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      KCI등재 SCOPUS SCIE

      The Analysis of Vitamin C Concentration in Organs of Gulo−/− Mice Upon Vitamin C Withdrawal

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      https://www.riss.kr/link?id=A103907934

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      다국어 초록 (Multilingual Abstract)

      Background: Vitamin C is an essential nutrient for maintaining human life. Vitamin C insufficiency in the plasma is closely related with the development of scurvy. However, in vivo kinetics of vitamin C regarding its storage and consumption is still largely unknown. Methods: We used Gulo−/− mice, which cannot synthesize vitamin C like human. Vitamin C level in plasma and organs from Gulo−/−mice was examined, and it compared with the level of wild-type mice during 5 weeks. Results: The significant weight loss of Gulo−/− mice was shown at 3 weeks after vitamin C withdrawal. However, there was no differences between wild-type and vitamin C-supplemented Gulo−/−mice (3.3 g/L in drinking water). The concentration of vitamin C in plasma and organs was significantly decreased at 1week after vitamin C withdrawal. Vitamin C is preferentially deposited in adrenal gland, lymph node, lung, and brain.
      There were no significant changes in the numbers and CD4/CD8 ratio of splenocytes in Gulo−/− mice with vitamin C withdrawal for 4 weeks. And the architecture of spleen in Gulo−/− mice was disrupted at 5 weeks after vitamin C withdrawal. Conclusion: The vitamin C level of Gulo−/− mice was considerably decreased from 1 week after vitamin C withdrawal. Vitamin C is preferentially stored in some organs such as brain, adrenal gland and lung.
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      Background: Vitamin C is an essential nutrient for maintaining human life. Vitamin C insufficiency in the plasma is closely related with the development of scurvy. However, in vivo kinetics of vitamin C regarding its storage and consumption is still l...

      Background: Vitamin C is an essential nutrient for maintaining human life. Vitamin C insufficiency in the plasma is closely related with the development of scurvy. However, in vivo kinetics of vitamin C regarding its storage and consumption is still largely unknown. Methods: We used Gulo−/− mice, which cannot synthesize vitamin C like human. Vitamin C level in plasma and organs from Gulo−/−mice was examined, and it compared with the level of wild-type mice during 5 weeks. Results: The significant weight loss of Gulo−/− mice was shown at 3 weeks after vitamin C withdrawal. However, there was no differences between wild-type and vitamin C-supplemented Gulo−/−mice (3.3 g/L in drinking water). The concentration of vitamin C in plasma and organs was significantly decreased at 1week after vitamin C withdrawal. Vitamin C is preferentially deposited in adrenal gland, lymph node, lung, and brain.
      There were no significant changes in the numbers and CD4/CD8 ratio of splenocytes in Gulo−/− mice with vitamin C withdrawal for 4 weeks. And the architecture of spleen in Gulo−/− mice was disrupted at 5 weeks after vitamin C withdrawal. Conclusion: The vitamin C level of Gulo−/− mice was considerably decreased from 1 week after vitamin C withdrawal. Vitamin C is preferentially stored in some organs such as brain, adrenal gland and lung.

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      다국어 초록 (Multilingual Abstract)

      Background: Vitamin C is an essential nutrient for maintaining human life. Vitamin C insufficiency in the plasma is closely related with the development of scurvy. However, in vivo kinetics of vitamin C regarding its storage and consumption is still largely unknown. Methods: We used Gulo−/− mice, which cannot synthesize vitamin C like human. Vitamin C level in plasma and organs from Gulo−/−mice was examined, and it compared with the level of wild-type mice during 5 weeks. Results: The significant weight loss of Gulo−/− mice was shown at 3 weeks after vitamin C withdrawal. However, there was no differences between wild-type and vitamin C-supplemented Gulo−/−mice (3.3 g/L in drinking water). The concentration of vitamin C in plasma and organs was significantly decreased at 1week after vitamin C withdrawal. Vitamin C is preferentially deposited in adrenal gland, lymph node, lung, and brain.
      There were no significant changes in the numbers and CD4/CD8 ratio of splenocytes in Gulo−/− mice with vitamin C withdrawal for 4 weeks. And the architecture of spleen in Gulo−/− mice was disrupted at 5 weeks after vitamin C withdrawal. Conclusion: The vitamin C level of Gulo−/− mice was considerably decreased from 1 week after vitamin C withdrawal. Vitamin C is preferentially stored in some organs such as brain, adrenal gland and lung.
      번역하기

      Background: Vitamin C is an essential nutrient for maintaining human life. Vitamin C insufficiency in the plasma is closely related with the development of scurvy. However, in vivo kinetics of vitamin C regarding its storage and consumption is still l...

      Background: Vitamin C is an essential nutrient for maintaining human life. Vitamin C insufficiency in the plasma is closely related with the development of scurvy. However, in vivo kinetics of vitamin C regarding its storage and consumption is still largely unknown. Methods: We used Gulo−/− mice, which cannot synthesize vitamin C like human. Vitamin C level in plasma and organs from Gulo−/−mice was examined, and it compared with the level of wild-type mice during 5 weeks. Results: The significant weight loss of Gulo−/− mice was shown at 3 weeks after vitamin C withdrawal. However, there was no differences between wild-type and vitamin C-supplemented Gulo−/−mice (3.3 g/L in drinking water). The concentration of vitamin C in plasma and organs was significantly decreased at 1week after vitamin C withdrawal. Vitamin C is preferentially deposited in adrenal gland, lymph node, lung, and brain.
      There were no significant changes in the numbers and CD4/CD8 ratio of splenocytes in Gulo−/− mice with vitamin C withdrawal for 4 weeks. And the architecture of spleen in Gulo−/− mice was disrupted at 5 weeks after vitamin C withdrawal. Conclusion: The vitamin C level of Gulo−/− mice was considerably decreased from 1 week after vitamin C withdrawal. Vitamin C is preferentially stored in some organs such as brain, adrenal gland and lung.

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      참고문헌 (Reference)

      1 Linster CL, "Vitamin C. Biosynthesis, recycling and degradation in mammals" 274 : 1-22, 2007

      2 Lee SK, "Vitamin C suppresses proliferation of the human melanoma cell SK-MEL-2 through the inhibition of cyclo oxygenase-2 (COX-2) expression and the modulation of insulin- like growth factor II (IGF-II) production" 216 : 180-188, 2008

      3 Levine M, "Vitamin C pharmacokinetics in healthy volunteers: evidence for a recommended dietary allowance" 93 : 3704-3709, 1996

      4 Harrison FE, "Vitamin C distribution and retention in the mouse brain" 1348 : 181-186, 2010

      5 Padayatty SJ, "Vitamin C as an antioxidant: evaluation of its role in disease prevention" 22 : 18-35, 2003

      6 Carr AC, "Toward a new recommended dietary allowance for vitamin C based on antioxidant and health effects in humans" 69 : 1086-1107, 1999

      7 Englard S, "The biochemical functions of ascorbic acid" 6 : 365-406, 1986

      8 Cameron E, "Supplemental ascorbate in the supportive treatment of cancer: Prolongation of survival times in terminal human cancer" 73 : 3685-3689, 1976

      9 Kang JS, "Sodium ascorbate (vitamin C) induces apoptosis in melanoma cells via the down-regulation of transferrin receptor dependent iron uptake" 204 : 192-197, 2005

      10 Chen Q, "Pharmacologic doses of ascorbate act as a prooxidant and decrease growth of aggressive tumor xenografts in mice" 105 : 11105-11109, 2008

      1 Linster CL, "Vitamin C. Biosynthesis, recycling and degradation in mammals" 274 : 1-22, 2007

      2 Lee SK, "Vitamin C suppresses proliferation of the human melanoma cell SK-MEL-2 through the inhibition of cyclo oxygenase-2 (COX-2) expression and the modulation of insulin- like growth factor II (IGF-II) production" 216 : 180-188, 2008

      3 Levine M, "Vitamin C pharmacokinetics in healthy volunteers: evidence for a recommended dietary allowance" 93 : 3704-3709, 1996

      4 Harrison FE, "Vitamin C distribution and retention in the mouse brain" 1348 : 181-186, 2010

      5 Padayatty SJ, "Vitamin C as an antioxidant: evaluation of its role in disease prevention" 22 : 18-35, 2003

      6 Carr AC, "Toward a new recommended dietary allowance for vitamin C based on antioxidant and health effects in humans" 69 : 1086-1107, 1999

      7 Englard S, "The biochemical functions of ascorbic acid" 6 : 365-406, 1986

      8 Cameron E, "Supplemental ascorbate in the supportive treatment of cancer: Prolongation of survival times in terminal human cancer" 73 : 3685-3689, 1976

      9 Kang JS, "Sodium ascorbate (vitamin C) induces apoptosis in melanoma cells via the down-regulation of transferrin receptor dependent iron uptake" 204 : 192-197, 2005

      10 Chen Q, "Pharmacologic doses of ascorbate act as a prooxidant and decrease growth of aggressive tumor xenografts in mice" 105 : 11105-11109, 2008

      11 Chojkier M, "Peterkofsky B: Specifically decreased collagen biosynthesis in scurvy dissociated from an effect on proline hydroxylation and correlated with body weight loss. In vitro studies in guinea pig calvarial bones" 72 : 826-835, 1983

      12 Ellis GR, "Neutrophil superoxide anion--generating capacity, endothelial function and oxidative stress in chronic heart failure: effects of short- and long-term vitamin C therapy" 36 : 1474-1482, 2000

      13 Burns JJ, "Missing step in man, monkey and guinea pig required for the biosynthesis of L-ascorbic acid" 180 : 553-, 1957

      14 Wintergerst ES, "Immune-enhancing role of vitamin C and zinc and effect on clinical conditions" 50 : 85-94, 2006

      15 Nishikimi M, "Guinea pigs possess a highly mutated gene for L-gulono-gamma-lactone oxidase, the key enzyme for L-ascorbic acid biosynthesis missing in this species" 267 : 21967-21972, 1992

      16 Koike K, "Complete lack of vitamin C intake generates pulmonary emphysema in senescence marker protein-30 knockout mice" 298 : L784-792, 2010

      17 Nishikimi M, "Cloning and chromosomal mapping of the human nonfunctional gene for L-gulono-gamma-lactone oxidase, the enzyme for L-ascorbic acid biosynthesis missing in man" 269 : 13685-13688, 1994

      18 Parsons KK, "Ascorbic acid-independent synthesis of collagen in mice" 290 : E1131-1139, 2006

      19 Peterkofsky B, "Ascorbate requirement for hydroxylation and secretion of procollagen: relationship to inhibition of collagen synthesis in scurvy" 54 (54): 1135S-1140S, 1991

      20 Frei B, "Ascorbate is an outstanding antioxidant in human blood plasma" 86 : 6377-6381, 1989

      21 Maeda N, "Aortic wall damage in mice unable to synthesize ascorbic acid" 97 : 841-846, 2000

      22 Odumosu A, "Anorectic drugs and vitamin C: role in appetite and brain ascorbic acid in guineapigs" 51 : 247-253, 1981

      23 Sauberlich HE, "A history of scurvy and vitamin C. Vitamin C in health and disease" Marcel Dekker 1-24, 1997

      24 Tsukaguchi H, "A family of mammalian Na+-dependent L-ascorbic acid transporters" 399 : 70-75, 1999

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2025 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2016-01-01 평가 우수등재학술지 선정 (계속평가)
      2012-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2009-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2008-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2007-01-01 평가 등재후보학술지 유지 (등재후보2차) KCI등재후보
      2006-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.36 0.36 0.29
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.24 0.2 0.636 0
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