药后测量的作用(DA释放增加)不同。因此,COMT的抑制可能是由于CGP 28014在外周而非脑内形成的代谢产物的作用。