Potential Root Cause of Depression Discovered by NARSAD Grantee

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Marina Picciotto, Ph.D. - Brain and behavior research expert on depression
Marina Picciotto, Ph.D.

From The Quarterly, Spring 2013

Marina Picciotto, Ph.D., leading a team of researchers at Yale University, has made an exciting discovery in the search for the biological causes of depression and anxiety. Their discovery points to the importance of a signaling system in the brain that was not previously believed to be central in causing depression.

For decades, many scientists have favored a theory of depression that stresses the impact of abnormally low levels of a signal-carrying chemical, called serotonin. The new research by Dr. Picciotto’s team shifts attention to a different signaling chemical, or neurotransmitter, called acetylcholine.

Millions of depressed people take anti-depressant drugs called SSRIs—an acronym for selective serotonin re-uptake inhibitors. Prozac®, Paxil®, Celexa®, Zoloft® and other SSRI medications act to keep message-carrying serotonin molecules from being rapidly reabsorbed by nerve cells. By allowing serotonin to float for longer periods of time in the tiny spaces between nerve cells, called synapses, scientists have theorized the SSRI drugs promote signaling by compensating for abnormally low serotonin levels.

Dr. Picciotto’s new research, published in Proceedings of the National Academy of Sciences in February, turns attention to fluctuations in levels of the neurotransmitter acetylcholine and the larger chemical signaling system it is part of, called the cholinergic system.

“Serotonin may be treating the problem,” Dr. Picciotto says, “but acetylcholine disruption may be a primary cause of depression. If we can treat the root cause, perhaps we can get a better response from the patient.”

Her team’s experiments demonstrate that abnormally high levels of acetylcholine in the brain can cause depression and anxiety symptoms in mice. In the brains of non-depressed mice—and people—an enzyme called acetyl- cholinesterase (AChE) is produced to lower acetylcholine levels. The team showed that when depressed mice were given Prozac®, AChE levels were raised, and abnormally high levels of acetylcholine were thus brought under control. This adds a new dimension to understanding how and why SSRI anti-depressants can alleviate depression.

Yet many depressed people do not get a therapeutic benefit from Prozac® or other SSRI medications. Dr. Picciotto’s research suggests this may be because the root problem is not, after all, low levels of serotonin, but rather, high levels of acetylcholine. By experimentally blocking the “ports,” called receptors, where acetylcholine molecules “dock” with nerve cells in the brain, the team was able to reverse depression in mice.

In still other experiments, the Yale team showed how interruptions in acetylcholine signaling in the brain area called the hippocampus—important in memory and mood—promotes depression and anxiety in mice.

While the relation between the serotonin and acetylcholine signaling systems is not yet fully clear, this new research opens a new possibility to treat the cause of depression and not just its symptoms. With the new hypothesis that it is the disruption of acetylcholine, and not serotonin, that sets depression in motion, further research studies can be undertaken to determine if medications that target acetylcholine rather than serotonin, are more effective in treating depression.

Marina Picciotto, Ph.D.
Charles B. G. Murphy Professor of Psychiatry,
Professor of Neurobiology and Pharmacology,
Assistant Chair for Basic Science Research, Psychiatry,
Yale University;
1996 NARSAD Young Investigator Grantee,
2004 NARSAD Independent Investigator Grantee

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I DONT KNOW HOW MUCH SUCH RESULTS ARE CORRECT, AT THE END OF IT, HOPEFULLY IT IS NOT AGAIN BLAMED OVER THE RESEARCH METHODOLOGY, EXTRANEOUS FACTORS, AND THE STUDY IS AGAIN CALLED DUBIOUS, ULTIMATELY INCREASING THE SUFFERING AND REDUCING HOPE OF THOSE SUFFERING FROM A DISEASE WHICH IS CHARACTERISED BY LACK OF HOPE.

THANK YOU, SHARIQ, FOR THAT.

Acetylcholine Receptors can be activated by Acetylcholine in both ways on binding and releasing from AchR. Artificial disrupting Acetylcholine activities acting to AchR, would disrupt human emotion balance. Have you seen when the Olympic sporters are extremely too happy to cry but unable to laugh when they are received the award for golden plates to their winedon the top of the first games in Olympic campaigning? This is a typical instance of when large amount of Acetylcholine are binding on AchR to cause caused too much activations of mAchR on activating releasing Acetylcholine to feedback suppressing AchR activities. Only at this point, AchE hydrolysis Acetylcholine from binding of AchR could moderately down the sportor’s emotions.

First, congratulations to Marina and the Team!! Way to go, folks!!! We who suffer from depression are eternally grateful for your work. You have no idea.

The conclusion I draw from these research results is that depression appears to arise from either too much acetylcholine or from too little acetylcholine. Therefore, would it not be ideal to seek within the cholinergic system for the REGULATOR and target how to ASSIST THAT? If we can understand the cholinergic system's acetylcholine regulator, someone might devise a treatment or medication that assists its stable functioning. That might help people prone to major depression AND those with bipolar mood disorder. (I'm guessing bipolars - or at least ultra-rapid cyclers - experience wildly swinging levels of acetylcholine, since clearly that too is some problem of dysregulation.) Even if I'm wrong about the bipolar mood disorder operating similarly, stabilizing the acetylcholine regulator would at least HELP MORE PEOPLE: those with too much acetylcholine AND those with too little acetylcholine.

Also, could you please, in conversations, advocate replacing the term "mental illness" with "neurological disorder?"I am not unusual in my experiences as a "mental patient." Like most "mental patients" (another goodie), I have been judged and abandoned by 99% of my (former) friends; and most of my family. Their brains work fine, and they assume mine is the same; so they don't see why I can't do what they do. Most people apparently see depressed peoples' negative thought patterns and words as an attitudinal issue, a thought-based or "mental" problem, so they expect us to just change it. They don't understand our attitudes and thoughts are just symptoms caused by a severe ORGANIC DYSFUNCTION.

"Mental illness" doesn't connote that to people. Identifying it more correctly as a Brain Disorder or Neurological Dysfunction reminds the listener that THE BRAIN IS AN ORGAN, A VERY IMPORTANT ORGAN that can render us pretty darn dysfunctional when it doesn't work right. It also indicates that depression is a MEDICAL condition, not laziness or a bad attitude, that actually does render us unable for long periods to think clearly, clean our homes, put things away, cook for ourselves, do laundry, keep up with bills, keep up our appearance, or even take baths.

Losing the respect of all my friends worsened my depression. I've lost all trust in people who claim to be loving. Everybody talks about love, but I have yet to find anybody willing to help me. I've turned to public and private agencies for help but do not meet their age or income guidelines (since they don't take into account the cost of prescription meds). I see a counselor thanks to insurance, but home care isn't covered by my insurance. I've spent entire days calling number after number suggested to me as a possible source of help but have over and over been denied access to desperately needed home support services. Some won't help because I have Medicare. Others won't help because I don't have Medicaid. And "Unless you are in a wheelchair," said the lady at the only local charity doing such work voluntarily, "you don't need help." This kind of ignorance is hurtful and harmful. When I began to develop sores that spiraled across my body , the dermatologist just snarled at me in disgust, "It isn't scabies. Go home and clean your house!" Her insult is typical - and frustrating. People just don't seem to know depression is a MEDICAL disorder, an organ dysfunction which renders us unable to solve problems, take action, seek happiness, etc. We deserve help just as much as people with different organ problems; for example, the pancreas. The world doesn't insult diabetics, refuse to help them, or demand that they just change themselves.

As for me, my doctor now reports I'm malnourished (affecting my decision making and increasing the fatigue from the depression). Bugs have been nesting in my skin and house seven months now. I am covered with large sores and scars despite four head-to-toe coatings of pyrethrin (poison) cream and four Ivermectin tablets (the poison in Frontline) the doctors prescribed. Despite my using bed bug spray and lice shampoo. Despite diatomaceous earth on my carpets. My house is nasty, the kitchen piked with unwashed dishes and rotting cat food; my piles of stuff continue to grow. I rarely eat real food, and the house has been more than I can handle for along time. I wander room to room trying to bring order but have trouble making decisions and never finish things I start. Haunted, haggard eyes stare back in the mirror. The ironic thing is I'm educated, I'm bright, and when I was well I was a teacher for many years at the toughest school in the city, upholding with love and dedication the safety net for "at-risk" teens. Now I'm the one "at-risk," but it seems there's no safety net for me. It's no wonder so many of us commit suicide.

So you see, it's very important to change what we call this. Until the public really groks that it's a medical condition, we who suffer depression will continue to be by and large treated with disdain.

Isabella Ringen How can I reach you? I don't know if you will see this or not but I am interested in this topic and would like to talk to you .

In your article you write: "For decades, many scientists have favored a theory of depression that stresses the impact of abnormally low levels of a signal-carrying chemical, called serotonin.". That is completely incorrect. The serotonin hypothesis of depression has been disproved over 30 years ago, before Prozac even came to market. There has been absolutely no conclusive or circumstantial evidence that serotonin and depression are linked.

Hundreds of clinical trials prove otherwise. Show me your studies and data from over thirty years ago, and tell me again how relevant that is in today's medicinal progressiveness.

I wonder how this relates to nicotine, seeing as how that boosts acetylcholine. I'm depressed, smoking helps ...sometimes.

The results of the study reported in this article are encouraging for increasing our understanding of the neurochemical mechanisms related to depression. However, there are many forms of depression and I suspect that most of the primary neurotransmitters act together and affect each other in myriad ways we still don't know about. In addition, the actions of secondary messengers and other possible influences must be taken into account. Psychiatric illness cannot be accurately pinned to any single neurotransmitter.

These findings might help explain why taking substantial doses of choline supplements over a course of months seemed to precipitate episodes of increased, chronic depression in me. I had started to take choline supplements as a possible aid to cognition and mood, but my mood worsened during the time I was taking these supplements. This is a casual observation. I'm not familiar with the science of how choline supplements might affect acetylcholine in the body, but my understanding is that there may be a correlation.

In line with the study reported in this article, it might be wise to observe and document the experience of people and animals treated with acetylcholine agonists like piracetam, celastrus paniculatus, and other nootropic compounds. The increased popularity of supplementation with alleged nootropic substances over the past few decades may have ramifications for this type of investigation. In addition, if supplementation with acetylcholine agonists were to lead to rising incidences of depression, as this study suggests it might, this could become a public health issue.

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