People who suffer from depression are also likely to face gastrointestinal distress as a study has pointed out that for some, both the conditions are triggered by the same glitch in neuron chemistry-low serotonin.
The study published in the journal Gastroenterology was conducted in mice.
The study showed that a shortage of serotonin in the neurons of the gut can cause constipation, just as a serotonin shortage in the brain can lead to depression.
The study also found that a treatment that raises serotonin in the gut and the brain may alleviate both conditions.
Up to a third of people with depression have chronic constipation, and a few studies reported that people with depression, rate their accompanying bowel difficulties as one of the biggest factors reducing their quality of life.
Severe constipation can obstruct the gastrointestinal (GI) tract and cause serious pain. The condition leads to 2.5 million physician visits and 100,000 hospitalisations each year.
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"Ultimately, many patients with depression are faced with limited treatment options and have to suffer from prominent GI dysfunction," said study leader Kara Gross Margolis.
Similarities between the gut and the brain suggest the two conditions may also share a common cause.
"The gut is often called the body's second brain. It contains more neurons than the spinal cord and uses many of the same neurotransmitters as the brain. So it shouldn't be surprising that the two conditions could be caused by the same process," said Margolis.
Because low levels of serotonin in the brain have been linked to depression and serotonin is also used by neurons in the gut, the researchers studied mice to determine if a serotonin shortage also plays a role in constipation.
The mice used in the study carry a genetic mutation (linked to severe depression in people) that impairs the ability of neurons in the brain and the gut to make serotonin.
The serotonin shortage in the gut, the researchers found, reduced the number of neurons in the gut, led to a deterioration of the gut's lining, and slowed the movement of contents through the GI tract.
"Basically, the mice were constipated and they showed the same kind of GI changes we see in people with constipation," said Margolis.
Encouragingly, an experimental drug treatment invented by two of the study's co-authors, Marc Caron and Jacob Jacobsen raised serotonin levels in the gut's neurons and alleviated constipation in the mice.
The treatment--slow-release drug-delivery of 5-HTP, a precursor of serotonin--works in part by increasing the number of GI neurons in adult mice.
The discovery of this connection between a brain and a gastrointestinal disorder suggests that new 5-HTP slow-release therapies could treat related brain-gut conditions simultaneously.
The study is also one of the first to show that neurogenesis in the gut is possible and can correct abnormalities in the gut. "Though it's been known for many years that neurogenesis occurs in certain parts of the brain, the idea that it occurs in the gut nervous system is relatively new," Margolis said.
Neurogenesis may help treat other types of constipation. "We see a reduction of neurons in the GI tract with age, and that loss is thought to be a cause of constipation in the elderly. The idea that we may be able to use slow-release 5-HTP to treat conditions that require the development of new neurons in the gut may open a whole new avenue of treatment," said Margolis.
Clinical studies are already planned for testing a slow-release 5-HTP drug in people with treatment-resistant depression.
Planning for testing a slow-release 5-HTP drug in constipation is in progress.
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