Evidence map›Paper›PMID 41204207›Full record

ArticleRespiratory research2025

Harnessing NLRX1: a new frontier in mitigating inflammation in pulmonary hypertension.

Yingchou Xiao, Zhigui Cai, Mengcai Bai, Xingan Wu, Wenlan Wang, Rongrong Liu, Ying Luo

Abstract read
In one paragraph

Article in Respiratory research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

7 authors.

Yingchou Xiao *Department of Physiology and Pathophysiology, School of Basic Medicine, Fourth Military Medical University, Changle West Road 169, Xian, 710032, People's Republic of China.
Zhigui Cai *Department of Pulmonary and Critical Care Medicine, Xijing Hospital, Fourth Military Medical University, Xian, China.
Mengcai BaiDepartment of Physiology and Pathophysiology, School of Basic Medicine, Fourth Military Medical University, Changle West Road 169, Xian, 710032, People's Republic of China.
Xingan WuDepartment of Microbiology, School of Basic Medicine, Fourth Military Medical University, Changle West Road 169, Xian, 710032, People's Republic of China.
Wenlan WangDepartment of Aerospace Hygiene, School of Aerospace Medicine, Fourth Military Mediacl University, Changle West Road 169, Xian, 710032, People's Republic of China. ypwl821@fmmu.edu.cn.
Rongrong LiuDepartment of Microbiology, School of Basic Medicine, Fourth Military Medical University, Changle West Road 169, Xian, 710032, People's Republic of China. rong4713@163.com.
Ying LuoDepartment of Physiology and Pathophysiology, School of Basic Medicine, Fourth Military Medical University, Changle West Road 169, Xian, 710032, People's Republic of China. luoying@fmmu.edu.cn.

Funding

Key Research and Development Project of Shanxi province 2023-YBSF-405National Nature Science Foundation of China 81770056
6 · The paper itself

Abstract

backgroundHypoxic pulmonary hypertension (HPH) serves as a crucial link in the pathogenesis of chronic high-altitude diseases and chronic obstructive pulmonary disease (COPD), and ultimately may lead to right heart failure. Hypoxia triggers immune responses and inflammatory processes, which contribute to vascular remodeling and elevated pulmonary artery pressure. NLRX1, a member of the Nod-like receptor family, plays a significant regulatory role in immunity, antioxidation, and apoptosis. However, its role in the occurrence and development of HPH remains unknown.

methodsWild type (WT) C57BL/6 mice and NLRX1 knockout (NLRX1

resultsHypoxia downregulates the expression of NLRX1 in the lung tissues of mice and bone marrow-derived macrophages (BMDM). Chronic hypoxia significantly increases right ventricular systolic pressure (RVSP), the ratio of right ventricle weight to left ventricle plus septum weight (RV/LV + S), and the medial width of pulmonary arterioles in NLRX1-knockout (NLRX1

conclusionsNLRX1 may suppress hypoxia-induced lung inflammation and alleviate hypoxia-induced pulmonary hypertension through its anti-inflammatory and antioxidant properties. Therefore, targeted up-regulation of NLRX1 may offer a new strategy for the treatment of HPH.

Indexed as

Hypertension, PulmonaryInflammation MediatorsMitochondrial ProteinsAnimalsCells, CulturedDisease Models, AnimalHypoxiaInflammationMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutOxidative StressRatsRats, Sprague-DawleyInflammation MediatorsMitochondrial ProteinsNLRX1 protein, mouseHypoxiaHypoxic pulmonary hypertension (HPH)InflammationNF-κBNLRX1Pulmonary vascular remodeling

Identifiers

PMID41204207
PMCPMC12595859

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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.