Yaksh T L, Chipkin R E
Anesthesiology Research Laboratory, University of California San Diego, La Jolla 92093.
Eur J Pharmacol. 1989 Aug 29;167(3):367-73. doi: 10.1016/0014-2999(89)90445-7.
SCH-34826 and thiorphan are inhibitors of the neutral endopeptidase (NEP; E.C. 3.4.24.11;) that cleaves the opiate peptides [Met5]- and [Leu5]enkephalin at the glycinylphenylalanine bond. These compounds were evaluated for their ability to affect the levels of [Met5]enkephalin-like immunoreactivity (MELI) in the brain and the spinal cord and the release into the extracellular space under resting and K+-evoked conditions. The results showed that oral administration of SCH-34826 (30-100 mg/kg p.o.) or thiorphan (10-30 mg/kg p.o.) had no effect on tissue levels of MELI. In contrast, both agents caused a dose-dependent increase in both the resting and the K+-evoked levels in spinal perfusates, which reached up to 10 times the control values. These data indicate that tissue (presumably intracellular) stores of [Met5]enkephalin are not affected by NEP inhibition and that it is the extracellular effects of the peptide that are potentiated by enzyme blockade. This agrees with the prior results demonstrating that NEP inhibitors require a nociceptive stimulus sufficient to release endogenous stores of [Met5]enkephalins for their actions to be observed.
SCH - 34826和硫磷酰胺是中性内肽酶(NEP;E.C. 3.4.24.11)的抑制剂,该酶可在甘氨酰苯丙氨酸键处切割阿片肽[Met5]-和[Leu5]脑啡肽。评估了这些化合物影响脑和脊髓中[Met5]脑啡肽样免疫反应性(MELI)水平以及在静息和钾离子诱发条件下释放到细胞外空间的能力。结果表明,口服SCH - 34826(30 - 100 mg/kg,口服)或硫磷酰胺(10 - 30 mg/kg,口服)对MELI的组织水平没有影响。相反,两种药物均导致脊髓灌流液中静息和钾离子诱发水平呈剂量依赖性增加,最高可达对照值的10倍。这些数据表明,[Met5]脑啡肽的组织(可能是细胞内)储存不受NEP抑制的影响,而肽的细胞外效应因酶阻断而增强。这与先前的结果一致,即NEP抑制剂需要足够的伤害性刺激以释放内源性[Met5]脑啡肽储存才能观察到其作用。