Evidence map›Paper›PMID 27656404›Full record

ArticleMolecular metabolism2016

Leptin and insulin engage specific PI3K subunits in hypothalamic SF1 neurons.

Jong-Woo Sohn, Youjin Oh, Ki Woo Kim, Syann Lee, Kevin W Williams, Joel K Elmquist

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. The metabolically protective energy expenditure increase ofAmerican journal of physiology. Endocrinology and metabolism · 2025
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  5. Population-Based Study of Rare Coding Variants inJournal of the Endocrine Society · 2024
    Article
  6. Subunit-Specific Developmental Roles of PI3K in SF1-Expressing Cells.Endocrinology and metabolism (Seoul, Korea) · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Leptin signaling and leptin resistance.Medical review (2021) · 2022
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Cellular and systemic mechanisms for glucose sensing and homeostasis.Pflugers Archiv : European journal of physiology · 2020
    Review
  19. Article
  20. Essential and sex-specific effects of mGluR5 in ventromedial hypothalamus regulating estrogen signaling and glucose balance.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Jong-Woo SohnDivision of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA; Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, South Korea. Electronic address: jwsohn@kaist.ac.kr.
Youjin OhDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, South Korea.
Ki Woo KimDivision of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA; Department of Pharmacology, Yonsei University Wonju College of Medicine, Wonju, 26426, South Korea.
Syann LeeDivision of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Kevin W WilliamsDivision of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA. Electronic address: Kevin.Williams@UTSouthwestern.edu.
Joel K ElmquistDivision of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA; Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
The University of Texas Southwestern Medical Center · USKorea Advanced Institute of Science and Technology · KR

Funding

Novel Mechanisms Regulating the Adipocyte-Brain-Hepatocyte AxisP01DK088761 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GORDILLO, RUTH · 2010 to 2019
$17.4M
SF1 neurons and sympathetic regulation of glucose homeostasisR01DK100659 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI JOEL K. ELMQUIST · 2014 to 2026
$4.8M
Leptin Action and Central Melanocortin SystemsR37DK053301 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ELMQUIST, JOEL K. · 2007 to 2016
$3.7M
NEUROANATOMIC MECHANIMS OF LEPTIN ACTIONR01DK053301 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ELMQUIST, JOEL K · 1998 to 2006
$3.0M
Central Mechanisms Regulating Acute Leptin and Insulin SignalingR01DK100699 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI WILLIAMS, KEVIN W · 2014 to 2018
$1.8M
Genetic dissection of endoplasmic reticulum stress in POMC neuronsK01DK087780 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI WILLIAMS, KEVIN W · 2010 to 2012
$354k
NIDDK NIH HHS K01 DK087780NIDDK NIH HHS P01 DK088761NIDDK NIH HHS R01 DK053301NIDDK NIH HHS R01 DK100659NIDDK NIH HHS R01 DK100699NIDDK NIH HHS R37 DK053301
6 · The paper itself

Abstract

objectiveThe ventromedial hypothalamic nucleus (VMH) regulates energy balance and glucose homeostasis. Leptin and insulin exert metabolic effects via their cognate receptors expressed by the steroidogenic factor 1 (SF1) neurons within the VMH. However, detailed cellular mechanisms involved in the regulation of these neurons by leptin and insulin remain to be identified.

methodsWe utilized genetically-modified mouse models and performed patch-clamp electrophysiology experiments to resolve this issue.

resultsWe identified distinct populations of leptin-activated and leptin-inhibited SF1 neurons. In contrast, insulin uniformly inhibited SF1 neurons. Notably, we found that leptin-activated, leptin-inhibited, and insulin-inhibited SF1 neurons are distinct subpopulations within the VMH. Leptin depolarization of SF1 neuron also required the PI3K p110β catalytic subunit. This effect was mediated by the putative transient receptor potential C (TRPC) channel. On the other hand, hyperpolarizing responses of SF1 neurons by leptin and insulin required either of the p110α or p110β catalytic subunits, and were mediated by the putative ATP-sensitive K(+) (KATP) channel.

conclusionsOur results demonstrate that specific PI3K catalytic subunits are responsible for the acute effects of leptin and insulin on VMH SF1 neurons, and provide insights into the cellular mechanisms of leptin and insulin action on VMH SF1 neurons that regulate energy balance and glucose homeostasis.

Indexed as

Cellular mechanismConditional knockout mouseFunctional heterogeneityHomeostasisPatch clamp technique

Identifiers

PMID27656404
PMCPMC5021675
OpenAlexW2431924510

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.