Evidence map›Paper›PMID 30498346›Full record

ArticleInternational journal of nanomedicine2018

Gold nanorods/siRNA complex administration for knockdown of PARP-1: a potential treatment for perinatal asphyxia.

Valentina Vio, Ana L Riveros, Andrea Tapia-Bustos, Carolyne Lespay-Rebolledo, Ronald Perez-Lobos, Luis Muñoz, Paola Pismante, Paola Morales, Eyleen Araya, Natalia Hassan and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  3. Nucleic acid drug vectors for diagnosis and treatment of brain diseases.Signal transduction and targeted therapy · 2023
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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

12 authors at 5 institutions in 2 countries.

Valentina VioDepartment of Pharmacological and Toxicology Chemistry, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago, Chile, mkogan@ciq.uchile.cl.
Ana L RiverosDepartment of Pharmacological and Toxicology Chemistry, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago, Chile, mkogan@ciq.uchile.cl.
Andrea Tapia-BustosProgram of Molecular and Clinical Pharmacology, Medical Faculty, Universidad de Chile, Santiago, Chile, mhmarschitz@gmail.com.
Carolyne Lespay-RebolledoProgram of Molecular and Clinical Pharmacology, Medical Faculty, Universidad de Chile, Santiago, Chile, mhmarschitz@gmail.com.
Ronald Perez-LobosProgram of Molecular and Clinical Pharmacology, Medical Faculty, Universidad de Chile, Santiago, Chile, mhmarschitz@gmail.com.
Luis MuñozChemical Meteorology Section, Comisión Chilena de Energía Nuclear, Santiago, Chile.
Paola PismanteChemical Meteorology Section, Comisión Chilena de Energía Nuclear, Santiago, Chile.
Paola MoralesProgram of Molecular and Clinical Pharmacology, Medical Faculty, Universidad de Chile, Santiago, Chile, mhmarschitz@gmail.com.
Eyleen ArayaDepartamento de Ciencias Quimicas, Facultad de Ciencias Exactas, Universidad Andres Bello, Santiago, Chile.
Natalia HassanDepartment of Pharmacological and Toxicology Chemistry, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago, Chile, mkogan@ciq.uchile.cl.
Mario Herrera-MarschitzProgram of Molecular and Clinical Pharmacology, Medical Faculty, Universidad de Chile, Santiago, Chile, mhmarschitz@gmail.com.
Marcelo J KoganDepartment of Pharmacological and Toxicology Chemistry, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago, Chile, mkogan@ciq.uchile.cl.
Universidad de Santiago de Chile · CLComisión Chilena de Energía Nuclear · CLUniversidad Andrés Bello · CLAdvanced Center for Chronic Diseases · CLUniversity of Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPerinatal asphyxia interferes with neonatal development, resulting in long-term deficits associated with systemic and neurological diseases. Despite the important role of poly (ADP-ribose) polymerase 1 (PARP-1) in the regulation of gene expression and DNA repair, overactivation of PARP-1 in asphyxia-exposed animals worsens the ATP-dependent energetic crisis. Inhibition of PARP-1 offers a therapeutic strategy for diminishing the effects of perinatal asphyxia.

methodsWe designed a nanosystem that incorporates a specific siRNA for PARP-1 knockdown. The siRNA was complexed with gold nanorods (AuNR) conjugated to the peptide CLPFFD for brain targeting.

resultsThe siRNA was efficiently delivered into PC12 cells, resulting in gene silencing. The complex was administered intraperitoneally in vivo to asphyxia-exposed rat pups, and the ability of the AuNR-CLPFFD/siRNA complex to reach the brain was demonstrated.

conclusionThe combination of a nanosystem for delivery and a specific siRNA for gene silencing resulted in effective inhibition of PARP-1 in vivo.

Indexed as

Gene Knockdown TechniquesAnimalsAnimals, NewbornAsphyxiaBrainCell SurvivalEndocytosisFemaleGoldHydrodynamicsNanotubesPC12 CellsPeptidesPoly(ADP-ribose) PolymerasesPregnancyRatsGoldPeptidesPoly(ADP-ribose) PolymerasesRNA, Small Interferinggold nanorodsin vivo administrationneonatal hypoxiaPARP-1 knockdownPC12ratssiRNA delivery

Identifiers

PMID30498346
PMCPMC6207385
OpenAlexW2898465879

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.