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Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring

OBJECTIVE(S): This study aimed to assess the impact of orally-administrated thymoquinone (TQ) during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring. MATERIALS AND METHODS: In this experimental study, 64 pregnant rats were divided into groups according t...

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Autores principales: Abdollahzade Fard, Amin, Saboory, Ehsan, Tahmazi, Yaghob, Rasmi, Yousef, Dindarian, Sina, Parsamanesh, Negin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894635/
https://www.ncbi.nlm.nih.gov/pubmed/33643567
http://dx.doi.org/10.22038/ijbms.2020.47479.10930
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author Abdollahzade Fard, Amin
Saboory, Ehsan
Tahmazi, Yaghob
Rasmi, Yousef
Dindarian, Sina
Parsamanesh, Negin
author_facet Abdollahzade Fard, Amin
Saboory, Ehsan
Tahmazi, Yaghob
Rasmi, Yousef
Dindarian, Sina
Parsamanesh, Negin
author_sort Abdollahzade Fard, Amin
collection PubMed
description OBJECTIVE(S): This study aimed to assess the impact of orally-administrated thymoquinone (TQ) during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring. MATERIALS AND METHODS: In this experimental study, 64 pregnant rats were divided into groups according to the doses of TQ (0,10, 40, and 80 mg/kg) and gestational week (GW2 and GW3) of TQ administration. After parturition, the pups were counted, weighed, and assessed for pentylenetetrazol (PTZ)-induced seizure on postnatal days 14 (P14) and 21 (P21). RESULTS: In GW2 treated rats, TQ 40 mg/kg decreased seizure stages compared with control only on P14 while seizure duration significantly decreased on P14 and P21. On P14, 40 mg/kg TQ increased latency to the first seizure but decreased it on P21. In addition, 40 mg/kg dose decreased body weight (BW) on P1, P14, and P21 compared with 10 mg/kg dose and control groups. The dose of 80 mg/kg led to a complete pregnancy loss. In GW3 treated rats, only 10 mg/kg TQ decreased the seizure stages on P14 and P21. None of the doses had a significant effect on seizure duration and latency. TQ 40 and 80 mg/kg led to a low birth weight while increased BW on P14 and P21. A 50% decrease in litter size was observed in 80 mg/kg treated rats. CONCLUSION: Prenatal TQ may have anticonvulsant effects. The effects of TQ on BW of offspring depend on its dose and administration time. Also, a high dose of TQ at GW2 can be severely toxic for pregnancy.
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spelling pubmed-78946352021-02-26 Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring Abdollahzade Fard, Amin Saboory, Ehsan Tahmazi, Yaghob Rasmi, Yousef Dindarian, Sina Parsamanesh, Negin Iran J Basic Med Sci Original Article OBJECTIVE(S): This study aimed to assess the impact of orally-administrated thymoquinone (TQ) during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring. MATERIALS AND METHODS: In this experimental study, 64 pregnant rats were divided into groups according to the doses of TQ (0,10, 40, and 80 mg/kg) and gestational week (GW2 and GW3) of TQ administration. After parturition, the pups were counted, weighed, and assessed for pentylenetetrazol (PTZ)-induced seizure on postnatal days 14 (P14) and 21 (P21). RESULTS: In GW2 treated rats, TQ 40 mg/kg decreased seizure stages compared with control only on P14 while seizure duration significantly decreased on P14 and P21. On P14, 40 mg/kg TQ increased latency to the first seizure but decreased it on P21. In addition, 40 mg/kg dose decreased body weight (BW) on P1, P14, and P21 compared with 10 mg/kg dose and control groups. The dose of 80 mg/kg led to a complete pregnancy loss. In GW3 treated rats, only 10 mg/kg TQ decreased the seizure stages on P14 and P21. None of the doses had a significant effect on seizure duration and latency. TQ 40 and 80 mg/kg led to a low birth weight while increased BW on P14 and P21. A 50% decrease in litter size was observed in 80 mg/kg treated rats. CONCLUSION: Prenatal TQ may have anticonvulsant effects. The effects of TQ on BW of offspring depend on its dose and administration time. Also, a high dose of TQ at GW2 can be severely toxic for pregnancy. Mashhad University of Medical Sciences 2021-01 /pmc/articles/PMC7894635/ /pubmed/33643567 http://dx.doi.org/10.22038/ijbms.2020.47479.10930 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Abdollahzade Fard, Amin
Saboory, Ehsan
Tahmazi, Yaghob
Rasmi, Yousef
Dindarian, Sina
Parsamanesh, Negin
Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring
title Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring
title_full Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring
title_fullStr Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring
title_full_unstemmed Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring
title_short Effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring
title_sort effect of orally-administrated thymoquinone during pregnancy on litter size, pentylenetetrazol-induced seizure, and body weight in rat offspring
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894635/
https://www.ncbi.nlm.nih.gov/pubmed/33643567
http://dx.doi.org/10.22038/ijbms.2020.47479.10930
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