Evidence map›Paper›PMID 34881424›Full record

ArticleCurrent medical science2022

Pachymic Acid Ameliorates Pulmonary Hypertension by Regulating Nrf2-Keap1-ARE Pathway.

Yuan He, Jian-Hua Zhong, Xiao-Dong Wei, Chu-Ying Huang, Pai-Lan Peng, Jun Yao, Xiu-Sheng Song, Wan-Li Fan, Guang-Cai Li

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Article in Current medical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Yuan He *Department of Ultrasound, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China.
Jian-Hua Zhong *Department of Neurology, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China.
Xiao-Dong WeiDepartment of Thoracic and Cardiovascular Surgery, Minda Hospital of Hubei Minzu University, Enshi, 445000, China.
Chu-Ying HuangDepartment of Pulmonary and Critical Care Medicine, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China.
Pai-Lan PengDepartment of Pulmonary and Critical Care Medicine, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China.
Jun YaoDepartment of Pulmonary and Critical Care Medicine, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China.
Xiu-Sheng SongDepartment of Pulmonary and Critical Care Medicine, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China.
Wan-Li FanDepartment of Pulmonary and Critical Care Medicine, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China.
Guang-Cai LiDepartment of Pulmonary and Critical Care Medicine, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, 445000, China. Guangcail66@aliyun.com.
The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture · CNMinda Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePulmonary hypertension (PH) is a severe pulmonary vascular disease that eventually leads to right ventricular failure and death. The purpose of this study was to investigate the mechanism by which pachymic acid (PA) pretreatment affects PH and pulmonary vascular remodeling in rats.

methodsPH was induced via hypoxia exposure and administration of PA (5 mg/kg per day) in male Sprague-Dawley rats. Hemodynamic parameters were measured using a right ventricular floating catheter and pulmonary vascular morphometry was measured by hematoxylin-eosin (HE), α-SMA and Masson staining. MTT assays and EdU staining were used to detect cell proliferation, and apoptosis was analyzed by TUNEL staining. Western blotting and immunohistochemistry were used to detect the expression of proteins related to the Nrf2-Keap1-ARE pathway.

resultsPA significantly alleviated hypoxic PH and reversed right ventricular hypertrophy and pulmonary vascular remodeling. In addition, PA effectively inhibited proliferation and promoted apoptosis in hypoxia-induced pulmonary artery smooth muscle cells (PASMCs). Moreover, PA pretreatment inhibited the expression of peroxy-related factor (MDA) and promoted the expression of antioxidant-related factors (GSH-PX and SOD). Furthermore, hypoxia inhibited the Nrf2-Keap1-ARE signaling pathway, while PA effectively activated this pathway. Most importantly, addition of the Nrf2 inhibitor ML385 reversed the inhibitory effects of PA on ROS generation, proliferation, and apoptosis tolerance in hypoxia-induced PASMCs.

conclusionOur study suggests that PA may reverse PH by regulating the Nrf2-Keap1-ARE signaling pathway.

Indexed as

AnimalsAntioxidant Response ElementsDisease Models, AnimalHypertension, PulmonaryKelch-Like ECH-Associated Protein 1MaleNF-E2-Related Factor 2Phospholipase A2 InhibitorsRatsRats, Sprague-DawleySignal TransductionTriterpenesKEAP1 protein, ratKelch-Like ECH-Associated Protein 1Nfe2l2 protein, ratNF-E2-Related Factor 2pachymic acidPhospholipase A2 InhibitorsTriterpenesantioxidant response elementsKelch-like epichlorohydrin-related protein 1nuclear factor erythroid 2-related factor 2pachymic acidpulmonary hypertension

Identifiers

PMID34881424
OpenAlexW4200288510

What OpenQuestion 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 OpenQuestion graph.