Evidence map›Paper›PMID 39401152›Full record

ArticlePharmacology research & perspectives2024

Study on the mechanism of echinacoside in preventing and treating hypoxic pulmonary hypertension based on proteomic analyses.

Xiangyun Gai, Qingqing Xia, Hongmai Wang, Hongtao Bi, Jinyu Wang, Yuefu Zhao

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Article in Pharmacology research & perspectives, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Xiangyun GaiDepartment of Pharmacy, Qinghai Minzu University, Xining, China.ORCID 0009-0006-8441-9715
Qingqing XiaDepartment of Pharmacy, Qinghai Minzu University, Xining, China.ORCID 0009-0004-8876-0414
Hongmai WangDepartment of Pharmacy, Qinghai Minzu University, Xining, China.ORCID 0009-0008-6095-7943
Hongtao BiQinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety Evaluation, Northwest Institute of Plateau Biology, Chinese Academy of Science, Xining, China.ORCID 0000-0002-5569-8552
Jinyu WangDepartment of Pharmacy, Qinghai Minzu University, Xining, China.ORCID 0009-0008-2669-1942
Yuefu ZhaoDepartment of Pharmacy, Qinghai Minzu University, Xining, China.ORCID 0009-0009-4414-857X

Funding

Application Foundation Project grant of Qinghai Province, China 2020-ZJ-703Kunlun Talents and High-level Innovative Entrepreneurship Program of Qinghai Province 2020
6 · The paper itself

Abstract

Hypoxic pulmonary hypertension (HPH), a chronic condition affecting the cardiopulmonary system, has high mortality. Echinacoside (ECH) is a phenylethanoid glycoside, which is used to ameliorate pulmonary vascular remodeling and pulmonary vasoconstriction in rats. Accordingly, we aimed to explore the mechanism of ECH in preventing and treating HPH. Sprague Dawley rats were housed in a hypobaric hypoxia chamber for 28 days to obtain the HPH model. The experimental rats were randomly allocated into the following several groups: normoxia group, chronic hypoxia group, and ECH group. The therapeutic results of ECH (10, 20, and 40 mg/kg) showed that ECH reduced mPAP, Hb, Hct, and RVHI in HPH rats. Then this work employed label-free quantitative proteomic analysis, western blotting, and RT-PCR to investigate the mechanism by which ECH prevents HPH. The results found that in the chronic hypoxia group, the levels of ACSL1, COL6A1, COL4A2, COL1A1, and PC increased compared to the normoxia group. However, the opposite effect was observed in the chronic hypoxia group treated with ECH. The study indicates that the administration of ECH may slow the pathological progression of HPH by suppressing the inflammatory response, inhibiting smooth muscle cell proliferation, and minimizing the deposition of extracellular matrix.

Indexed as

GlycosidesHypertension, PulmonaryHypoxiaProteomicsRats, Sprague-DawleyAnimalsCell ProliferationDisease Models, AnimalMaleMyocytes, Smooth MuscleRatsVascular RemodelingechinacosideGlycosidescell proliferationechinacosidehypoxic pulmonary hypertensioninflammationproteomics

Identifiers

PMID39401152
PMCPMC11472809

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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.