TY - JOUR
T1 - PACAP neurons in the hypothalamic ventromedial nucleus are targets of central leptin signaling
AU - Hawke, Zoe
AU - Ivanov, Tina R.
AU - Bechtold, David A.
AU - Dhillon, Harveen
AU - Lowell, Brad B.
AU - Luckman, Simon M.
N1 - , Biotechnology and Biological Sciences Research Council, United Kingdom
PY - 2009/11/25
Y1 - 2009/11/25
N2 - The adipose-derived hormone, leptin, was discovered over 10 years ago, but only now are we unmasking its downstream pathways which lead to reduced energy intake (feeding) and increased energy expenditure (thermogenesis). Recent transgenic models have challenged the longstanding supposition that the hypothalamic arcuate nucleus (Arc) is omnipotent in the central response to leptin, and research focusis beginning to shift to examine roles of extra-arcuate sites. Dhillon et al. (2006) demonstrated that targeted knock out of the signaling form of the leptin receptor (lepr-B) in steroidogenic factor 1 (SF-1) cells of the hypothalamic ventromedial nucleus (VMN) produces obesity of a similar magnitude to the proopiomelanocortin (POMC)-driven lepr-B deleted mouse, via a functionally distinct mechanism. These findings reveal that SF-1 cells of the VMN could be equally as important as POMC cells in mediating leptin's anti-obesity effects. However, the identification of molecular and cellular correlates of this relationship remains tantalizingly unknown. Here, we have shown that mRNA expression of the VMN-expressed neuropeptide pituitary adenylate cyclase-activating polypeptide (PACAP) is regulated according to energy status and that it exerts catabolic effects when administered centrally to mice. Furthermore, we have shown that SF-1 and PACAP mRNAs are colocalized in the VMN, and that leptin signaling via lepr-B is required for normal PACAP expressionin these cells. Finally, blocking endogenous central PACAP signaling with the antagonist PACAP6-38 markedly attenuates leptin-induced hypophagia and hyperthermia in vivo. Thus, it appears that PACAP is an important mediator of central leptin effects on energy balance. Copyright © 2009 Society for Neuroscience.
AB - The adipose-derived hormone, leptin, was discovered over 10 years ago, but only now are we unmasking its downstream pathways which lead to reduced energy intake (feeding) and increased energy expenditure (thermogenesis). Recent transgenic models have challenged the longstanding supposition that the hypothalamic arcuate nucleus (Arc) is omnipotent in the central response to leptin, and research focusis beginning to shift to examine roles of extra-arcuate sites. Dhillon et al. (2006) demonstrated that targeted knock out of the signaling form of the leptin receptor (lepr-B) in steroidogenic factor 1 (SF-1) cells of the hypothalamic ventromedial nucleus (VMN) produces obesity of a similar magnitude to the proopiomelanocortin (POMC)-driven lepr-B deleted mouse, via a functionally distinct mechanism. These findings reveal that SF-1 cells of the VMN could be equally as important as POMC cells in mediating leptin's anti-obesity effects. However, the identification of molecular and cellular correlates of this relationship remains tantalizingly unknown. Here, we have shown that mRNA expression of the VMN-expressed neuropeptide pituitary adenylate cyclase-activating polypeptide (PACAP) is regulated according to energy status and that it exerts catabolic effects when administered centrally to mice. Furthermore, we have shown that SF-1 and PACAP mRNAs are colocalized in the VMN, and that leptin signaling via lepr-B is required for normal PACAP expressionin these cells. Finally, blocking endogenous central PACAP signaling with the antagonist PACAP6-38 markedly attenuates leptin-induced hypophagia and hyperthermia in vivo. Thus, it appears that PACAP is an important mediator of central leptin effects on energy balance. Copyright © 2009 Society for Neuroscience.
U2 - 10.1523/JNEUROSCI.1526-09.2009
DO - 10.1523/JNEUROSCI.1526-09.2009
M3 - Article
C2 - 19940178
SN - 0270-6474
VL - 29
SP - 14828
EP - 14835
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 47
ER -