• 한국축산식품학회지
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• 제30권6호
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• pp.923-929
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• 2010

Colostral whey prepared from colostrum (pooled from first six post-partum milkings) was heated for 10 min at $100^{\circ}C$ Heated colostral whey was incubated with 1% enzymes (protein equivalent basis) for 15, 30, 60, 90, and 120 min at $50^{\circ}C$. Papain, pepsin, trypsin, and alcalase produced different degrees of hydrolysis (DH), 10.66%, 12.42%, 10.83%, and 25.31%, respectively, at an incubation time of 120 min. The SDS-PAGE reveals that significant amounts of bovine serum albumin (BSA), ${\beta}$-lactoglobulin (${\beta}$-LG), and ${\alpha}$-lactalbumin (${\alpha}$-LA) survived papain digestion. In contrast, pepsin completely removed BSA but not ${\beta}$-LG present in heated colostral whey. Alcalase completely eliminated BSA, ${\beta}$-LG, and ${\alpha}$-LA. This differential hydrolysis was confirmed by reversed-phase HPLC analysis. Using ion-exchange chromatography, fraction-1 (F-1) was obtained from alcalase hydrolysate at a NaCl gradient concentration of 0.25 M. Reversed-phase HPLC chromatograms of alcalase F-1 showed numerous small peaks, which probably indicate that a variety of new peptides were produced. Iron content of alcalase F-1 was 28.94 ppm, which was the highest among all enzyme fractions, whereas iron content of colostral whey was 36.56 ppm. Main amino acids contained in alcalase F-1 were Thr (15.45%), Glu (14.12%), and Ser (10.39%). Therefore, alcalase can be used to generate good iron-binding peptides in heated colostral whey, and the resulting iron-binding peptides could be suitable as a value-added food ingredient for food supplements.

• 한국수정란이식학회지
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• 제33권4호
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• pp.245-254
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• 2018

Pigs are considered as optimal donor animal for the successful xenotransplantation. To increase the possibility of clinical application, genetic modification to increase compatibility with human is an important and essential process. Genetic modification technique has been developed and improved to produce genetically modified pigs rapidly. CRISPR/Cas9 system is widely used in various fields including the production of transgenic animals and also can be enable multiple gene modifications. In this study, we developed new gene targeting vector and enrichment system for the rapid and efficient selection of genetically modified cells. We conducted co-transfection with two targeting vectors for simultaneous inactivation of two genes and enrichment of the genetically modified cells using MACS. After this efficient enrichment, genotypic analysis of each colony showed that colonies which have genetic modifications on both genes were confirmed with high efficiency. Somatic cell nuclear transfer was conducted with established donor cells and genetically modified pigs were successfully produced. Genotypic and phenotypic analysis of generated pigs showed identical genotypes with donor cells and no surface expression of ${\alpha}$-Gal and HD antigens. Furthermore, functional analysis using pooled human serum revealed dramatically reduction of human natural antibody (IgG and IgM) binding level and natural antibody-mediated cytotoxicity. In conclusion, the constructed vector and enrichment system using MACS used in this study is efficient and useful to generate genetically modified donor cells with multiple genetic alterations and lead to an efficient production of genetically modified pigs.

• Journal of Veterinary Science
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• 제21권6호
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• pp.81.1-81.10
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• 2020

Background: Although previous in vivo studies explored urinary microRNA (miRNA), there is no agreement on nephrotoxicity-specific miRNA biomarkers. Objectives: In this study, we assessed whether urinary miRNAs could be employed as biomarkers for nephrotoxicity. Methods: For this, literature-based candidate miRNAs were identified by reviewing the previous studies. Female Sprague-Dawley rats received subcutaneous injections of a single dose or repeated doses (3 consecutive days) of gentamicin (GEN; 137 or 412 mg/kg). The expression of miRNAs was analyzed by real-time reverse transcription-polymerase chain reaction in 16 h pooled urine from GEN-treated rats. Results: GEN-induced acute kidney injury was confirmed by the presence of tubular necrosis. We identified let-7g-5p, miR-21-3p, 26b-3p, 192-5p, and 378a-3p significantly upregulated in the urine of GEN-treated rats with the appearance of the necrosis in proximal tubules. Specifically, miR-26-3p, 192-5p, and 378a-3p with highly expressed levels in urine of rats with GEN-induced acute tubular injury were considered to have sensitivities comparable to clinical biomarkers, such as blood urea nitrogen, serum creatinine, and urinary kidney injury molecule protein. Conclusions: These results indicated the potential involvement of urinary miRNAs in chemical-induced nephrotoxicity, suggesting that certain miRNAs could serve as biomarkers for acute nephrotoxicity.

• 한국산업보건학회지
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• 제8권2호
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• pp.296-305
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• 1998

흰쥐에 있어서 toluene 또는 ethanol 전처치가 toluene 대사에 어떠한 영향을 미치는지를 검토하는 일환으로 흰쥐에 toluene 또는 ethanol을 경시별로 4주간 투여한 다음, 톨루엔을 1회 재투여한 후 처치하여 다음과 같은 결과를 얻었다. 즉, 간조직의 광학 및 전자현미경을 통한 병리조직학적 소견과 체중당 간무게, 혈청 alanine aminotransferase 활성 및 간조직 중 glutathione 함량 변동을 관찰한 결과, toluene 및 ethanol 전처치군 모두 가역적 간손상 정도가 관찰되었으며 톨루엔 및 에탄올 전처치군 간에 간손상 정도 차이는 볼 수 없었다. 이러한 실험동물 모델에서 toluene 및 ethanol 전처치군 모두 요 중 마뇨산 농도가 대조군 보다 높게 나타났으며 toluene 대사에 관여하는 간조직의 cytochrome P-450 함량 및 benzylacohol(BAD) 또는 benzaldehyde dehydrogenase(BzAD) 활성치가 대조군 보다 높게 나타났다. 그리고 요 중 마뇨산 농도와 BAD 및 BzAD 의 활성치는 톨루엔 전처치군이 에탄올 전처치군 보다 전 실험기간 동안 대체로 다소 높게 나타났다. 또한 간조직의 benzylalcohol dehydrogenase의 반응속도를 관찰한 결과 $V_{max}$치는 toluene 및 alcohol 전처치군 모두 대조군 보다 높게 나타났다. 이상 실험결과를 종합해 볼 때 실험동물에 toluene 및 ethanol 전처치가 toluene 대사를 촉진시키며 이는 toluene 대사에 관여하는 효소활성에 영향을 미쳐 나타난 결과로 생각된다.

• 한국발생생물학회지:발생과생식
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• 제7권2호
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• pp.105-112
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• 2003

최근 사람의 난포액에 존재하는 gelatinase 중 EDTA처리에 의해 활성이 크게 증가하는 GA110을 발견하였으며, 본 연구에서는 이러한 GA110이 만들어지는 기작을 알아보고자 하였다. 먼저, protein disulfide isomerase(PDI)가 관여하는지 알아보기 위해 PDI 저해제를 처리하여 GA110의 활성을 조사하였다. 난포액에 EDTA를 처리하기 전에 저해제를 첨가하여 반응시키면 저해제 의 농도가 증가할수록 GA110의 활성 이 감소하였으나 반면 72 kDa gelatinase의 활성은 증가하였다. 그러나 EDTA를 처 리 한 후 저해제를 첨가하여 반응시키면 GA110의 활성에 영 향을 주지 못하였다. 다음으로 72 kDa gelatinase로부터 GA110이 만들어지는 과정에 관여하는 효소를 분리하기 위하여 chromatography 방법을 이용하였으며 이렇게 분리한 효소와 기질을 반응시켜 GA110이 만들어지는 것을 확인하였다. 또한 PDI 항체를 이용하여 immunoblotting을 수행한 결과 난포액 내에 PDI보다 분자량은 약간 작지만 항체와 반응하는 단백질이 존재하는 것으로 나타났다. 이러한 결과로 보아 EDTA 처리로 인해 난포액에서 나타나는 GA110은 난포액 내에 존재하는 PDI와 유사한 효소의 활성화로 인해 72 kDa gelatinase 서로간에 이황화 결합이 형성되어 결국 72 kDa gelatinase dimer인 GA110이 만들어지는 것으로 추측된다.

• 대한지역사회영양학회지
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• 제21권4호
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• pp.378-385
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• 2016

Objectives: This study was conducted to investigate the association between sarcopenia and sarcopenic obesity and cardiovascular disease risk in Korean postmenopausal women. Methods: We analyzed data of 2,019 postmenopausal women aged 50-64 years who participated in the Korea National Health and Nutrition Examination Survey in 2008-2011 and were free of cardiovascular disease history. Blood pressure, height, and weight were measured. We analyzed the serum concentrations of glucose, total cholesterol, high density lipoprotein cholesterol, low density lipoprotein cholesterol and triglyceride levels. Waist circumference was used to measure obesity. Appendicular skeletal muscle mass was measured by dual-energy X-ray absorptiometry. Sarcopenia was defined as the appendicular skeletal muscle mass/body weight<1 standard deviation below the gender-specific means for healthy young adults. The estimated 10-year risk of cardiovascular disease risk was calculated by Pooled Cohort Equation. Subjects were classified as non-sarcopenia, sarcopenia, or sarcopenic obesity based on status of waist circumference and appendicular skeletal muscle mass. Results: The prevalence of sarcopenia and sarcopenic obesity was 16.3% (n=317) and 18.3% (n=369), respectively. The 10-year risk of cardiovascular disease risk in the sarcopenic obesity group was higher ($3.82{\pm}0.22%$) than the normal group ($2.73{\pm}0.09%$) and sarcopenia group ($3.17{\pm}0.22%$) (p < 0.000). The odd ratios (ORs) for the ${\geq}7.5%$ 10-year risk of cardiovascular disease risk were significantly higher in the sarcopenic obesity group (OR 3.609, 95% CI: 2.030-6.417) compared to the sarcopenia group (OR 2.799, 95% CI: 1.463-5.352) (p for trend < 0.000) after adjusting for independent variables (i.e., exercise, period of menopausal, alcohol use disorders identification test (AUDIT) score, income, education level, calorie intake, %fat intake and hormonal replacement therapy). Conclusions: Sarcopenia and sarcopenic obesity appear to be associated with higher risk factors predicting the 10-year risks of cardiovascular disease risk in postmenopausal women. These findings imply that maintaining normal weight and muscle mass may be important for cardiovascular disease risk prevention in postmenopausal women.

• Current Research on Agriculture and Life Sciences
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• 제8권
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• pp.45-50
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• 1990

본 실험은 성선(性腺)자극호르몬과 우태아혈청(牛胎兒血淸) 첨가가 돼지 난포란(卵胞卵)의 체외성숙(體外成熟) 및 체외수정(體外受精)에 미치는 영향을 조사하기 위하여 실시하였다. 미경산돈(未經産豚)(체중 80~90kg)의 난소(卵巢)를 도살된 직후에 절취하여 $37{\sim}39^{\circ}C$의 보온병에 담아 실험실로 운반하여 난포(卵胞)직경이 3~5mm되는 것만을 골라 난포(卵胞)를 찔러서 난포란(卵胞卵)을 채취하였다. 성숙모돈(成熟牡豚)(체중 130~150kg)의 정소상체미부정자(精巢上體尾部精子)를 $4{\times}10^8cells/m{\ell}$ 농도로 희석하여 체외수정(體外受精)에 이용하였다. 본 실험의 경과를 요약하면 다음과 같다. 1. m-KRB와 10% FCS를 m-KRB에 첨가한 경우 성숙율(成熟率)은 82.37%이며, 10% FCS가 첨가된 배양액에 PMSG, hCG 그리고 PMSG와 hCG를 각각 $10IU/m{\ell}$ 첨가한 경우 66, 58, 68%로서 성숙율(成熟率)이 향상되었다. 2. 난구세포(卵丘細胞)의 팽화(膨化)는 m-KRB와 10% FCS가 첨가된 배양액에서 일어나지 않았으나 10% FCS가 첨가된 배양액에 PMSG, hCG 그리고 PMSG와 hCG를 각각 $10IU/m{\ell}$ 첨가시 92, 13, 91%로서 팽화율(膨化率)이 향상되었다. 3. m-KRB에서 성숙된 난포란(卵胞卵)의 체외수정(體外受精)에서 정자침입율과 웅성전핵(雄性前核) 형성율은 각각 93.7%였으나 FCS와 성선(性腺)자극호르몬을 첨가한 경우 각각 100, 80%로서 웅성전핵(雄性前核) 형성율이 향상되었다.