Evidence map›Paper›PMID 36750092›Full record

ArticleCurrent biology : CB2023

A carotid body-brainstem neural circuit mediates sighing in hypoxia.

Yilong Yao, Jingwen Chen, Xingyu Li, Zhou-Feng Chen, Peng Li

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  9. Functional modulation of retrotrapezoid neurons drives fentanyl-induced respiratory depression.American journal of physiology. Lung cellular and molecular 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

5 authors at 2 institutions in 2 countries.

Yilong YaoLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA; Department of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Jingwen ChenLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Xingyu LiLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.
Zhou-Feng ChenDepartment of Anesthesiology, Center for the Study of Itch and Sensory Disorders, Washington University School of Medicine, St. Louis, MO 63110, USA.
Peng LiLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA; Department of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI 48109, USA; Department of Molecular and Integrative Physiology, School of Medicine, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: penglium@umich.edu.
University of Michigan · USWashington University in St. Louis · US

Funding

Dissecting neural circuits for breathing patternsR01AT011652 · NCCIH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, PENG · 2021 to 2025
$2.1M
Neural circuit control of sighingR01HL156989 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, PENG · 2022 to 2025
$1.5M
NCCIH NIH HHS R01 AT011652NHLBI NIH HHS R01 HL156989
6 · The paper itself

Abstract

Increased ventilation is a critical process that occurs when the body responds to a hypoxic environment. Sighs are long, deep breaths that prevent alveolar collapse, and their frequency is significantly increased by hypoxia. In this study, we first show that sighing is induced by hypoxia as a function of increased hypoxic severity and that hypoxia-induced sighing is capable of increasing the oxygen saturation in a mouse model. We next found that the gastrin-releasing peptide (Grp) expressing neurons in the nucleus of the solitary tract (NTS) are important in mediating hypoxia-induced sighing. Retrograde tracing from these Grp neurons reveals their direct afferent input from the petrosal ganglion neurons that innervate the carotid body, the major peripheral chemoreceptor that senses blood oxygen. Acute hypoxia preferentially activates these Grp neurons in the NTS. Photoactivation of these neurons through their projections in the inspiratory rhythm generator in the ventral medulla induces sighing, whereas genetic ablation or chemogenetic silencing of these neurons specifically diminishes the sighs, but not other respiratory responses, induced by hypoxia. Finally, the mice with reduced sighing in hypoxia exhibit an elevated heart-rate increase, which may compensate for maintaining the blood oxygen level. Therefore, we identified a neural circuit that connects the carotid body to the breathing control center in the ventral medulla with a specific function for hypoxia-induced sighing, which restores the oxygen level.

Indexed as

Carotid BodyAnimalsBrain StemGastrin-Releasing PeptideHypoxiaMiceOxygenSolitary NucleusGastrin-Releasing PeptideOxygenblood oxygenbreathingcarotid bodygastrin-releasing peptidehypoxiahypoxic ventilatory responseneural circuitsighingthe nucleus of the solitary tract

Identifiers

PMID36750092
PMCPMC10337290
OpenAlexW4319312976

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.