Radiation workers, especially those dealing with Uranium isotopes, can potentially intake Uranium -containing materials through their respiratory and digestive systems. According to the “Regulations on the Measurement and Calculation of Internal Exposure” from Nuclear Safety and Security Commission (NSSC), those who intend to work in or enter the nuclear facilities with a risk of exceeding 2 mSv exposure per year should be examined the internal exposure. However, when it comes to in-vitro bioassay, Uranium intake through drinking water can affect the quantitative analysis. The International Commission on Radiological Protection (ICRP) reported in ICRP Publication 23 (Report on the Task Group on Reference Man) that the reference man excretes Uranium in the urine (0.05-0.5 μg/day) and feces (1.4-1.8 μg/day). Korea Atomic Energy Research Institute (KAERI) set the 90.5 ng/day as the 238U background of workers handing Uranium based on the daily Uranium intake of Koreans. In this research, we examined the possible effects of Uranium in drinking water on internal exposure by analyzing the concentration of Uranium in bottled waters from various water sources sold in the domestic market and a water from the water purifier. The 238U concentration results of analyzing 11 bottled waters and 1 purified water, were ranged from 0 to 10.2 μg/L. All the results were satisfied the standard of 30 μg/L according to “Regulations for Drinking Water Quality Standards and Inspection” enacted by the Ministry of Environment. However, various concentrations were shown depending on the water sources. Assuming that these concentrations of water are consumed by drinking 1 L per day, the internal dose assessment result is 0 to 0.94 mSv. On the other hand, if it is assumed to be inhaled, it can be an overestimated because the dose coefficient of inhalation, Type M is higher than that of ingestion, f1=0.02 which are the values recommended by ICRP Publication 78 (Individual Monitoring for Internal Exposure of Workers) when the Uranium compound is unspecified. In case of two workers at KAERI, the daily excretion of urine was 151 and 120 ng/day respectively in the first quarter monitoring. However after changing the kind of drinking water in the second quarter monitoring, it dropped to 17.4 and 15.4 ng/day respectively. Through this study, it is confirmed that the Uranium background in urine can be analyzed differently depending on the kind of drinking water consumed by each worker. Depending on the Uranium concentration of drinking water, the internal exposure dose assessment can be overestimated or underestimated. Therefore, the Uranium concentration and intake amount according to the kind of drinking water should be considered for in-vitro bioassays of Uranium handlers. Furthermore, if necessary, the Uranium isotope ratio analysis in urine and the handling information should be comprehensively considered. In addition, in order to exclude the effect of intake through the digestive system, replacing the kind of drinking water can be considered. The additional analysis such as in-vivo bioassay and 24 hours urine analysis rather than spot samples can be also recommended.

세리신은 누에고치에서 추출한 단백질로 많은 건강상의 이점을 가지고 있다. 본 연구는 화장품 소재로서 누에고치에서 유래된 세리신 표준품의 항주름 활성 및 항염증 활성을 평가하기 위해 수행되었다. 세리신의 항산화 효과는 DPPH 및 ABTS 측정법에 의해 측정되었다. 또한 대식세포인 Raw 264.7 cell에서 의 세포 생존율을 확인하였으며, lipoplyscaccharide를 이용하여 유도된 염증반응을 이용하여 세리신의 항 염증 효과를 조사하였다. 그 결과 세리신은 DPPH, ABTS에서 항산화 활성을 보였으며 세포 독성을 가지지 않은 1,000 μg/mL의 농도에서 NO를 억제하였다. 종합하여 세리신은 항산화 활성을 가지며 항노화 및 항 염증 화장품의 우수한 소재가 될 수 있음을 보여준다.

In the early development of parthenogenetic embryo, cytoplasm and nucleic acid fragmentation may be a cause of lower embryo development. The purpose of this study was to evaluate whether embryonic development and apoptosis factors can be reduced by controlling the in-vitro culture environment by the addition of hormones, pregnancy serum and uterine milk. Our study showed that the activity of Casp-3 increased within the cytoplasm when artificially used hormones to induce the incubation environment, and PCNA's manifestation was low. However, the addition of pregnant serum appeared to lower the Casp-3 activity compared to the other groups. In addition, MMP-9 activity was increased and early embryo development and cytoplasmic fidelity were also increased. Therefore, the results of the present study showed that the use of gestational serum in the development of parthenogenetic embryo inhibit apoptosis and increases cytoplasmic reorganization by natural environmental control in in vitro culture.

반하(Pinellia ternata(Thunb.) Breit)는 천남성과에 속하는 다년생 초본식물로서 조직배양을 이용하 여 대량번식 방법 연구가 활발히 진행되어 왔다. 하지만 대량생산된 괴경들의 토양 순화 및 적응을 위 한 환경 조건의 확립의 연구는 미비하다. 따라서 본 연구에서는 기내에서 증식된 반하의 괴경을 이용하 여 우수한 품질의 약재와 건전묘의 대량생산을 위해 생육에 적합한 토양조건을 탐색하였다. 본 연구에 서는 액체배지에서 현탁배양 한 괴경(Type 1)과 고체배지에 치상하여 배양된 괴경(Type 2)두 종류를 비 교하였다. 토양은 3개의 조성으로 조합하여 생육을 비교하였으며, 코코피트, 피트모스, 버미큘라이트, 펄라이트 및 제오라이트를 배합하여 사용하였다. 기내 배양 조건이 다른 처리구들의 토양 조성별 순화 율 측정하였으며, 생육의 차이를 확인하기 위해 8주동안 생육 후 초장, 잎 수, 마른잎 수, 괴경 수, 괴 경 크기, 생체중 및 건물중을 측정하였다. 또한 주아의 생성율을 확인하기 위하여 4주와 8주에 측정을 진행하였다. 그 결과 Type 2가 펄라이트를 20%증량한 상토 B에서 가장 우수한 생육을 보였다. 괴경의 비대에 영향을 주고 묘로서 이용을 위하여 필요한 잎의 수는 상토 B에서 가장 많은 1.7개로 나타났고 가장 잎의 출현이 없었던 Type 1의 상토 C가 0.9개로 나타나 1.8배의 차이를 나타냈다. 또한 같은 처 리구에서 건물중이 통계적으로 유의한 차이를 보이며 우수한 것으로 나타났다. 반하의 주아 생성율의 차이는 상토 B에서 1.1개로 우수하였으며, 가장 저조한 처리구의 수치보다 1.2배 높은 생성율을 확인할 수 있었다. 이러한 결과로 기내에서 배양된 반하의 토양 순화 및 적응기에 괴경의 비대를 유도하여 우 수한 한약재 생산이 가능 할 것으로 생각되며 차후 토양에서 재배 시 반하의 대량번식에도 도움이 될 것이라 사료된다.

The gastro-intestinal behaviors of foods influence their physiological functions in the human body. In-vitro methods simulating digestion processes have been extensively used to study the gastro-intestinal behaviors of foods due to more rapid and less expensive advantages. However, there is a lack of systematic studies to monitor the rheological changes of the food digesta in real time. In this study, rice-based products (specifically, extruded noodles) were prepared with three varieties of rice flours with different contents of amylose and their physicochemical properties and in-vitro digestibility were then characterized from a rheological point of view. The rice flours with higher amylose contents exhibited greater stability to dual mixing and higher degrees of starch gelatinization and retrogradation in thermo-mechanical measurements. In addition, greater elastic properties were clearly observed in the high amylose rice samples. The noodles which were produced with high amylose rice flour had a harder texture and reduced cooking loss. When the rheological changes of the extruded rice noodles were monitored in real time during the in-vitro starch digestion, the rice noodle digesta with higher amylose content exhibited greater viscosities throughout the simulated oral-gastric-intestinal digestion steps. The flow behavior of the rice noodle digesta consisted of the Power-law region and infinite shear plateau that were satisfactorily characterized by the Sisko model (R2>0.99). Hence, this study was conducted to investigate the physicochemical and in-vitro digestibility of extruded rice noodles with different amylose contents. These results can provide a promising opportunity for the food industry to research in-vitro digestion and physicochemical characteristics of rice-based products.

This study was to research the relationships between rice straw degradation and changes of fibrolytic bacteria population during the in vitro rumen fermentation. Dry matter(DM) digestion of rice straw and population of fibrolytic bacteria were measured at the 0. 4, 8, 12 and 48 hours during the incubation. The populations of F. succinogenes. R. albus and R. flavefaciens were defined as log copy number of 16S rDNA by technical method of Quantitative real-time PCR. Total population of F. succinogenes, R. flavefaciens and R. albus was sum of bactera attached on rice straw and suspended in medium. It's population was increased with incubation, reached top level of 29.0 Log copy No at the 24 hour and then decreased. In the meantime, DM digestion of rice straw showed the higher increasement from the 8 hour to the 24 hour than from the 0 hour to the 8 hour, and then a slowdown in increasing trend of digestibility. Attachments of F. succinogenes, R. flavefaciens and R. albus were detected immediately after start of in vitro rumen incubation. At the same time, the colonized bacterial share were respectively 34.5%, 84.4% and 67.9% in total population. All of them was reached the highest colonized bacterial share above 94.7% at the 4 hour incubation. However population of attached bacteria was shown the highest level at the 12 hour or the 24 hour incubation. Kinetics of colonization were formed area of top speed from the 12 hour to the 24 hour and respectively reached 10.33, 9.28 및 8.30 Log copy No/h/g DM at the 24 hour by F. succinogenes, R. flavefaciens and R. albus. The kinetics of rice straw degradation was formed top level of 0.95% DM/h at the 24 hour. The present results gave clear evidence that degradation of rice straw was increased with the development of total fibrolytic bacteria in process of rumen fermentation. Also, their attachment was largely occurred immediately after insertion of rice straw, the colonized bacteria was actively proliferated, and then degradation of rice straw was maximized.

NNK (4-(methylnitrosamino)―1-(3-pyridyl)-1-butanone) is a major form of nitrosamine abundant in cigarette smoke and is a powerful carcinogen. Mercury is a major component of the amalgam that is widely used as dental filling material. Concurrent exposure to these two agents may result in their interaction and alter their carcinogenic potential. The present study used an immortalized human epithelial cell system that allows continuous exposure to potential carcinogens, in an attempt to elaborate the carcinogenic potential of mercury and NNK in humans. Cytotoxicity of mercury chloride and NNK was measured by an MTT assay. Parameters of neoplastic cellular transformation such as cell saturation density, soft-agar colony formation, and cell aggregation were analyzed to examine the carcinogenic potential of mercury chloride and NNK. The study showed that exposure to mercury chloride with NNK resulted in increased soft agar colony formation and cell aggregation. ROS generation by mercury chloride was further enhanced by treatment with NNK. The apoptosis that was observed following mercury chloride exposure was further increased upon co-treatment with NNK. The interaction between these two agents was also observed in cytokine mRNA induction. In the present study, mercury alone did not seem to pose a significant threat as a carcinogen, but it may have potential to enhance the carcinogenic potential of a known carcinogen from cigarette smoke. The present study provides valuable data regarding the evaluation of potential carcinogenic risk of mercury chloride and NNK on concurrent exposure.

Atopic dermatitis (AD) is usually caused by foods such as wheat, egg, milk, and peanuts, leading to common health problems in early childhood with complications like urtication. The aim of this study was to evaluate ethanol extracts of rice and rice snacks concentrated until the ethanol was completely eliminated and hot-air dried. In vitro analyses were carried out using murine macrophage RAW 264.7 cells. We measured cytotoxicity, nitric oxide (NO) production, and inflammatory cytokine level. The NO level of the cells exposed to lipopolysaccharide (LPS) was significantly reduced by rice and rice snack extracts. TNF-α level decreased in contrast to the LPS group, although a significant difference was not observed. On the other hand, IL-6 significantly decreased in both rice and rice snack extracts in a dose-dependent manner. The results of the present study suggest that rice and rice snack decreased NO and inflammatory cytokine levels. Therefore, rice could be useful as a raw material for relieving child atopic dermatitis caused by snacks made from wheat.

These study was to investigate the in vitro fertilization and viability of fresh and vitrified oocytes. Also, the developmental capacity of IVF and intracytoplasmic sperm injection (ICSI) oocytes were investigated. Then vitrification was performed with the use of 20% ethylene glycol + 20% DMSO + 0.5 M sucrose + 10% FCS + TCM-199 medium. Vitrification immature oocytes are cultured in vitrification solution for 10 min afterwards transferred to expose at room temperature for 5 min. and transferred to the ice water for 5 min. The oocytes were sealed in a 1.0 mm straw and placed in a LN2 container. Frozen oocytes were rapidly thawed in a water bath at 30～35℃, and then placed in TCM-199 medium containing 0.5 M sucrose for 5 min each, respectively, at 38℃. After being washed for 2～3 times, using fresh medium the oocytes were cultured in TCM-199 medium supplemented with 5% FCS at 38℃ in 5% CO2 and air. The normal morphology of fresh and vitrified-thawed oocytes were 87.1±2.1% and 54.8±2.5%, respectively. The viability rates of fresh and vitrified-thawed oocytes were 70.0±2.2% and 41.9±2.6%, respectively. Viability rates of vitrified-thawed oocytes were lower than that of fresh follicular oocytes (p<0.05). The in vitro maturation rates of fresh and vitrified oocytes were 45.1±3.6% and 28.9±4.4%, respectively. The IVF rates of fresh follicular and vitrified-thawed oocytes were 34.0±2.2% and 20.2±2.6%, respectively. The in vitro maturation and fertilization rates of vitrified-thawed oocytes were lower than those of the fresh follicular oocytes (p<0.05). A total of 350 oocytes were fixed and stained after co-incubation with spermatozoa, of which 88 had identifiable nuclear material. After IVF for 20 hrs, 25.1±3.4% of the oocytes found to have been penetrated by spermatozoas. Oocytes were fixed and stained after ICSI, and 105 oocytes contained identifiable nuclear material. After IVF and ICSI for 20 hrs, 34.3±3.4% and 59.0±2.0% of the oocytes were found to have been penetrated by spermatozoas. The developmental rates upon ICSI were significantly higher than those of the IVF method (p<0.05).

These study was carried out to investigate the effects of the recovery time, diameter of oocytes on in vitro fertilization or intracytoplasmic sperm injection (ICSI). The in vitro maturation rates to MII stage of oocytes recovered at the inactive, follicular and luteal stages matured for 72 h were 1.4±0.0%, 43.4±3.2% and 10.8±2.7%, respectively. The fertilization rates of in vitro cultured oocytes recovered from ovaries at the in active, follicular and luteal stages were 0.0±0.0%, 15.7±3.4% and 7.6±3.5%, respectively. The in vitro maturation rate of oocytes recovered from ovaries at the follicular stage of the reproductive cycle was significantly higher than those at the inactive and luteal stages (p<0.05). The penetration rate determined that the percentages of oocytes with diameters in the <100 μm, 100 to 100 μm and 110 to 120 μm ranges were 17.5±4.7%, 43.9±4.5%, 21.3±3.4%, respectively. The penetration rate of oocytes with diameters between 100 to 110 μm was significantly higher than that of oocytes whose diameters were 100< μm and 110～120 μm (p<0.05). The penetration rate of oocytes determined that the percentages of ovaries with diameters between 1 to 5 mm and 6 to 10 mm were 32.9±3.2% and 17.5±3.7%, respectively. Thus, the diameters of the ovaries were significantly higher at 1 to 5 mm (p<0.05). A total of 264 oocytes were fixed and stained after co-incubation with sperm, of which 72 had identifiable nuclear material. After in vitro fertilization for 20 hrs, 27.3% of oocytes were penetrated by spermatozoas. Oocytes were fixed and stained after ICSI, of which 38 oocytes contained identifiable nuclear material. After in vitro fertilization and ICSI for 20 hrs, to 27.3% and 67.9% of oocytes were penetrated by spermatozoas. The in vitro fertilization rates by ICSI was significantly higher than that in vitro fertilization method (p<0.05).

The purpose of this study was to investigate the effects of the collection time, co-culture and sperm penetration of canine oocytes on in vitro maturation and fertilization. The oocytes were cultured in TCM-199 media containing hormonal supplements (10% FCS, 10 IU/ml HCG, 10 IU/ml PMSG) at 5% CO2, 95% air, 38℃. The in vitro maturation rate to MⅡ stage of in vitro oocytes recovered from ovaries that collected at follicular, luteal and inactive phases of the reproductive phase for 44～72 hrs were 19.2%, 12.2%, and 6.0%, respectively. Follicular phases oocytes had a significantly higher in vitro maturation rate than oocytes collected at luteal and anestrus stage (p<0.05). The in vitro maturation rates to the MII stage of canine oocytes after 48 hrs of culture with glutathione, pyruvate, or glutathione + pyruvate were 12.5%, 10.7%, and 17.5%, respectively. This was higher than that in both alone or the combination of the two compared to the control group (19.0%). The sperm penetration rates of in vitro matured oocytes by fresh and frozen semen were 29/80 (36.3%) and 18/80 (22.5%), respectively. Although there are limited reports about canine oocytes co-culture and in vitro fertilization, our results on in vitro maturation is comparable to the results from other researches.

Beef marbling is known as one of the most important beef-quality traits in Korea. It is likely that marbling derived from fatty acids, mainly propionate, is mediated by rumen. Recently micro-agents were studied to enhance marbling, although many parts of that were digested in rumen. Therefore, this study was conducted to screen candidate materials to effect on beef quality with in vitro ruminal incubation. The materials such as saponin, chitosan, Zn compounds (4), vitamin C sources (2), Korean herb cocktail and garlic sources (2) were added to rumen fluid to 1.25% of substrate volume at 0 and 24 h incubation time. Total gas production in intact vitamin C source increased but that in all Zn compounds decreased (P＜0.05). Total gas production in Zn sulfate compound less decreased than in other Zn sources. Propionate in Zn sulfate increased than the other candidate compounds at all incubation time (P＜0.05). Experiment two was conducted to clarified effect of additives such as vitamin C sources (2), garlic lyophilized, Korea herb cocktail and Zn sulfate were supplemented with 2.5% volume at the 0, 3, 6, 12 and 24 h incubation time. Total gas in Zn sulfate was lower than any other treatments. Propionate in garlic, herb and Zn sulfate appeared to be lower than control and vitamin C sources at all incubation time, although significant difference was not observed in total VFA among control and all treatment. This study suggested that micro-agent might be used to improve beef quality with minute level.

In the present study, effects of concentration of cryoprotectant solutions on the nuclear maturation of vitrifiedthawed porcine oocytes were examined. Oocytes were cultured in TCM-199 medium supplemented with 5% FBS at C in 5% and air. The percentage of monospermy in the toxicity group and vitrification group (22.0 3.0% and 31.5 3.5%) was decreased compared with that of the control group (44.0 4.0%). The percentage of in vitro development to blastocyst in the toxicity group and vitrification group (12.0 2.5% and 14.8 2.8%) was decreased compared with that of the control group (28.0 3.0%, p<0.05). The survival and in vitro developmental rate of oocytes vitrification-thawed with EDS and EDT + TCM-199 medium supplemented with 0.1% PVA were 46.3 3.0%, 54.5 3.8% and 14.8 2.5%, 16.4 2.7%, respectively. This results were lower than the control group (28.0 3.5%). The in vitro developmental rate of embryos vitrified with EDS and EDT supplemented PVA did not have a significant difference. The survival and in vitro developmental rate of vitrified-thawed morula and blastocyst embryos were 44.2 3.5%, 17.3 3.0% and 48.1 4.2%, 18.5 3.5%, respectively. Vitrified morulae and blastcyst embryos had a lower survival and developmental rates than their control counterparts.

This study was carried out to investigate the effect of morphology of oocytes, kinds of media, cysteine and myo-inositol supplementation on IVM rate of porcine oocytes. Cumulus- enclosed oocytes were incubated in maturation NCSU-23 and TCM-199 medium with supplementation with 3, 5, 10, 20 mM myo-inositol and 0.05, 0.1, 0.5, 1.0 mM cysteine. 1. When classified by morphology, excellent, good and fair of cumulus-enclosed oocytes were incubated for 48 hrs and the IVM rate were , respectively. The rate were greater in oocytes with excellent cumulus cells than those without cumulus cells. 2. The IVM rate of oocytes cultured in TCM-199 and NCSU- 23 medium supplementation or non-supplementation with 1.0 mM myo-inositol were , respectively. Supplementation with myo-inositol significantly increased the IVM rate of oocytes. 3. The IVM rate of oocytes cultured in NCSU-23 medium supplementation of 3, 5, 10, 20 mM myo-inositol for 48 hrs were , respectively. The IVM rate of oocytes in NCSU-23 medium supplemented with 10 mM myo-inositol were significantly increased compared to control (). 4. The IVM rate of oocytes cultured for 48 hrs in NCSU-23 media supplement with 0.3, 0.5, 1.0, 2.0 mM myo-inositol were , respectively. The IVM rate of oocytes in NCSU-23 medium supplemented with 10 mM cysteine were significantly increased compared to control ().

식용꽃인 꽃베고니아(Begonia semperflorens ‘Superolympia White’), 토레니아(Torenia fournieri ‘Crown Pink’), 팬지(Viola tricolor ‘Solvetsunny Royal’) 및 펠라고니움(Pelargonium grandiflorum ‘Jessie Jarrett’) 추출물의 총페놀 함량, 전자공여능 및 세포독성에 미치 는 영향을 조사하였다. 에탄올 추출물의 총 페놀함량은 펠라고니움의 경우 531.57mg/100g으로 높게 나타났으 나 토레니아는 30.98mg/100g, 팬지는 14.62mg/100g, 꽃베고니아는 5.77mg/100g으로 낮게 나타났다. 전자공 여능은 꽃베고니아, 토레니아, 팬지의 열수 및 에탄올 추출물은 500g·mL-1에서는 모두 69.4% 이하를 나타 냈으나 펠라고니움의 열수 및 에탄올 추출물은 125g·mL-1에서도 각각 94% 내외를 나타내었다. 세포 생존율은 토레니아와 팬지의 열수 및 에탄올 추출물 처리구에서는 95% 이하를 나타내어 세포사가 일어난 것으로 추정되었다. 히스타민 억제효과는 펠라고니움 추출물의 경우 91% 이상을 나타냈으나 토레니아 추출 물은 51-66%, 팬지 추출물은 14-24%, 꽃베고니아 추 출물은 1~2%의 억제 효과만 나타났다.

The propagation of light radiation within tissues is an important problem that confronts the dosimetry of therapeutic laser delivery and the development of diagnostic spectroscopy. In the clinical application of photodynamic therapy(PDT) and in photobiology, the photon deposition within a tissue determines the spatial distribution of photochemical reactions. Scattered light is measured as a function of the distance (r) between the axis of the incident beam and the detection spot. Consequently, knowledge of the photosensitizer(Chlorophyll-a) function that characterizes a phantom is important. To obtain the results of scattering coefficients(μs) of a turbid material from diffusion described by experimental approach. It was measured the energy fluency of photon radiation at the position of penetration depth. From fluorescence experimental method obtained the analytical expression for the scattered light as the values of (I /Io)wavelength vs the distance between the center of the incident beam and optical fiber in terms of the condition of "in situ spectroscopy(optically thick)" and real time by fluorometric measurements.