Abstract

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 (P < 0.01) 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 (P < 0.01) 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.

Highlights

  • Human beings and wild life are constantly exposed to environmental contaminants

  • The pregnant females administered with Ni+2 during organogenetic period revealed an almost significant (P < 0.05) decrease in diet consumption after 92.25 mg Ni/kg b.wt

  • Similar pattern of decrease was evident in intake of water

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Summary

Introduction

Human beings and wild life are constantly exposed to environmental contaminants. Nickel widely used in industries for various processes such as catalysts, dye mordant, electroplating, and so forth [1] has become a serious problem throughout the world. Cardiovascular disease, kidney diseases, asthma, inflammatory reactions, and hematopoiesis have been reported on exposure to nickel compounds [6,7,8]. A case report of occupational exposure of Russian women to nickel hydrometallurgy refinery plant resulted in complications during pregnancy with high incidence of spontaneous and threatening abortions, congenital malformations, and cardiovascular and musculoskeletal defects [9,10,11,12]. Embryotoxicity and fetotoxicity have been reported using nickel salts [17]. Keeping in view the adverse impact of Ni upon human health, a study was planned to evaluate the embryotoxic and teratogenic potentials of Ni+2 as NiCl2⋅6H2O during organogenetic period in Swiss albino mice

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