Mouse Study Helps Nail Down How Antidepressants Work
Researchers theorize that antidepressants such as Prozac, Lexapro and Paxil work by blocking the serotonin transporter, a brain protein that normally clears away the mood-regulating chemical serotonin — but in fact, no one really knows how such drugs work.
Now, a new research effort by neuroscientists at Vanderbilt University is aimed at determining how selective serotonin reuptake inhibitors (SSRIs) actually interact with neurotransmitters.
The key to the study is use of a genetically altered mouse. These mice, described in the online edition of the Proceedings of the National Academy of Sciences (PNAS), express a serotonin transporter that has been genetically altered so that it does not respond to many SSRIs or cocaine.
In addition to testing the theory about how SSRIs work, the new mouse model could lead to the development of entirely new classes of antidepressant medications, said Randy Blakely, Ph.D., senior author of the PNAS paper.
In the world of medicine and pharmacology, some of the most prominent theories on how or why something works the way it does are based on expert conjecture, rather than hard proof.
“Many antidepressants have been shown to target other proteins besides the serotonin transporter and … their efficacy in treating depression takes many weeks to develop,” Blakely said. “There is likely a lot that we don’t know about how these drugs act.”
To generate the mouse model, Blakely and colleagues at Vanderbilt and the University of Texas Health Science Center at San Antonio first determined exactly which parts of the serotonin transporter protein interact with SSRIs. They took advantage of the fact that the fruit fly expresses a serotonin transporter that is relatively insensitive to the drugs.
By changing the protein’s amino acid building blocks, they converted parts of the human serotonin transporter into its fruit fly equivalent, and in so doing identified the single amino acid required for potent binding to many SSRIs as well as to cocaine.
As predicted, the genetically-modified mice displayed normal serotonin transporter levels, and their transporter exhibited normal activity in clearing serotonin from the synapses between nerve cells. But the mice did not respond to Prozac or Lexapro, indicating that the transporter is indeed the specific target of these medications for blocking serotonin inactivation.
“Interestingly, one SSRI, paroxetine (Paxil), retains its normal powerful action on the transporter, revealing that — at a molecular level — different antidepressants interact with the transporter in different ways,” Blakely said.
The researchers are now evaluating chronic administration of SSRIs to determine how much the transporter contributes to the more clinically relevant, delayed effects of these drugs — how they alter mood — as well as for the side effects experienced with antidepressant medications.
Because the serotonin transporter in the mouse also lost cocaine sensitivity, the model also may help researchers determine exactly how cocaine acts in the brain.
“Perhaps what started as a hunt for better ways to treat depression may also spill over into a better understanding of addiction,” Blakely said.
Nauert PhD, R. (2015). Mouse Study Helps Nail Down How Antidepressants Work. Psych Central. Retrieved on March 22, 2018, from https://psychcentral.com/news/2011/02/21/mouse-study-helps-nail-down-how-antidepressants-work/23717.html