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The effect of prolyl oligopeptidase inhibition on extracellular acetylcholine and dopamine levels in the rat striatum

机译:脯氨酰寡肽酶抑制对大鼠纹状体细胞外乙酰胆碱和多巴胺水平的影响

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摘要

Prolyl oligopeptidase (PREP, EC 3.4.21.26) inhibitors have potential as cognition enhancers, but the mechanism of action behind the cognitive effects remains unclear. Since acetylcholine (ACh) and dopamine (DA) are known to be associated with the regulation of cognitive processes, we investigated the effects of two PREP inhibitors on the extracellular levels of ACh and DA in the rat striatum using in vivo microdialysis. KYP-2047 and JTP-4819 were administered either as a single systemic dose (50 μmol/kg~17 mg/kg i.p.) or directly into the striatum by retrodialysis via the microdialysis probe (12.5, 37.5 or 125 μM at 1.5 μl/min for 60 min). PREP inhibitors had no significant effect on striatal DA levels after systemic administration. JTP-4819 significantly decreased ACh levels both after systemic (by ~25%) and intrastriatal (by ~30-50%) administration. KYP-2047 decreased ACh levels only after intrastriatal administration by retrodialysis (by ~40-50%) when higher drug levels were reached, indicating that higher brain drug levels are needed to modulate ACh levels than to inhibit PREP. This result does not support the earlier hypothesis that the positive cognitive effects of PREP inhibitors in rodents would be mediated through the cholinergic system. In vitro specificity studies did not reveal any obvious off-targets that could explain the observed effect of KYP-2047 and JTP-4819 on ACh levels, instead confirming the concept that these compounds have a high selectivity towards PREP.
机译:脯氨酰寡肽酶(PREP,EC 3.4.21.26)抑制剂具有作为认知增强剂的潜力,但认知作用背后的作用机制仍不清楚。由于已知乙酰胆碱(ACh)和多巴胺(DA)与认知过程的调节有关,因此我们使用体内微透析技术研究了两种PREP抑制剂对大鼠纹状体中ACh和DA细胞外水平的影响。 KYP-2047和JTP-4819可以单次全身剂量(50μmol/ kg〜17 mg / kg ip)给药,也可以通过微量透析探针(12.5、37.5或125μM,以1.5μl/ min的速度通过逆向透析)直接注射到纹状体中60分钟)。全身给药后,PREP抑制剂对纹状体DA水平无明显影响。 JTP-4819在全身(约25%)和纹状体内(约30-50%)给药后均显着降低ACh水平。当达到更高的药物水平时,KYP-2047仅在通过逆透析进行纹状体内给药后才降低ACh水平(降低约40-50%),这表明与抑制PREP相比,调节ACh水平需要更高的脑部药物水平。该结果不支持先前的假设,即PREP抑制剂在啮齿动物中的积极认知作用将通过胆碱能系统介导。体外特异性研究未发现任何明显的脱靶现象可以解释KYP-2047和JTP-4819对ACh水平的影响,而是证实了这些化合物对PREP具有高选择性的概念。

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