Drp1 is required for AgRP neuronal activity and feeding

Author:

Jin Sungho1ORCID,Yoon Nal Ae1,Liu Zhong-Wu23,Song Jae Eun23,Horvath Tamas L23ORCID,Kim Jung Dae1,Diano Sabrina145ORCID

Affiliation:

1. Institute of Human Nutrition, Columbia University Irving Medical Center, New York, United States

2. Department of Comparative Medicine, Yale University School of Medicine, New Haven, United States

3. Program in Integrative Cell Signaling and Neurobiology of Metabolism, Yale University School of Medicine, New Haven, United States

4. Department of Molecular Pharmacology and Therapeutics, Columbia University Irving Medical Center, New York, United States

5. Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, United States

Abstract

The hypothalamic orexigenic Agouti-related peptide (AgRP)-expressing neurons are crucial for the regulation of whole-body energy homeostasis. Here, we show that fasting-induced AgRP neuronal activation is associated with dynamin-related peptide 1 (DRP1)-mediated mitochondrial fission and mitochondrial fatty acid utilization in AgRP neurons. In line with this, mice lacking Dnm1l in adult AgRP neurons (Drp1 cKO) show decreased fasting- or ghrelin-induced AgRP neuronal activity and feeding and exhibited a significant decrease in body weight, fat mass, and feeding accompanied by a significant increase in energy expenditure. In support of the role for mitochondrial fission and fatty acids oxidation, Drp1 cKO mice showed attenuated palmitic acid-induced mitochondrial respiration. Altogether, our data revealed that mitochondrial dynamics and fatty acids oxidation in hypothalamic AgRP neurons is a critical mechanism for AgRP neuronal function and body-weight regulation.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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