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Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor
BACKGROUND: The aim of study was to evaluate the single oral dose and 28 day repeated oral administration toxicity profile of the synthetic compound Gαq-RGS2 signaling inhibitor, (1-(5-chloro-2-hydroxyphenyl)-3-(4-(trifluoromethyl)phenyl)-1 H-1,2,4-triazol-5(4 H)-one) as per OECD guideline 425 (2008...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314442/ https://www.ncbi.nlm.nih.gov/pubmed/34311782 http://dx.doi.org/10.1186/s42826-021-00093-1 |
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author | Beladiya, Jayesh V. Mehta, Anita A. |
author_facet | Beladiya, Jayesh V. Mehta, Anita A. |
author_sort | Beladiya, Jayesh V. |
collection | PubMed |
description | BACKGROUND: The aim of study was to evaluate the single oral dose and 28 day repeated oral administration toxicity profile of the synthetic compound Gαq-RGS2 signaling inhibitor, (1-(5-chloro-2-hydroxyphenyl)-3-(4-(trifluoromethyl)phenyl)-1 H-1,2,4-triazol-5(4 H)-one) as per OECD guideline 425 (2008a) and 407 (2008b), respectively. RESULTS: In acute toxicity study, a single oral dose administration of Gαq-RGS2 signaling inhibitor did not show any mortality at doses of 5, 50, 300 and 2000 mg/kg within 24 h and 14 days. The treatment of Gαq-RGS2 signaling inhibitor at dose 10 and 100 mg/kg for 28 days did not show any mortality, significant changes in the increase of body weight, various organ damage markers, hematological parameters, relative organ/body weight ratio and microscopic anatomical texture of essential organs as compared to vehicle and normal control. CONCLUSIONS: A single oral administration of Gαq-RGS2 signaling inhibitor up to dose of 2000 mg/kg in mice and repeated administration of Gαq-RGS2 signaling inhibitor at higher dose 100 mg/kg for 28 days in the rats is safe. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42826-021-00093-1. |
format | Online Article Text |
id | pubmed-8314442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83144422021-07-27 Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor Beladiya, Jayesh V. Mehta, Anita A. Lab Anim Res Research BACKGROUND: The aim of study was to evaluate the single oral dose and 28 day repeated oral administration toxicity profile of the synthetic compound Gαq-RGS2 signaling inhibitor, (1-(5-chloro-2-hydroxyphenyl)-3-(4-(trifluoromethyl)phenyl)-1 H-1,2,4-triazol-5(4 H)-one) as per OECD guideline 425 (2008a) and 407 (2008b), respectively. RESULTS: In acute toxicity study, a single oral dose administration of Gαq-RGS2 signaling inhibitor did not show any mortality at doses of 5, 50, 300 and 2000 mg/kg within 24 h and 14 days. The treatment of Gαq-RGS2 signaling inhibitor at dose 10 and 100 mg/kg for 28 days did not show any mortality, significant changes in the increase of body weight, various organ damage markers, hematological parameters, relative organ/body weight ratio and microscopic anatomical texture of essential organs as compared to vehicle and normal control. CONCLUSIONS: A single oral administration of Gαq-RGS2 signaling inhibitor up to dose of 2000 mg/kg in mice and repeated administration of Gαq-RGS2 signaling inhibitor at higher dose 100 mg/kg for 28 days in the rats is safe. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42826-021-00093-1. BioMed Central 2021-07-26 /pmc/articles/PMC8314442/ /pubmed/34311782 http://dx.doi.org/10.1186/s42826-021-00093-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Beladiya, Jayesh V. Mehta, Anita A. Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor |
title | Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor |
title_full | Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor |
title_fullStr | Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor |
title_full_unstemmed | Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor |
title_short | Acute and 28-days subacute toxicity studies of Gαq-RGS2 signaling inhibitor |
title_sort | acute and 28-days subacute toxicity studies of gαq-rgs2 signaling inhibitor |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314442/ https://www.ncbi.nlm.nih.gov/pubmed/34311782 http://dx.doi.org/10.1186/s42826-021-00093-1 |
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