Teratogenic effects of the anticonvulsant gabapentin in mice

<p><b>INTRODUCTION</b>We aim to study and elucidate the safety profile of the antiepileptic doses of gabapentin during pregnancy, and to evaluate gabapentin-induced murine fetotoxicity at different dose levels.</p><p><b>METHODS</b>A total of 60 pregnant mice, divided into 12 groups of five mice each, were exposed to gabapentin in four different doses of 0 (control), 113, 226, or 452 mg/kg body weight per day, at three different gestational stages including early gestation (1-6 days), mid-gestation (7-12 days), and late gestation (13-17 days). The pregnant mice were euthanized on day 18 of gestation, and foetuses were examined for teratogenic manifestations. Their brains were dissected and examined for gross changes, malformations, histological changes, and quantitative protein estimation.</p><p><b>RESULTS</b>Foetal resorptions were observed in all treated groups with gabapentin administration at early gestation (1-6 days), and mid-gestation (7-12 days). On the other hand, growth retardation along with stunting in size of live foetuses were observed in all the mid-gestation (7-12 days), and late gestation (13-17 days) treated groups. Various gross malformations were observed with all the three doses (113, 226, and 452 mg/kg body weight per day) when gabapentin was administered at mid-gestation (7-12 days). The same trends were confirmed by gross and microscopic examination of brains along with quantitative protein estimation.</p><p><b>CONCLUSION</b>Gabapentin should not be prescribed during pregnancy, as no therapeutic dose of gabapentin is safe during this period as far as the foetal well-being is concerned.</p>

Cytological effects of the aqueous fruit extracts of emblica officinalis on allium sativum root tips

The cytological effects of E. Officinalis fruit extract on root tips of Allium Sativum have been studied; three concentrations of the extract [1, 5 and 10 percent] for 12 h treatment and for three recovery periods [24, 48 and 72 h] were used, All the three concentrations suppress cell division significantly and cause chromosomal abnormalities such as scattering, stickiness, bridges, fragments and laggards. The lower concentration appears to be more effective and the effects are stable during the recovery periods. This fruit extract appears to be mutagenic and have mitodepressive and mitoclastic effects