The science behind giving up

Summary: Pnoc neurons in the paranigral ventral tegmental area become active when mice seek rewards. Stimulating these neurons with optogenetics promotes avoidance behaviors. Researchers say ventral tegmental area dopamine neuron NOPR expression is necessary to limit reward-seeking behavior.

Source: UW Medicine

What happens when we give up?

Inside the brain, a group of cells known as nociceptin neurons get very active before a mouse’s breakpoint. They emit nociceptin, a complex molecule that suppresses dopamine, a chemical largely associated with motivation.

The findings, reported July 25 in Cell, offer new insight into the complex world of motivation and reward.

The nociceptin neurons are located near an area of the brain known as the ventral tegmental area. The VTA contains neurons that release dopamine during pleasurable activities. Although scientists have previously studied the effects of fast, simple neurotransmitters on dopamine neurons, this study is among the first to describe the effects of this complex nociception modulatory system.

“We are taking an entirely new angle on an area of the brain known as VTA,” said co-lead author Christian Pedersen, a fourth-year Ph.D. student in bioengineering at the University of Washington School of Medicine and the UW College of Engineering.

Researchers at the UW School of Medicine and at Washington University School of Medicine as well as colleagues at other universities spent four years looking at the role of nociceptin in regulating motivation.

“The big discovery is that large complex neurotransmitters known as neuropeptides have a very robust effect on animal behavior by acting on the VTA,” said Pedersen.

The researchers said this discovery could lead to helping people find motivation when they are depressed and conversely decrease motivation for drugs in substance- abuse disorders, like addiction.

The discovery came by looking at the neurons in mice seeking sucrose. The mice had to poke their snout into a port to get sucrose. At first, it was easy, then it became two pokes, then five, increasing exponentially, and so on. Eventually, all the mice gave up. Neural activity recordings revealed that these “demotivation” or “frustration” neurons became most active when mice stopped seeking sucrose.

In mammals, the neural circuits that underlie reward-seeking are regulated by mechanisms to keep homeostasis – the tendency to maintain internal stability to compensate for environmental changes. In the wild, animals are less motivated to seek rewards in environments where resources are scarce. Persistence in seeking uncertain rewards can be disadvantageous due to risky exposure to predators or from energy expenditure, the researchers noted.

This is an illustration of VTA neurons

At the point of giving up, neurons in green get very active and suppress dopamine, a chemical associated with motivation, researchers found. The image is credited to Max Huffman.

Deficits within these regulatory processes in humans can manifest as behavioral dysfunctions, including depression, addiction, and eating disorders.

Senior author Michael Bruchas, professor of anesthesiology and pain medicine and of pharmacology at the University of Washington School of Medicine is one of the principal faculty in UW’s new Center for Neurobiology of Addiction, Pain, and Emotion. He said the findings could go a long way into finding help for patients whose motivation neurons are not functioning correctly.

“We might think of different scenarios where people aren’t motivated like depression and block these neurons and receptors to help them feel better,” he said. “That’s what’s powerful about discovering these cells. Neuropsychiatric diseases that impact motivation could be improved.”

Looking to the future, he said, these neurons could perhaps be modified in people seeking drugs or those that have other addictions.

About this neuroscience research article

Source:
UW Medicine
Media Contacts:
Bobbi Nodell – UW Medicine
Image Source:
The image is credited to Max Huffman.

Original Research: Closed access
“A Paranigral VTA Nociceptin Circuit that Constrains Motivation for Reward”. Christian Pedersen et al.
Cell. doi:10.1016/j.cell.2019.06.034

Abstract

A Paranigral VTA Nociceptin Circuit that Constrains Motivation for Reward

Highlights
• pnVTA Pnoc neurons project locally onto VTA dopamine neurons
• pnVTA Pnoc neurons become active when animals are demotivated to seek rewards
• Stimulation of pnVTA Pnoc neurons reduces breakpoint and promotes avoidance behavior
• VTA dopamine neuron NOPR expression is necessary to limit reward-seeking behavior

Summary
Nociceptin and its receptor are widely distributed throughout the brain in regions associated with reward behavior, yet how and when they act is unknown. Here, we dissected the role of a nociceptin peptide circuit in reward seeking. We generated a prepronociceptin ( Pnoc)-Cre mouse line that revealed a unique subpopulation of paranigral ventral tegmental area (pnVTA) neurons enriched in prepronociceptin. Fiber photometry recordings during progressive ratio operant behavior revealed pnVTA Pnoc neurons become most active when mice stop seeking natural rewards. Selective pnVTA Pnoc neuron ablation, inhibition, and conditional VTA nociceptin receptor (NOPR) deletion increased operant responding, revealing that the pnVTA Pnoc nucleus and VTA NOPR signaling are necessary for regulating reward motivation. Additionally, optogenetic and chemogenetic activation of this pnVTA Pnoc nucleus caused avoidance and decreased motivation for rewards. These findings provide insight into neuromodulatory circuits that regulate motivated behaviors through identification of a previously unknown neuropeptide-containing pnVTA nucleus that limits motivation for rewards.

Feel free to share this Neuroscience News.
Join our Newsletter
I agree to have my personal information transferred to AWeber for Neuroscience Newsletter ( more information )
Sign up to receive the latest neuroscience headlines and summaries sent to your email daily from NeuroscienceNews.com
We hate spam and only use your email to contact you about newsletters. We do not sell email addresses. You can cancel your subscription any time.
No more articles