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Acne drug’s link to depression

posted Tuesday, 13 November 2007

A team of American and British researchers has found that a drug used to treat severe acne may reduce the availability of the neurotransmitter serotonin, low levels of which are linked to aggression and clinical depression.

In a study published in the journal Experimental Biology and Medicine, scientists reveal a potential mechanism that might link the drug isotretinoin (Roaccutane®, Accutane®) to reported cases of depression in some patients taking the medication.

The researchers had previously reported that the drug caused depressive behavior in mice but, until now, the mechanism by which this might happen was unknown.

Using cells cultured in a laboratory, the researchers from the University of Bath (UK) and University of Texas at Austin (USA) were able to monitor the effect of the drug on the chemistry of the cells that produce serotonin.

They found that the cells significantly increased production of proteins and cell metabolites that are known to reduce the availability of serotonin.

This, says scientists, could disrupt the process by which serotonin relays signals between neurons in the brain and may be the cause of depression-related behavior.

"Serotonin is an important chemical that relays signals from nerve cells to other cells in the body," said Dr Sarah Bailey from the Department of Pharmacy & Pharmacology at the University of Bath.

"In the brain it is thought to play an important role in the regulation of a range of behaviors, such as aggression, anger and sleep.

"Low levels of serotonin have been linked to depression, as well as bipolar and anxiety disorders.

"Many medications aimed at treating depression seek to increase levels of serotonin to help overcome these problems.

"Our findings suggest that Roaccutane might disrupt the way serotonin is produced and made available to the cells. This could result in problems associated with low levels of serotonin, which might include depression.

The researchers now plan to study the mechanism in more detail.

The study is funded by the U.S. National Institute of Environmental Health Sciences, the U. S. National Institutes of Health and the University of Texas at Austin.


O'Reilly KC, Trent S, Bailey SJ, Lane MA. 13-cis-Retinoic acid alters intracellular serotonin, increases 5-HT1A receptor, and serotonin reuptake transporter levels in vitro. Exp Biol Med. 2007;232(9):1195-203.   [Abstract]
Comment:  
While the results of this study provide a possible explanation for isotretinoin's depressive effects, it may not be the last word on the matter.

Variations in brain serotonin have been implicated in both depression and anxiety, however, there is in fact little evidence to support the theory. True, one of the most immediate effects of serotonergic antidepressants is to boost serotonin levels in the synapses. But this, in itself, does not alleviate depression (or anxiety). Indeed, both synthesis and brain levels of this neurotransmitter drop to baseline levels or below after a few weeks just as the drugs become effective. Furthermore, the novel antidepressant tianeptine (Stablon®), which enhances serotonin removal from synapses, appears to be as effective as SSRI class antidepressants which impede its removal.

It should also be noted that this study was carried out on cultured cells. Results of such in vitro (in glass) tests often cannot be replicated in whole organisms.

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