• 한국독성학회:학술대회논문집
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• 한국독성학회 2003년도 춘계학술대회 논문집
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• pp.45-45
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• 2003

The present study was conducted to investigate the potential embryo-fetal toxicity of Artesunate, an antimalarial drug, in Sprague-Dawley rats. The test item was orally administered by gavage to pregnant rats (22 females per group) from days 6 through 15 of gestation at dose levels of 0, 2, 4 and 8 mg/kg/ day. (omitted)

• 한국독성학회:학술대회논문집
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• 한국독성학회 2003년도 추계학술대회
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• pp.157-157
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• 2003

Recently we have demonstrated that a 12-day s.c. dose of 2-Bromopropane(2-BP) to pregnant mice during pregnancy resulted in significant developmental toxicity at dose levels of above 1250 mg/kg/day. However, the cause and effect relationship between maternal and developmental toxicities could not be elucidated in the previous study.(omitted)

• 한국수정란이식학회지
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• 제9권2호
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• pp.173-180
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• 1994

The present experirnents on cryopreservation were carried out to investigate effect of solution toxicity, equilibration time and cell stages on the post-thaw survival of mouse morulae and blastocyst embryos cryopreserved by vitrification in EFS solution. The mouse embryos were exposed to the EFS solution in one step at room temperature, kept in the EFS solution during different period for toxicity test, vitrified in liquid nitrogen and thawed rapidly. After the mouse morulae embryos were exposed to EFS solution for 2 and 5 ruin. at room temperature and then they were washed in 0.5 M sucrose solution and basal mediurn(D-PBS + 10% FCS), they were cultured to examined cryoprotectant toxicity induced injury during exposure, most of embryos developed to expanded blastocysts(100 and 90.0%). However, when the exposure time was extended to 10 and 20 min, these development rates dropped dramatically in 10 ruin. (75.0%) and 20 ruin. (4.5%), respectively. When the compacted morulae were vitrified in EFS solution after equilibration for 2 and 5 min, the embryos have developed to normal blastocyst following thawing, washing and culture processes was 89.3 and 89.6%. However, when the exposure time was expanded to 10 ruin, this survival rate dropped to 68.8%. When the blastocyst were vitrified in EFS solution after equilibration for 2, 5 and 10 minutes, the survival rate of embryos which developed to normal blastocyst following thawing and culture processing were 58.5, 46.7 and 22.4%, respectively. The optimal time of equilibration of mouse morula and blastocysts in EFS solution seemed o be 2 and 5 ruin.

• 약학회지
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• 제42권5호
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• pp.534-539
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• 1998

Effect of recombinant human epidermal growth factor (rhEGF, DWP401) on fetal external, visceral and skeletal malformation during organogenesis was examined. Pregnant Sprauge-Daw ley rats were administered with 0.2, 1 and 5mg/kg/day subcutaneously on gestation day 6 through 16. Dams were sacrified at 20th day of gestation. Materal body weight, food consumption and clinical observation were not changed. Significant dose-dependent increase of relative and absolute liver weight were observed in the treatment group, whereas other organ weights were not changed. Placental weight of 1 and 5mg/kg/day group and number of resorption in 5mg/kg/day treatment group were significantly increased. External and visceral malformation of fetuses were not observed with treatment. However, skeletal variations(increase of asymmetry sternebrae, decrease of dumb-bell and asymmetry sternbrae at 5mg/kg/day, and fused stemebrae at 5mg/kg/day) were observed. These results showed that rhEGF (DWP401) may not have embryo and/or fetal developmental toxicity effect in rats.

• 한국환경성돌연변이발암원학회:학술대회논문집
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• 한국환경성돌연변이발암원학회 2004년도 춘계학술대회
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• pp.115-115
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• 2004

• 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.

• 한국환경생태학회지
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• 제26권5호
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• pp.675-681
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• 2012

국내에 서식하는 개구리의 배아를 이용하여 화학물질의 독성평가에 대한 가능성을 파악하기 위해 FETAX(Frog Embryo Teratogenesis Assay-Xenopus) 기법에 따라 청개구리(Hyla japonica)의 배아를 배양하면서 $Cu^{2+}$과 Tebuconazole의 효과를 probit 분석법으로 조사하였다. 그 결과, $Cu^{2+}$과 Tebuconazole의 농도에 의존하여 유생의 체장 길이는 감소하고 치사율과 기형율은 증가하였으며 $Cu^{2+}$과 Tebuconazole의 teratogenic concentration($EC_{50}$)은 각각 0.05, 5.0mg/L을 나타내었고 embryo lethal concentrations($LC_{50}$)은 0.16, 39.1mg/L을 나타내었다. Teratogenic index($TI=LC_{50}/EC_{50}$)는 $Cu^{2+}$의 경우 3.0, Tebuconazole의 경우 7.7을 나타내어 청개구리 배아 발달에 최기형성 물질로 작용함을 알 수 있었다. 이상의 결과들로 보아 $Cu^{2+}$과 Tebuconazole 모두 낮은 농도에서 청개구리 배아의 발달에 민감하게 반응하였으며 다량의 배아 확보가 가능하였고 배양이 용이하였으며 치사율, 기형율, 성장률, 기형양상 등이 기존의 연구들과 비교하였을 때 유사한 결과를 나타내어 청개구리 배아를 활용한 시험기법은 화학물질 및 환경오염물질의 독성검정에 활용할 수 있을 것으로 판단된다.

• Toxicological Research
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• 제16권3호
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• pp.229-238
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• 2000

The purpose of reproductive toxicity studies is to evaluate all effects resulting from paternal or maternal exposure that interfere with conception, development, birth, and maturation of offspring. In 1966, the US Food and Drug Administration (US FDA) published guidelines for a three-segment study for drug testing to examine adverse effects on fertility and pregnancy. Three segments were proposed: Segment I, Study of Fertility and General Reproductive Performance, to provide information on breeding, fertility, nidation, parturition, neonatal effects and lactation: Segment II, Teratological study, to provide information on embryo toxicity and teratogenicity: and Segment III. perinatal and Postnatal Study, to provide information on late fetal development, labour and delivery, neonatal viability, and growth and lactation. The classic guideline is still used to this day with only monor modification throughout the world. In the present review, the principles and methods of reproductive toxicity studies are discussed with special attention given to scientific issues.

• Toxicological Research
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• 제14권2호
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• pp.193-203
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• 1998

The toxicity of DA-125. a new anthracycline anticancer agent, on the male reproductive system was studied in Sprague-Dawley rats. Forty male rats were rando$m\ell$y assigned to Jour groups with ten rats in each group and given single intraveneous doses of DA-125 at dose levels of 0. 12.5. 25. and 50 mg/kg body weight. On day 56 after treatment the animals were allowed to mate. and their male reproductive Junctions and organs were examined in detail. Copulated females were sacrificed on day 20 of gestation for examination of embryo-fetal development. One out of ten rats in the 50 mg/kg group died on day 12 after treatment. Clinical signs such as emaciation. sedation, anorexia. swelling. dark material around eye. alopecia. and diarrhea were observed in the 25 and/or 50 mg/kg groups. Reduction in the body weight gain. decrease in the absolute weights of testes. epididymis and seminal vesicles. and/or decrease in the number of testicular sperm heads were also found. Although histopathological changes such as atrophy of seminiferous tubules. loss or decrease of spermatogenic cells. exfoliation of spermatogenic cells. vacuolization of Sertoli cells. decrease of sperm. and/or increase of necrotic spermatogenic cells in epididymal ducts were observed. no adverse effects on the motility and morphology of epididymal sperm. copulation index. fertility index. and embryo-fetal development were detected in the 25 and 50 mg/kg groups. There were no evidences of male reproductive toxicity in the 12.5 mg/kg group. These results show that single intravenouse doses of DA-125 produce significant dose-related testicular atrophy. histopathological changes. and oligozoospermia in rats and $LD_{10}$ for DA-125 appears to be 50 mg/kg body weight.

• 한국응용과학기술학회지
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• 제40권3호
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• pp.570-578
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• 2023

커피 부산물을 이용하여 대체실험동물 모델인 제브라피쉬 배아 독성 및 미백 효능에 대한 실험을 진행하였다. 커피 부산물 추출물을 처리한 배아 독성 실험의 결과 24, 48, 72hpf에서 125ppm 농도에서는 각각 3, 3, 5%로 응고율을 나타냈다. 배아의 부화율은 최고 농도인 125ppm에서 73%를 나타냈다. 제브라피쉬 치어의 심장 박동수 실험에서 72hpf 후 심박수가 125ppm 농도에서 153회/60s'로 확인되었다. 음성대조군은 148회/60s'으로 대조군의 비해 심박수의 변화가 크지 않았으며, 낮은 독성을 나타냈다. 또한 미백효능을 평가한 결과 커피 부산물 추출물의 농도가 증가할수록 멜라닌 형성이 저해되는 것으로 나타났다. 본 연구 결과를 통해 천연 유래 부산물 소재가 화장품 원료로 활용할 수 있다는 가능성을 제안하며, 천연 부산물의 부가가치를 높이는 연구 예시로서 화장품 산업에 활용되기를 기대한다.