The acute effects of leptin require PI3K signaling in the hypothalamic ventral premammillary nucleus

Kevin W. Williams, Jong Woo Sohn, Jose Donato, Charlotte E. Lee, Jean J. Zhao, Joel K. Elmquist, Carol F. Elias

Research output: Contribution to journalArticle

48 Scopus citations

Abstract

Evidence suggests that the role playedby the adipocyte-derived hormone leptin in female reproductive physiologyis mediated in part by neurons located within the ventral premammillary nucleus (PMV). Leptin activates PMV neurons; however, the intracellular signaling pathway and channel(s) involved remain undefined. Notably, leptin's excitatory and inhibitory effects within hypothalamic and brains-tem nuclei share the intracellular signaling cascade phosphoinositide 3 kinase (PI3K). Therefore, we assessed whether PI3K signaling is required for the acute effect of leptin to alter cellular activity of PMV neurons that express leptin receptors (LepR PMV neurons). Leptin caused a rapid depolarization in the majority of LepR PMV neurons in patch-clamp recordings of hypothalamic slices, while a subset of LepR PMV neurons were hyperpolarized in response to leptin. Data were obtained from both male and female mice and results demonstrate that the acute effect of leptinon LepR PMV neurons was identical for both sexes. Pharmacological inhibitionof PI3K prevented the acute leptin-induced change in neuronal activity of LepR PMV neurons, indicating a PI3K-dependent mechanism of leptin action. Similarly, mice with genetically disrupted PI3K signaling in LepR PMV neurons failed to alter cellular activity in response to leptin. Moreover, the leptin-induced depolarization was dependent on a putative TRPC channel. In contrast, the leptin-induced-hyper polarization required the activation of a putative Katp channel. Collectively, these results suggest that PI3K signalingin LepR PMV neurons is essential for leptin-induced alteration in cellular activity, and these data may suggest a cellular correlate in which leptin contributes to the initiation of reproductive development.

Original languageEnglish (US)
Pages (from-to)13147-13156
Number of pages10
JournalJournal of Neuroscience
Volume31
Issue number37
DOIs
StatePublished - Sep 14 2011

ASJC Scopus subject areas

  • Neuroscience(all)

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