• 제목/요약/키워드: c-KIT

검색결과 566건 처리시간 0.024초

가공공유의 품질개선을 위한 Chitosan의 이용 (Utilization of Chitosan to Improve the Quality of Processed Milk)

  • 하태조;이신호
    • 한국식품영양과학회지
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    • 제30권4호
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    • pp.630-634
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    • 2001
  • 가공유는 우유에 과즙 등을 첨가하여 우유의 성분을 변화시킨 우유로서 백색 시유와는 달리 가공공정 중 각종 첨가물에 의해 미생물이 오염되어 품질악화를 초래할 수도 있다. 미생물 오염에 의한 가공유의 품질악화를 방지하고 품질개선을 위해 chitosan의 이용 가능성을 검토하였다. 시판 가공유에서 api 20E kit 와 api 20C AUX kit 로 동정한 결과 Saccharomyces cerevisiae와 Pseudomonas fluorescence를 분리동정하였다. 0.01%, 0.03%, 0.05%, 0.1% chitosan 을 함유한 YM broth에서 분리 yeast의 성장을 측정한 결과 0.03% chitosan 첨가구에서 배양 12시간후 성장이 완전히 저해되었다. 분리 P. fluorescence는 chitosan 0.03%를 함유한 TSB 에서 2~3 l$og_{10}$ cycle 성장이 억제되었다. Chitosan 0.03%를 첨가한 가공 시유를 제조하여 15일 동안 $4^{\circ}C$, 1$0^{\circ}C$, $25^{\circ}C$에서 저장하면서 품질특성을 조사한 결과 $4^{\circ}C$와 1$0^{\circ}C$에서는 대조구와 뚜렷한 차이를 나타내지 않았으나 $25^{\circ}C$ 저장의 경우 대조구는 저장 2일째부터 이화학적 변화(pH, 산도)를 나타낸 반면 chitosan 첨가구의경우 저장 15일 동안 저장초기와 거의 같은 수준을 나타내었다. Chitosan 첨가 가공유는 5% 유의수준에서 taste는 감소하였으며 texture는 증가하여, chitosan 첨가에 의한 가공유의 기호성 저하는 없었다.

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D-갈락토스 유도 C2C12 근원세포에 대한 자소엽 추출물의 세포 노화 억제 효과 (Cellular Aging Inhibitory Effect of Perilla Leaf Extract on D-Galactose Induced C2C12 Myoblasts)

  • 박송미;조성우;최영현
    • 한방재활의학과학회지
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    • 제34권2호
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    • pp.15-28
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    • 2024
  • Objectives We used the D-galactose (D-gal) induced C2C12 myoblast senescence model to investigate whether ethanol extract of Perilla. fructescens leaves (EEPF) could delay cellular senescence and regulate related mechanisms. Methods C2C12 myogenic cells were cultured in an incubator under 37 ℃ and 5% CO2 conditions. EEPF, dried perilla leaves were pulverized and extracted at 1:10 (v/v) at 50 ℃ for 4 hours. Cell counting kit-8 and western blot analysis was performed. Annexin V-FITC apoptosis detection kit and DAPI staining was applied. Catalase (CAT), glutathione peroxidase (GSH-Px), total antioxidant capacity (T-AOC), superoxide dismutase (SOD), and malondialdehyde analysis kits were used. To measure the level of reactive oxygen species generation, staining and flow cytometry was used. To analyze the mitochondrial activity, membrane potential changes were measured using JC-1. 𝛽-gal activity was analyzed using SA-𝛽-gal staining solution, and DNA damage was analyzed by using 𝛾-H2AX. Quantikine ELISA kit was used to analyze inflammatory cytokine production. Results According to the results of this study, EEPF significantly alleviated the decrease in cell viability in C2C12 cells treated with D-gal and suppressed the decrease in the expression of proliferating cell nuclear antigen. EEPF also markedly blocked D-gal-induced C2C12 cell apoptosis and restored reduced activity of CAT, GSH-Px, T-AOC, SOD. In addition, EEPF suppressed the decrease in 𝛽-galactosidase activity, the induction of DNA damage and the increase in expression of senescence-associated secretory phenotype proteins such as p16, p53 and p21 in D-gal-treated C2C12 cells. Furthermore, EEPF significantly attenuated D-gal-induced production and expression of inflammatory cytokines such as interleukin (IL)-6 and IL-18. Conclusions The results of this study indicate that EEPF can be used as a potential candidate for the prevention and treatment of muscle aging.

병렬신호처리시스템을 위한 성능 모니터의 구현 및 검증 (An Implementation and Verification of Performance Monitor for Parallel Signal Processing System)

  • 이원주;김효남
    • 한국컴퓨터정보학회논문지
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    • 제10권5호
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    • pp.313-322
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    • 2005
  • 본 논문에서는 TMS302C6711을 기본 프로세서로 사용하는 DSP Starter Kit(DSK)를 이용하여 병렬신호처리시스템의 성능을 측정하는 성능 모니터를 구현하고 검증한다. 이 성능 모니터의 특징은 DSP/BIOS의 기능 및 실시간 데이터 전송을 위한 RTDX(Real Time Data Exchange)를 사용하여 DSP 작업부하, 메모리 이용률, 그리고 브릿지 트래픽 등과 같은 병렬신호처리시스템의 성능 평가 척도를 측정할 수 있다는 것이다. 시뮬레이션에서는 DSP 알고리즘에서 널리 사용하는 FFT, 2D FFT, Matrix Multiplication, Fir Filter를 사용한다. 하나의 웨이브 파일에서 각각 다른 주기와 데이터 크기, 버퍼크기에 따른 결과를 성능 모니터와 TI(Texas Instrument)사의 코드 컴포저 스투디오로 측정한다. 그리고 그 결과를 비교함으로써 본 논문에서 구현한 성능 모니터의 정확성을 검증한다.

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Voltage-dependent $Ca^{2+}$ Current Identified in Freshly Isolated Interstitial Cells of Cajal (ICC) of Guinea-pig Stomach

  • Kim, Young-Chul;Suzuki, Hikaru;Xu, Wen-Xie;Hashitani, Hikaru;Choi, Woong;Yun, Hyo-Yung;Park, Seon-Mee;Youn, Sei-Jin;Lee, Sang-Jeon;Lee, Sang-Jin
    • The Korean Journal of Physiology and Pharmacology
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    • 제12권6호
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    • pp.323-330
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    • 2008
  • The properties of voltage dependent $Ca^{2+}$ current (VDCC) were investigated in interstitial cells of Cajal (ICC) distributed in the myenteric layer (ICC-MY) of guinea-pig antrum. In tissue, ICC-MY showed c-Kit positive reactions and produced driving potentials with the amplitude and frequency of about 62 mV and 2 times $min^{-1}$ respectively, in the presence of $1{\mu}M$ nifedipine. Single ICC-MY isolated by enzyme treatment also showed c-Kit immunohistochemical reactivity. These cells were also identified by generation of spontaneous inward current under $K^+$ -rich pipette solution. The voltage clamp experiments revealed the amplitude of - 329 pA inward current at irregular frequency. With $Cs^+$-rich pipette solution at $V_h=-80\;mV$, ICC-MY produced voltage-dependent inward currents (VDIC), and nifedipine ($1{\mu}M$) blocked VDIC. Therefore, we successfully isolated c-Kit positive single ICC from guinea-pig stomach, and found that ICC-MY potently produced dihydropiridine sensitive L-type voltage-dependent $Ca^{2+}$ currents ($VDCC_L$).

홍화씨가 신생골 형성에 미치는 영향 (Effects of Safflower Seed on New Bone formation)

  • 송해룡;라도경;김종수;정태성;김용환;강호조;강정부;연성찬;김은희
    • 한국임상수의학회지
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    • 제19권1호
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    • pp.66-72
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    • 2002
  • Korean safflower seed has been known to have healing effects on both bone fracture and osteoporosis. On the base of such a notice, this experiment was carried out to explore the effects of safflower seed on bone formation and bone repair. The toxicity test and the effect of Korean safflower seed were evaluated with 60 rats, 3-month old. Forty Sprague-Dawley rats composed of 20 male and 20 female were underwent unilateral tibial defect and then fastened with unilateral fixators. The operated rats were divided into two groups depending on the composition of diet, such as positive control group fed normal diet(C-OP group) and safflower seed group fed 30% of safflower seed diet and 70% of normal diet(S-OP group). Another 20 rats without operation were maintained, each 10 rats were fed either normal diet or 30% of safflower seed diet and 70% of normal diet, and observed the toxicity of safflower seed by measuring weight and urine parameters. Postoperative radiography were taken once in 2 weeks to evaluate callus formation for operated groups and blood collection via heart puncture were carried out once in 3 weeks for 3 groups. The concentration of Ca and Pi in serum were measured using both auto Kit and $^{31}$ P Nuclear Magnetic Resonance(NMR). At present study, no toxic effect was observed from both weight increment and urine index after feeding the safflower seed diet. The comparison of the radiography between C-OP and S-OP group were showed that the safflower seed diet appeared to stimulate the formation of callus in the rat. The ratio of Ca/P in serum was low in S-OP group compared to C-OP group with the auto Kit, but there were no significant differences between two groups (p < 0.05). In addition, the variations of Pi values in NMR examination were also confirmed based on the result of auto Kit. In conclusion, this study implied that safflower seed might influence to bone formation and shorten the periods of remedy by stimulating the calcification of bone

자궁경부상피내종양과 침윤성 편평상피암종의 혈관신생에서 비만세포와 혈관내피성장인자의 발현 (Mast Cells and Vascular Endothelial Growth Factor Expression in Neoangiogenesis of Cervical Intraepithelial Neoplasia and Invasive Squamous Cell Carcinomas of the Uterine Cervix)

  • 제갈승주;이정아;노종섭
    • 대한임상검사과학회지
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    • 제37권3호
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    • pp.197-206
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    • 2005
  • To determine the correlation between mast cells(MCs) and neoangiogenesis in the growth and progression of cervical cancer, we investigated mast cell density(MCD), microvessel density(MVD) and the expression of vascular epithelial growth factor(VEGF) in cervical intraepithelial neoplasia and invasive suqamous cell carcinoma of the uterine cervix. Forty-five cervical intraepithelial neoplasia(CIN I, II and III), 15 microinvasive carcinomas, 15 invasive squamous cell carcinomas and 20 normal cervical epithelia were included in this study. MCs were stained with anti-c-Kit antibody and alcian blue, microvessels with anti-factor VIII antibody and VEGF with anti-VEGF antibody. The adjacent fields of both normal and neoplastic epithelium were used for counting MCs and microvessels. Computerized image analysis was used to evaluate MCD and MVD. MCD and MVD were the mean numbers per $1mm^2$ counted in 5-10 high and low power fields respectively. In both c-Kit and alcian blue stained sections, MCD progressively increased along the continuum from CIN I to invasive squamous cell carcinoma(p<0.001). MVD increased significantly with cervical neoplasia progression, from CIN to invasive squamous cell carcinoma (p<0.001). In double c-Kit and Factor VIII-stained sections, MCs were mainly present in the areas adjacent to newly formed blood vessels. However, there were no significant differences in MCD and MVD between normal epithelum and CIN I. A strong correlation was also observed between MCD and MVD. In double VEGF and alcian blue-stained sections, VEGF was expressed in only MCs. Strong VEGF-positive MCs were particularly abundant around the tumorous region. Our results suggest that MCs may upregulate neoangiogenesis by VGEF secretion in the development and progression of cervical neoplasia.

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Immunohistochemical Expression of Receptor Tyrosine Kinase (RTK) in Canine Brain Tumors

  • Jung, Hae-Won;Song, Joong-Hyun;Yu, Do-Hyeon;An, Su-Jin;Sur, Jung-Hyang;Kim, Young Joo;Han, Donghyun;Jung, Dong-In
    • 한국임상수의학회지
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    • 제36권6호
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    • pp.319-324
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    • 2019
  • Receptor tyrosine kinases (RTK) are major promising targets in anticancer therapy in human and veterinary medicine. Using immunohistochemistry method, we evaluated the expressionof five types RTK (PDGFR-α, PDGFR-β, VEGFR 2, c-Kit and Abl) in the six canine brain tumor samples (2 meningioma, 2 astrocytoma, 1 ependymoma and 1 choroid plexus papilloma). A total of five samples expressed PDGFR-β (5/6), one sample, the choroid plexus papilloma, expressed c-Kit (1/6), and a total of two samples expressed Abl (2/6). None of the samples showed expression of PDGFR-α and VEGFR 2. We demonstrate that a significant portion of canine brain tumors express tyrosine receptors for growth factors and show that these receptors generally localize to tumor cell membranes and the cytoplasm. Evaluation of immunohistochemical expression for the RTKs PDGFR-β, c-Kit, and Alb in canine brain samples reveals an interesting potential for molecular targeting by TKIs in therapeutic studies of canine brain tumors, and more studies will be needed to assess the interactions and efficacy of these RTKs and TKIs. Based on these results, we have some evidence for novel chemotherapeutic trials using TKIs for canine nervous tumors.

당화혈색소 측정을 위한 Norudia® HbA1c 키트의 평가 (Evaluation of Norudia® HbA1c Kit for Glycohemoglobin Assay)

  • 홍승복;김은중
    • 대한임상검사과학회지
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    • 제41권1호
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    • pp.37-41
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    • 2009
  • Measurement of hemoglobin A1c is used as an objective indicator of long-term blood glucose control in diabetic patients. We evaluated recently introduced Norudia$^{(R)}$ HbA1c (Daiichi Pure Chemical Co. Ltd, Tokyo, Japan) test reagent using enzyme method for HbA1c assay. Linearity, precision and correlation with VARIANT$^{TM}$ II Turbo HbA1c analyzer (BIO-RAD, Hercules, CA, USA) were evaluated. The reference range was determined from 201 healthy subjects. The Norudia$^{(R)}$ HbA1c test reagent was founded to be linear in a range of 5.6% to 14.0% ($r^2=0.9885$). The within-run and between-day precision were 0.954% and 1.03% for low level (HbA1c 5.24%), 0.67% and 1.28% for high level (HbA1c 9.01%), respectively. Comparison study between Norudia$^{(R)}$ HbA1c test reagent and VARIANT$^{TM}$ II Turbo showed good correlation with a slope of 1.0489. an intercept at -0.9717, and coefficient of correlation was 0.9907. The reference range of HbA1c obtained from this reagent was 4.07-5.50%. The Norudia$^{(R)}$ HbA1c test reagent showed good linearity, precision and correlation with HbA1c analyzer with HPLC method. In addition, the exclusive analyzer is not required for assay and then this kit may be useful for HbA1c assay in clinical laboratory.

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네발나비과 나비류의 계대사육법 체계확립 (Establishment of the Successive Rearing System of Brush-footed Butterflies (Lepidoptera: Nymphalidae))

  • 설광열;김남정;홍성진
    • 한국응용곤충학회지
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    • 제44권4호
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    • pp.257-264
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    • 2005
  • 곤충관의 연중 전시용으로서 붉은 색 계통의 화려한 나비로서 공급하기 위하여 네발나비류의 계대사육법 체계확립을 위해 일련의 시험을 수행하였다. 먼저 실내 제대사육용 인공사료를 개발하기 위해 3종의 사료를 공시한 결과 종에 따라 선호하는 사료의 종류가 달랐으나 Bu사료가 대체로 사육 성적이 양호하였으며 사료 중 기주잎 분말은 냉동 건조한 것이 좋았으며 C/N율은 1:1이 가장 양호한 결과로 나타났다. 또한 발육단계 별 냉장가능기간을 조사한 결과 알의 경우 $5^{\circ}C$에서는 3일간, $15^{\circ}C$에서는 5일간 저장이 가능하였고 번데기의 경우에는 저온에 오래 보관할수록 기형 나비의 출현율이 높아 $15^{\circ}C$에서 최대 15일간 냉장 가능한 것으로 판단되었다. 나비의 장기 저온보호시험을 통해 냉장전의 흡밀기간, 냉장 온도에는 관계없이 법 장기간이 생존을, 산란전기간 및 산란수에 영향하였으며 60일까지 냉장이 가능한 것으로 나타났다. 네발나비는 기주식물의 자극없이는 산란하지 않아 페트리 접시를 이용한 간이 인공산란용 키트를 개발하여 기주식물(한삼덩굴)잎의 에테르 물추출물을 처리한 결과 암컷 1마리 당 평균 $278{\pm}27$개를 산란하였다. 이러한 결과들을 종합하여 네발나비류의 연중 실내제대사육 체계도를 완성하였다.