Evidence map›Paper›PMID 39456189›Full record

ArticleBiomolecules2024

Cellular Profile of Subfornical Organ Insulin Receptors in Mice.

Han-Rae Kim, Jin-Kwon Jeong, Colin N Young

Abstract read
In one paragraph

Article in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

3 authors.

Han-Rae KimDepartment of Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA.ORCID 0000-0002-9108-2421
Jin-Kwon JeongDepartment of Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA.
Colin N YoungDepartment of Pharmacology and Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA.

Funding

Brain endoplasmic reticulum stress in non-alcoholic fatty liver diseaseR01DK117007 · NIDDK · GEORGE WASHINGTON UNIVERSITY · PI YOUNG, COLIN NEAL · 2018 to 2022
$2.5M
Forebrain-hypothalamic mechanisms in obesity-induced hypertensionR01HL141393 · NHLBI · GEORGE WASHINGTON UNIVERSITY · PI YOUNG, COLIN NEAL · 2018 to 2022
$2.4M
American Heart Association 19CDA34630010American Heart Association AHA932522American Heart Association-American Stroke Association 932522National Institue of Health, NHLBI R01HL141393National Institute of Health, NIDDK R01DK117007NHLBI NIH HHS R01 HL141393NIDDK NIH HHS R01 DK117007
6 · The paper itself

Abstract

Brain insulin receptor signaling is strongly implicated in cardiovascular and metabolic physiological regulation. In particular, we recently demonstrated that insulin receptors within the subfornical organ (SFO) play a tonic role in cardiovascular and metabolic regulation in mice. The SFO is a forebrain sensory circumventricular organ that regulates cardiometabolic homeostasis due to its direct exposure to the circulation and thus its ability to sense circulating factors, such as insulin. Previous work has demonstrated broad distribution of insulin receptor-expressing cells throughout the entire SFO, indirectly indicating insulin receptor expression in multiple cell types. Based on this, we sought to determine the cellular phenotypes that express insulin receptors within the SFO by combining immunohistochemistry with genetically modified reporter mouse models. Interestingly, SFO neurons, including both excitatory and inhibitory types, were the dominant cell site for insulin receptor expression, although a weak degree of insulin receptor expression was also detected in astrocytes. Moreover, SFO angiotensin type 1a receptor neurons also expressed insulin receptors. Collectively, these anatomical findings indicate the existence of potentially complex cellular networks within the SFO through which insulin signaling can influence physiology and further point to the SFO as a possible brain site for crosstalk between angiotensin-II and insulin.

Indexed as

NeuronsReceptor, InsulinSubfornical OrganAnimalsAstrocytesInsulinMaleMiceMice, Inbred C57BLReceptor, Angiotensin, Type 1Signal TransductionInsr protein, mouseInsulinReceptor, Angiotensin, Type 1Receptor, Insulinangiotensin-IIastrocytescircumventricular organinsulinneurons

Identifiers

PMID39456189
PMCPMC11506324

What OpenQuestion holds

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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.