Evidence map›Paper›PMID 37574117›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2023

Rolipram-loaded PgP nanoparticle reduces secondary injury and enhances motor function recovery in a rat moderate contusion SCI model.

Jun Gao, Min Kyung Khang, Zhen Liao, Ken Webb, Megan Ryan Detloff, Jeoung Soo Lee

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Article
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

6 authors at 2 institutions in 1 country.

Jun GaoDrug Design Delivery and Development (4D) Laboratory, Department of Bioengineering, Clemson University, Clemson, SC, USA.
Min Kyung KhangDrug Design Delivery and Development (4D) Laboratory, Department of Bioengineering, Clemson University, Clemson, SC, USA.
Zhen LiaoDrug Design Delivery and Development (4D) Laboratory, Department of Bioengineering, Clemson University, Clemson, SC, USA. Electronic address: liao4@g.clemson.edu.
Ken WebbMicroEnvironmental Laboratory, Department of Bioengineering, Clemson University, Clemson, SC, USA. Electronic address: kwebb@clemson.edu.
Megan Ryan DetloffDepartment of Neurobiology & Anatomy, Marion Murray Spinal Cord Research Center, College of Medicine, Drexel University, Philadelphia, PA 19129, USA. Electronic address: mrd64@drexel.edu.
Jeoung Soo LeeDrug Design Delivery and Development (4D) Laboratory, Department of Bioengineering, Clemson University, Clemson, SC, USA. Electronic address: ljspia@clemson.edu.
Clemson University · USDrexel University · US

Funding

Targeted Nano-therapeutics for Neural RegenerationP20GM103444 · NIGMS · CLEMSON UNIVERSITY · PI MARKWALD, ROGER R, VYAVAHARE, NAREN R · 2012 to 2018
$14.9M
Validation of Targeting Macrophage-Mediated Events in the DRG to Alleviate Chronic Spinal Cord Injury PainR01NS097880 · NINDS · DREXEL UNIVERSITY · PI MEGAN R DETLOFF · 2017 to 2026
$4.0M
Neuron-specific nanotherapeutics for spinal cord injury repairR01NS111037 · NINDS · CLEMSON UNIVERSITY · PI LEE, JEOUNG SOO · 2019 to 2022
$1.3M
NIGMS NIH HHS P20 GM103444NINDS NIH HHS R01 NS097880NINDS NIH HHS R01 NS111037
6 · The paper itself

Abstract

Spinal cord injury (SCI) results in immediate axonal damage and cell death, as well as a prolonged secondary injury consist of a cascade of pathophysiological processes. One important aspect of secondary injury is activation of phosphodiesterase 4 (PDE4) that leads to reduce cAMP levels in the injured spinal cord. We have developed an amphiphilic copolymer, poly (lactide-co-glycolide)-graft-polyethylenimine (PgP) that can deliver Rolipram, the PDE4 inhibitor. The objective of this work was to investigate the effect of rolipram loaded PgP (Rm-PgP) on secondary injury and motor functional recovery in a rat moderate contusion SCI model. We observed that Rm-PgP can increase cAMP level at the lesion site, and reduce secondary injury such as the inflammatory response by macrophages/microglia, astrogliosis by activated astrocytes and apoptosis as well as improve neuronal survival at 4 weeks post-injury (WPI). We also observed that Rm-PgP can improve motor functional recovery after SCI over 4 WPI.

Indexed as

ContusionsNanoparticlesSpinal Cord InjuriesAnimalsRatsRats, Sprague-DawleyRecovery of FunctionRolipramRolipramcAMPMotor functionNeuropathic painPgP nanocarrierRolipramSecondary injurySpinal cord injury

Identifiers

PMID37574117
PMCPMC12207785
OpenAlexW4385752784

What OpenQuestion holds

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LicenceTDM
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.