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CLA 첨가사료가 감성돔(Acanthopagrus schlegeli) 성장과 지방산 조성 및 내장 추출지방이 지방세포 3T3-L1에 미치는 영향
Influence of Dietary Conjugated Linoleic Acid (CLA) and Carotenoids on Growth, Fatty Acid Composition, and 3T3-L1 Cells in Black Seabream (Acanthopagrus schlegeli) 원문보기

생명과학회지 = Journal of life science, v.25 no.5 = no.181, 2015년, pp.548 - 556  

곽뢰 (경상대학교 해양식품생명의학과) ,  쥴리야티 로마 (경상대학교 해양식품생명의학과) ,  최광수 (경상대학교 해양환경공학과) ,  박시향 (선마린바이오) ,  하영래 (경상 대학교 환경생명화학과) ,  강석중 (경상대학교 해양식품생명의학과) ,  최병대 (경상대학교 해양식품생명의학과)

초록
AI-Helper 아이콘AI-Helper

공액리놀레산(CLA)과 카로테노이드 일정량을 함유하는 두 가지 사료구와 대조구를 감성돔(Acanthopagrus schlegeli)에 급여하였다. 대조구에는 CLA와 카로테노이드가 포함되지 않았고, CP10구에는 CLA 1%와 카로테노이드 0.1%가 포함되었고, CP25구에는 CLA 2.5%와 카로테노이드 0.1%가 포함되었다. 대조구, CP10 및 CP25구의 일일성장률(SGR)은 0.74, 0.81, 0.97이었고, 사료요구율은 2.65, 2.46 및 2.04이었다. 사육 후 근육 내에 축적된 CLA 함량은 CP10 및 CP25구에서 각각 2.8% 및 5.6%였으며, 내장에 축적된 CLA 함량은 4.0% 및 8.3%였다. 한편, CP25구의 에서 추출된 지용성 물질(VLE)을 첨가한 3T3-L1 지방세포 생존율은 대조구와 비교하였을 때 처리량에 따라 영향을 받는 것으로 나타났다. 따라서 CP25구의 VLE 추출물 농도를 1, 10, 50 및 $100{\mu}g/ml$으로 처리하였을때 각각 $85.9{\pm}0.8%$, $74.8{\pm}0.9%$, $75.5{\pm}0.6%$$72.1{\pm}0.7%$ 감소시켰다. 이와 같은 사료로 감성돔을 사육하는 경우 CP10 및 CP25구의 내장에서 추출한 지질함량 중 CLA함량은 각각 4.0% 및 8.5%, 카로테노이드는 각각 0.62 mg/g 및 0.56 mg/g, EPA 및 DHA는 각각 11.7%와 10.8% 및 11.8%와 12.7%로 증가하였고, 총 PUFA 함량도 각각 48.4% 및 50.5%로 증가하여 인체에 긍정적인 영향을 미치는 성분을 동시에 섭취할 수 있어 기능성 어류의 생산이 가능한 것으로 나타났다.

Abstract AI-Helper 아이콘AI-Helper

Three groups of black seabream (Acanthopagrus schlegeli) were fed with treatment diets containing certain concentrations of conjugated linoleic acid (CLA) and carotenoids. The control group feed contained 0% CLA and 0% carotenoids, the CP10 group feed contained 1% CLA and 0.1% carotenoids, and the C...

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제안 방법

  • In addition of inducer mixture, 1, 10, 50, 100 μg/ml of black seabream viscera’s lipid extract (VLE) from control and CP25 group were added respectively. After 48 hr in- cubation, the medium was replaced with DMEM plus 10% BCS, 5 μg/ml insulin and VLE of control and CP25 0, 1, 10, 50, 100 μg/ml respectively. Reference group was a cul- ture without addition of VLE.
  • However, this method has a drawback, since CLA has prominent effect as body fat reducer thus it will lower harvest weight. This study aims are to inves- tigate the influence of dietary conjugated linoleic acid (CLA) in alliance with carotenoids on growth and fatty acid composition in black seabream, and to examine the impact of black seabream lipid extract on 3T3-L1 cells. The addition of carotenoids will feasibly maintain the weight of the fish as well as enhance meat coloring.
  • size. Treatments were conducted for 8 weeks, feed were given 3% of fish body weight, twice a day at 10:00 am and 17:00 pm until satiation. The experiment was conducted during summer (June-August) in sea area of Tongyeong, Korea.

대상 데이터

  • 1% carotenoids). CLA (purity ≥ 77%) was supplied by HK Biotech Co. (Jinju, Korea), which consisted: 39% cis-9, trans-11 CLA; 39% trans-10, cis-12 CLA; and 2% other CLA isomers (cis-9, cis-11; cis-10, cis-12; trans- 9, trans-11, and trans-10, trans-12 CLA). Commercial car- otenoids that being used in this study was Carophyll Pink® (contained 10% astaxanthin) obtained from Vixxol Co.
  • One thousand and five hundred fishes were randomly distributed into three groups (Control, CP10 and CP25) and allotted to cages of 175 m3 (5 m × 5 m × 7 m) in size. Treatments were conducted for 8 weeks, feed were given 3% of fish body weight, twice a day at 10:00 am and 17:00 pm until satiation.
  • Treatments were conducted for 8 weeks, feed were given 3% of fish body weight, twice a day at 10:00 am and 17:00 pm until satiation. The experiment was conducted during summer (June-August) in sea area of Tongyeong, Korea. Water quality was monitored twice a week at 08:00-09:00 am.

데이터처리

  • Hepatosomatic index (HI) was equal to viscera weight over body weight times 100. Data were analyzed for the degree of variation and significant differences, based on Analysis of Variance (ANOVA), along with the Tukey’s pair-wise comparison test between treatment means and Duncan’s multiple range test (DMRT) to determine the differences. Analyses were conducted by using the JMP statistical soft- ware (SAS Institute Inc.

이론/모형

  • hr during differentiation steps. Cells viability was de- termined with MTS assay. Fig.
  • were analyzed. Protein content was determined with Kjeldahl method [1]. Total Lipid content was analyzed with Bligh and Dyer [4] method.
  • Total Lipid content was analyzed with Bligh and Dyer [4] method. The moisture and ash of the samples were determined with methods according to AOAC [1]. For fatty acid methyl ester (FAME) analysis, Park et al.
  • Protein content was determined with Kjeldahl method [1]. Total Lipid content was analyzed with Bligh and Dyer [4] method. The moisture and ash of the samples were determined with methods according to AOAC [1].
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