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Tuning cocaine addiction

David Mazoor, M.D.Published July 20, 20102 min read

Key points

  • Reducing the abundance of a set of microRNAs – small bits of genetic material that influence gene expression – reduces the urge for a cocaine fix in mice, according to a paper published online on July 19 in the Journal of Experimental Medicine (http://www.jem.org).
  • Among the 23 Ago2-dependent microRNAs whose expression increased after cocaine administration in normal mice, several regulate the expression of genes known to be involved in drug addiction.
  • The Journal of Experimental Medicine (JEM) is published by The Rockefeller University Press.
  • As mice become addicted to cocaine, characteristic changes in gene expression occur in the brain.

Reducing the abundance of a set of microRNAs – small bits of genetic material that influence gene expression – reduces the urge for a cocaine fix in mice, according to a paper published online on July 19 in the Journal of Experimental Medicine (http://www.jem.org).

As mice become addicted to cocaine, characteristic changes in gene expression occur in the brain. To determine if this process is influenced by microRNAs, a team led by Anne Schaefer and Paul Greengard at Rockefeller University offered cocaine to mice whose neurons lack Ago2, a protein essential for the production and function of certain microRNAs.

Ago2-deficient mice consumed less cocaine. Among the 23 Ago2-dependent microRNAs whose expression increased after cocaine administration in normal mice, several regulate the expression of genes known to be involved in drug addiction.

Additional work is needed to determine which of these microRNAs control cocaine addiction in mice and whether similar pathways operate in the human brain.

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About The Journal of Experimental Medicine

The Journal of Experimental Medicine (JEM) is published by The Rockefeller University Press. All editorial decisions on manuscripts submitted are made by active scientists in conjunction with our in-house scientific editors. JEM content is posted to PubMed Central, where it is available to the public for free six months after publication. Authors retain copyright of their published works and third parties may reuse the content for non-commercial purposes under a creative commons license. For more information, please visit http://www.jem.org.

Schaefer, A., et al. 2010. J. Exp. Med. doi:10.1084/jem.20100451.

Contact: Rita Sullivan
news@rupress.org
212-327-8603
Rockefeller University Press

Revised and edited by

David Mazoor, M.D.

Medically reviewedLast reviewed

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