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Median eminence blood flow influences food intake by regulating ghrelin access to the metabolic brain
Nicola Romanò, Chrystel Lafont, Pauline Campos, Anne Guillou, Tatiana Fiordelisio, David J. Hodson, Patrice Mollard, Marie Schaeffer
Nicola Romanò, Chrystel Lafont, Pauline Campos, Anne Guillou, Tatiana Fiordelisio, David J. Hodson, Patrice Mollard, Marie Schaeffer
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Research Article Metabolism

Median eminence blood flow influences food intake by regulating ghrelin access to the metabolic brain

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Abstract

Central integration of peripheral appetite-regulating signals ensures maintenance of energy homeostasis. Thus, plasticity of circulating molecule access to neuronal circuits involved in feeding behavior plays a key role in the adaptive response to metabolic changes. However, the mechanisms involved remain poorly understood despite their relevance for therapeutic development. Here, we investigated the role of median eminence mural cells, including smooth muscle cells and pericytes, in modulating gut hormone effects on orexigenic/anorexigenic circuits. We found that conditional activation of median eminence vascular cells impinged on local blood flow velocity and altered ghrelin-stimulated food intake by delaying ghrelin access to target neurons. Thus, activation of median eminence vascular cells modulates food intake in response to peripheral ghrelin by reducing local blood flow velocity and access to the metabolic brain.

Authors

Nicola Romanò, Chrystel Lafont, Pauline Campos, Anne Guillou, Tatiana Fiordelisio, David J. Hodson, Patrice Mollard, Marie Schaeffer

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Figure 1

NG2-expressing cells line capillaries in the ME/ARH region.

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NG2-expressing cells line capillaries in the ME/ARH region.
(A) Confocal...
(A) Confocal images depicting a ventral view of the ME in an NG2DsRed mouse (left panel, scale: 100 μm, 50 μm Z-projection; red: NG2DsRed, green: FITC-lectin, blue: DAPI), showing NG2DsRed cellular bodies and processes line ME capillaries. Right panels (scale: 20 μm, 15 μm Z-projection) correspond to an enlargement of the boxed area on left. (B) Confocal images depicting a coronal view of the ME in an NG2DsRed mouse (left panel, scale: 100 μm, 200 μm Z-projection; red: NG2DsRed, green: FITC-lectin, blue: DAPI). Arrows indicate the position of NG2DsRed cells along capillary loop projections within the ME. (C) Confocal images depicting a coronal view of the ME in an NG2DsRed mouse (scale: 50 μm, 20 μm Z-projection; red: NG2DsRed, green: PDGFR-β, white: α-SMA; 3°V: third ventricle). (D) Enlargements of boxed areas in C (scale: 10 μm, 15 μm Z-projection; red: NG2DsRed, green: PDGFR-β, white: α-SMA). Arrows indicate NG2DsRed cell projections labeled with PDGFR-β and α-SMA.

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