Department of Behavioral Neurogenomics, Institute of Cytology and Genetics, Siberian Division of the Russian Academy of Science, Novosibirsk, Russia.
Neurosci Lett. 2012 Jul 26;522(1):52-6. doi: 10.1016/j.neulet.2012.06.015. Epub 2012 Jun 15.
Among serotonin (5-HT) receptors, the 5-HT(3) receptor is the only ligand-gated ion-channel. Little is known about the interaction between the 5-HT(3) receptor and other 5-HT receptors and influence of 5-HT(3) chronic activation on other 5-HT receptors and the expression of key genes of 5-HT system. Chronic activation of 5-HT(3) receptor with intracerebroventricularly administrated selective agonist 1-(3-chlorophenyl)biguanide hydrochloride (m-CPBG) (14 days, 40 nmol, i.c.v.) produced significant desensitization of 5-HT(3) and 5-HT(1A) receptors. The hypothermic responses produced by acute administration of selective agonist of 5-HT(3) receptor (m-CPBG, 40 nmol, i.c.v.) or selective agonist of 5-HT(1A) receptor (8-hydroxy-2-(di-n-propylamino)tetralin) (8-OH-DPAT, 1mg/kg, i.p.) was significantly lower in m-CPBG treated mice compared with the mice of control groups. Chronic m-CPBG administration failed to induce any significant change in the 5-HT(2A) receptor functional activity and in the expression of the gene encoding 5-HT(2A) receptor. Chronic activation of 5-HT(3) receptor produced no considerable effect on the expression on 5-HT(3), 5-HT(1A), and 5-HT transporter (5-HTT) and tryptophan hydroxylase-2 (TPH-2) genes - the key genes of brain 5-HT system, in the midbrain, frontal cortex and hippocampus. In conclusion, chronic activation of ionotropic 5-HT(3) receptor produced significant desensitization of 5-HT(3) and postsynaptic 5-HT(1A) receptors but caused no considerable changes in the expression of key genes of the brain 5-HT system.
在血清素(5-HT)受体中,5-HT(3)受体是唯一的配体门控离子通道。关于 5-HT(3)受体与其他 5-HT 受体的相互作用以及 5-HT(3)受体的慢性激活对其他 5-HT 受体和 5-HT 系统关键基因表达的影响知之甚少。用选择性激动剂 1-(3-氯苯基)双胍盐酸盐(m-CPBG)(40nmol,iv)经侧脑室给药对 5-HT(3)受体进行慢性激活会导致 5-HT(3)和 5-HT(1A)受体明显脱敏。与对照组相比,急性给予 5-HT(3)受体选择性激动剂(m-CPBG,40nmol,iv)或 5-HT(1A)受体选择性激动剂(8-羟基-2-(二正丙基氨基)四氢萘)(8-OH-DPAT,1mg/kg,ip)引起的解热反应在 m-CPBG 处理的小鼠中明显降低。慢性 m-CPBG 给药并未引起 5-HT(2A)受体功能活性或编码 5-HT(2A)受体的基因表达发生任何显著变化。5-HT(3)受体的慢性激活对中脑、前额叶皮层和海马体中 5-HT(3)、5-HT(1A)和 5-HT 转运体(5-HTT)以及色氨酸羟化酶-2(TPH-2)基因(脑 5-HT 系统的关键基因)的表达没有产生显著影响。总之,离子型 5-HT(3)受体的慢性激活导致 5-HT(3)和突触后 5-HT(1A)受体明显脱敏,但对脑 5-HT 系统关键基因的表达没有产生显著变化。