Center for Molecular Medicine Cologne

No more binge eating: signal pathway in the brain that controls food intake discovered


A group of Cologne scientists and their cooperating partners demonstrated that the brain controls our body’s lysophospholipids, which in turn control a programme that activates nutritional intake / specific inhibitors of lipid synthesis could serve as new obesity therapies / publication in ‘Nature Metabolism’.

Nerve cells of a mouse brain (green) and the protein PRG-1 (red). If the nerve cellls contain PRG-1, the cell appear in yellow. © Johannes Vogt

An interdisciplinary research team led by Professor Johannes Vogt (Faculty of Medicine, University of Cologne) has developed an entirely novel approach to treating eating disorders. The scientists showed that a group of nerve cells in the hypothalamus (so-called AgRP, agouti-related peptide neurons) control the release of endogenous lysophospholipids, which in turn control the excitability of nerve cells in the cerebral cortex, which stimulates food intake. In this process, the crucial step of the signalling pathway is controlled by the enzyme autotaxin, which is responsible for the production of lysophosphatidic acid (LPA) in the brain as a modulator of network activity.

The administration of autotaxin inhibitors can thereby significantly reduce both excessive food intake after fasting and obesity in animal models. The article ‘AgRP neurons control food intake behaviour at cortical synapses via peripherally-derived lysophospholipids’ has now appeared in Nature Metabolism with following titel:  AgRP neurons control feeding behaviour at cortical synapses via peripherally derived lysophospholipids, Nature Metabolismvolume 4, pages 683–692 (2022) - DOI: 10.1038/s42255-022-00589-7 .

Eating disorders and especially obesity are one of the most common causes of a variety of diseases in industrialized societies worldwide, especially cardiovascular diseases with permanent disabilities or fatal outcomes such as heart attacks, diabetes, or strokes. The Robert Koch Institute reported in 2021 that 67% of men and 53% of women in Germany are overweight. 23% of adults are severely overweight (obese). Attempts to influence eating behaviour with medication have so far proved ineffective. A novel therapy that modulates the excitability of networks that control eating behaviour would be a decisive step towards controlling this widespread obesity.

The research team found an increased rate of obesity and the attendant type II diabetes in people with impaired synaptic LPA signalling. A group led by Professor Johannes Vogt (Molecular and Transltional Neuroscience, Institute for Anatomy II affiliated with CECAD and CMMC), Professor Robert Nitsch (Faculty of Medicine, University of Münster) und Professor Thomas Horvath (Yale School of Medicine, New Haven, USA) has now shown that control of the excitability of neurons in the cerebral cortex by LPA plays an essential role in the control of eating behaviour: AgRP neurons regulate the amount of lysophosphatidylcholine (LPC) in the blood. Through active transport, LPC reaches the brain, where it is converted by the enzyme autotaxin (ATX) into LPA, which is active at the synapse. Synaptic LPA signals stimulate specific networks in the brain, thus leading to increased food intake.

In the mouse model, after a period of fasting, an increase in LPC in the blood led to an increase in stimulating LPA in the brain. These mice showed typical food-seeking behavior. Both could be normalized by administrating autotaxin inhibitors. Obese mice, on the other hand, lost weight when these inhibitors were administered continuously.

Johannes Vogt explained: ‘We saw a significant reduction in excessive food intake and obesity through gene mutation and pharmacological inhibition of ATX. Our fundamental findings on the LPA-controlled excitability of the brain, which we have worked on for years, therefore also play a central role for eating behaviour.’
Robert Nitsch sees the findings as an important step towards new drug development: ‘The data show that people with a disturbed synaptic LPA signalling pathway are more likely to be overweight and suffer from type II diabetes. This is a strong indication of a possible therapeutic success of ATX inhibitors, which we are currently developing together with the Hans Knöll Institute in Jena for use in humans.’

These findings on the excitation control of neuronal networks in eating behaviour through lysophospholipids and the new therapeutic possibilities they suggest could in future contribute not only to treating eating disorders, but also neurological and psychiatric illnesses.

AgRP neurons control feeding behaviour at cortical synapses via peripherally derived lysophospholipids
Heiko Endle #, Guilherme Horta #, Bernardo Stutz #, Muthuraman Muthuraman, Irmgard Tegeder, Yannick Schreiber, Isabel Faria Snodgrass, Robert Gurke, Zhong-Wu Liu, Matija Sestan-Pesa, Konstantin Radyushkin, Nora Streu, Wei Fan , Jan Baumgart, Yan Li , Florian Kloss, Sergiu Groppa, Nils Opel, Udo Dannlowski, Hans J Grabe, Frauke Zipp, Bence Rácz, Tamas L Horvath, Robert Nitsch and Johannes Vogt.
Nature Metabolismvolume 4, pages 683–692 (2022) - DOI: 10.1038/s42255-022-00589-7 .


Media Contact:
Prof. Dr. Johannes Vogt
Molecular and Translational Neurosciences
Institute for Anatomy II, CECAD Cluster of Excellence in Aging Research, Center for Molecular Medicine Cologne (CMMC)
University of Cologne

Prof. Dr. Robert Nitsch
Director of the Institute for Translational Neurosciences
Faculty of Medicine, University of Münster

Original Press release - University of Cologne
provided by Robert Hahn - Press and Communications Team, University of Cologne