Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic Period
The present study evaluates potential hazardous of nickel (Ni+2 as NiCl2·6H2O) to Swiss albino mice fetus. Ni was administered orally on body weight base from days 6 to 13 of gestation period. Based on LD50, Ni doses (46.125, 92.25, and 184.5) mg Ni/kg b.wt. were used. On day 18 of gestation, uteri...
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2013-01-01
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doaj-72fe5ae340c54aeab5b5ecde31571c252020-11-24T23:06:23ZengHindawi LimitedBioMed Research International2314-61332314-61412013-01-01201310.1155/2013/701439701439Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic PeriodShivi Saini0Neena Nair1Mali Ram Saini2Cell and Molecular Biology Laboratory, Department of Zoology, University of Rajasthan, Jaipur, Rajasthan 302055, IndiaCell and Molecular Biology Laboratory, Department of Zoology, University of Rajasthan, Jaipur, Rajasthan 302055, IndiaRadiation and Cancer Biology Laboratory, Department of Zoology, University of Rajasthan, Jaipur, Rajasthan, IndiaThe present study evaluates potential hazardous of nickel (Ni+2 as NiCl2·6H2O) to Swiss albino mice fetus. Ni was administered orally on body weight base from days 6 to 13 of gestation period. Based on LD50, Ni doses (46.125, 92.25, and 184.5) mg Ni/kg b.wt. were used. On day 18 of gestation, uteri of the sacrificed dams were examined. A dose-dependent decrease () in the body weight of the pregnant females and fetuses during the gestation period was observed. Number of implant sites and placental weight at all the three dose levels was lower compared with their respective control groups. Average number of live fetuses/dams reduced significantly () at 184.5 mg Ni/kg b.wt. with concomitant increase in the percentage of postimplantation death and percentage of resorbed, macerated, and dead fetuses, respectively. Exposure increased the fetal malformations, namely, hydrocephaly, open eyelids, microphthalmia, exophthalmia, club foot, umbilical hernia, and skeletal anomalies. Reduced ossification of nasal, frontal, parietal, intraparietal, and supraoccipital bones, absence/gap between the ribs, reduced/fused sternebrae, vertebral centra, and caudal vertebrae, reduced pelvic elements, absence of carpals, metacarpals, tarsals, metatarsals, and phalanges were distinct. This indicates vulnerability of the mice fetus to nickel during prenatal exposure.http://dx.doi.org/10.1155/2013/701439 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shivi Saini Neena Nair Mali Ram Saini |
spellingShingle |
Shivi Saini Neena Nair Mali Ram Saini Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic Period BioMed Research International |
author_facet |
Shivi Saini Neena Nair Mali Ram Saini |
author_sort |
Shivi Saini |
title |
Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic Period |
title_short |
Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic Period |
title_full |
Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic Period |
title_fullStr |
Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic Period |
title_full_unstemmed |
Embryotoxic and Teratogenic Effects of Nickel in Swiss Albino Mice during Organogenetic Period |
title_sort |
embryotoxic and teratogenic effects of nickel in swiss albino mice during organogenetic period |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2013-01-01 |
description |
The present study evaluates potential hazardous of nickel (Ni+2 as NiCl2·6H2O) to Swiss albino mice fetus. Ni was administered orally on body weight base from days 6 to 13 of gestation period. Based on LD50, Ni doses (46.125, 92.25, and 184.5) mg Ni/kg b.wt. were used. On day 18 of gestation, uteri of the sacrificed dams were examined. A dose-dependent decrease () in the body weight of the pregnant females and fetuses during the gestation period was observed. Number of implant sites and placental weight at all the three dose levels was lower compared with their respective control groups. Average number of live fetuses/dams reduced significantly () at 184.5 mg Ni/kg b.wt. with concomitant increase in the percentage of postimplantation death and percentage of resorbed, macerated, and dead fetuses, respectively. Exposure increased the fetal malformations, namely, hydrocephaly, open eyelids, microphthalmia, exophthalmia, club foot, umbilical hernia, and skeletal anomalies. Reduced ossification of nasal, frontal, parietal, intraparietal, and supraoccipital bones, absence/gap between the ribs, reduced/fused sternebrae, vertebral centra, and caudal vertebrae, reduced pelvic elements, absence of carpals, metacarpals, tarsals, metatarsals, and phalanges were distinct. This indicates vulnerability of the mice fetus to nickel during prenatal exposure. |
url |
http://dx.doi.org/10.1155/2013/701439 |
work_keys_str_mv |
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