A USC study shows the brain's plumbing system serves double duty, flushing waste and channeling a hunger molecule that tells you when you should eat.

"People usually think of brain cells as communicating signals through the synapses between them," said Emily Noble. "We are showing that the brain has another complementary way to communicate by sending these signals into the cerebrospinal fluid." In cell-to-cell communication, the neurons are discretely passing notes to individual neurons or other cells. However, cerebrospinal fluid distributes a newsletter to many subscribers.

Scientists have long known that signals are sent from cell to cell, or through release into blood vessels. The study shows that the brain regulates some processes by releasing and dispersing molecules, and in this case, a Neuropeptide, through cerebrospinal fluid. Drug developers are interested in creating pharmaceuticals that would target the MCH system to control appetite, and thereby address obesity and other weight-related health problems.

Cerebrospinal fluid has three chief assignments. First, its grueling eternal task is buoyancy, like the Greek Titan Atlas, supporting the brain. Second, it acts as a cushion after a blow to the head. Third, it is the brain's sewer system, clearing away metabolic waste. As neuroscience technologies have advanced, scientists have seen indications that what is sometimes dismissed as sewage actually has a role in the brain's regulation of behaviors such as stress, energy balance and reproduction.

"The cerebrospinal fluid had been historically thought more of as a metabolic wasteland," said Scott Kanoski. "But what we are showing is that the fluid is an active mechanism for communication in the brain." For their study, the researchers focused on the molecule "melanin-concentrating hormone" (MCH). This neuropeptide is generated by neurons in the brain's hunger center, the lateral hypothalamus, at the base of the brain just above the pituitary gland. A protein molecule, MCH stimulates appetite. It also can slow energy expenditure.

Through a series of experiments with rats, the researchers stimulated release of the hunger peptide and then tracked it in the cerebrospinal fluid. "When we released MCH into the cerebrospinal fluid, the animals would start eating," Kanoski said. "When we reduced the levels of the molecule, then we saw the opposite effect and the animals would eat less."

Based on their findings, the researchers determined the peptide's release is likely influenced by circadian clock and a daily mealtime routine. The study has been published in the journal Cell Metabolism.