» Articles » PMID: 18382766

Acute Effects of Leptin Require PI3K Signaling in Hypothalamic Proopiomelanocortin Neurons in Mice

Overview
Journal J Clin Invest
Specialty General Medicine
Date 2008 Apr 3
PMID 18382766
Citations 197
Authors
Affiliations
Soon will be listed here.
Abstract

Normal food intake and body weight homeostasis require the direct action of leptin on hypothalamic proopiomelanocortin (POMC) neurons. It has been proposed that leptin action requires PI3K activity. We therefore assessed the contribution of PI3K signaling to leptin's effects on POMC neurons and organismal energy balance. Leptin caused a rapid depolarization of POMC neurons and an increase in action potential frequency in patch-clamp recordings of hypothalamic slices. Pharmacologic inhibition of PI3K prevented this depolarization and increased POMC firing rate, indicating a PI3K-dependent mechanism of leptin action. Mice with genetically disrupted PI3K signaling in POMC cells failed to undergo POMC depolarization or increased firing frequency in response to leptin. Insulin's ability to hyperpolarize POMC neurons was also abolished in these mice. Moreover, targeted disruption of PI3K blunted the suppression of feeding elicited by central leptin administration. Despite these differences, mice with impaired PI3K signaling in POMC neurons exhibited normal long-term body weight regulation. Collectively, these results suggest that PI3K signaling in POMC neurons is essential for leptin-induced activation and insulin-induced inhibition of POMC cells and for the acute suppression of food intake elicited by leptin, but is not a major contributor to the regulation of long-term organismal energy homeostasis.

Citing Articles

KCNB1-Leptin receptor complexes couple electric and endocrine function in the melanocortin neurons of the hypothalamus.

Forzisi-Kathera-Ibarra E, Jo C, Castillo L, Gaur A, Lad P, Bortolami A FASEB J. 2024; 38(20):e70111.

PMID: 39436109 PMC: 11556505. DOI: 10.1096/fj.202401931R.


Upregulation of Xbp1 in NPY/AgRP neurons reverses diet-induced obesity and ameliorates leptin and insulin resistance.

Ajwani J, Hwang E, Portillo B, Lieu L, Wallace B, Kabahizi A Neuropeptides. 2024; 108:102461.

PMID: 39180950 PMC: 11568921. DOI: 10.1016/j.npep.2024.102461.


Molecular and functional mapping of the neuroendocrine hypothalamus: a new era begins.

Lee T, Nicolas J, Quarta C J Endocrinol Invest. 2024; 47(11):2627-2648.

PMID: 38878127 DOI: 10.1007/s40618-024-02411-5.


Body fat and circulating leptin levels in the captive short-beaked echidna (Tachyglossus aculeatus).

Dutton-Regester K, Roser A, Meer H, Hill A, Pyne M, Al-Najjar A J Comp Physiol B. 2024; 194(4):457-471.

PMID: 38748188 PMC: 11316712. DOI: 10.1007/s00360-024-01559-z.


Canonical transient receptor potential channels and hypothalamic control of homeostatic functions.

Kelly M, Wagner E J Neuroendocrinol. 2024; 36(10):e13392.

PMID: 38631680 PMC: 11444909. DOI: 10.1111/jne.13392.


References
1.
Luo J, Cantley L . The negative regulation of phosphoinositide 3-kinase signaling by p85 and it's implication in cancer. Cell Cycle. 2005; 4(10):1309-12. DOI: 10.4161/cc.4.10.2062. View

2.
Morrison C, Morton G, Niswender K, Gelling R, Schwartz M . Leptin inhibits hypothalamic Npy and Agrp gene expression via a mechanism that requires phosphatidylinositol 3-OH-kinase signaling. Am J Physiol Endocrinol Metab. 2005; 289(6):E1051-7. DOI: 10.1152/ajpendo.00094.2005. View

3.
Williams K, Zsombok A, Smith B . Rapid inhibition of neurons in the dorsal motor nucleus of the vagus by leptin. Endocrinology. 2006; 148(4):1868-81. PMC: 3761087. DOI: 10.1210/en.2006-1098. View

4.
Powis J, Bains J, Ferguson A . Leptin depolarizes rat hypothalamic paraventricular nucleus neurons. Am J Physiol. 1998; 274(5):R1468-72. DOI: 10.1152/ajpregu.1998.274.5.R1468. View

5.
Luo J, Field S, Lee J, Engelman J, Cantley L . The p85 regulatory subunit of phosphoinositide 3-kinase down-regulates IRS-1 signaling via the formation of a sequestration complex. J Cell Biol. 2005; 170(3):455-64. PMC: 2171479. DOI: 10.1083/jcb.200503088. View