Evidence map›Paper›PMID 26790434›Full record

ArticleJournal of molecular neuroscience : MN2016

Determination of the Best Concentration of Streptozotocin to Create a Diabetic Brain Using Histological Techniques.

Marzieh Dehghan-Shasaltaneh, Nasser Naghdi, Samira Choopani, Leila Alizadeh, Bahram Bolouri, Ali Masoudi-Nejad, Gholam Hossein Riazi

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Article in Journal of molecular neuroscience : MN, 2016. 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
0.6field-weighted citation impact, top 30% 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, 16 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

7 authors at 3 institutions in 1 country.

Marzieh Dehghan-ShasaltanehLaboratory of Neuro-Organic Chemistry, Institute of Biochemistry and Biophysics (IBB), University of Tehran, Tehran, Iran.
Nasser NaghdiDepartment of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran.
Samira ChoopaniDepartment of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran.
Leila AlizadehDepartment of Physiology and Pharmacology, Pasteur Institute of Iran, Tehran, Iran.
Bahram BolouriSchool of Advanced Medical Technologies, Iran University of Medical Sciences, Tehran, Iran.
Ali Masoudi-NejadLaboratory of Systems Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, 1417614411, Iran.
Gholam Hossein RiaziLaboratory of Neuro-Organic Chemistry, Institute of Biochemistry and Biophysics (IBB), University of Tehran, Tehran, Iran. ghriazi@ut.ac.ir.
Pasteur Institute of Iran · IRUniversity of Tehran · IRIran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is one of the most important disorders among neurodegenerative diseases which is characterized by neurofibrillary tangles and senile plagues. Intercerebroventricular (ICV) streptozotocin administration is a form of sAD which was applied to examine different factors following AD. Previous reports used different doses of streptozotocin (STZ) to create Alzheimer's model, but no standard dose has been introduced. Therefore, we decided to investigate the best concentration of STZ to induce a diabetic brain with lowest mortality rate and high severity of destruction. We treated rats with three different doses of STZ (STZ 1.5, 2.25, and 3 mg/kg, ICV). Spatial memory for treated rats was evaluated by Morris water maze (MWM). Locomotor activities of rats were assessed by open field test. Histological observation such as immunohistochemistry, immunofluorescence, and Nissl staining were performed on the brain especially in CA1, CA3, and DG regions of hippocampal neurons at residues P-ser396 and P-ser404. Our data suggest that although the percentage hyperphosphorylation of tau protein by injection of STZ 3 mg/kg was about 10 % more than STZ 2.25 mg/kg compared to the control group, we considered the latter doses due to no effect on motor activities and enhance the number of glial cells.

Indexed as

Alzheimer DiseaseAnimalsDiabetes Mellitus, ExperimentalDiabetic NeuropathiesDisease Models, AnimalDose-Response Relationship, DrugHippocampusLocomotionMaleMaze LearningRatsRats, WistarStreptozocinToxicity TestsStreptozocinAlzheimer’s diseaseHyperphosphorylated tauImmunofluorescenceImmunohistochemistryNissl staining

Identifiers

PMID26790434
OpenAlexW2296466390

What OpenQuestion holds

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Registered trials

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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.