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Cited by 256

The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.

Leptin action in the forebrain regulates the hindbrain response to satiety signals

Open access
Morton, Gregory J., Blevins, James E., Williams, Diana L., Niswender, Kevin D., Gelling, Richard W., Rhodes, Christopher J., Baskin, Denis G., Schwartz, Michael W.·2005·Journal of Clinical Investigation

Abstract

The capacity to adjust energy intake in response to changing energy requirements is a defining feature of energy homeostasis. Despite the identification of leptin as a key mediator of this process, the mechanism whereby changes of body adiposity are coupled to adaptive, short-term adjustments of energy intake remains poorly understood. To investigate the physiological role of leptin in the control of meal size and the response to satiety signals, and to identify brain areas mediating this effect, we studied Koletsky (fa(k)/fa(k)) rats, which develop severe obesity due to the genetic absence of leptin receptors. Our finding of markedly increased meal size and reduced satiety in response to the gut peptide cholecystokinin (CCK) in these leptin receptor-deficient animals suggests a critical role for leptin signaling in the response to endogenous signals that promote meal termination. To determine if the hypothalamic arcuate nucleus (ARC) (a key forebrain site of leptin action) mediates this leptin effect, we used adenoviral gene therapy to express either functional leptin receptors or a reporter gene in the area of the ARC of fa(k)/fa(k) rats. Restoration of leptin signaling to this brain area normalized the effect of CCK on the activation of neurons in the nucleus of the solitary tract and area postrema, key hindbrain areas for processing satiety-related inputs. This intervention also reduced meal size and enhanced CCK-induced satiety in fa(k)/fa(k) rats. These findings demonstrate that forebrain signaling by leptin, a long-term regulator of body adiposity, limits food intake on a meal-to-meal basis by regulating the hindbrain response to short-acting satiety signals.

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Metadata

Authors
Morton, G. J., Blevins, J. E., Williams, D. L., Niswender, K. D., Gelling, R. W., Rhodes, C. J., Baskin, D. G., & Schwartz, M. W.
Venue
Journal of Clinical Investigation
Published
2005-03-01
Volume
115
Issue
3
Pages
703-710
ISSN
0021-9738 (ISSN-L)
OpenAlex
W1986299003
Cited by
256
References
10
FWCI
7.04
Type
journal article
Language
en
Open access
bronze

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