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How Cocaine Cues Get Planted in the Brain

September 06, 2018
By Stacey C. Tobin, Ph.D., ELS, NIDA Notes Contributing Writer

This research found that:

  • An epigenetic mechanism underlies the powerful cocaine–environment associations that promote relapse.
  • The mechanism may be instrumental in all drug reward–based learning.

A NIDA-sponsored study sheds light on how cocaine creates the powerful drug–environment associations that underlie cue-induced drug seeking and relapse. Researchers found that cocaine blocks an epigenetic process which limits the strength of synapses that link rewarding experiences with associated environments. The new findings suggest that a gene regulator called histone deacetylase 5 (HDAC5) may offer new opportunities for reducing relapse risk.

Cocaine and HDAC5

Drs. Makoto Taniguchi and Christopher Cowan from the Medical University of South Carolina and Harvard Medical School and colleagues have been investigating HDAC5 and its role in responses to cocaine. HDAC5 is one of a group of enzymes that enhance or reduce transcription, and hence expression, of their target genes. The enzyme is found both inside and outside the cell nucleus, but only has access to its target genes when it is inside.

The researchers previously showed that cocaine causes HDAC5 molecules in the nucleus accumbens (NAc) to pick up phosphate groups that lock it out of the cell nucleus. They now report that excluding HDAC5 from NAc nuclei bolsters cocaine–environment associations and cue-induced responses to the drug. The researchers exposed two groups of mice with different levels of NAc nuclear HDAC5 to cocaine in a test chamber. When they later gave the animals the option of returning to the chamber in which they had received the drug or another chamber, the group with less NAc nuclear HDAC5 was more likely to prefer the chamber associated with exposure. These mice also exhibited more cue-induced relapse-like behavior when re-exposed to the cocaine-associated test chamber after a period without access to the drug.

HDAC5 and Its Target Gene

Further experiments revealed the mechanism by which cocaine’s exclusion of HDAC5 from NAc nuclei strengthens drug–environment associations.

First, Drs. Taniguchi and Cowan and colleagues conducted a screen to identify HDAC5's target genes. Among the many genes that HDAC5 affected, one stood out. Npas4 encodes a protein, NPAS4, that promotes the strengthening of neural connections.

Figure. Cocaine Strengthens Synaptic Connections by Preventing HDAC5 From Suppressing Npas4 Expression in the Nucleus Accumbens (NAc) (Left) In the absence of cocaine, HDAC5 enters the nucleus of cells in the NAc, where it interacts with transcription factors (TFs) to block production of NPAS4. (Right) In the presence of cocaine, HDAC5 picks up phosphate groups, which prevent it from entering the cell nucleus. Consequently, no blockage of Npas4 occurs. NPAS4 levels rise and facilitate expression of plasticity genes that promote neuronal connections presumed to underlie cocaine–environment associations and cue-induced responses.
Text Description of Graphic

The researchers demonstrated that when HDAC5 interacts with Npas4, it reduces expression of the gene. Conversely, when cocaine prevents HDAC5 from entering the nucleus and interacting with Npas4, the gene is robustly expressed (see Figure). Thus, administering cocaine to mice or placing the animals in a test chamber where they previously received the drug resulted in a rapid increase in Npas4 expression.

The researchers next linked the cocaine-induced increase in Npas4 expression to the formation of strong drug–environment associations. In these experiments, blocking Npas4 expression in the NAc of mice weakened the animals’ attraction to a chamber in which they had received the drug and slowed their acquisition of other drug-reinforced actions.

Drs. Taniguchi and Cowan and colleagues concluded that cocaine’s effects on HDAC5 and Npas4 are keys to the powerful drug–environment associations that drive cue-induced drug seeking and relapse. By excluding HDAC5 from cell nuclei, the drug removes a brake on Npas4 expression in the NAc. NPAS4 levels rise and enhance synaptic changes that are presumed to be the physical basis for the associations. The researchers suggest that this same NAc mechanism may be instrumental in all learning that involves linking drug reward experiences and their associated circumstances in memory.

"Nuclear shuttling of HDAC5 is an unexpected and exciting neuroregulatory mechanism," says Dr. John Satterlee from the Division of Neuroscience and Behavior in NIDA's Genetics, Epigenetics, and Developmental Neuroscience Branch. "In the long term, this foundational knowledge could even lead to the development of a novel therapeutic to treat cocaine use disorder."

This study was supported by NIH grants DA027664, DA032708, DA10460, DA003906, DA007288, and DA036319.

Source:

Taniguchi, M., Carreira, M.B., Cooper, Y.A., et al. HDAC5 and its target gene, Npas4, function in the nucleus accumbens to regulate cocaine-conditioned behaviors. Neuron 96(1):130-144.e6, 2017.

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    NIDA. (2018, September 6). How Cocaine Cues Get Planted in the Brain. Retrieved from https://www.drugabuse.gov/news-events/nida-notes/2018/09/how-cocaine-cues-get-planted-in-brain

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