Davis J P, Vo X T, Sulakhe P V
College of Medicine, University of Saskatchewan, 107 Wiggins Road, Saskatoon, Saskatchewan, S7N-5E, Canada.
Biochem Biophys Res Commun. 1997 Sep 18;238(2):351-6. doi: 10.1006/bbrc.1997.7278.
The stimulation of cardiomyocyte guanylyl cyclase by nitric oxide (NO)-donor drugs was examined before and after exposure of these cells to the NO-donor drugs: S-nitroso-d,l-acetylpenicillamine (SNAP) and sodium nitroprusside (SNP). Short- (2-hr) and long-term (24-hr) exposure attenuated the maximal stimulation of GC by either SNAP or SNP by up to 80% ("desensitization"). However this "desensitization" of the myocardial GC was atypical in nature in that the reduction in maximal NO-stimulated GC activity was associated with an increase in the affinity of the GC towards either NO-donor, a finding not as yet reported. There was also evidence of "cross-desensitization" of GC (e.g., SNAP exposure decreasing the stimulatory effect of SNP). Further, this is the first time that SNAP-induced desensitization of GC has been observed.
在将心肌细胞暴露于一氧化氮(NO)供体药物:S-亚硝基-d,l-乙酰青霉胺(SNAP)和硝普钠(SNP)之前和之后,检测了这些药物对心肌细胞鸟苷酸环化酶(GC)的刺激作用。短期(2小时)和长期(24小时)暴露使SNAP或SNP对GC的最大刺激作用减弱高达80%(“脱敏”)。然而,心肌GC的这种“脱敏”本质上是非典型的,因为最大NO刺激的GC活性降低与GC对任一NO供体的亲和力增加有关,这一发现尚未见报道。也有GC“交叉脱敏”的证据(例如,SNAP暴露降低了SNP的刺激作用)。此外,这是首次观察到SNAP诱导的GC脱敏。