Evidence map›Paper›PMID 27642592›Full record

ArticleBioMed research international2016

Myoinositol Attenuates the Cell Loss and Biochemical Changes Induced by Kainic Acid Status Epilepticus.

Lia Tsverava, Tamar Lordkipanidze, Eka Lepsveridze, Maia Nozadze, Marina Kikvidze, Revaz Solomonia

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Frontiers in neuroscience · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Myo-Inositol Limits Kainic Acid-Induced Epileptogenesis in Rats.International journal of molecular sciences · 2022
    Article
  9. 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 1 institution in 1 country.

Lia TsveravaInstitute of Chemical Biology, Ilia State University, 3/5 K. Cholokashvili Avenue, 0162 Tbilisi, Georgia.ORCID 0000-0001-5545-8009
Tamar LordkipanidzeInstitute of Chemical Biology, Ilia State University, 3/5 K. Cholokashvili Avenue, 0162 Tbilisi, Georgia; I. Beritashvili Center of Experimental Biomedicine, 14 L. Gotua Street, 0160 Tbilisi, Georgia.ORCID 0000-0002-5567-2678
Eka LepsveridzeInstitute of Chemical Biology, Ilia State University, 3/5 K. Cholokashvili Avenue, 0162 Tbilisi, Georgia.ORCID 0000-0001-8991-4666
Maia NozadzeInstitute of Chemical Biology, Ilia State University, 3/5 K. Cholokashvili Avenue, 0162 Tbilisi, Georgia; I. Beritashvili Center of Experimental Biomedicine, 14 L. Gotua Street, 0160 Tbilisi, Georgia.ORCID 0000-0002-7713-5945
Marina KikvidzeInstitute of Chemical Biology, Ilia State University, 3/5 K. Cholokashvili Avenue, 0162 Tbilisi, Georgia.
Revaz SolomoniaInstitute of Chemical Biology, Ilia State University, 3/5 K. Cholokashvili Avenue, 0162 Tbilisi, Georgia; I. Beritashvili Center of Experimental Biomedicine, 14 L. Gotua Street, 0160 Tbilisi, Georgia.ORCID 0000-0003-4798-6762
Ilia State University · GE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identification of compounds preventing or modifying the biochemical changes that underlie the epileptogenesis process and understanding the mechanism of their action are of great importance. We have previously shown that myoinositol (MI) daily treatment for 28 days prevents certain biochemical changes that are triggered by kainic acid (KA) induced status epilepticus (SE). However in these studies we have not detected any effects of MI on the first day after SE. In the present study we broadened our research and focused on other molecular and morphological changes at the early stages of SE induced by KA and effects of MI treatment on these changes. The increase in the amount of voltage-dependent anionic channel-1 (VDAC-1), cofilin, and caspase-3 activity was observed in the hippocampus of KA treated rats. Administration of MI 4 hours later after KA treatment abolishes these changes, whereas diazepam treatment by the same time schedule has no significant influence. The number of neuronal cells in CA1 and CA3 subfields of hippocampus is decreased after KA induced SE and MI posttreatment significantly attenuates this reduction. No significant changes are observed in the neocortex. Obtained results indicate that MI posttreatment after KA induced SE could successfully target the biochemical processes involved in apoptosis, reduces cell loss, and can be successfully used in the future for translational research.

Indexed as

AnimalsBlotting, WesternCalibrationCaspase 3Cell CountHippocampusInositolKainic AcidMaleMitochondrial MembranesNerve Tissue ProteinsNeuronsRats, WistarStatus EpilepticusCaspase 3InositolKainic AcidNerve Tissue Proteins

Identifiers

PMID27642592
PMCPMC5011512
OpenAlexW2517426177

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.