• 한국동물학회지
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• 제37권2호
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• pp.182-202
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• 1994

마우스(ICR mouse)의 줄생전 ·후 발생에 따른 설점막에서 설유두와 미뢰의 발생, 미뢰를 구성하는 미각세포들의 각 형별 미세구조적인 특징 및 미각세포와 신경종말과의 관계를 광학 및 전자현미경으로 관찰하였다. 유곽유두는 임신 17일 심상유두와 엽상유두는 출생 후 0일, 사상유두는 출생후 1일에 출현하였으며, 유곽유두와 심상유두에서의 미뢰는 출생 후 0일, 엽상유두에서의 미뢰는 출생후 1일에 관찰되었다. 유곽유두에서는 유두벽 상피 뿐만 아니라 유두 표면상피에서도 성체에서와는 다르게 미뢰가 출현하였다. 출생후 7일과 15일에서 유곽유두의 미뢰에 대한 미세구조적 관찰에서 미각세포는 중간형 세포. 암세포, 명세포, 기저세포 및 주변세포로 구분되었다 중간형 세포는 암세포와 명세포의 중간정도의 전자밀도를 보이는 세포로서 세포질에서는 활면 및 조면소포체가 다수 관찰되었고. 세포질 및 핵질내에서 다소포성소체와 유사한 구조물들이 관찰되었다. 암세포는 전자밀도가 높아 어둡게 보였고. 핵막은 깊은 함입을 보였다 이 세포의 핵주변 세포질에는 미토콘드리아, 섬유상 물질, 조면소포체 및 폴리솜들이 다수 관찰되었으며, 첨부 세포질에서는 전자밀도가 높아 어둡게 보이는 과립들이 다수 관찰되었다. 명세포는 전자밀도가 낮아 밝게 보였고, 크고 등근 핵을 갖고 있었으며. 세포질내에서 활면소포체, 폴리솜 그리고 크고 작은 공포들이 다수, 조면소포체들은 소수 관찰되었다. 기저세포는 핵질이 풍부한 난원형의 핵을 갖고 있었으며, 전자밀도가 낮아 밝게 보였고, 유리리보솜들은 많았으나, 활면 및 조면소포체들은 소수 관찰되었다 주변세포는 비교적 긴 방추형의 세포로 얕은 핵막 함입들을 보였고, 대부분의 세포소기 관들은 미약하였으나 유리리보솜들은 다소 많이 관찰되었다. 출생후 7일에는 명세포, 15일에는 중간형 세포들이 다른 세포에 비하여 다수 출현하였다 출생후 미각세포들의 형태적 특징 및 세포소기 관들의 분화들로 미루어 암세포 주변세포 및 기저세포는 미성숙세포, 중간형 세포는 미각기능이 활발한 성숙한 세포 그리고 명세포는 퇴행성 세포로 생각된다.

• 한국발생생물학회지:발생과생식
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• 제23권3호
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• pp.255-262
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• 2019

Previously, we reported negative effects of low-dose nonylphenol (NP) exposure on the reproductive organs of F1 male mice. In the present study was further investigated the endocrine disrupting effect of NP exposure to F2 generation male mice. Mice were divided into 2 groups; (1) CON, control animals and (2) NP-50 ($50{\mu}g/L$), animals were treated with NP via drinking water. NP exposures were continuously conducted from parental pre-mating period until the postnatal day (PND) 55 of F2 offsprings. Mice were sacrificed on PND 55 and the reproductive tissue weights were measured. The initial (at PND 21) and terminal (PND 55) body weights of the NP-50 group animals were not significantly different from those of control group animals. NP exposure fail to induce a significant weight change of the testes, seminal vesicle and prostate except absolute epididymal weight (p<0.05). However, pathohistological studies revealed that NP-treated F2 animals showed evident decrease in seminiferous tubule diameters, reduced luminal area and number of germ cells. Also, sloughing morphologies in the tubules were notable. In the caudal epididymis, fewer mature sperms and swollen epithelial cells were found in the NP-treated group. The present study demonstrated that the subchronic low-dose NP exposure induced pathohistological abnormalities in testis and epididymis of F2 mice, and we assumed that these 'qualitative' changes in reproductive tissues could be derived from the epigenetic modifications such as DNA methylation, histone modification, altered DNA accessibility and chromatin structure. Further studies are needed to achieve a better understanding on the multi- or trans-generational effects of NP on the reproductive health and a human application.

• 한국발생생물학회지:발생과생식
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• 제24권3호
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• pp.159-165
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• 2020

Previously, we reported adverse effects of low-dose nonylphenol (NP) exposure on the reproductive parameters of F1 female mice. In the present study we further investigated the pathohistological effect of NP exposure on the reproductive organs in F1 female mice. NP exposures were continuously conducted from parental pre-mating period until the postnatal day (PND) 33 of F1 offspring for vaginal examination. Mice were sacrificed on PND 30 and the reproductive tissue weights were measured. The initial (at PND 21) body weights of the NP-50 group animals were significantly lower than those of control group animals, and the weight deficit were recovered when the terminal (PND 33) body weights were measured. Early vaginal opening was found in NP group animals (p<0.05). Pathohistological studies revealed that NP-treated F1 animals showed prominent increase in the ovarian follicle numbers (p<0.01), and decrease in the diameter of uterine myometrium (p<0.01), and increase in the diameter of luminal epithelium (p<0.05). The present study demonstrated that the subchronic low-dose NP exposure induced early beginning of puberty and pathohistological abnormalities in ovary and uterus of F1 mice. Further studies are needed to achieve a better understanding on the action mechanism of NP in pubertal onset and to find a way to avoid a hazardous situation provoked by NP exposure.

• 한국발생생물학회지:발생과생식
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• 제23권2호
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• pp.93-99
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• 2019

Nonylphenols (NPs) are widely used industrial materials, and are considered as potent endocrine disrupting chemical. Present study was undertaken to clarify the effect of subchronic low-dose NP exposure to F1 generation male mice. Mice were divided into 2 groups; (1) CON, control animals and (2) NP-50 ($50{\mu}g/L$), animals were treated with NP via drinking water. NP exposures were continuously conducted from parental pre-mating period until the postnatal day (PND) 55 of F1 offsprings. Mice were sacrificed on PND 55 and the tissue weights were measured. The initial body weights (at PND 21) and terminal body weights (PND 55) of the NP-50 animals were significantly lower than those of control animals (p<0.05). NP exposure induced a significant increase in the absolute weight of the testes (p<0.05). Conversely, the NP exposure caused significant decrease in the absolute weights of the epididymis (p<0.01), prostate (p<0.05) and seminal vesicle (p<0.05). Histopathological studies revealed that NP-treated animals exerted decreased seminiferous tubule diameters, reduced luminal area, and lower number of germ cells. Also some sloughing morphologies in the tubules were observed. In the caudal epididymis, fewer mature sperms and swollen epithelial cells were found in the NP-treated group. Our results confirmed that the subchronic low-dose NP exposure altered some male parameters and induced histopathological abnormalities in testis and epididymis of F1 mice. Since the NP dose used in this study is close to the average human daily NP exposure, our results could provide practically meaningful understanding of adverse effect of EDC in human.

• 한국수정란이식학회지
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• 제28권2호
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• pp.157-162
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• 2013

Methoxychlor (MXC) was developed to be a replacement for the banned pesticide DDT. HPTE [2,2-bis (p-hydroxyphenyl)-1,1,1-trichloroethane], which is an in vivo metabolite of MXC, has strong oestrogenic and anti-androgenic effects. MXC and HPTE are thought to produce potentially adverse effects by acting through oestrogen and androgen receptors. Of the two, HPTE binds to sex-steroid receptors with greater affinity, and it inhibits testosterone biosynthesis in Leydig cells by inhibiting cholesterol side-chain cleavage enzyme activity and cholesterol utilisation. In a previous study, MXC was shown to induce Leydig cell apoptosis by decreasing testosterone concentrations. I focused on the effects of MXC on male mice that resulted from interactions with sex-steroid hormone receptors. Sex-steroid hormones affect other organs including the kidney and liver. Accordingly, I hypothesised that MXC can act through sex-steroid receptors to produce adverse effects on the testis, kidney and liver, and I designed our experiments to confirm the different effects of MXC exposure on the male reproductive system, kidney and liver. In these experiments, I used pre-pubescent ICR mice; the puberty period in ICR mice is from postnatal day (PND) 45 to PND60. I treated the experimental group with 0, 100, 200, 400 mg MXC/kg b.w. delivered by an intra-peritoneal injection with sesame oil used as vehicle for 4 weeks. At the end of the experiment, the mice were sacrificed under anaesthesia. The testes and accessory reproductive organs were collected, weighed and prepared for histological investigation. I performed a chemiluminescence immune assay to observe the serum levels of testosterone, LH and FSH. Blood biochemical determination was also performed to check for other effects. There were no significant differences in our histological observations or relative organ weights. Serum testosterone levels were decreased in a dose-dependent manner; a greater dose resulted in the production of less testosterone. Compared to the control group, testosterone concentrations differed in the 200 and 400 mg/kg dosage groups. In conclusion, I observed markedly negative effects of MXC exposure on testosterone concentrations in pre-pubescent male mice. From our biochemical determinations, I observed some changes that indicate renal and hepatic failure. Together, these data suggest that MXC produces adverse effects on the reproductive system, kidney and liver.