Evidence map›Paper›PMID 32020309›Full record

ArticlePharmaceutical research2020

Neuroprotective Effect of New Nanochelating-Based Nano Complex, ALZc3, Against Aβ

Ramin Karimi-Sales, Mehrafarin Ashiri, Maryam Hafizi, Somayeh Kalanaky, Amir Hossein Maghsoudi, Saideh Fakharzadeh, Nader Maghsoudi, Mohammad Hassan Nazaran

Abstract read
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Article in Pharmaceutical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. 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

8 authors at 2 institutions in 1 country.

Ramin Karimi-SalesNeuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mehrafarin AshiriNeuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Maryam HafiziDepartment of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran.
Somayeh KalanakyDepartment of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran.
Amir Hossein MaghsoudiDepartment of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran.
Saideh FakharzadehDepartment of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran.
Nader MaghsoudiNeuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. nmaghsoudi@sbmu.ac.ir.
Mohammad Hassan NazaranDepartment of Research and Development, Sodour Ahrar Shargh Company, Tehran, Iran. mnazaran@nanochelatingtechnology.com.
Shahid Beheshti University of Medical Sciences · IRIslamic Azad University, Science and Research Branch · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe current drugs for Alzheimer's disease (AD) are only used to slow or delay the progression of the pathology. So using a novel technology is a necessity to synthesize more effective medications to control this most common cause of dementia. In this study, using nanochelating technology, ALZc3 was synthesized and its therapeutic effects were evaluated in comparison with memantine on a well-known rat model of AD, which is based on Amyloid-βeta (Aβ) injection into the brain. MATERIALS AND

methodsAβ (1-42) was injected bilaterally into the CA1 area of the hippocampus of male rats and then animals were treated daily by oral administration of Alz-C3, memantine or their vehicles. Activities of antioxidant enzymes catalase and superoxide dismutase (SOD), glutathione (GSH) and malondialdehyde (MDA) levels, as well as Bax/Bcl-2 ratio, caspase-3 activation, and TNF-α expression were evaluated 7 days after Aβ injection. Finally, learning and memory of the rats were assessed by Morris water maze test.

resultsALZc3 and memantine improved memory impairment and antioxidant activity and reduced TNF-α expression, caspase-3 activity and Bax/Bcl-2 ratio in the rat's hippocampus. The results showed a superiority of ALZC3 compared to memantine in reducing caspase-3, increasing CAT activity in Aβ (1-42)-injected groups and improving apoptosis factor in healthy mice.

conclusionThese results indicated that ALZc3 could significantly prevent the memory impairment and Aβ (1-42) toxicity. Thus, ALZc3 could be a promising novel anti-AD agent.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsCaspase 3GlutathioneHippocampusMagnesiumMaleMalondialdehydeMemantineModels, AnimalMorris Water Maze TestNanoparticlesNeuroprotective AgentsOxidative StressProto-Oncogene Proteins c-bcl-2Amyloid beta-PeptidesCaspase 3GlutathioneMagnesiumMalondialdehydeMemantineNeuroprotective AgentsProto-Oncogene Proteins c-bcl-2Superoxide DismutaseTumor Necrosis Factor-alphaALZc3alzheimer’s diseasedendrimernanochelating technologynano complex

Identifiers

PMID32020309
OpenAlexW3004880038

What OpenQuestion holds

Textmetadata
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.