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Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models

Indigenous preparations(IPs) for a male child is reported from some parts of India. The present study aims to explore the effects of IPs for sex selection or sex selection drugs (SSDs) on pregnancy outcomes in rat models. SSDs contain Bryonia laciniosa, Quercus infectoria and Putranjiva roxburghii a...

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Autores principales: Bandyopadhyay Neogi, Sutapa, Roy, Dilip Kumar, Sachdeva, Anand Kamal, Sharma, Rashmi, Gupta, Rakesh, Ganguli, Abhijit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102661/
https://www.ncbi.nlm.nih.gov/pubmed/32292714
http://dx.doi.org/10.1016/j.jtcme.2019.09.005
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author Bandyopadhyay Neogi, Sutapa
Roy, Dilip Kumar
Sachdeva, Anand Kamal
Sharma, Rashmi
Gupta, Rakesh
Ganguli, Abhijit
author_facet Bandyopadhyay Neogi, Sutapa
Roy, Dilip Kumar
Sachdeva, Anand Kamal
Sharma, Rashmi
Gupta, Rakesh
Ganguli, Abhijit
author_sort Bandyopadhyay Neogi, Sutapa
collection PubMed
description Indigenous preparations(IPs) for a male child is reported from some parts of India. The present study aims to explore the effects of IPs for sex selection or sex selection drugs (SSDs) on pregnancy outcomes in rat models. SSDs contain Bryonia laciniosa, Quercus infectoria and Putranjiva roxburghii along with other ingredients. METHODS: An experimental design with successfully mated female rats were randomized into control and treatment groups. Phase 1 had 2 interventional arms while phase 2 had 3 interventional arms (12 rats/arm) besides control arm. In phase-1, pregnant females were dosed two SSDs(1000 mg/kg) on gestation days 1–5 whereas, in phase-2, on gestation days 6–19 to correlate the effect of the SSDs (500/1000/1500 mg/kg) consumption during different stages of pregnancy. Pregnant females were observed for clinical signs following treatment. The rats were sacrificed one day before expected day of delivery for evaluation. Pregnancy rate, gestation index, number of corpora lutea, and litter size were assessed. Foetuses were examined for sex, skeletal and soft tissue alterations. DISCUSSION AND CONCLUSION: In phase 1, no appreciable findings were there with SSD exposure. In phase 2, intrauterine growth and survival of foetuses were affected when SSDs were administered during organogenesis period. Decreased number of live foetuses and increased incidence of early and late resorption, reduced fetal growth with significant alteration in skeleton and viscera were found in treatment groups in a dose-dependent manner. This correlates well with findings from observational studies in pregnant women. However, such treatment at any dose did not effect sex differentiation.
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spelling pubmed-71026612020-03-31 Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models Bandyopadhyay Neogi, Sutapa Roy, Dilip Kumar Sachdeva, Anand Kamal Sharma, Rashmi Gupta, Rakesh Ganguli, Abhijit J Tradit Complement Med Original Article Indigenous preparations(IPs) for a male child is reported from some parts of India. The present study aims to explore the effects of IPs for sex selection or sex selection drugs (SSDs) on pregnancy outcomes in rat models. SSDs contain Bryonia laciniosa, Quercus infectoria and Putranjiva roxburghii along with other ingredients. METHODS: An experimental design with successfully mated female rats were randomized into control and treatment groups. Phase 1 had 2 interventional arms while phase 2 had 3 interventional arms (12 rats/arm) besides control arm. In phase-1, pregnant females were dosed two SSDs(1000 mg/kg) on gestation days 1–5 whereas, in phase-2, on gestation days 6–19 to correlate the effect of the SSDs (500/1000/1500 mg/kg) consumption during different stages of pregnancy. Pregnant females were observed for clinical signs following treatment. The rats were sacrificed one day before expected day of delivery for evaluation. Pregnancy rate, gestation index, number of corpora lutea, and litter size were assessed. Foetuses were examined for sex, skeletal and soft tissue alterations. DISCUSSION AND CONCLUSION: In phase 1, no appreciable findings were there with SSD exposure. In phase 2, intrauterine growth and survival of foetuses were affected when SSDs were administered during organogenesis period. Decreased number of live foetuses and increased incidence of early and late resorption, reduced fetal growth with significant alteration in skeleton and viscera were found in treatment groups in a dose-dependent manner. This correlates well with findings from observational studies in pregnant women. However, such treatment at any dose did not effect sex differentiation. Elsevier 2019-09-17 /pmc/articles/PMC7102661/ /pubmed/32292714 http://dx.doi.org/10.1016/j.jtcme.2019.09.005 Text en © 2019 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Bandyopadhyay Neogi, Sutapa
Roy, Dilip Kumar
Sachdeva, Anand Kamal
Sharma, Rashmi
Gupta, Rakesh
Ganguli, Abhijit
Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models
title Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models
title_full Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models
title_fullStr Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models
title_full_unstemmed Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models
title_short Evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models
title_sort evidence of prenatal toxicity of herbal based indigenous formulations for sex selection in rat models
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102661/
https://www.ncbi.nlm.nih.gov/pubmed/32292714
http://dx.doi.org/10.1016/j.jtcme.2019.09.005
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