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Article
Peer-Review Record

In Vivo Neuropharmacological Effects of Neophytadiene

Molecules 2023, 28(8), 3457; https://doi.org/10.3390/molecules28083457
by Maria L. Gonzalez-Rivera 1,†, Juan Carlos Barragan-Galvez 1,†, Deisy Gasca-Martínez 2, Sergio Hidalgo-Figueroa 3, Mario Isiordia-Espinoza 4 and Angel Josabad Alonso-Castro 1,*
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Reviewer 3: Anonymous
Molecules 2023, 28(8), 3457; https://doi.org/10.3390/molecules28083457
Submission received: 3 March 2023 / Revised: 3 April 2023 / Accepted: 11 April 2023 / Published: 14 April 2023
(This article belongs to the Special Issue Natural Bioactive Compounds and Human Health)

Round 1

Reviewer 1 Report

The manuscript must be corrected as indicated.

Comments for author File: Comments.pdf

Author Response

Please see the attachment

Author Response File: Author Response.pdf

Reviewer 2 Report

Castro and his co-worker reported the "In vivo Neuropharmacological Effects of Neophytadiene" in which they reveal that the NPT has anxiolytic-like activity and anticonvulsant effects without sedative-locomotor effects. By using molecular docking studies they determined the mechanism of neuropharmacological actions using inhibitors like flumazenil and analyzed the interaction of neophytadiene with the GABA receptor which is another addition to in vivo studies and gives a good understanding to readers. Whereas the author should conclude the future direction of the current work in the conclusion. I recommend manuscripts to publish in the given format.

Author Response

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Author Response File: Author Response.pdf

Reviewer 3 Report

 

The manuscript presented In vivo study on the anxiolytic, antidepressant, anticonvulsant and sedative effects of neophytadiene using mouse models. While the study reported interesting observations, more convincing data and conclusions are required to warrant a good publication.

1.      A more scientific rendering of the chemical structure of neophytadiene is recommended.

2.      Number of mice need to be specified in each experiment.

3.  Should neophytadiene exert its pharmacological effect through its interaction with GABAA receptor, would flumazenil have similar effect given it has tighter binding affinity?

4.      Benzodiazepine family have been replaced by more effective compounds with fewer side effects. The less effective neophytadiene with reference to benzodiazepine as demonstrated herein does not lend credence to further investigation on neophytadiene as an anxiolytic candidate.

Author Response

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Author Response File: Author Response.pdf

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