Evidence map›Paper›PMID 31235716›Full record

ArticleScientific reports2019

gH625-liposomes as tool for pituitary adenylate cyclase-activating polypeptide brain delivery.

Giuseppina Iachetta, Annarita Falanga, Yves Molino, Maxime Masse, Francoise Jabès, Yasmine Mechioukhi, Vincenza Laforgia, Michel Khrestchatisky, Stefania Galdiero, Salvatore Valiante

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 28 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

10 authors at 4 institutions in 2 countries.

Giuseppina IachettaDepartment of Biology, University of Naples "Federico II", Via Cinthia, 80126, Naples, Italy.
Annarita FalangaDepartment of Agricultural Sciences, University of Naples "Federico II", Via Università, 100, 80055, Portici, Italy.
Yves MolinoVect-Horus SAS, Marseille, France.
Maxime MasseVect-Horus SAS, Marseille, France.
Francoise JabèsVect-Horus SAS, Marseille, France.
Yasmine MechioukhiVect-Horus SAS, Marseille, France.
Vincenza LaforgiaDepartment of Biology, University of Naples "Federico II", Via Cinthia, 80126, Naples, Italy.
Michel KhrestchatiskyAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, Marseille, France.
Stefania GaldieroCiRPEB- University of Naples "Federico II", Via Mezzocannone 16, 80134, Napoli, Italy.ORCID http://orcid.org/0000-0002-7849-7024
Salvatore ValianteDepartment of Biology, University of Naples "Federico II", Via Cinthia, 80126, Naples, Italy. valiante@unina.it.
Centro Interuniversitario di Ricerca sui Peptidi Bioattivi · ITUniversity of Naples Federico II · ITCentre National de la Recherche Scientifique · FRIstituto Nazionale Biostrutture e Biosistemi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The blood-brain barrier (BBB) regulates the traffic of molecules into the central nervous system (CNS) and also limits the drug delivery. Due to their flexible properties, liposomes are an attractive tool to deliver drugs across the BBB. We previously characterized gH625, a peptide derived from Herpes simplex virus 1. The present study investigates the efficiency of liposomes functionalized on their surface with gH625 to promote the brain uptake of neuroprotective peptide PACAP (pituitary adenylate cyclase-activating polypeptide). Using a rat in vitro BBB model, we showed that the liposomes preparations were non-toxic for the endothelial cells, as assessed by analysis of tight junction protein ZO1 organization and barrier integrity. Next, we found that gH625 improves the transfer of liposomes across endothelial cell monolayers, resulting in both low cellular uptake and increased transport of PACAP. Finally, in vivo results demonstrated that gH625 ameliorates the efficiency of liposomes to deliver PACAP to the mouse brain after intravenous administration. gH625-liposomes improve both PACAP reaching and crossing the BBB, as showed by the higher number of brain cells labelled with PACAP. gH625-liposomes represent a promising strategy to deliver therapeutic agents to CNS and to provide an effective imaging and diagnostic tool for the brain.

Indexed as

Drug Delivery SystemsAdministration, IntravenousAnimalsBiological TransportBlood-Brain BarrierCells, CulturedEndothelial CellsLiposomesMicePeptidesPituitary Adenylate Cyclase-Activating PolypeptideRatsRats, WistarViral Envelope ProteinsgH625 peptide, Herpes simplex virus type ILiposomesPeptidesPituitary Adenylate Cyclase-Activating PolypeptideViral Envelope Proteins

Identifiers

PMID31235716
PMCPMC6591382
OpenAlexW2954231282

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.