Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice

Swainsonine is the primary toxin in locoweeds. It causes intention tremors, reproductive dysfunction, emaciation, and death. The objective of the present study was to evaluate the potential reproductive and developmental toxicities caused by swainsonine in mice. The treatment groups consisting of th...

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Main Authors: Chenchen Wu, Ke Feng, Dezhang Lu, Dujian Yan, Tiesuo Han, Baoyu Zhao
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2016/6824374
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spelling doaj-e1dbacb4906d428f9132b3d588e830792020-11-24T22:55:57ZengHindawi LimitedBioMed Research International2314-61332314-61412016-01-01201610.1155/2016/68243746824374Reproductive Toxicities Caused by Swainsonine from Locoweed in MiceChenchen Wu0Ke Feng1Dezhang Lu2Dujian Yan3Tiesuo Han4Baoyu Zhao5College of Animal Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, ChinaLhasa City Animal Disease Prevention Control Center, Lhasa 851000, ChinaCollege of Animal Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, ChinaAKS Vocational and Technical College, Aksu, Xinjiang 843000, ChinaAnimal Health Center, Lanzhou Chia Tai Food Co., Ltd., Charoen Pokphand Group, Lanzhou, Gansu 730200, ChinaCollege of Animal Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, ChinaSwainsonine is the primary toxin in locoweeds. It causes intention tremors, reproductive dysfunction, emaciation, and death. The objective of the present study was to evaluate the potential reproductive and developmental toxicities caused by swainsonine in mice. The treatment groups consisting of three generations of mice were given a range of concentrations of swainsonine by intraperitoneal injection (2.50 mg/kg body weight (BW), 1.20 mg/kg BW, 0.60 mg/kg BW, and 0 mg/kg BW). The 0 mg/kg BW group exhibited significantly fewer estrous cycles and an increased number of estrous ones compared to the 2.50 mg/kg BW, 1.20 mg/kg BW, and 0.60 mg/kg BW groups (P<0.05). All three generations of mice treated with swainsonine had significantly higher spleen, liver, and kidney indices and significantly lower body weights compared to the 0 mg/kg BW group (P<0.05). For the first and second generations of treatment group, the copulation indices and the numbers of live pups on postnatal days (PND) 0, 4, and 15 were significantly decreased compared to those of the 0 mg/kg BW group (P<0.05). The fertility and gestation indices of the treatment group of the first generation were significantly increased compared to the 2.50 mg/kg BW, 1.20 mg/kg BW, and 0.60 mg/kg BW groups of the second generation (P<0.05). Cumulatively, these results indicate that swainsonine may cause reproductive and developmental toxicities in mice in both parents and offspring.http://dx.doi.org/10.1155/2016/6824374
collection DOAJ
language English
format Article
sources DOAJ
author Chenchen Wu
Ke Feng
Dezhang Lu
Dujian Yan
Tiesuo Han
Baoyu Zhao
spellingShingle Chenchen Wu
Ke Feng
Dezhang Lu
Dujian Yan
Tiesuo Han
Baoyu Zhao
Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice
BioMed Research International
author_facet Chenchen Wu
Ke Feng
Dezhang Lu
Dujian Yan
Tiesuo Han
Baoyu Zhao
author_sort Chenchen Wu
title Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice
title_short Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice
title_full Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice
title_fullStr Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice
title_full_unstemmed Reproductive Toxicities Caused by Swainsonine from Locoweed in Mice
title_sort reproductive toxicities caused by swainsonine from locoweed in mice
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2016-01-01
description Swainsonine is the primary toxin in locoweeds. It causes intention tremors, reproductive dysfunction, emaciation, and death. The objective of the present study was to evaluate the potential reproductive and developmental toxicities caused by swainsonine in mice. The treatment groups consisting of three generations of mice were given a range of concentrations of swainsonine by intraperitoneal injection (2.50 mg/kg body weight (BW), 1.20 mg/kg BW, 0.60 mg/kg BW, and 0 mg/kg BW). The 0 mg/kg BW group exhibited significantly fewer estrous cycles and an increased number of estrous ones compared to the 2.50 mg/kg BW, 1.20 mg/kg BW, and 0.60 mg/kg BW groups (P<0.05). All three generations of mice treated with swainsonine had significantly higher spleen, liver, and kidney indices and significantly lower body weights compared to the 0 mg/kg BW group (P<0.05). For the first and second generations of treatment group, the copulation indices and the numbers of live pups on postnatal days (PND) 0, 4, and 15 were significantly decreased compared to those of the 0 mg/kg BW group (P<0.05). The fertility and gestation indices of the treatment group of the first generation were significantly increased compared to the 2.50 mg/kg BW, 1.20 mg/kg BW, and 0.60 mg/kg BW groups of the second generation (P<0.05). Cumulatively, these results indicate that swainsonine may cause reproductive and developmental toxicities in mice in both parents and offspring.
url http://dx.doi.org/10.1155/2016/6824374
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