• 생약학회지
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• 제13권3호
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• pp.116-121
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• 1982

In order to investigate the side-effects of crude drugs, twenty drugs have been tested for the teratogenic effect in rats. Among seven drugs contained alkaloid as their ingredients, no one showed teratogenic effect, but Veratri rhizoma showed embryo-toxic as revealed by severe retardation in growth of the fetuses. The other thirteen drugs which have been used freguently in oriental medicines exhibited no teratogenic effect. Cyclophosphamide used as a reference compound showed severe malformation and retardation in the growth of rat fetuses. These findings suggest that the drug extracts adopted for the study might have no teratogenic effect in the rats.

• 생물정신의학
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• 제5권2호
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• pp.283-287
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• 1998

The mother was 24 years old, primipara, and had been taking carbamazepine 400mg(serum concentration $5.0-8.5{\mu}g/ml$) during pregnancy without any clinical seizures. A male baby with physical malformation was delivered on week 39. The malformation is extradigit(polydactily) on X-ray of right foot and left mild hydronephrosis on ultrasonography and renal scan with radioactive material. We reported this rare case and reviewed related articles about teratogenic effect of carbamazepine, mechanism of action and prevention of teratogenesis.

• Toxicological Research
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• 제14권3호
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• pp.357-363
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• 1998

The teratogenic potential of the anticonvulsant drug phenytoin (PHT) has been well documented both in the human and in the experimental animals. However there are few reports on the effects of PHT on embryonic development in rats in vitro. The present study was performed to evaluate the teratogenic effects of PHT using whole-embryo culture system in rats. Sprague-Dawley rat embryos were explanted on gestational day (GD) 9.5 and cultured for 48 hrs in the immediately centrifuged and heat-inactivated rat serum containing 0,25,50, or $100{\mu}g$ PHT/mL. At the end of culture period the embryos were scored for morphological development according to the procedure of Van Maele-Fabry, and their total protein contents were determined. At 100 ${\mu}$g/mL of culture medium. PHT caused significant reduction in developmental score and protein content of embryos and a high incidence morphological abnormalities (100%). Characteristic malformations included altered yolk and embryonic circulation, craniofacial hypoplasia, neural tube schisis, branchial arch defects, abnormal ratation, and limb bud hypoplasia, among others. There were no adverse effects on embryonic growth and development at concentrations of 25 and 50 ${\mu}$g /mL of culture medium. The results indicated that the dysmorphogenic effect of PHT on cultured embryos is due to a direct interference with embryonic development.

• 한국환경생태학회지
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• 제30권4호
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• pp.705-711
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• 2016

국내에 서식하는 두꺼비의 배아를 이용하여 화학물질의 독성평가에 대한 가능성을 파악하기 위해 FETAX(Frog Embryo Teratogenesis Assay-Xenopus) 기법에 따라 두꺼비(Bufo gargarizans)의 배아를 배양하면서 Zn과 Benomyl의 효과를 probit 분석법으로 조사하였다. 그 결과, Zn과 Benomyl의 농도에 의존하여 유생의 체장 길이는 감소하고 치사율과 기형율은 증가하였으며 Zn과 Benomyl의 teratogenic concentration($EC_{50}$)은 각각 2.3, $1.0mg/{\ell}$을 나타내었고 embryo lethal concentrations($LC_{50}$)은 10.3, $6.9mg/{\ell}$을 나타내었다. Teratogenic index($TI=LC_{50}/EC_{50}$)는 Zn의 경우 4.4, Benomyl의 경우 6.7을 나타내어 Zn과 Benomyl은 두꺼비 배아 발달에 최기형성 물질로 작용함을 알 수 있었다. 이상의 결과들로 보아 Zn과 Benomyl 모두 낮은 농도에서 두꺼비 배아발달에 민감하게 반응하였다. 이는 다량의 배아 확보가 가능하며 배양이 용이하고 치사율, 기형율, 성장률, 기형양상 등을 기존의 연구들과 비교하였을 때 유사한 결과를 나타내어 두꺼비 배아를 활용한 시험기법은 화학물질 및 환경오염물질의 독성검정에 활용할 수 있을 것으로 판단된다.

• Toxicological Research
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• 제11권1호
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• pp.37-42
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• 1995

Effect of cadmium on the early amphibian development was analyzed through FETAX (Frog Embryo Teratogenesis Assay: Xenopus). Embryos manifested concentration-dependent mortality and realformations; shortage of anterior-posterior axis gut realformation, ocular anomalies, bent notochord, misshapen dorsal fin, and derreal blisters. The treatment with 1.5ppm cadmium solution caused 100% mortality and concentration of lppm did not kill the embryos that caused 100% anomaly. The teratogenic index (TI = LC50 /EC50) was 2.8 indicating that $CdCl_2$ is teratogenic for Xenopus laevis. Embryos that were pulsetreated with at early to late blastula stage (St. 3-9) and mid to late blastula stage (St. 6-10) showed relatively strong resistance to cadmium, but the embryos treated at gastrula stage (St. 10-13) showed high mortality. And the embryos treated at tailbud stage (after St. 25) showed highest mortality of any other early stages. Effects of temperature were studied through pulse- treatment during gastrula stage at $20^{\circ}C$ and $30^{\circ}C$. The embryos treated with 7.5ppm at $30^{\circ}C$ and 15ppm at $20^{\circ}C$ caused 100% mortality respectively, indicating that higher temperature had more severe toxic effect. One of the most peculiar effect of cadmium at gastrulation was distortion of the tail. The probable cause of toxic effect of Cd was discussed.

• 대한수의학회지
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• 제34권4호
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• pp.821-831
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• 1994

Phenytoin(PHT), a commonly prescribed anticonvulsant, has been known as a teratogen in experimental animals and human. However, PHT has strain-specific teratogenic effects for mice and human. Dimethyl sulfoxids(DMSO) has been known to antagonize the teratogenic effects of secalonic acid D, a toxic mold metabolite that has similar teratogenic effects to PHT. Therefore, this study was performed to examine the embryopathic effects of PHT in terms of treatment period and the antiteratogenic effect of DMSO in ICR mice. PHT(75mg/kg, BW) was administered intrapetitoneally on day 10, 10-11 and 10-12 of gestation with or without DMSO(2ml/kg, BW), and the fetal malformation was observed on day 18. Major malformation of fetuses treated with PHT on day 10, 10-11 and 10-12 of gestation was cleft palate, and the percentages of fetus with cleft palate were 14.5%, 31.7% and 51.7%, respectively. Also, there was a significant decrease of cleft palate from 51.7% in PHT alone group to 30.8% in PHT plus DMSO group. Our findings suggest that cleft palate is one of major malformation by PHT treatment in ICR mouse and DMSO has strong antiteratogenic effect.

• 한국환경생태학회지
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• 제34권3호
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• pp.207-215
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• 2020

농약류 3종의 독성평가를 위해 FETAX(Frog Embryo Teratogenesis Assay-Xenopus) 기법에 따라 국내에 서식 중인 두꺼비(Bufo gargarizans)의 배아를 배양하면서 Benomyl(살균제), Carbofuran(살충제), Thiobencarb(제초제)의 영향을 probit 분석법으로 조사하였다. 그 결과, Benomyl, Carbofuran, Thiobencarb의 농도에 의존하여 유생의 체장 길이는 감소하고 치사율과 기형율은 증가하였다. Benomyl, Carbofuran, Thiobencarb의 teratogenic concentration(EC₅₀)은 각각 1.03, 8.74, 4.98mg/ℓ을 나타내어 Benomyl이 기형 유발에 가장 민감하게 반응하였으며, embryo lethal concentrations(LC₅₀)은 7.26, 560.72, 16.87mg/ℓ을 나타내어 Benomyl이 가장 낮은 농도에서 배아가 치사되는 것으로 나타났다. Teratogenic index (TI=LC₅₀/EC₅₀)는 Benomyl 7.05, Carbofuran 64.16, Thiobencarb 3.39를 나타내어 TI값이 모두 기형유발물질로 판단되는 기준인 1.5이상으로 시험에 사용된 농약류 3종은 최기형성 물질로 판단된다. Carbofuran이 가장 강력한 최기형성물질로 작용함을 알 수 있었으며, 농약류가 두꺼비 및 양서류의 배아 발달에 미치는 영향과 그 작용기작을 규명하기 위해서는 보다 구체적인 연구가 필요할 것으로 판단된다.

• 환경생물
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• 제39권3호
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• pp.311-318
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• 2021

국내에 서식하는 개구리들의 배아를 이용하여 살균제인 tebucoanzole의 독성을 파악하기 위해 FETAX (Frog Embryo Teratogenesis Assay-Xenopus) 기법에 따라 두꺼비(Bufo gargarizans), 청개구리(Hyla japonica), 참개구리(Pelophylax nigromaculatus)의 배아를 배양하면서 tebuconazole의 효과를 probit 분석법으로 조사하였다. 그 결과, tebuconazole의 농도에 의존하여 유생의 체장 길이는 감소하고 치사율과 기형률은 증가하였으며 tebuconazole의 teratogenic concentration (EC₅₀)은 각각 34.4, 10.6, 14.9 mg kg^-1을 나타내었고 embryo lethal concentrations (LC₅₀)은 75.4, 38.2, 39.6 mg kg^-1 을 나타내었다. Teratogenic index (TI=LC₅₀/EC₅₀)는 각각 2.19, 3.58, 2.65을 나타내어 두꺼비, 청개구리, 참개구리 배아 발달에 최기형성 물질로 작용함을 알 수 있었다. 이상의 결과들로 보아 tebuconazole은 낮은 농도에서 개구리 배아의 발달에 민감하게 반응하였으며 치사율, 기형률, 성장률, 기형양상 등을 기존의 연구들과 비교하였을 때 유사한 결과를 나타내어 국내 서식하는 개구리류 배아발달에 영향을 미칠 수 있는 것으로 여겨지며, 종에 따라 치사율 및 기형률, 기형양상 등의 차이를 나타내는 원인 등을 명확히 파악하기 위해서 종 특이적 특성 등을 규명하는 연구가 더 필요할 것으로 여겨진다.

• Biomolecules & Therapeutics
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• 제30권6호
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• pp.562-569
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• 2022

Etretinate, an acitretin metabolite, has a long retention duration in adipose tissues with a teratogenic potential. FDA advises a contraceptive period of at least three years after discontinuing acitretin. However, the effect of accumulated etretinate in adipose tissues on fetus is unknown. Although the teratogenic threshold for serum concentration of etretinate has been presented as higher than 2 ng/mL, that of acitretin is unknown. To examine factors affecting body retention of acitretin and etretinate, effects of acitretin dosage, acitretin-taking duration, elapsed time after stopping acitretin, age, sex, concomitant alcohol consumption, and foods and supplements rich in vitamin A intake on serum concentrations of acitretin and etretinate were analyzed in 14 acitretin-taken patients and 58 controls without taking acitretin or etretinate. Serum concentrations of acitretin, but not etretinate, tended to be inversely related to the discontinuation duration. They were also related to old age. Different from a published result that alcohol consumption could promote the metabolism of acitretin into etretinate, alcohol intake did not affect serum concentrations of etretinate. Unexpectedly, more frequent intake of vitamin A or provitamin A-rich food and supplements was associated with higher serum acitretin, whereas less frequent intake of vitamin A or provitamin A-rich food and supplements was associated with higher serum levels of etretinate in acitretin-taken patients. Despite preliminary data, inter-individual variations in serum retention of etretinate suggest the necessity of further research before applying the same guidelines to everyone to minimize unnecessary contraception.

• 대한한의학방제학회지
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• 제31권1호
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• pp.21-28
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• 2023

Objective : Scolopendra, a dried body of Scolopendra subspinipes mutilans, is one of Korean medicine. Several reports revealed that Scolopendra has therapeutic effects for arthritis, neuroinflammatory diseases and neuropathic pain. However, the fetal adaptive response or teratogenicity associated with administration of Scolopendra is unclear. Therefore, this study aimed to investigate the fetal toxicity effects that were induced following oral administration of Scolopendra water extract (SWE) in pregnant mice. Methods : The pregnant mice were administrated SWE at dosed of 0, 100, 500 and 1000 mg/kg/day during gestation day 0-18. The mortality, body weight and clinical signs of pregnant mice were observed throughout experimental period. Also, the mortality and malformations in foetus were examined. Results : No meaningful changes were observed in the mortality and clinical signs of pregnant mice between the normal control group and SWE administrated groups. Additionally, there are no significant changes in fetal mortalities, and malformations by SWE administration. conclusion : These results suggest that oral exposure to SWE during pregnancy at oral dosages up to 1000 mg/kg/day did not induce teratogenic toxicity in regard to fetal mortality and morphology.