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PUBLIC RELEASE DATE:
4-Sep-2014

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Contact: Joe Miksch
jmiksch@pitt.edu
412-624-4356
University of Pittsburgh

The yin and yang of overcoming cocaine addiction

Pitt scientists discover that the brain already has an 'anti-relapse' circuit. Research could lead to treatments for boosting the brain's existing resistance to relapse.

PITTSBURGH—Yaoying Ma says that biology, by nature, has a yin and a yang—a push and a pull.

Addiction, particularly relapse, she finds, is no exception.

Ma is a research associate in the lab of Yan Dong, assistant professor of neuroscience in the University of Pittsburgh's Kenneth P. Dietrich School of Arts and Sciences. She is the lead author of a paper published online today in the journal Neuron that posits that it may be possible to ramp up an intrinsic anti-addiction response as a means to fight cocaine relapse and keep the wolves of relapse at bay.

This paper is the first to establish the existence of a brain circuitry that resists a relapse of cocaine use through a naturally occurring neural remodeling with "silent synapses."

The work is a follow-up on a recent study conducted by Dong and his colleagues, which was published in Nature Neuroscience last November. The team used rat models to examine the effects of cocaine self-administration and withdrawal on nerve cells in the nucleus accumbens, a small region in the brain that is commonly associated with reward, emotion, motivation, and addiction. Specifically, they investigated the roles of synapses—the structures at the ends of nerve cells that relay signals.

The team reported in its Nature Neuroscience study that when a rat uses cocaine, some immature synapses are generated, which are called "silent synapses" because they are semifunctional and send few signals under normal physiological conditions. After that rat stops using cocaine, these "silent synapses" go through a maturation phase and acquire their full function to send signals. Once they can send signals, the synapses will send craving signals for cocaine if the rat is exposed to cues previously associated with the drug.

The current Neuron paper shows that there's another side of "silent synapse" remodeling. Silent synapses that are generated in a specific cortical projection to the nucleus accumbens by cocaine exposure become "unsilenced" after cocaine withdrawal, resulting in a profound remodeling of this cortical projection. Additional experiments show that silent synapse-based remodeling of this cortical projection decreases cocaine craving. Importantly, this anti-relapse circuitry remodeling is induced by cocaine exposure itself, suggesting that our body has its own way to fight addiction.

Dong, the paper's senior author, says that the pro-relapse response is predominant after cocaine exposure. But since the anti-relapse response exists inside the brain, it could possibly be clinically tweaked to achieve therapeutic benefits.

Ma notes that this finding "may provide insight into ways to manipulate this yin-yang balance and hopefully provide new neurobiological targets for interventions designed to decrease relapse."

"The story won't stop here," Ma adds. "Our ongoing study is exploring some unusual but simple ways to beef up the endogenous anti-relapse mechanism."

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Others contributing to the study are Susan Sesack, Pitt professor of neuroscience; Yanhua Huang, Pitt assistant professor of psychiatry; Xiusong Wang, a postdoctoral associate in Pitt's psychiatry department; Changyong Guo, a postdoctoral associate in Dong's lab; Yan Lan, a visiting postdoctoral associate in Dong's lab; Judith Balcita-Pedicino, a technician in Sesack's lab; Brian Lee, a former member of Dong's lab who is now at the Allen Institute for Brain Science in Seattle; Lei Liu and Ranji Cui of Northeastern Normal University in China; Marina Wolf of Rosalind Franklin University of Medicine and Science in Illinois; Yavin Shaham of the National Institutes of Health; and Oliver Schlüter of the European Neuroscience Institute in Germany.

Contact: Joe Miksch, University of Pittsburgh News Services

[412-624-4356 (office); 412-997-0314 (cell); jmiksch@pitt.edu]

9/4/14/klf/cjhm



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