VGF is required for obesity induced by diet, gold thioglucose treatment, and agouti and is differentially regulated in pro-opiomelanocortin- and neuropeptide Y-containing arcuate neurons in response to fasting

Seung Hahm, Csaba Fekete, Tooru M. Mizuno, Joan Windsor, Hai Yan, Carol N. Boozer, Charlotte Lee, Joel K. Elmquist, Ronald M. Lechan, Charles V. Mobbs, Stephen R J Salton

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Abstract

Targeted deletion of the gene encoding the neuronal and neuroendocrine secreted polypeptide VGF (nonacronymic) produces a lean, hypermetabolic mouse. Consistent with this phenotype, VGF mRNA levels are regulated in the hypothalamic arcuate nucleus in response to fasting. To gain insight into the site(s) and mechanism(s) of action of VGF, we further characterized VGF expression in the hypothalamus. Double-label studies indicated that VGF and pro-opiomelanocortin were coexpressed in lateral arcuate neurons in the fed state, and that VGF expression was induced after fasting in medial arcuate neurons that synthesize neuropeptide Y (NPY). Like NPY, VGF mRNA induction in this region of the hypothalamus in fasted mice was inhibited by exogenous leptin. In leptin-deficient ob/ob and receptor-mutant db/db mice, VGF mRNA levels in the medial arcuate were elevated. To identify neural pathways that are functionally compromised by Vgf ablation, VGF mutant mice were crossed with obese Ay/a (agouti) and ob/ob mice. VGF deficiency completely blocked the development of obesity in Ay/a mice, whereas deletion of Vgf in ob/ob mice attenuated weight gain but had no impact on adiposity. Hypothalamic levels of NPY and agouti-related polypeptide mRNAs in both double-mutant lines were dramatically elevated 10- to 15-fold above those of wild-type mice. VGF-deficient mice were also found to resist diet- and gold thioglucose-induced obesity. These data and the susceptibility of VGF mutant mice to monosodium glutamate-induced obesity are consistent with a role for VGF in outflow pathways, downstream of hypothalamic and/or brainstem melanocortin 4 receptors, that project via the autonomic nervous system to peripheral metabolic tissues and regulate energy homeostasis.

Original languageEnglish (US)
Pages (from-to)6929-6938
Number of pages10
JournalJournal of Neuroscience
Volume22
Issue number16
StatePublished - Aug 15 2002

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Aurothioglucose
Pro-Opiomelanocortin
Fasting
Obesity
Diet
Neurons
Neuropeptide Y
Messenger RNA
Leptin
Hypothalamus
proneuropeptide Y
Dasyproctidae
Receptor, Melanocortin, Type 4
Neural Pathways
Sodium Glutamate
Arcuate Nucleus of Hypothalamus
Peptides
Autonomic Nervous System
Gene Deletion
Adiposity

Keywords

  • Agouti
  • Hypothalamus
  • Leptin
  • Melanocortin
  • Neurotrophin
  • NPY
  • Obesity
  • POMC
  • VGF

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

VGF is required for obesity induced by diet, gold thioglucose treatment, and agouti and is differentially regulated in pro-opiomelanocortin- and neuropeptide Y-containing arcuate neurons in response to fasting. / Hahm, Seung; Fekete, Csaba; Mizuno, Tooru M.; Windsor, Joan; Yan, Hai; Boozer, Carol N.; Lee, Charlotte; Elmquist, Joel K.; Lechan, Ronald M.; Mobbs, Charles V.; Salton, Stephen R J.

In: Journal of Neuroscience, Vol. 22, No. 16, 15.08.2002, p. 6929-6938.

Research output: Contribution to journalArticle

Hahm, Seung ; Fekete, Csaba ; Mizuno, Tooru M. ; Windsor, Joan ; Yan, Hai ; Boozer, Carol N. ; Lee, Charlotte ; Elmquist, Joel K. ; Lechan, Ronald M. ; Mobbs, Charles V. ; Salton, Stephen R J. / VGF is required for obesity induced by diet, gold thioglucose treatment, and agouti and is differentially regulated in pro-opiomelanocortin- and neuropeptide Y-containing arcuate neurons in response to fasting. In: Journal of Neuroscience. 2002 ; Vol. 22, No. 16. pp. 6929-6938.
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abstract = "Targeted deletion of the gene encoding the neuronal and neuroendocrine secreted polypeptide VGF (nonacronymic) produces a lean, hypermetabolic mouse. Consistent with this phenotype, VGF mRNA levels are regulated in the hypothalamic arcuate nucleus in response to fasting. To gain insight into the site(s) and mechanism(s) of action of VGF, we further characterized VGF expression in the hypothalamus. Double-label studies indicated that VGF and pro-opiomelanocortin were coexpressed in lateral arcuate neurons in the fed state, and that VGF expression was induced after fasting in medial arcuate neurons that synthesize neuropeptide Y (NPY). Like NPY, VGF mRNA induction in this region of the hypothalamus in fasted mice was inhibited by exogenous leptin. In leptin-deficient ob/ob and receptor-mutant db/db mice, VGF mRNA levels in the medial arcuate were elevated. To identify neural pathways that are functionally compromised by Vgf ablation, VGF mutant mice were crossed with obese Ay/a (agouti) and ob/ob mice. VGF deficiency completely blocked the development of obesity in Ay/a mice, whereas deletion of Vgf in ob/ob mice attenuated weight gain but had no impact on adiposity. Hypothalamic levels of NPY and agouti-related polypeptide mRNAs in both double-mutant lines were dramatically elevated 10- to 15-fold above those of wild-type mice. VGF-deficient mice were also found to resist diet- and gold thioglucose-induced obesity. These data and the susceptibility of VGF mutant mice to monosodium glutamate-induced obesity are consistent with a role for VGF in outflow pathways, downstream of hypothalamic and/or brainstem melanocortin 4 receptors, that project via the autonomic nervous system to peripheral metabolic tissues and regulate energy homeostasis.",
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AU - Hahm, Seung

AU - Fekete, Csaba

AU - Mizuno, Tooru M.

AU - Windsor, Joan

AU - Yan, Hai

AU - Boozer, Carol N.

AU - Lee, Charlotte

AU - Elmquist, Joel K.

AU - Lechan, Ronald M.

AU - Mobbs, Charles V.

AU - Salton, Stephen R J

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AB - Targeted deletion of the gene encoding the neuronal and neuroendocrine secreted polypeptide VGF (nonacronymic) produces a lean, hypermetabolic mouse. Consistent with this phenotype, VGF mRNA levels are regulated in the hypothalamic arcuate nucleus in response to fasting. To gain insight into the site(s) and mechanism(s) of action of VGF, we further characterized VGF expression in the hypothalamus. Double-label studies indicated that VGF and pro-opiomelanocortin were coexpressed in lateral arcuate neurons in the fed state, and that VGF expression was induced after fasting in medial arcuate neurons that synthesize neuropeptide Y (NPY). Like NPY, VGF mRNA induction in this region of the hypothalamus in fasted mice was inhibited by exogenous leptin. In leptin-deficient ob/ob and receptor-mutant db/db mice, VGF mRNA levels in the medial arcuate were elevated. To identify neural pathways that are functionally compromised by Vgf ablation, VGF mutant mice were crossed with obese Ay/a (agouti) and ob/ob mice. VGF deficiency completely blocked the development of obesity in Ay/a mice, whereas deletion of Vgf in ob/ob mice attenuated weight gain but had no impact on adiposity. Hypothalamic levels of NPY and agouti-related polypeptide mRNAs in both double-mutant lines were dramatically elevated 10- to 15-fold above those of wild-type mice. VGF-deficient mice were also found to resist diet- and gold thioglucose-induced obesity. These data and the susceptibility of VGF mutant mice to monosodium glutamate-induced obesity are consistent with a role for VGF in outflow pathways, downstream of hypothalamic and/or brainstem melanocortin 4 receptors, that project via the autonomic nervous system to peripheral metabolic tissues and regulate energy homeostasis.

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