• Toxicological Research
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• 제29권1호
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• pp.53-60
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• 2013

Studies on milk transfer of drugs in non-human primates (NHPs) are among the crucial components in the assessment of peri- and postnatal toxicity because of the similarity between NHPs and humans. To evaluate the milk transfer of valproic acid (VPA) in NHPs, the toxicokinetics of VPA, an antiepileptic drug, were studied in pregnant cynomolgus monkeys. VPA was administered once daily to pregnant cynomolgus monkeys at doses of 0, 30, 90, and 270 mg/kg by oral gavage from Day 100 of gestation (GD 100) to Day 31 of lactation (LD 31). Concentrations of VPA and its metabolite, 4-ene-VPA, in the maternal plasma on GD 100, GD 140, and LD 30, and concentrations of VPA and 4-ene-VPA in the offspring plasma and milk on LDs 30 and 31, respectively, were quantified using liquid chromatography tandem mass spectrometry (LC/MS/MS). After administration of a single oral dose of VPA to pregnant monkeys on GD 100, the concentrations of VPA and 4-ene-VPA were generally quantifiable in the plasma of all treatment groups up to 24 hr after administration, which showed that VPA was absorbed and that the monkeys were systemically exposed to VPA and 4-ene-VPA. After administration of multiple doses of VPA to the monkeys, VPA was detected in the pup's plasma and in milk taken on LD 30 and LD 31, respectively, which showed that VPA was transferred via milk, and the pup was exposed to VPA. Further, the concentration of VPA in the milk increased with an increase in the dose. Extremely low concentrations of 4-ene VPA were detected in the milk and in the pup plasma. In conclusion, pregnant monkeys were exposed to VPA and 4-ene-VPA after oral administration of VPA at doses of 30, 90, and 270 mg/kg/day from GD 100 to LD 31. VPA was transferred via milk, and the VPA exposure to the pup increased with an increase in the dose of VPA. The metabolite, 4-ene VPA, was present in extremely low concentrations (< 0.5 ${\mu}g/ml$) in the milk and in the pup plasma. In this study, we established methods to confirm milk transfer in NHPs, such as mating and diagnosis of pregnancy by examining gestational sac with ultrasonography, collection of milk and pup plasma and determination of toxicokinetics, using cynomolgus monkeys.

• 한국발생생물학회지:발생과생식
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• 제21권2호
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• pp.157-165
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• 2017

One of the reasons to causing blood coagulation in the tissue of xenografted organs was known to incompatibility of the blood coagulation and anti-coagulation regulatory system between TG pigs and primates. Thus, overexpression of human CD73 (hCD73) in the pig endothelial cells is considered as a method to reduce coagulopathy after pig-to-non-human-primate xenotransplantation. This study was performed to produce and breed transgenic pigs expressing hCD73 for the studies immune rejection responses and could provide a successful application of xenotransplantation. The transgenic cells were constructed an hCD73 expression vector under control porcine Icam2 promoter (pIcam2-hCD73) and established donor cell lines expressing hCD73. The numbers of transferred reconstructed embryos were $127{\pm}18.9$. The pregnancy and delivery rate of surrogates were 8/18 (44%) and 3/18 (16%). The total number of delivered cloned pigs were 10 (2 alive, 7 mummy, and 1 died after birth). Among them, three live hCD73-pigs were successfully delivered by Caesarean section, but one was dead after birth. The two hCD73 TG cloned pigs had normal reproductive ability. They mated with wild type (WT) MGH (Massachusetts General Hospital) female sows and produced totally 16 piglets. Among them, 5 piglets were identified as hCD73 TG pigs. In conclusion, we successfully generated the hCD73 transgenic cloned pigs and produced their litters by natural mating. It can be possible to use a mate for the production of multiple transgenic pigs such as ${\alpha}-1,3-galactosyltransferase$ knock-out /hCD46 for xenotransplantation.

• Reproductive and Developmental Biology
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• 제39권4호
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• pp.127-132
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• 2015

To overcome the hyperacute immune rejection during pig-to-non-human primates xenotranasplantation, we have produced and bred ${\alpha}$-1,3-galactosyltransferase knock-out ($GalT^{-/-}$) pigs. In this study, the somatic cells and tissues from the $GalT^{-/-}$ pigs were characterized by an analysis of the expression of Gal${\alpha}$-1,3-Gal (${\alpha}-Gal$) epitope. Briefly, ear fibroblast cell lines of 19 homozygous $GalT^{-/-}$ pigs were established and cryopreserved. The expression of ${\alpha}-Gal$ epitope in the cells was measured by fluorescence activated cell sorter (FACS) analysis using BS-I-B4 lectin. Also, the homozygous ($GalT^{-/-}$) cells and tissues samples were immunostained with BS-I-B4 lectin for analysis of ${\alpha}-Gal$ epitope expression. The results showed that the expression of ${\alpha}-Gal$ epitope in $GalT^{-/-}$ cells (0.2 %) were significantly (p<0.05) down-regulated to the range of cynomolgus monkey fibroblast (0.2 %) cells compared to heterozygous ($GalT^{-/+}$) (9.3 %) and wild type ($GalT^{+/+}$) (93.7 %) fibroblast cells. In the immunostaining results, while the expression of ${\alpha}-Gal$ epitope was detected a partly in $GalT^{-/+}$ cells and mostly in $GalT^{+/+}$ cells, it was almost not detected in the $GalT^{-/-}$ cells. Also, immunostaining results from various tissues of the $GalT^{-/-}$ pig showed that the expression of ${\alpha}-Gal$ epitope was not detectable, whereas various tissues from $GalT^{+/+}$ pig showed a strong expression of ${\alpha}-Gal$ epitope. Our results demonstrated that ${\alpha}-Gal$ epitope expressions from $GalT^{-/-}$ pigs were successfully knocked out to prevent hyperacute immune rejection for further study of xenotransplantation.

• Investigative Magnetic Resonance Imaging
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• 제9권1호
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• pp.30-35
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• 2005

목적 : 본 논문은 뇌 기능 자기공명영상(Brain Functional Magnetic Resonance Imaging: Brain fMRI)을 이용하여 짠 맛 자극에 대한 인지활동으로 뇌 신경세포의 활성화에 따른 국소 대사 및 혈류역학적 변화가 일어나는 뇌 영역을 분석 및 가시화함으로써 맛에 대한 뇌 활성화 부위의 기초자료를 마련하고자 하였다. 대상 및 방법 : 건강한 비흡연 남자 12명을 대상으로 1.5T MRI 장치에서 혈액산소수준의존(Blood Oxygen Level Dependent, 이하 BOLD) 방법을 이용한 fMRI 실험을 수행하여 인간의 미각 중 짠맛에 대한 반응을 관찰하였다. 잔 맛의 자극은 $3\%$ 농도의 소금물(NaCl)을 미각 자극기를 이용하여 혀 전체에 자극을 주었다. 미각 자극기인 Auto Syringe Pump는 일정한 자극을 반복적으로 가할 수 있도록 마이크로프로세서를 이용하여 연구실에서 자체 제작되었다. 자극의 패러다임은 5회의 휴식기간과 4회의 자극기간으로 구성되었으며, 자극기간은 15초씩 진행되고 휴식기간은 30초로 하여 각 slice당 42 영상을 연속적으로 획득하였다. 자극에 대해 얻은 fMRI 영상은 SPM99'(Statistical Parametric Mapping, UCL)를 이용하여 분석하였다. 활성화 영상은 EPI 영상과 동일한 부위의 T1 강조영상에 registration 기법을 이용하여 overlapping시켜 활성화 부위의 해부학적 판별을 용이하도록 하였다. 결과 : 농도 $3\%$ 소금물의 짠맛 자극에 대해서 insula, amygdala, frontal opercular taste cortex (OFC), orbitofrontal cortex 영역에서 활성화 영역을 fMRI로 확인하였으며, dorsolateral prefrontal cortex (DLPFC) 영역에서도 유효한 신호를 관찰하였다. 결론 : 본 연구의 결과는 미각의 주요 신경이 뇌의 insula, OFC 그리고 DLPFC 영역에 주로 분포한다는 기존의 결과와 잘 일치하고 있다. 마이크로 프로세서로 동작하는 자동펌프를 미각 자극기로 사용함으로써 미각자극에 대한 뇌의 활성화 영역을 안정되게 관찰할 수 있었다. 본 연구의 결과는 fMRI를 이용한 고차원적 미각작용 과정 연구에 튼튼한 밑거름이 될 것으로 생각된다.