Showing 4 results for Teratogen
Takzare N, Bakhtiarian A, Saeedi E, Nekoui V,
Volume 68, Issue 10 (1-2011)
Abstract
Background: Alprazolam belongs to benzodiazepine family and is increasingly used these days
by pregnant women. It should be noticed that alprazolam exposure during
pregnancy may have teratogenic effects on the fetus. Till now, limited studies
have been conducted on the teratogenic effect of alprazolam. In this study,
teratogenicity of alprazolam intake during pregnancy and its effects on fetus
development was investigated.
Methods: About 20 virgin rats of known age and weight were
selected. After being pregnant, they were divided into four groups which
contained five animals in each group: Negative and positive control groups. The
case group exposed to 1 to 6
mg/kg/day alprazolam. The fetuses were first studied macroscopically regarding
anomalies, and then histologically and histochemically to inspect the defects
of tissue organogenesis.
Results: Our results show that there was significant difference especially at the dose 6
mg/kg weight and length of the cases compared to the control group.
It appeared that at the dose of 6 mg/kg/day, cleft lip
and palates were seen in the animals. The highest anomalies of limbs were also
seen at the dose of 6 mg/kg/day. The statistical results indicate that
alprazolam intake during the second half of pregnancy can lead to irreversible
anomalies.
Conclusion: Our results indicate that alprazolam in doses higher than 4
mg/kg/day might cause teratogenic effect. It seems that benzodiazepine therapy
among pregnant woman would be better to avoid during the first trimester and
multidrug regimens.
Takzare N, Nikoui V, Ostadhadi S, Nabavi Sma, Bakhtiarian A,
Volume 70, Issue 6 (9-2012)
Abstract
Background: Obsessive-compulsive disorders and depression have a high prevalence during pregnancy therefore, pregnant women may take clomipramine and also take other drugs or consume foods that contain caffeine. As investigations about the teratogenic effects of clomipramine and its concurrent administration with caffeine during organogenesis period are scarce, we aimed to study the teratogenicity of simultaneous administration of clomipramine and caffeine in rat fetus.
Methods: After dividing 42 pregnant rats to several case and control groups, we injected different doses of caffeine and clomipramine to the animals. All the injections were performed on the eighth until the 15th day of pregnancy. We removed the fetuses on the 17th day of pregnancy and studied the morphological features and apparent anomalies of the fetuses macroscopically.
Results: We found a significant rate of mortality, apparent anomalies, abnormal torsion, shrinkage of skin and subcutaneous bleeding in fetuses of rats receiving high doses of caffeine or a combination of caffeine and clomipramine. Statistical analysis of the data revealed a significant increase (P?0.001) in teratogenicity of high doses of caffeine and its combination with clomipramine.
Conclusion: This study implies simultaneous intake of high amounts of caffeine and clomipramine lead to teratogenicity. We recommend pregnant women to avoid uncontrolled consumption of foods that contain caffeine or drugs that contain high amounts of this substance. They should not also take clomipramine with caffeine in the first trimester of pregnancy.
Abdolmaleki A, Zahri S, Bezaatpour A,
Volume 71, Issue 1 (4-2013)
Abstract
Background: Salen metal complexes are used successfully in a wide range of asymmet-ric reactions and important in the pharmaceutical and industry. On the toxicity of salen vanadium oxide (VOsalen) on embryo and cell cultures, little information is available. In the present study, the toxic and teratogenic effects of VOsalen was evaluated against chicken embryos as a animal model and liver and fibroblast cell cultures which was derived from the embryo.
Methods: The VOsalen compound was synthesized. The compound solution was inject-ed in triplicate examination, in the air sac of the eggs, at third day of incubation. Treat-ed and control eggs, on day 19 of incubation opened and embryos were weighted, then mortality rate was recorded. The liver and fibroblast cell culture were treated by this and survival fraction was recorded.
Results: The survived fraction of the embryos depends on the compound concentration. In concentration of 300μM/egg, 36/32% of the embryos survived and the Lethal dose 50% (LD50) was 226/37 μM/egg. Morphological study of the treated embryos showed retarded growth, and skeletal staining showed the deletion of caudal vertebrate. The compound was inhibited liver and fibroblast cells growth with IC50 1047/25 and 1036/82μM respectively. The cytoplasm of treated cells became dense and their interco-nnections were loosed.
Conclusion: The VOsalen compound had low toxic effects against the embryos and the cultured cells at the concentrations. Significant cytotoxic effect was not observed in the treated cells. However the proliferative cells were affected significantly in comparison with the cells which their growth was stopped. The effect of VOsalen compound against replication of liver cells were lower than fibroblast cells.
Iraj Ragerdi Kashani , Mohammad Ansari , Kobra Mehrannia , Kasra Moazzemi , Safura Vardasbi Joybary ,
Volume 71, Issue 8 (11-2013)
Abstract
Background: A number of studies on reproduction have mentioned Origanum Vulgare extract’s ability to reduce mortality rates and improve fertility rates. However, other studies have suggested that it is possible to use Origanum Vulgare extract to induce abortion. The aim of this study was to investigate the effect of different doses of Origanum Vulgare on embryo survival and macroscopic abnormalities in mice.
Methods: In this study, 24 mice Balb/c female weighting approximately 25-30 g were divided into 4 groups. Origanum Vulgare extract was prepared different concentrations (2.5, 12.5, and 25 mg in 0.25 ml distilled water) were administered, by oral gavage, to three experimental groups of mice between day 6 (starting gastrulation) until day 15 of pregnancy (end of organogenesis). The control group consisted of six mice that received 0.25 ml of distilled water daily. On day 16 of study, pregnant mice were anesthetized by chloroform and fetuses were removed and stained with Alcian Blue, Alizarin Red s and microwave irradiation. Morphological and skeletal abnormalities were investigated by light and stereomicroscopes.
Results: The results of this study showed that high doses of the Origanum Vulgare extract significantly decreased the mean number of embryos (100.5, P>0.05), mean number of live embryos (70.5, P>0.05) in each mouse and resulted in significant reduction in mean weight(11848 mg, P>0.05) and crown-rump length(11.90.23 mm, P>0.05) and the overall size of fetuses compared to control group, whereas there was no significant difference between the groups receiving low dose of Origanum Vulgare extract with control group. In addition, under the effect of the Origanum Vulgare extract the subcutaneous bleeding seemed (20.1, P>0.05) significantly more frequent compared to the control group.
Conclusion: Origanum Vulgare extract did not have any positive effect on fetal development and high dosages led to an increased incidence rate of abortion and fetal malformations in the fetuses of women who received it.
