Evidence map›Paper›PMID 38136603›Full record

ArticleBiomolecules2023

Imipramine Treatment Alters Sphingomyelin, Cholesterol, and Glycerophospholipid Metabolism in Isolated Macrophage Lysosomes.

Jacob M Albright, Matthew J Sydor, Jonathan Shannahan, Christina R Ferreira, Andrij Holian

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. The miR-214-3p/Biology · 2026
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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

5 authors at 3 institutions in 1 country.

Jacob M AlbrightDepartment of Biomedical and Pharmaceutical Sciences, Center for Environmental Health Sciences (CEHS), University of Montana, Missoula, MT 59812, USA.ORCID 0009-0008-5063-899X
Matthew J SydorDepartment of Biomedical and Pharmaceutical Sciences, Center for Biomolecular Structure and Dynamics, University of Montana, Missoula, MT 59812, USA.
Jonathan ShannahanSchool of Health Sciences, Purdue University, West Lafayette, IN 47907, USA.
Christina R FerreiraMetabolite Profiling Facility, Bindley Bioscience Center, Center for Analytical Instrumentation Development, Purdue University, West Lafayette, IN 47907, USA.
Andrij HolianDepartment of Biomedical and Pharmaceutical Sciences, Center for Environmental Health Sciences (CEHS), University of Montana, Missoula, MT 59812, USA.
Center for Environmental Health · USPurdue University West Lafayette · USUniversity of Montana · US

Funding

Surveillance genome sequencing to detect SARS-CoV-2 virus variants in MontanaP30GM140963 · NIGMS · UNIVERSITY OF MONTANA · PI BOWLER, BRUCE E · 2021 to 2025
$6.9M
Role of particle surface functionalization in inflammationR01ES033533 · NIEHS · UNIVERSITY OF MONTANA · PI Andrij Holian · 2022 to 2026
$2.7M
Compromised Resolution of Inflammation following Nanoparticle Exposure in Metabolic SyndromeR01ES033173 · NIEHS · PURDUE UNIVERSITY · PI Jonathan Henry Shannahan · 2022 to 2026
$1.7M
NIEHS NIH HHS R01 ES033173NIEHS NIH HHS R01ES033173NIEHS NIH HHS R01 ES033533NIEHS NIH HHS R01ES033533NIGMS NIH HHS P30 GM140963NIGMS NIH HHS P30GM140963
6 · The paper itself

Abstract

Lysosomes are degradative organelles that facilitate the removal and recycling of potentially cytotoxic materials and mediate a variety of other cellular processes, such as nutrient sensing, intracellular signaling, and lipid metabolism. Due to these central roles, lysosome dysfunction can lead to deleterious outcomes, including the accumulation of cytotoxic material, inflammation, and cell death. We previously reported that cationic amphiphilic drugs, such as imipramine, alter pH and lipid metabolism within macrophage lysosomes. Therefore, the ability for imipramine to induce changes to the lipid content of isolated macrophage lysosomes was investigated, focusing on sphingomyelin, cholesterol, and glycerophospholipid metabolism as these lipid classes have important roles in inflammation and disease. The lysosomes were isolated from control and imipramine-treated macrophages using density gradient ultracentrifugation, and mass spectrometry was used to measure the changes in their lipid composition. An unsupervised hierarchical cluster analysis revealed a clear differentiation between the imipramine-treated and control lysosomes. There was a significant overall increase in the abundance of specific lipids mostly composed of cholesterol esters, sphingomyelins, and phosphatidylcholines, while lysophosphatidylcholines and ceramides were overall decreased. These results support the conclusion that imipramine's ability to change the lysosomal pH inhibits multiple pH-sensitive enzymes in macrophage lysosomes.

Indexed as

ImipramineSphingomyelinsCholesterolGlycerophospholipidsHumansInflammationLipid MetabolismLysosomesMacrophagesCholesterolGlycerophospholipidsImipramineSphingomyelinsanisotropyceramidelipidomicslipidslysophosphatidylcholinephosphatidylcholinesphingolipids

Identifiers

PMID38136603
PMCPMC10742328
OpenAlexW4389225372

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.