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Cancer-induced anorexia and malaise are mediated by CGRP neurons in the parabrachial nucleus
- Source :
- Nature neuroscience. 20(7)
- Publication Year :
- 2016
-
Abstract
- Anorexia is a common manifestation of chronic diseases, including cancer. Here we investigate the contribution to cancer anorexia made by calcitonin gene-related peptide (CGRP) neurons in the parabrachial nucleus (PBN) that transmit anorexic signals. We show that CGRPPBN neurons are activated in mice implanted with Lewis lung carcinoma cells. Inactivation of CGRPPBN neurons before tumor implantation prevents anorexia and loss of lean mass, and their inhibition after symptom onset reverses anorexia. CGRPPBN neurons are also activated in Apcmin/+ mice, which develop intestinal cancer and lose weight despite the absence of reduced food intake. Inactivation of CGRPPBN neurons in Apcmin/+ mice permits hyperphagia that counteracts weight loss, revealing a role for these neurons in a 'nonanorexic' cancer model. We also demonstrate that inactivation of CGRPPBN neurons prevents lethargy, anxiety and malaise associated with cancer. These findings establish CGRPPBN neurons as key mediators of cancer-induced appetite suppression and associated behavioral changes.
- Subjects :
- 0301 basic medicine
Male
Cachexia
Calcitonin Gene-Related Peptide
Adenomatous Polyposis Coli Protein
Mice, Transgenic
Anorexia
Calcitonin gene-related peptide
Malaise
03 medical and health sciences
Carcinoma, Lewis Lung
Mice
Tetanus Toxin
Neoplasms
medicine
Tumor Cells, Cultured
Animals
Clozapine
Illness Behavior
2. Zero hunger
Parabrachial Nucleus
Behavior, Animal
business.industry
General Neuroscience
digestive, oral, and skin physiology
Body Weight
Lewis lung carcinoma
Cancer
Metalloendopeptidases
medicine.disease
3. Good health
030104 developmental biology
Neuroimmunology
nervous system
Calcitonin
Female
medicine.symptom
business
Energy Metabolism
Neuroscience
Subjects
Details
- ISSN :
- 15461726
- Volume :
- 20
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- Nature neuroscience
- Accession number :
- edsair.doi.dedup.....8b773b41a826a5a7ad3e5d65558b9251