Urban Daniel J, Zhu Hu, Marcinkiewcz Catherine A, Michaelides Michael, Oshibuchi Hidehiro, Rhea Darren, Aryal Dipendra K, Farrell Martilias S, Lowery-Gionta Emily, Olsen Reid H J, Wetsel William C, Kash Thomas L, Hurd Yasmin L, Tecott Laurence H, Roth Bryan L
Department of Pharmacology and National Institute of Mental Health Psychoactive Drug Screening Program, Chapel Hill, NC, USA.
Bowles Center for Alcohol Studies and Department of Pharmacology, School of Medicine, University of North Carolina, Chapel Hill, NC, USA.
Neuropsychopharmacology. 2016 Apr;41(5):1404-15. doi: 10.1038/npp.2015.293. Epub 2015 Sep 18.
Elucidating how the brain's serotonergic network mediates diverse behavioral actions over both relatively short (minutes-hours) and long period of time (days-weeks) remains a major challenge for neuroscience. Our relative ignorance is largely due to the lack of technologies with robustness, reversibility, and spatio-temporal control. Recently, we have demonstrated that our chemogenetic approach (eg, Designer Receptors Exclusively Activated by Designer Drugs (DREADDs)) provides a reliable and robust tool for controlling genetically defined neural populations. Here we show how short- and long-term activation of dorsal raphe nucleus (DRN) serotonergic neurons induces robust behavioral responses. We found that both short- and long-term activation of DRN serotonergic neurons induce antidepressant-like behavioral responses. However, only short-term activation induces anxiogenic-like behaviors. In parallel, these behavioral phenotypes were associated with a metabolic map of whole brain network activity via a recently developed non-invasive imaging technology DREAMM (DREADD Associated Metabolic Mapping). Our findings reveal a previously unappreciated brain network elicited by selective activation of DRN serotonin neurons and illuminate potential therapeutic and adverse effects of drugs targeting DRN neurons.
阐明大脑的血清素能网络如何在相对较短的时间(几分钟至几小时)和较长的时间段(几天至几周)内介导多种行为反应,仍然是神经科学面临的一项重大挑战。我们对此相对缺乏了解,很大程度上是由于缺乏具有稳健性、可逆性和时空可控性的技术。最近,我们已经证明,我们的化学遗传学方法(例如,仅由设计药物激活的设计受体(DREADDs))为控制基因定义的神经群体提供了一种可靠且稳健的工具。在此,我们展示了中缝背核(DRN)血清素能神经元的短期和长期激活如何诱导强烈的行为反应。我们发现,DRN血清素能神经元的短期和长期激活均能诱导出抗抑郁样行为反应。然而,只有短期激活会诱导出焦虑样行为。同时,通过最近开发的非侵入性成像技术DREAMM(与DREADD相关的代谢图谱),这些行为表型与全脑网络活动的代谢图谱相关联。我们的研究结果揭示了由DRN血清素神经元的选择性激活引发的一个此前未被认识的脑网络,并阐明了靶向DRN神经元的药物的潜在治疗作用和不良反应。