Serotonin - a brain chemical known to help regulate emotion, mood and sleep - might also have anti-diabetic properties, says new research.
The findings by the researchers at the University of Texas Southwestern Medical Center also offer a potential explanation for why individuals prescribed certain kinds of anti-psychotic drugs that affect serotonin signalling sometimes have problems with their metabolism, including weight gain and the development of diabetes.
Advertisement"In this paper, we describe a circuit in the brain that may explain the anti-diabetic actions of serotonin-receptor signalling," said Dr Joel Elmquist, professor of internal medicine and pharmacology at UT Southwestern and senior author of the study.
"This discovery tells us that drugs that affect serotonin action can have anti-diabetic actions independent of body weight and feeding," he added.
For the current study, the researchers engineered a mouse model in which the expression of a serotonin receptor called 5-hydroxytryptamine 2C was blocked throughout the entire body.
Without functioning receptors, the mice developed insulin resistance in their livers.
Previous research has implicated these receptors in the brain in the regulation of energy balance and glucose metabolism throughout the body.
When activated by serotonin, this receptor also suppressed the appetite.
Until now, however, it was unclear which type of neuron in the brain mediated the effects of serotonin to regulate glucose, or blood sugar, levels.
The study authors engineered another set of mice in which the same serotonin receptor was blocked everywhere except within a group of brain cells called pro-opiomelanocortin, or POMC, neurons.
The POMC neurons, which are found in the hypothalamus, are also known to play an important role in suppressing appetite and inducing weight loss.
The researchers found that when they reactivated the serotonin receptor only in the POMC neurons, the mice no longer displayed insulin resistance in the liver.
Restoring the receptor essentially protected the mice from developing the metabolic problems usually found in mice which lack the receptor throughout the body.
Elmquist said that even though the findings are in mice, they do provide potential insight into blood glucose control in humans.
"It also further reinforces our previous findings that specific subsets of POMC neurons within the brain are responsible for the regulation of liver function and blood sugar metabolism," Elmquist said.
The findings are published in Nature Neuroscience.