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Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats
CONTEXT: Glycoside-based standardized fenugreek seed extract (SFSE-G) demonstrated promising efficacy in animal models of immune-inflammatory conditions. AIM: The present study was aimed at embryo-fetal development toxicity evaluation of SFSE-G in Wistar rats as per guideline No. 414 of the Organiza...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407105/ https://www.ncbi.nlm.nih.gov/pubmed/28479738 http://dx.doi.org/10.4103/0973-1296.203978 |
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author | Deshpande, Pallavi O. Mohan, Vishwaraman Pore, Mukul P. Gumaste, Shailesh Thakurdesai, Prasad A. |
author_facet | Deshpande, Pallavi O. Mohan, Vishwaraman Pore, Mukul P. Gumaste, Shailesh Thakurdesai, Prasad A. |
author_sort | Deshpande, Pallavi O. |
collection | PubMed |
description | CONTEXT: Glycoside-based standardized fenugreek seed extract (SFSE-G) demonstrated promising efficacy in animal models of immune-inflammatory conditions. AIM: The present study was aimed at embryo-fetal development toxicity evaluation of SFSE-G in Wistar rats as per guideline No. 414 of the Organization for Economic Co-operation and Development (OECD). MATERIAL AND METHODS: Mated female rats were randomized into four groups of 30 each and received oral doses of either SFSE-G at 250, 500, and 1000 mg/kg or vehicle (water) during the period of gestation (postconception) from gestational day 5 (GD5, an implantation day) until 1 day before cesarean sections (GD19). Maternal food consumption, body weights, and clinical signs were monitored throughout gestation. Cesarean sections were performed on GD20 and fetal observations (gravid uterine weight, implantation sites, early and late resorptions, live and dead fetuses) were recorded. Live fetuses were weighed and examined for external, visceral, and skeletal variations and malformations. RESULTS: None of the SFSE-G-treated groups showed maternal and embryo–fetal toxicity. Occasional and incidental skeletal and visceral malformations were observed and found to be spontaneous and unrelated to the treatment. CONCLUSION: Oral exposure of SFSE-G during the prenatal period did not show significant maternal and embryo-fetal toxicity up to a dose of 1000 mg/kg in rats. Therefore, the no-observed-adverse-effect level for SFSE-G for prenatal oral exposure was considered to be 1000 mg/kg. SUMMARY: Prenatal toxicity of glycoside-based standardized fenugreek seed extract (SFSE-G) was evaluated. SFSE-G was orally gavaged to rats on gestational days 5-19 with a limit dose of 1000 mg/kg. SFSE-G did not show maternal or developmental toxicity. SFSE-G showed NOAEL of 1000 mg/kg for prenatal exposure in female rats. Abbreviations used: CPCSEA: Committee for the Purpose of Control and Supervision of Experiments on Animals; GD: Gestational day; GRAS: Generally recognized as safe; HED: Human equivalent dose; NOAEL: No-observed adverse effect levels; OECD: Organization for Economic Co-operation and Development; SFSE-G: glycoside-based standardized fenugreek seed extract. |
format | Online Article Text |
id | pubmed-5407105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54071052017-05-05 Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats Deshpande, Pallavi O. Mohan, Vishwaraman Pore, Mukul P. Gumaste, Shailesh Thakurdesai, Prasad A. Pharmacogn Mag Original Article CONTEXT: Glycoside-based standardized fenugreek seed extract (SFSE-G) demonstrated promising efficacy in animal models of immune-inflammatory conditions. AIM: The present study was aimed at embryo-fetal development toxicity evaluation of SFSE-G in Wistar rats as per guideline No. 414 of the Organization for Economic Co-operation and Development (OECD). MATERIAL AND METHODS: Mated female rats were randomized into four groups of 30 each and received oral doses of either SFSE-G at 250, 500, and 1000 mg/kg or vehicle (water) during the period of gestation (postconception) from gestational day 5 (GD5, an implantation day) until 1 day before cesarean sections (GD19). Maternal food consumption, body weights, and clinical signs were monitored throughout gestation. Cesarean sections were performed on GD20 and fetal observations (gravid uterine weight, implantation sites, early and late resorptions, live and dead fetuses) were recorded. Live fetuses were weighed and examined for external, visceral, and skeletal variations and malformations. RESULTS: None of the SFSE-G-treated groups showed maternal and embryo–fetal toxicity. Occasional and incidental skeletal and visceral malformations were observed and found to be spontaneous and unrelated to the treatment. CONCLUSION: Oral exposure of SFSE-G during the prenatal period did not show significant maternal and embryo-fetal toxicity up to a dose of 1000 mg/kg in rats. Therefore, the no-observed-adverse-effect level for SFSE-G for prenatal oral exposure was considered to be 1000 mg/kg. SUMMARY: Prenatal toxicity of glycoside-based standardized fenugreek seed extract (SFSE-G) was evaluated. SFSE-G was orally gavaged to rats on gestational days 5-19 with a limit dose of 1000 mg/kg. SFSE-G did not show maternal or developmental toxicity. SFSE-G showed NOAEL of 1000 mg/kg for prenatal exposure in female rats. Abbreviations used: CPCSEA: Committee for the Purpose of Control and Supervision of Experiments on Animals; GD: Gestational day; GRAS: Generally recognized as safe; HED: Human equivalent dose; NOAEL: No-observed adverse effect levels; OECD: Organization for Economic Co-operation and Development; SFSE-G: glycoside-based standardized fenugreek seed extract. Medknow Publications & Media Pvt Ltd 2017-01 2017-04-07 /pmc/articles/PMC5407105/ /pubmed/28479738 http://dx.doi.org/10.4103/0973-1296.203978 Text en Copyright: © 2017 Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Deshpande, Pallavi O. Mohan, Vishwaraman Pore, Mukul P. Gumaste, Shailesh Thakurdesai, Prasad A. Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats |
title | Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats |
title_full | Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats |
title_fullStr | Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats |
title_full_unstemmed | Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats |
title_short | Prenatal Developmental Toxicity Study of Glycosides-based Standardized Fenugreek Seed Extract in Rats |
title_sort | prenatal developmental toxicity study of glycosides-based standardized fenugreek seed extract in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407105/ https://www.ncbi.nlm.nih.gov/pubmed/28479738 http://dx.doi.org/10.4103/0973-1296.203978 |
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