• 제목/요약/키워드: PGC-1

검색결과 138건 처리시간 0.025초

태생 경골어류, 망상어(Ditrema temmincki)의 초기생식소 형성 및 성분화 (Early Gonadogenesis and Sex Differentiation in the Viviparous Teleost, Ditrema temmincki)

  • 이정식;이영돈
    • 한국수산과학회지
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    • 제29권1호
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    • pp.35-43
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    • 1996
  • 망상어, Ditrema temmincki이 시원생식세포의 출현, 원시생식소와 초기생식소의 형성, 정소와 난소의 분화 및 체내자어의 성비조성을 조직학적으로 조사하였다. 시원생식세포는 부화전 배의 초기소화관과 등쪽 체벽사이의 섬유성 간충직에서 처음 식별되었다. 부화후부터 전장 4.0mm 까지 소화관과 체벽사이의 섬유성 간충직에 고르게 분포하던 시원생식세포들은 간충직이 등쪽 체벽으로 부터 분리되는 전장 5.0 mm 시기를 전후해서 간충직의 후방으로 이동하여 원시생식소를 형성하게 된다. 초기생식소 형성과정 동안 정소와 난소의 분화는 생식세포와 체세포의 배열 상태에 의하여 구분되며, 전장 10.0mm 부터 생식소는 외부형태에 의하여 정소와 난소로 구분되는데, 정소는 한쌍으로 분리된 형태이고 난소는 후반부가 융합된 형태이다. 정소의 분화는 체내자어의 크기가 전장 25.0mm를 전후해서 정소에 곡정세관의 조직상이 나타나고, 전장 30.0mm를 전후해서 수정관이 형성되며, 전장 45.0 mm를 전후해서 외부형태와 내부 구조적으로 성어와 유사한 정소로 분화된다. 난소의 분화는 체내자어의 크기가 전장 30.0mm를 전후해서 난소습곡과 난소강의 형성이 명확하며, 전장 60.0mm를 전후해서 외부형태와 내부 구조적으로 성어와 유사한 난소로 분화된다. 체내자어의 출산시 전장은 63.0mm 전후이고, 이때 정소와 난소에는 각각 정원세포와 염색인기 단계의 생식세포를 보유하며, 암 : 수 성비는 약 1.65 : 1이었다. 망상어의 성은 자웅이체이며, 성분화 양식은 분화형에 속한다.

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황련-감초 추출물의 지방축적 감소를 통한 비알콜성지방간 개선 효과 (The Effect of Coptidis Rhizoma and Glycyrrhiza Uralensis on Lipid Deposition with Nonalcoholic Fatty Liver Disease (NAFLD))

  • 안상현;김기봉
    • 대한한방소아과학회지
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    • 제33권2호
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    • pp.12-21
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    • 2019
  • Objectives Coptidis Rhizoma and Glycyrrhiza Uralensis are herbs that treat obesity and dampness-phlegm. The aim of this study is to investigate the efficacy of Coptidis Rhizoma and Glycyrrhiza Uralensis on lipid deposition with nonalcoholic fatty liver disease (NAFLD). Methods Male 6-week-old C57BL/6 male mice were divided into three groups: control group (Ctrl), high fat diet group (HFF), and high fat diet with Coptidis Rhizoma and Glycyrrhiza Uralensis extract administration group (CGT). Each 10 mice were allocated to each group (total of 30 mice). All mice were allowed to eat fat rich diet freely throughout the experiment. To examine the effect of Coptidis Rhizoma and Glycyrrhiza Uralensis, we observed weight changes, total cholesterol and glucose levels, lipid blot distributions, PGC-1, p-$I{\kappa}B$, and p-JNK. Results Body weights for all mice were measured and analyzed the difference between the groups. Weight gain was significantly lower in CGT group than the HFF group. Total cholesterol and glucose levels were significantly lower in CGT group. The distribution of lipid blots and positive reaction of PGC-1 were significantly lower in CGT group. The positive reaction of p-$I{\kappa}B$ in hepatic tissues was significantly lower in CGT group. The positive reaction of p-JNK in hepatic tissues was significantly lower in CGT group. Conclusions Coptidis Rhizoma and Glycyrrhiza Uralensis have the effect of improving non - alcoholic fatty liver induced insulin resistance through regulation of lipid metabolism.

고지방식이로 유발된 비만에 대한 택사의 항비만 효과 (Efficacy of Alismatis Orientale Rhizoma on Obesity induced by High Fat Diet)

  • 정향숙
    • 대한본초학회지
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    • 제28권3호
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    • pp.95-106
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    • 2013
  • Objectives : The researcher investigated the anti-obesity effect of Alismatis Orientale Rhizoma(AP) water extract in mice fed a high fat diet and focused on the analysis of local area adipose tissue. Methods : Male ICR mice were divided into three groups, which were fed either a normal AIN diet, a 45% high fat diet (CT group), or a high fat diet and orally administration with a concentrations of 100 mg/kg (AP100 group) and 300 mg/kg body weight (AP300 group) for eight weeks. Results : As compared with CT group, AP100 group showed significant reductions in absolute weight of liver. As compared with CT group, AP100 group and AP300 group showed significant reductions in weight gain and relative weight of total fat. AST, triglyceride, total-cholesterol levels from the AP 100 group and 300 group were significantly lower than those of the CT, and ALT, LDL-cholesterol levels from the AP 100 group was significantly lower than those of the CT. But serum HDL-cholesterol levels from the AP 100 group and 300 group were significantly higher than those of the CT. And serum adiponectin levels from the AP 100 group was significantly higher than those of the CT. In result of real time PCR, all mRNA expression(PEPCK, G6Pase, PGC-$1{\alpha}$ and $ERR{\gamma}$) of two experimental groups were significantly decreased compared to those of CT group. The treatment with AP on local abdominal area made a fat cell size lessen on the fat tissue in the abdominal cavity and subcutaneous area. Conclusions : These results suggest that AP has an anti-obesity effect and the effect is mediated by inhibition of fat gain.

공정 트러블에 따른 안전장치 선택방법에 관한 연구 (A study on Selection Method of Safety Devices According to Process Trouble)

  • 고재욱;정인희;정상용
    • 한국가스학회지
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    • 제13권1호
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    • pp.52-60
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    • 2009
  • 본 논문에서는 Risk-based design개념을 반영하여 체계적인 설계방향을 제시하고 현존하는 법에 더욱 안전한 방향으로 법안이나 규격을 수정할 수 있는 방안을 제시하려고 한다. 안전설계 부분의 초기설계 집중도 및 수준을 향상시키기 위하여 설계 초기단계에서부터 체계화된 안전설계 요소의 정보를 제공할 수 있는 새로운 Advanced Safety Analysis Table(ASAT)을 개발하였다. 또한 ASAT를 토대로 공정 트러블에 따른 안전장치를 선택하는 방법에 대한 가이드라인을 개발하였다. 개발된 ASAT, 공정 트러블에 따른 안전장치를 선택방법의 사례 연구로 NCC(Naphtha Cracking Center) 공정의 PGC(Process Gas Compressor)에 대한 ASAT를 구축하고 공정 트러블에 따른 안전장치를 선택한 결과를 분석하였다.

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메추리의 발달 중 배자 생식선에서 분리한 원시생식세포의 이동능에 대한 연구 (Studies on the Migratory Ability of Primordial Germ Cells from Embryonic Gonads at Different Developmental Stages in Quail)

  • D. K. Kim;G. H. Song;J. N. Kim;D. K. Jeong;K. D. Kim
    • 한국가금학회지
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    • 제28권1호
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    • pp.69-76
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    • 2001
  • Avian primordial germ cells (PGCs) originate from the epiblast and appear in the germinal crescent. These PGCs enter the developing blood vessels during stage 10∼12 (H&H), circulate in the blood stream, migrate into the developing gonadal anlage and differentiate into germ cells. However, it is not clear until when the migratory ability of PGC is maintained. This study was conducted to examine whether migratory ability is present in PGCs from the gonad at later embryonic developmental stages. In the present study, gonads were dissected from 5-, 6- and 10-day old quail embryos and treated with trypsin-EDTA. Gonadal PGCs (gPGCs) were purified by Ficoll-density-gradient-centrifugation and labeled with PKH26 fluorescent dye. The PKH26-labeled gPGCs were microinjected into the blood vessel of the recipient quail embryo. Manipulated recipients were incubated for 3 days, embedded in paraffin and sdctioned. The foreign gPGCs were detected by fluorescent and confocal laser microscopy. As a result, quail gPGCs, from 10, 6 and 5 day old embryos could migrate through the recipient blood stream at early stage and settle in the gonads. Thus, results suggest that gPGCs from upto 10-day old embryos keep properties seen in circulating PGC. Therefore, the PGCs of 10-day old embryonic gonads can be used for the tools of genetic manipulation.

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나노 액체크로마토그래피-텐덤 질량분석기를 이용하여 N-당질화 위치 및 N-당사슬 구조 규명을 위한 방법 (A Sensitive Method for Identification of N-Glycosylation Sites and the Structures of N-Glycans Using Nano-LC-MS/MS)

  • 조영은;김숙경;백문창
    • 약학회지
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    • 제57권4호
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    • pp.250-257
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    • 2013
  • Biosimilars are important drugs in medicine and contain many glycosylated proteins. Thorough analysis of the glycosylated protein is a prerequisite for evaluation of biosimilar glycan drugs. A method to assess the diversity of N-glycosylation sites and N-glycans from biosimilar glycan drugs has been developed using two separate methods, LC-MS/MS and MALDI-TOF MS, respectively. Development of sensitive, accurate, and efficient methods for evaluation of glycoproteins is still needed. In this study, analysis of both N-glycosylation sites and N-glycans of glycoprotein was performed using the same LC-MS/MS with two different nano-LC columns, nano-C18 and nano-porous graphitized carbon (nano-PGC) columns. N-glycosylated proteins, including RNAse B (one N-glycosylation site), Fetuin (three sites), and ${\alpha}$-1 acid glycoprotein (four sites), were used, and small amounts of each protein were used for identification of N-glycosylation sites. In addition, high mannose N-glycans (one type of typical glycan structure), Mannose 5 and 9, eluted from RNAse B, were successfully identified using nano-PGC-LC MS/MS analysis, and the abundance of each glycan from the glycoprotein was calculated. This study demonstrated an accurate and efficient method for determination of N-glycosylation sites and N-glycans of glycoproteins based on high sensitive LC-MS/MS using two different nano-columns; this method could be applied for evaluation of the quality of various biosimilar drugs containing N-glycosylation groups.

열분해-가스크로마토그라피에 의한 자동차 페인트 분석 (Analysis of Automotive Paints using Pyrolysis-Gas Chromatography)

  • 손성건;박하선;이진숙;홍성욱;박성우;조성희
    • 분석과학
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    • 제13권1호
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    • pp.101-107
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    • 2000
  • 자동차 페인트는 안료층과 도색된 페인트층의 색상, 도막층의 배열 및 화학적 성분에 의해 구별되어 질 수 있다. 법과학 시료로 채택된 페인트 도막의 미세편에 의한 뺑소니 차량의 성공적인 확인은 표준시료의 포괄적인 수집 및 전처리 과정 없이 직접 분석하는 기법이 무엇보다 중요하다. 열분해 가스크로마토그래피는 고분자 시료뿐만 아니라 법과학적 시료의 정성 및 정량분석을 수행하는데 정확하고 신뢰성 있는 방법으로 널리 이용되고 있다. 본 실험실은 국내에서 선호도가 높은 각 자동차 회사의 4개 색상 73종에 대해 Curie Point Pyrolyzer(JHP-3) 및 Capillary Column(Ultra Alloy-5)이 장착된 가스크로마토그래프를 이용하여 실험을 진행하였다. 이 분석방법은 용의차량의 페인트와 유류된 페인트의 비교뿐만 아니라 자동차의 제조회사, 차종검객까지 확인하는 데에 이용이 가능하였다.

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HPLC/ELSD Analysis of ginseng saponins with PGC column

  • Shin, Byong-Kyu;Piao, Xiang-Lan;Yoo, Hye-Hyun;Park, Yun-Kyung;Baek, Seung-Hoon;Kim, Bak-Kwang;Park, Man-Ki;Park, Jeong-Hill
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.218.1-218.1
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    • 2003
  • Saponins are known to be the major constituent of Panax ginseng. More than 30 kinds of ginseng saponins are reported so far. The major saponins in white ginseng (WG) or red ginseng (RG) are ginsenosides Rb1, Rb2, Rc, Rd, Rg1, and Re. HPLC method with ELSD or UV detection was used to analyze ginsenosides. Recently, a new processed ginseng with fortified activity, named as Sun Ginseng (SG), was reported. The major ginsenosides of SG are totally different from that of WG or RG, i.e., ginsenoside Rg3, Rk1, and Rg5 are the major constituents of SG. (omitted)

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Sarcopenia targeting with autophagy mechanism by exercise

  • Park, Sung Sup;Seo, Young-Kyo;Kwon, Ki-Sun
    • BMB Reports
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    • 제52권1호
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    • pp.64-69
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    • 2019
  • The loss of skeletal muscle, called sarcopenia, is an inevitable event during the aging process, and significantly impacts quality of life. Autophagy is known to reduce muscle atrophy caused by dysfunctional organelles, even though the molecular mechanism remains unclear. Here, we have discuss the current understanding of exercise-induced autophagy activation in skeletal muscle regeneration and remodeling, leading to sarcopenia intervention. With aging, dysregulation of autophagy flux inhibits lysosomal storage processes involved in muscle biogenesis. AMPK-ULK1 and the $FoxO/PGC-1{\alpha}$ signaling pathways play a critical role in the induction of autophagy machinery in skeletal muscle, thus these pathways could be targets for therapeutics development. Autophagy has been also shown to be a critical regulator of stem cell fate, which determines satellite cell differentiation into muscle fiber, thereby increasing muscle mass. This review aims to provide a comprehensive understanding of the physiological role of autophagy in skeletal muscle aging and sarcopenia.

창출·지모·육계 복합추출물의 고지방식이 유도 당뇨병 마우스에서의 항당뇨 효능 및 C2C12 골격근세포에서의 조절기전 연구 (Anti-diabetic effects of the extract from Atractylodes lancea, Anemarrhena asphodeloides and Cinnamomum Cassia mixture in high fat diet-induced diabetic mice and regulation of the function in C2C12 mouse skeletal muscle cells)

  • 박기호;강석용;강안나;정효원;박용기
    • 대한본초학회지
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    • 제34권6호
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    • pp.79-89
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    • 2019
  • Objective : This study investigated the anti-diabetic effects of DM1, a herbal mixture with Atractylodis Rhizoma, Anemarrhenae Rhizoma, and Cinnamomi Cortex in high fat diet (HFD)-induced diabetic mice and the mechanism in C2C12 mouse skeletal muscle cells. Methods : The C57B/6 mice were fed high fat for 12 weeks, and then administrated DM1 extract (500 mg/kg, p.o.) for 4 weeks. The changes of body weight, calorie and water intakes, fasting blood glucose levels and the serum levels of glucose, insulin, triglyceride, HDL-cholesterol, AST and ALT were measured in mice. The histological changes of liver and pancreas tissues were also observed by H&E stain. C2C12 myoblasts were differentiated into myotubes and then treated with DM1 extract (0.5, 1, and 2 mg/㎖) for 24 hr. The expression of myosin heavy chain (MHC), PGC1α, Sirt1 and NRF1, and the AMPK phosphorylation were determined in the myotubes by western blot, respectively. Results : The DM1 extract administration significantly decreased the calorie and water intakes, glucose, triglyceride, AST and ALT levels and increased insulin and HDL-cholesterol in HFD-induced diabetic mice. DM1 extract inhibited lipid accumulation in liver tissue and improved glucose tolerance. In C2C12 myotubes, DM1 treatment increased the expression of MHC, PGC1α, Sirt-1, NRF-1 and the AMPK phosphorylation. Conclusion : In our results indicate that DM1 can improve diabetic symptoms by decreasing the obesity, glucose tolerance and fatty liver in HFD-induced diabetic mice, and responsible mechanism is might be related with energy enhancement.