Evidence map›Paper›PMID 35535222›Full record

ArticleDrug design, development and therapy2022

Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis.

Leila Gobejishvili, Walter E Rodriguez, Philip Bauer, Yali Wang, Chirag Soni, Todd Lydic, Shirish Barve, Craig McClain, Claudio Maldonado

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  6. Review
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 3 institutions in 1 country.

Leila GobejishviliDepartment of Medicine, School of Medicine, University of Louisville, Louisville, KY, USA.
Walter E RodriguezDepartment of Medicine, School of Medicine, University of Louisville, Louisville, KY, USA.
Philip BauerEndoprotech, Inc., Louisville, KY, USA.
Yali WangDepartment of Medicine, School of Medicine, University of Louisville, Louisville, KY, USA.
Chirag SoniEndoprotech, Inc., Louisville, KY, USA.
Todd LydicLipidomics Center, Michigan State University, East Lansing, MI, USA.
Shirish BarveDepartment of Medicine, School of Medicine, University of Louisville, Louisville, KY, USA.
Craig McClainDepartment of Medicine, School of Medicine, University of Louisville, Louisville, KY, USA.
Claudio MaldonadoDepartment of Physiology, School of Medicine, University of Louisville, Louisville, KY, USA.ORCID 0000-0002-2034-2273
University of Louisville · USEndoProtech (United States) · USMichigan State University · US

Funding

Phosphodiesterase 4 mediated pathogenic mechanisms in alcohol associated liver diseaseR01AA029798 · NIAAA · UNIVERSITY OF LOUISVILLE · PI GOBEJISHVILI, LEILA · 2021 to 2025
$2.2M
Novel Drug Carrier System for the Treatment of Alcoholic Liver DiseaseR44AA021331 · NIAAA · ENDOPROTECH, INC. · PI BAUER, PHILIP, GOBEJISHVILI, LEILA · 2015 to 2016
$1.4M
Device for Delivery of Rolipram to Liver for Treatment of Alcoholic Liver DiseaseR43AA021331 · NIAAA · ENDOPROTECH, INC. · PI BAUER, PHILIP, GOBEJISHVILI, LEILA · 2012 to 2012
$278k
NIAAA NIH HHS R01 AA029798NIAAA NIH HHS R43 AA021331NIAAA NIH HHS R44 AA021331
6 · The paper itself

Abstract

Introduction: The phosphodiesterase 4 (PDE4) inhibitor, rolipram, has beneficial effects on tissue inflammation, injury and fibrosis, including in the liver. Since rolipram elicits significant CNS side-effects in humans (ie, nausea and emesis), our group developed a fusogenic lipid vesicle (FLV) drug delivery system that targets the liver to avoid adverse events. We evaluated whether this novel liposomal rolipram formulation reduces emesis. Methods: C57Bl/6J male mice were used to compare the effect of three doses of free and FLV-delivered (FLVs-Rol) rolipram in a behavioral correlate model of rolipram-induced emesis. Tissue rolipram and rolipram metabolite levels were measured using LC-MS/MS. The effect of FLVs-Rol on brain and liver PDE4 activities was evaluated. Results: Low and moderate doses of free rolipram significantly reduced anesthesia duration, while the same doses of FLVs-Rol had no effect. However, the onset and duration of adverse effects (shortening of anesthesia period) elicited by a high dose of rolipram was not ameliorated by FLVs-Rol. Post-mortem analysis of brain and liver tissues demonstrated that FLVs affected the rate of rolipram uptake by liver and brain. Lastly, administration of a moderate dose of FLVs-Rol attenuated endotoxin induced PDE4 activity in the liver with negligible effect on the brain. Discussion: The findings that the low and moderate doses of FLVs-Rol did not shorten the anesthesia duration time suggest that FLV delivery prevented critical levels of drug from crossing the blood-brain barrier (BBB) to elicit CNS side-effects. However, the inability of high dose FLVs-Rol to prevent CNS side-effects indicates that there was sufficient unencapsulated rolipram to cross the BBB and shorten anesthesia duration. Notably, a moderate dose of FLVs-Rol was able to decrease PDE4 activity in the liver without affecting the brain. Taken together, FLVs-Rol has a strong potential for clinical application for the treatment of liver disease without side effects.

Indexed as

Phosphodiesterase 4 InhibitorsTandem Mass SpectrometryAnimalsChromatography, LiquidMaleMiceMice, Inbred C57BLRolipramVomitingPhosphodiesterase 4 InhibitorsRolipramliposomesliverPDE4rolipramside-effects

Identifiers

PMID35535222
PMCPMC9078351
OpenAlexW4225277596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.