Developmental toxicity evaluation of oral aluminum in rats

ABSTRACT

The present study was designed to elucidate the adverse effects of the orally administered aluminum [Al] on the growing fetus and consequently on the animal wealth in our country. This aim has been achieved by studying the teratogenic, perinatal and postnatal effects of aluminum chloride when administered orally at 345 mg/kg body weight to female rats during organogenesis, fetal and/ or lactation periods. The results showed that Al chloride exposure on days 6-15 of gestation produced a significantly higher percentage of postimplantation death, resorptions, morphological, visceral and skeletal anomalies in the obtained fetuses compared to the control group. In addition, the live fetuses' percentage, mean fetal body weight and placental weights were significantly decreased. The obtained data revealed also that Al chloride exposure on 6[th] day of gestation till weaning induced significant increase in the percentage of dams showed delayed birth date and signs of dystocia. In addition, it induced a significant increase in the percentage of postimplantation loss, dead fetuses; fetuses showing neurobehavioral and respiratory symptoms and those born with morphological abnormalities. Moreover, it decreased the live/ birth, survival and viability indices and weight gain of these fetuses compared with control. The Al- induced effects on the obtained fetuses from Al chloride treated dams through lactation period included significant increase in the percentage of postnatal deaths, fetal stunted growth with a significantly increased percentage of nervous and respiratory symptoms prior to death. Consequently, the survival and viability indices were reduced. Moreover, the weight gain during lactation was significantly reduced. Brain examination of the obtained fetuses from all exposed dams throughout this study showed different histopathological changes. It can be concluded that Al chloride exposure of female rats during gestation and/ or lactation periods caused teratogenic, perinatal and postnatal adverse effects on their progeny