Enhancing Depression Mechanisms in Midbrain Dopamine Neurons Achieves Homeostatic Resilience

Allyson K. Friedman(Icahn School of Medicine at Mount Sinai), Jessica J. Walsh(Icahn School of Medicine at Mount Sinai), Barbara Juarez(Icahn School of Medicine at Mount Sinai), Stacy M. Ku(Icahn School of Medicine at Mount Sinai), Dipesh Chaudhury(Icahn School of Medicine at Mount Sinai), Jing Wang(Icahn School of Medicine at Mount Sinai), Xianting Li(Icahn School of Medicine at Mount Sinai), David Dietz(Allen Institute for Brain Science), Nina Pan(Icahn School of Medicine at Mount Sinai), Vincent F. Vialou(Allen Institute for Brain Science), Rachael L. Neve(McGovern Institute for Brain Research), Zhenyu Yue(Allen Institute for Brain Science), Ming‐Hu Han(Allen Institute for Brain Science)
Science
April 17, 2014
Cited by 493Open Access
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Abstract

Typical therapies try to reverse pathogenic mechanisms. Here, we describe treatment effects achieved by enhancing depression-causing mechanisms in ventral tegmental area (VTA) dopamine (DA) neurons. In a social defeat stress model of depression, depressed (susceptible) mice display hyperactivity of VTA DA neurons, caused by an up-regulated hyperpolarization-activated current (I(h)). Mice resilient to social defeat stress, however, exhibit stable normal firing of these neurons. Unexpectedly, resilient mice had an even larger I(h), which was observed in parallel with increased potassium (K(+)) channel currents. Experimentally further enhancing Ih or optogenetically increasing the hyperactivity of VTA DA neurons in susceptible mice completely reversed depression-related behaviors, an antidepressant effect achieved through resilience-like, projection-specific homeostatic plasticity. These results indicate a potential therapeutic path of promoting natural resilience for depression treatment.


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