Evidence map›Paper›PMID 39899532›Full record

ArticleAmerican journal of respiratory cell and molecular biology2025

Inhalation of the Novel Tryptophan Hydroxylase 1 Inhibitor TPT-004 Alleviates Pulmonary Arterial Hypertension.

Ekaterina Legchenko, Philippe Chouvarine, Klea Hysko, Fatimunnisa Qadri, Radoslaw Wesolowski, Edgar Specker, Silke Glage, Martin Meier, Katharina Schwarz, Joerg Heineke and 4 more

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Article in American journal of respiratory cell and molecular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Ekaterina LegchenkoDepartment of Pediatric Cardiology and Critical Care.
Philippe ChouvarineDepartment of Pediatric Cardiology and Critical Care.
Klea HyskoDepartment of Pediatric Cardiology and Critical Care.
Fatimunnisa QadriMax-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.
Radoslaw WesolowskiMax-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.
Edgar SpeckerTrypto Therapeutics GmbH, Berlin, Germany.
Silke GlagePathohistological Diagnostics, Central Animal Facility, and.
Martin MeierSmall Animal Imaging Centre, Central Animal Facility, Hannover Medical School, Hannover, Germany.
Katharina SchwarzFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Hannover, Germany.
Joerg HeinekeDepartment of Cardiovascular Physiology, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.
Gerhard PohlmannFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Hannover, Germany.
Mehmet RamazanogluFraunhofer Institute for Toxicology and Experimental Medicine ITEM, Hannover, Germany.
Michael BaderMax-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.
Georg HansmannDepartment of Pediatric Cardiology and Critical Care.ORCID 0000-0003-0709-3935

Funding

Bundesministerium für Bildung und Forschung 01KC2001ABundesministerium für Bildung und Forschung 01KC2001BBundesministerium für Bildung und Forschung 03VP08051Bundesministerium für Bildung und Forschung 03VP08053Bundesministerium für Bildung und Forschung 16GW0298Deutsche Forschungsgemeinschaft HA4348/2-2
6 · The paper itself

Abstract

Inhaled pharmacotherapies are promising treatment options for patients with pulmonary arterial hypertension (PAH), as they minimize extrapulmonary adverse effects. Recently, we developed a highly specific tryptophan hydroxylase 1 inhibitor (TPHi): TPT-004. We hypothesized that repetitive nose-only inhalation of TPT-004 alleviates PAH and pulmonary vascular remodeling in the Sugen 5416/hypoxia (SuHx) rat model. Male Sprague Dawley rats were divided into three groups: ConNx (control animals kept in room air during the study); SuHx+vehicle (rats injected with the VEGFR2 inhibitor SU5416 and then exposed to chronic hypoxia for 3 weeks, followed by 10 days recovery and subsequent 4 weeks of daily vehicle inhalations; and SuHx+TPHi (SuHx-exposed rats after recovery treated with daily inhalations of the TPH1 inhibitor, TPT-004, for 4 weeks). Closed-chest right-left heart catheterization and cardiac magnetic resonance imaging were performed in spontaneously breathing rats. Histological and mRNA-sequencing analyses were performed on lungs. SuHx-exposed rats had severe PAH, right ventricle (RV) hypertrophy, and RV dilation. In comparison with SuHx-exposed rats, TPHi-treated SuHx rats had significantly lower RV systolic pressure (67.25 vs. 51.47 mm Hg;

Indexed as

Enzyme InhibitorsHypertension, PulmonaryPulmonary Arterial HypertensionTryptophan HydroxylaseAdministration, InhalationAnimalsDisease Models, AnimalHypoxiaIndolesLungMalePulmonary ArteryPyrrolesRatsRats, Sprague-DawleyVascular RemodelingEnzyme InhibitorsIndolesPyrrolesSemaxinibTryptophan Hydroxylaseinhaled therapypulmonary hypertensionpulmonary vascular diseaseserotonintryptophan hydroxylase 1 inhibitor

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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.