Evidence map›Paper›PMID 37440208›Full record

ReviewPhysiological reviews2024

Sympathetic circuits regulating hepatic glucose metabolism: where we stand.

Andrea Zsombok, Lucie D Desmoulins, Andrei V Derbenev

Open access · greenAbstract readReview
In one paragraph

Review in Physiological reviews, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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  16. Midlife estradiol treatment reduces the firing rate of liver-related PVN neurons in ovariectomized high-fat diet-fed mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
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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 at 1 institution in 1 country.

Andrea ZsombokDepartment of Physiology, School of Medicine, Tulane University, New Orleans, Louisiana, United States.ORCID 0000-0002-1412-0041
Lucie D DesmoulinsDepartment of Physiology, School of Medicine, Tulane University, New Orleans, Louisiana, United States.
Andrei V DerbenevDepartment of Physiology, School of Medicine, Tulane University, New Orleans, Louisiana, United States.
Tulane University · US

Funding

Brain Circuits Involved in the Sympathetic Control of the LiverR01DK122842 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI DERBENEV, ANDREI, ZSOMBOK, ANDREA · 2020 to 2023
$2.4M
Brain Circuits Involved in the Sympathetic Control of the LiverR56DK122842 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI ZSOMBOK, ANDREA · 2019 to 2019
$152k
HHS | NIH | NIDDK | Division of Diabetes, Endocrinology, and Metabolic Diseases (DEM) DK122842NIDDK NIH HHS R01 DK122842NIDDK NIH HHS R56 DK122842
6 · The paper itself

Abstract

The prevalence of metabolic disorders, including type 2 diabetes mellitus, continues to increase worldwide. Although newer and more advanced therapies are available, current treatments are still inadequate and the search for solutions remains. The regulation of energy homeostasis, including glucose metabolism, involves an exchange of information between the nervous systems and peripheral organs and tissues; therefore, developing treatments to alter central and/or peripheral neural pathways could be an alternative solution to modulate whole body metabolism. Liver glucose production and storage are major mechanisms controlling glycemia, and the autonomic nervous system plays an important role in the regulation of hepatic functions. Autonomic nervous system imbalance contributes to excessive hepatic glucose production and thus to the development and progression of type 2 diabetes mellitus. At cellular levels, change in neuronal activity is one of the underlying mechanisms of autonomic imbalance; therefore, modulation of the excitability of neurons involved in autonomic outflow governance has the potential to improve glycemic status. Tissue-specific subsets of preautonomic neurons differentially control autonomic outflow; therefore, detailed information about neural circuits and properties of liver-related neurons is necessary for the development of strategies to regulate liver functions via the autonomic nerves. This review provides an overview of our current understanding of the hypothalamus-ventral brainstem-liver pathway involved in the sympathetic regulation of the liver, outlines strategies to identify organ-related neurons, and summarizes neuronal plasticity during diabetic conditions with a particular focus on liver-related neurons in the paraventricular nucleus.

Indexed as

Diabetes Mellitus, Type 2GlucoseHumansHypothalamusLiverParaventricular Hypothalamic NucleusGlucoseglucose homeostasishypothalamus-ventral brainstem neurocircuitsliversympathetic nervous systemviral tracing

Identifiers

PMID37440208
PMCPMC11281813
OpenAlexW4384120679

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.