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Brain receptor that regulates body heat may also help accelerate weight loss

November 27, 2019

LA JOLLA, CA - The brain mechanism that enables us to maintain a constant body temperature may also be the key to rapid weight loss, a new study finds. In experiments involving mice that were given a calorie-restricted diet, scientists at Scripps Research discovered that blocking a brain receptor that normally regulates body heat resulted in significant weight reductions.

The findings will be further explored as a potential treatment approach for obesity, which the World Health Organization has called a global epidemic. Obesity affects virtually all age and socioeconomic groups--increasing risk for heart disease, stroke, diabetes, cancer and many other serious health conditions.

The new study, led by Scripps Research Professor Bruno Conti, PhD, appears in Current Biology.

"Up to 50 percent of what we eat every day is used as energy to maintain body temperature," Conti says. "But when food is scarce, mammals adapt by lowering their temperature, limiting energy expenditure and the loss of body weight."

Some species, he notes, can go into complete hibernation. Of course, humans don't hibernate when they're on a calorie-restricted diet, but they do naturally experience a lower body temperature just like other mammals. And that makes it harder to lose weight when on a diet.

"It's a basic survival mechanism," Conti says. "The body is saying: Let's save energy today and maybe we will find food tomorrow."

In a continuation of their earlier research on lifespan and aging, Conti and his team investigated the cellular mechanisms that regulate the body's cooling response to calorie restriction. Biological data obtained in collaboration with the Scripps Research lab of Gary Siuzdak, PhD, suggested the possibility that opioid compounds that naturally occur within the body could be mediating these effects.

Next, the team tested whether blocking the activity of opioid receptors would affect body temperature during calorie restriction. It did. They also determined that this mechanism was uniquely regulated by one of the three known opioid receptor types: the kappa opioid receptor. The finding made sense, as the kappa receptor is the most abundant opioid receptor in the hypothalamus, the part of the brain already known to play a role in regulating both body temperature and feeding.

Conti's team then wondered if by blocking the kappa receptor, the body would continue to burn up calories to regulate heat even when food was restricted. "We developed an experimental protocol that would allow us to determine what changes were happening as a result of body heat regulation, not diet," says Rigo Cintron-Colon, PhD, first author of the study.

In one set of experiments, the scientists observed two groups of lean mice that had already been on calorie-restricted diets for six weeks. One group was then treated with a drug to block the kappa receptor. The control group had adapted to the new diet and weight loss plateaued, while the experimental group showed greater energy expenditure and lost an additional 6 percent of body weight.

"When we blocked the kappa receptor, the animals did not lower their temperature during calorie restriction and lost more body weight," Conti says.

Similar results were obtained with mice that had developed diet-induced obesity. Blocking the kappa opioid receptor during calorie restriction nearly doubled the body weight loss that the obese animals would normally undergo if their receptor was functional. However, when animals were allowed to eat freely, blocking the kappa opioid receptor had no effects on body temperature and did not alter the normal rate of body weight loss.

This is important, Conti says, as it tells us that kappa opioid blockers are effective in both lean mice and obese mice, but that the medicine is able to affect body weight only in animals that are dieting.

The findings suggest a possibility that by translating these findings into humans, a pharmaceutical product may be able to help those who are struggling to lose weight, despite their adherence to a calorie-restricted diet. As a next step, Conti would like to explore whether existing medicines that are known to block the kappa receptor could be repurposed and refined to safely treat obesity.

"The tools to interact with this mechanism may already be available, and if they are, they may be able to translate quickly into a medicine," he says. "Unfortunately, for many people who are obese, losing weight isn't as simple as eating less."
Authors of the article, "Activation of Kappa Opioid Receptor Regulates the Hypothermic Response to Calorie Restriction and Limits Body Weight Loss," include Rigo Cintron-Colon, Christopher W. Johnson, J. Rafael Montenegro-Burke, Carlos Guijas, Lila Faulhaber, Manuel Sanchez-Alavez, Carlos A. Aguirre, Kokila Shankar, Mona Singh, Andrea Galmozzi, Gary Siuzdak, Enrique Saez and Bruno Conti.

This work was supported by the National Institutes of Health (GM113894, RC2 DK114785, R01 GM114368-03, P30 MH062261-17, P01 DA026146-02) and the Cloud Credits Model Pilot, a component of the NIH Big Data to Knowledge program.

Scripps Research Institute

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