Evidence map›Paper›PMID 37041718›Full record

ArticleCardiovascular research2023

Corticotropin-releasing hormone neurons in the central nucleus of amygdala are required for chronic stress-induced hypertension.

Zhao-Fu Sheng, Hua Zhang, Jeffery G Phaup, PeiRu Zheng, XunLei Kang, Zhenguo Liu, Hui-Ming Chang, Edward T H Yeh, Alan Kim Johnson, Hui-Lin Pan and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cardiovascular research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Targeting Histamine H4 Receptor in the Rostral Ventromedial Medulla to Relieve Hypertension.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  5. Article
  6. Cardiac vagal motor neurons.Current opinion in neurobiology · 2025
    Review
  7. Characteristics of the amygdala and its subregions in premenstrual syndrome/premenstrual dysphoric disorder patients.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Review
  8. Article
  9. Article
  10. 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

11 authors at 4 institutions in 1 country.

Zhao-Fu ShengCenter for Precision Medicine, Department of Medicine, School of Medicine University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.
Hua ZhangCenter for Precision Medicine, Department of Medicine, School of Medicine University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.ORCID 0000-0002-5532-1659
Jeffery G PhaupCenter for Precision Medicine, Department of Medicine, School of Medicine University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.
PeiRu ZhengCenter for Precision Medicine, Department of Medicine, School of Medicine University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.
XunLei KangCenter for Precision Medicine, Department of Medicine, School of Medicine University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.
Zhenguo LiuCenter for Precision Medicine, Department of Medicine, School of Medicine University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.
Hui-Ming ChangDepartment of Pharmacology, The University of Arkansas for Medical Sciences, 4301 West Markham Street, Little Rock, AR 72205, USA.
Edward T H YehDepartment of Pharmacology, The University of Arkansas for Medical Sciences, 4301 West Markham Street, Little Rock, AR 72205, USA.
Alan Kim JohnsonDepartment of Psychological and Brain Sciences, The University of Iowa, G60 Psychological and Brain Sciences Building, Iowa City, IA 52242, USA.
Hui-Lin PanDepartment of Anesthesiology and Perioperative Medicine, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
De-Pei LiCenter for Precision Medicine, Department of Medicine, School of Medicine University of Missouri, One Hospital Drive, Columbia, MO 65212, USA.ORCID 0000-0003-1478-3854
University of Missouri Hospital · USUniversity of Arkansas for Medical Sciences · USThe University of Texas MD Anderson Cancer Center · USUniversity of Iowa · US

Funding

Neuroendocrine dysfunction and hypertensionR01HL159157 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI LI, DE-PEI · 2021 to 2024
$2.7M
Mechanisms of Stress-Induced HypertensionR01HL139523 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, DE-PEI, PAN, HUI-LIN · 2018 to 2021
$1.8M
Synaptic Mechanisms of Stress-Induced HypertensionR01HL142133 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, DE-PEI, PAN, HUI-LIN · 2018 to 2021
$1.8M
NHLBI NIH HHS R01 HL139523NHLBI NIH HHS R01 HL142133NHLBI NIH HHS R01 HL159157
6 · The paper itself

Abstract

aimsChronic stress is a well-known risk factor for the development of hypertension. However, the underlying mechanisms remain unclear. Corticotropin-releasing hormone (CRH) neurons in the central nucleus of the amygdala (CeA) are involved in the autonomic responses to chronic stress. Here, we determined the role of CeA-CRH neurons in chronic stress-induced hypertension. METHODS AND

resultsBorderline hypertensive rats (BHRs) and Wistar-Kyoto (WKY) rats were subjected to chronic unpredictable stress (CUS). Firing activity and M-currents of CeA-CRH neurons were assessed, and a CRH-Cre-directed chemogenetic approach was used to suppress CeA-CRH neurons. CUS induced a sustained elevation of arterial blood pressure (ABP) and heart rate (HR) in BHRs, while in WKY rats, CUS-induced increases in ABP and HR quickly returned to baseline levels after CUS ended. CeA-CRH neurons displayed significantly higher firing activities in CUS-treated BHRs than unstressed BHRs. Selectively suppressing CeA-CRH neurons by chemogenetic approach attenuated CUS-induced hypertension and decreased elevated sympathetic outflow in CUS-treated BHRs. Also, CUS significantly decreased protein and mRNA levels of Kv7.2 and Kv7.3 channels in the CeA of BHRs. M-currents in CeA-CRH neurons were significantly decreased in CUS-treated BHRs compared with unstressed BHRs. Blocking Kv7 channel with its blocker XE-991 increased the excitability of CeA-CRH neurons in unstressed BHRs but not in CUS-treated BHRs. Microinjection of XE-991 into the CeA increased sympathetic outflow and ABP in unstressed BHRs but not in CUS-treated BHRs.

conclusionsCeA-CRH neurons are required for chronic stress-induced sustained hypertension. The hyperactivity of CeA-CRH neurons may be due to impaired Kv7 channel activity, which represents a new mechanism involved in chronic stress-induced hypertension.

Indexed as

Central Amygdaloid NucleusHypertensionAnimalsAnthracenesCorticotropin-Releasing HormoneNeuronsRatsRats, Inbred WKY10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenoneAnthracenesCorticotropin-Releasing HormoneCentral nucleus of the amygdalaChronic stressCorticotropin-releasing hormoneHypertensionKv7 channel

Identifiers

PMID37041718
PMCPMC10325697
OpenAlexW4365135631

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.