Abstract
The mammalian (or mechanistic) target of rapamycin (mTOR) complex 1 (mTORC1) is a serine and threonine kinase that regulates cell growth, survival, and proliferation. mTORC1 is a master controller of the translation of a subset of mRNAs. In the central nervous system mTORC1 plays a crucial role in mechanisms underlying learning and memory by controlling synaptic protein synthesis. Here, we review recent evidence suggesting that the mTORC1 signaling pathway promotes neuroadaptations following exposure to a diverse group of drugs of abuse including stimulants, cannabinoids, opiates, and alcohol. We further describe potential molecular mechanisms by which drug-induced mTORC1 activation may alter brain functions. Finally, we propose that mTORC1 is a focal point shared by drugs of abuse to mediate drug-related behaviors such as reward seeking and excessive drug intake, and offer future directions to decipher the contribution of the kinase to mechanisms underlying addiction.
| Original language | English |
|---|---|
| Pages (from-to) | 172-184 |
| Number of pages | 13 |
| Journal | Journal of Neurochemistry |
| Volume | 130 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jul 2014 |
Funding
| Funders | Funder number |
|---|---|
| National Institute on Alcohol Abuse and Alcoholism | P50AA017072 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- addiction
- alcohol
- drugs of abuse
- limbic system
- mTOR
- translation
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