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Article
Peer-Review Record

Antiepileptic Effect of Neuroaid® on Strychnine-Induced Convulsions in Mice

Pharmaceuticals 2022, 15(12), 1468; https://doi.org/10.3390/ph15121468
by Ahmed Salim Mahmood 1,*, Afaq M. Ammoo 1, Mayssam Hussein Mohammed Ali 1, Tiba M. Hameed 1, Hany A. Al-Hussaniy 2, Abdulla Amer Abbas Aljumaili 3, Mohammed Hussein Alaa Al-Fallooji 4 and Ali Hakim Kadhim 1
Reviewer 2: Anonymous
Pharmaceuticals 2022, 15(12), 1468; https://doi.org/10.3390/ph15121468
Submission received: 11 October 2022 / Revised: 13 November 2022 / Accepted: 23 November 2022 / Published: 26 November 2022
(This article belongs to the Special Issue Therapeutic Agents for Neurological Disorders 2022)

Round 1

Reviewer 1 Report

The manuscript provides interesting information, nevertheless some aspects should be addressed, i.e. please provide information about mice sex (males/females). An interesting addition to the study could be to investigate the oxidative status of brain tissues and the level of lipid peroxidation?

Author Response

 

"Please see the attachment"

Author Response File: Author Response.pdf

Reviewer 2 Report

In the present study, the authors demonstrated an anticonvulsive effect of NeuroAid in a mouse model of seizure induced by strychnine. Several measures including seizure onset, duration, number of seizures, and mortality were assessed. Additionally, it was found that the seizure-induced mRNA overexpression of hippocampal GluR1 as well as brain histopathological changes were reduced by NeuroAid and also topiramate as control anti-seizure medication. Overall, the study is well designed and well written. I have few minor recommendations to improve the quality of paper.

Comment 1. An explanation about different glutamate receptors (especially, NMDAR and AMPA) and their subtypes in the CNS and their role in epilepsy is necessary in the Introduction. This helps readers understand better the rationale behind choosing GluR1 as target receptor in this study as well as they would know which glutamatergic receptors GluR1 belongs to!

Comment 2. The abbreviation for glutamate receptor should be either GluR or GlutR throughout the manuscript, not both. Please unify this in all manuscript.

Comment 3. If it is not against the journal guideline for authors, it would be better to have material and methods section prior to results section.

Author Response

"Please see the attachment."

Author Response File: Author Response.pdf

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