McCall Jordan G, Al-Hasani Ream, Siuda Edward R, Hong Daniel Y, Norris Aaron J, Ford Christopher P, Bruchas Michael R
Division of Basic Research, Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110, USA; Washington University Pain Center, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO 63110, USA; Division of Biology and Biomedical Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA.
Division of Basic Research, Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110, USA; Washington University Pain Center, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Neuron. 2015 Aug 5;87(3):605-20. doi: 10.1016/j.neuron.2015.07.002. Epub 2015 Jul 23.
The locus coeruleus noradrenergic (LC-NE) system is one of the first systems engaged following a stressful event. While numerous groups have demonstrated that LC-NE neurons are activated by many different stressors, the underlying neural circuitry and the role of this activity in generating stress-induced anxiety has not been elucidated. Using a combination of in vivo chemogenetics, optogenetics, and retrograde tracing, we determine that increased tonic activity of the LC-NE system is necessary and sufficient for stress-induced anxiety and aversion. Selective inhibition of LC-NE neurons during stress prevents subsequent anxiety-like behavior. Exogenously increasing tonic, but not phasic, activity of LC-NE neurons is alone sufficient for anxiety-like and aversive behavior. Furthermore, endogenous corticotropin-releasing hormone(+) (CRH(+)) LC inputs from the amygdala increase tonic LC activity, inducing anxiety-like behaviors. These studies position the LC-NE system as a critical mediator of acute stress-induced anxiety and offer a potential intervention for preventing stress-related affective disorders.
蓝斑去甲肾上腺素能(LC-NE)系统是应激事件发生后最早被激活的系统之一。尽管许多研究小组已经证明LC-NE神经元会被多种不同的应激源激活,但其潜在的神经回路以及这种活动在引发应激诱导的焦虑中所起的作用尚未阐明。通过结合体内化学遗传学、光遗传学和逆行追踪技术,我们确定LC-NE系统紧张性活动的增强对于应激诱导的焦虑和厌恶是必要且充分的。在应激期间选择性抑制LC-NE神经元可预防随后出现的焦虑样行为。外源性增加LC-NE神经元的紧张性活动而非相位性活动,就足以引发焦虑样和厌恶行为。此外,杏仁核中内源性促肾上腺皮质激素释放激素(CRH)阳性的LC输入会增加LC的紧张性活动,诱发焦虑样行为。这些研究将LC-NE系统定位为急性应激诱导焦虑的关键调节因子,并为预防与应激相关的情感障碍提供了一种潜在的干预手段。