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Antidepressant-like and anxiolytic-like effects of YL-IPA08, a potent ligand for the translocator protein (18 kDa)

机译:YL-IPA08的抗抑郁药和抗焦虑药作用,YL-IPA08是易位蛋白(18 kDa)的有效配体

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It has been demonstrated that the translocator protein (18 kDa) (TSPO) plays an important role in stress-response and stress-related disorders, such as anxiety and depression, by affecting the production of neurosteroids, supporting the potential use of selective TSPO ligands as antidepressant or anxiolytic drugs. N-ethyl-N-(2-pyridinylmethyl)- 2-(3,4-ichlorophenyl)- 7-methylimidazo [1,2-a] pyridine-3-acetamide hydrochloride (YL-IPA08), a novel TSPO ligand that has been synthesized at our institute, exerted a high affinity for TSPO in a crude mitochondrial fraction prepared from rat cerebellum but exhibited only a negligible affinity for the central benzodiazepine receptor. As expected, YL-IPA08 incubation with the cultured rat astrocyte cells increased the pregnenolone and progesterone concentration from the cultured medium. Moreover, YL-IPA08 produced significant antidepressant-like and anxiolytic-like effects in a series of mouse and rat behavior models. In addition, the antidepressant-like behavior of YL-IPA08 was totally blocked by the TSPO antagonist PK11195 in a tail suspension test, and the anxiolytic effect was blocked by PK11195 but not by a CBR antagonist in the elevated plus-maze test. Furthermore, compared with the CBR agonist diazepam, YL-IPA08 had no myorelaxant effects and did not affect the motor coordination, memory or hexobarbitone-induced sleep in mice. Overall, these results indicate that YL-IPA08 is a more potent and selective TSPO ligand, which exerts antidepressant-like and anxiolytic-like effects on behaviors that are mediated by TSPO but does not cause the side effects that are typically associated with conventional benzodiazepines.
机译:已经证明,易位蛋白(18 kDa)(TSPO)通过影响神经类固醇的产生,在应激反应和应激相关疾病(如焦虑和抑郁)中起重要作用,支持选择性TSPO配体的潜在用途作为抗抑郁药或抗焦虑药。 N-乙基-N-(2-吡啶基甲基)-2-(3,4-氯苯基)-7-甲基咪唑并[1,2-a]吡啶-3-乙酰胺盐酸盐(YL-IPA08),具有新颖的TSPO配体在我们研究所合成的这种化合物对从大鼠小脑制备的粗线粒体级分中的TSPO具有很高的亲和力,但对中央苯并二氮杂receptor受体的亲和力却微不足道。如预期的那样,将YL-IPA08与培养的大鼠星形胶质细胞一起孵育会增加培养基中孕烯醇酮和孕酮的浓度。此外,YL-IPA08在一系列小鼠和大鼠行为模型中产生了明显的抗抑郁样和抗焦虑样作用。此外,在尾部悬吊试验中,TSPO拮抗剂PK11195完全阻止了YL-IPA08的抗抑郁样行为,而在高迷宫试验中,PK11195阻止了抗焦虑作用,但CBR拮抗剂没有阻止其抗焦虑作用。此外,与CBR激动剂地西epa相比,YL-IPA08没有肌肉松弛作用,并且不影响小鼠的运动协调,记忆或六巴比妥诱导的睡眠。总体而言,这些结果表明YL-IPA08是更有效和更具选择性的TSPO配体,可对TSPO介导的行为发挥抗抑郁样和抗焦虑样作用,但不会引起通常与常规苯二氮卓类药物相关的副作用。

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