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富含纹状体的蛋白酪氨酸磷酸酶抑制剂,8-(三氟甲基)-1,2,3,4,5-苯并五噻吩-6-胺盐酸盐(TC-2153),具有抗抑郁作用,并降低大脑中 5-HT 受体的功能活性和蛋白水平。

Inhibitor of Striatal-Enriched Protein Tyrosine Phosphatase, 8-(Trifluoromethyl)-1,2,3,4,5-Benzopentathiepin-6-Amine hydrochloride (TC-2153), Produces Antidepressant-Like Effect and Decreases Functional Activity and Protein Level of 5-HT Receptor in the Brain.

机构信息

Federal Research Center Institute of Cytology and Genetics, Siberian Division of the Russian Academy of Science, Novosibirsk, Russia.

Federal Research Center Institute of Cytology and Genetics, Siberian Division of the Russian Academy of Science, Novosibirsk, Russia.

出版信息

Neuroscience. 2018 Dec 1;394:220-231. doi: 10.1016/j.neuroscience.2018.10.031. Epub 2018 Oct 24.

DOI:10.1016/j.neuroscience.2018.10.031
PMID:30367948
Abstract

The serotoninergic 5-HT receptor is involved in the mechanism of depression and antidepressant drugs action. Earlier we showed that striatal-enriched protein tyrosine phosphatase (STEP) inhibitor - 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153) affects both the brain serotoninergic system and the brain-derived neurotropic factor that are known to be involved in the psychopathology of depression. In the present study we investigated the effects of chronic TC-2153 administration on behavior in the standard battery of tests as well as the effects of acute and chronic TC-2153 treatment on the brain 5-HT receptors in mice. We obtained a prominent antidepressant-like effect of chronic TC-2153 treatment in the forced swim test without any adverse side effects on locomotor activity, anxiety, exploration, motor skill and obsessive-compulsive-like behavior. Moreover, both acute and chronic TC-2153 administration inhibited the functional activity of 5-HT receptors estimated by the number of 2,5-dimethoxy-4-iodoamphetamine (DOI, agonist of 5-HT receptors)-induced head-twitches. TC-2153 treatment also attenuated the DOI-induced c-fos expression in cortical and hippocampal neurons and reduced the 5-HT receptor protein level in the hippocampus and frontal cortex, but not in the striatum. Taken together, our combined data demonstrate that the antidepressant effect of STEP inhibitor TC-2153 could be mediated by its inhibitory properties towards the 5-HT receptor-mediated signaling.

摘要

5-羟色胺能 5-HT 受体参与抑郁症的发病机制和抗抑郁药物的作用。我们之前的研究表明,富含纹状体的蛋白酪氨酸磷酸酶(STEP)抑制剂-8-(三氟甲基)-1,2,3,4,5-苯并戊噻嗪-6-胺盐酸盐(TC-2153)可同时影响脑内 5-羟色胺能系统和脑源性神经营养因子,这两者均与抑郁症的发病机制有关。在本研究中,我们研究了慢性 TC-2153 给药对标准行为测试组合中行为的影响,以及急性和慢性 TC-2153 治疗对小鼠脑内 5-HT 受体的影响。我们发现慢性 TC-2153 治疗在强迫游泳试验中表现出明显的抗抑郁样作用,而对运动活动、焦虑、探索、运动技能和强迫样行为没有任何不良的副作用。此外,急性和慢性 TC-2153 给药均抑制了 5-HT 受体的功能活性,这是通过 2,5-二甲氧基-4-碘苯丙胺(DOI,5-HT 受体激动剂)诱导的摇头次数来估计的。TC-2153 治疗还减弱了 DOI 诱导的皮质和海马神经元中 c-fos 的表达,并降低了海马和额叶皮质中的 5-HT 受体蛋白水平,但对纹状体没有影响。总之,我们的综合数据表明,STEP 抑制剂 TC-2153 的抗抑郁作用可能与其对 5-HT 受体介导的信号的抑制特性有关。

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