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Cancer-induced anorexia and malaise are mediated by CGRP neurons in the parabrachial nucleus.


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.

SUBMITTER: Campos CA 

PROVIDER: S-EPMC5538581 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature

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Cancer-induced anorexia and malaise are mediated by CGRP neurons in the parabrachial nucleus.

Campos Carlos A CA   Bowen Anna J AJ   Han Sung S   Wisse Brent E BE   Palmiter Richard D RD   Schwartz Michael W MW  

Nature neuroscience 20170605 7


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 CGRP<sup>PBN</sup> neurons are activated in mice implanted with Lewis lung carcinoma cells. Inactivation of CGRP<sup>PBN</sup> neurons before tumor implantation prevents anorexia and loss of lean mass, and their inhibition after symptom  ...[more]

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