Evidence map›Paper›PMID 34830481›Full record

ReviewInternational journal of molecular sciences2021

PSD-95: An Effective Target for Stroke Therapy Using Neuroprotective Peptides.

Lola Ugalde-Triviño, Margarita Díaz-Guerra

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 4% 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.

NCT05849805 nacompletednot on this mapstarted 2023, after this paper: background citation

The Feasibility, Safety and Efficacy of Y-3 Injection Through Skull Bone Marrow Bypassing Blood-brain Barrier in the Treatment of Acute Malignant Middle Cerebral Artery Infarction(SOLUTION)

TypeinterventionalSponsorBeijing Tiantan HospitalRan2023 to 2024Enrolled20ConditionsStroke, Acute IschemicArmsIntracalvaria bone marrow injection, Conventional treatment
NCT07514949 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

The Feasibility and Safety of RK-4 Injection Bypassing Blood-brain Barrier in the Treatment of Acute Large Hemispheric Infarction Using Intracalvariosseous Injection Device

TypeinterventionalSponsoryilong WangRan2026 to 2026Enrolled6ConditionsStroke, Acute Ischemic Stroke, Blood-Brain BarrierArmsRK-4 ICO injection, Conventional treatment
3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 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

2 authors at 1 institution in 1 country.

Lola Ugalde-TriviñoInstituto de Investigaciones Biomédicas "Alberto Sols", Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), Arturo Duperier 4, 28029 Madrid, Spain.ORCID 0000-0002-0911-8043
Margarita Díaz-GuerraInstituto de Investigaciones Biomédicas "Alberto Sols", Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid (CSIC-UAM), Arturo Duperier 4, 28029 Madrid, Spain.ORCID 0000-0002-4478-0956
Consejo Superior de Investigaciones Científicas · ES

Funding

Agencia Estatal de Investigación PID2019-105784RB-100/AEI/10. 13039/501100011033
6 · The paper itself

Abstract

Therapies for stroke have remained elusive in the past despite the great relevance of this pathology. However, recent results have provided strong evidence that postsynaptic density protein-95 (PSD-95) can be exploited as an efficient target for stroke neuroprotection by strategies able to counteract excitotoxicity, a major mechanism of neuronal death after ischemic stroke. This scaffold protein is key to the maintenance of a complex framework of protein interactions established at the postsynaptic density (PSD) of excitatory neurons, relevant to neuronal function and survival. Using cell penetrating peptides (CPPs) as therapeutic tools, two different approaches have been devised and advanced to different levels of clinical development. First, nerinetide (Phase 3) and AVLX-144 (Phase 1) were designed to interfere with the coupling of the ternary complex formed by PSD-95 with GluN2B subunits of the N-methyl-D-aspartate type of glutamate receptors (NMDARs) and neuronal nitric oxide synthase (nNOS). These peptides reduced neurotoxicity derived from NMDAR overactivation, decreased infarct volume and improved neurobehavioral results in different models of ischemic stroke. However, an important caveat to this approach was PSD-95 processing by calpain, a pathological mechanism specifically induced by excitotoxicity that results in a profound alteration of survival signaling. Thus, a third peptide (TP95

Indexed as

CalpainCell-Penetrating PeptidesDisks Large Homolog 4 ProteinHumansIschemic StrokeNeuroprotective AgentsProtein Interaction MapsCalpainCell-Penetrating PeptidesDisks Large Homolog 4 ProteinNeuroprotective AgentsAVLV-144calpaincell-penetrating peptidesexcitotoxicityischemiaNA-1nerinetideneuroprotectionPSD-95strokeTP95414

Identifiers

PMID34830481
PMCPMC8618101
OpenAlexW3215402778

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.