Espinoza Stefano, Sukhanov Ilya, Efimova Evgeniya V, Kozlova Alena, Antonova Kristina A, Illiano Placido, Leo Damiana, Merkulyeva Natalia, Kalinina Daria, Musienko Pavel, Rocchi Anna, Mus Liudmila, Sotnikova Tatiana D, Gainetdinov Raul R
Department of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genova, Italy.
Department of Pharmacology, St. Petersburg State Medical University, St. Petersburg, Russia.
Front Mol Neurosci. 2020 Mar 5;13:18. doi: 10.3389/fnmol.2020.00018. eCollection 2020.
Trace amine-associated receptors (TAARs) are a class of G-protein-coupled receptors found in mammals. While TAAR1 is expressed in several brain regions, all the other TAARs have been described mainly in the olfactory epithelium and the glomerular layer of the olfactory bulb and are believed to serve as a new class of olfactory receptors sensing innate odors. However, there is evidence that TAAR5 could play a role also in the central nervous system. In this study, we characterized a mouse line lacking TAAR5 (TAAR5 knockout, TAAR5-KO) expressing beta-galactosidase mapping TAAR5 expression. We found that TAAR5 is expressed not only in the glomerular layer in the olfactory bulb but also in deeper layers projecting to the limbic brain olfactory circuitry with prominent expression in numerous limbic brain regions, such as the anterior olfactory nucleus, the olfactory tubercle, the orbitofrontal cortex (OFC), the amygdala, the hippocampus, the piriform cortex, the entorhinal cortex, the nucleus accumbens, and the thalamic and hypothalamic nuclei. TAAR5-KO mice did not show gross developmental abnormalities but demonstrated less anxiety- and depressive-like behavior in several behavioral tests. TAAR5-KO mice also showed significant decreases in the tissue levels of serotonin and its metabolite in several brain areas and were more sensitive to the hypothermic action of serotonin 5-HT1A receptor agonist 8-hydroxy-2-(di--propilamino)tetralin (8-OH-DPAT). These observations indicate that TAAR5 is not just innate odor-sensing olfactory receptor but also serves to provide olfactory input into limbic brain areas to regulate emotional behaviors likely modulation of the serotonin system. Thus, anxiolytic and/or antidepressant action of future TAAR5 antagonists could be predicted. In general, "olfactory" TAAR-mediated brain circuitry may represent a previously unappreciated neurotransmitter system involved in the transmission of innate odors into emotional behavioral responses.
痕量胺相关受体(TAARs)是一类在哺乳动物中发现的G蛋白偶联受体。虽然TAAR1在几个脑区表达,但所有其他TAARs主要在嗅上皮和嗅球的肾小球层中被描述,并且被认为是一类新的感知先天气味的嗅觉受体。然而,有证据表明TAAR5在中枢神经系统中也可能发挥作用。在本研究中,我们对一种缺乏TAAR5的小鼠品系(TAAR5基因敲除,TAAR5-KO)进行了表征,该品系表达β-半乳糖苷酶以定位TAAR5的表达。我们发现TAAR5不仅在嗅球的肾小球层中表达,还在投射到边缘脑嗅觉回路的更深层中表达,在许多边缘脑区有显著表达,如前嗅核、嗅结节、眶额叶皮质(OFC)、杏仁核、海马体、梨状皮质、内嗅皮质、伏隔核以及丘脑和下丘脑核。TAAR5-KO小鼠没有表现出明显的发育异常,但在几项行为测试中表现出较少的焦虑样和抑郁样行为。TAAR5-KO小鼠在几个脑区的血清素及其代谢物的组织水平也显著降低,并且对血清素5-HT1A受体激动剂8-羟基-2-(二丙基氨基)四氢萘(8-OH-DPAT)的低温作用更敏感。这些观察结果表明,TAAR5不仅是先天气味感知嗅觉受体,还用于向边缘脑区提供嗅觉输入以调节情绪行为,可能是通过调节血清素系统。因此,可以预测未来TAAR5拮抗剂的抗焦虑和/或抗抑郁作用。一般来说,“嗅觉”TAAR介导的脑回路可能代表了一个以前未被认识的神经递质系统,参与将先天气味传递到情绪行为反应中。