Analysis of S-methylmethionine and S-adenosylmethionine in plant tissue by a dansylation, dual-isotope method

1986 ◽  
Vol 158 (1) ◽  
pp. 93-97 ◽  
Author(s):  
Peter K. Macnicol
1992 ◽  
Vol 13 (6) ◽  
pp. 432-439 ◽  
Author(s):  
M. J. SMITH ◽  
J. JOSEPH ◽  
W. D. FLATMAN ◽  
G. S. BASRAN

2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Romain Tessier ◽  
Nadezda Khodorova ◽  
Juliane Calvez ◽  
Daniel Tomé ◽  
Claire Gaudichon

Abstract Objectives In order to establish DIAAS in humans, the FAO recommended to develop a new method to measure indispensable amino acid (IAA) digestibility. This method uses two isotopic labeling, one for the protein to test and one for a reference protein. Spirulina was chosen as the 13C reference protein due to its commercial availability and affordability. However, the real digestibility of spirulina protein has not been measured in vivo. This work aims to assess the digestibility of spirulina and its repeatability in different meal tests in rats. Methods 23 Wistar male rats were fed a test meal containing 0.5 g of 15 N protein from either spirulina (n = 7), sunflower n = 8) or goat milk isolate (n = 8) and 10 mg of 13C labeled spirulina. Rats were euthanized 6 h after the meal and their digestive luminal contents (stomach, small intestine, ileum, caecum, colon) were collected. Protein digestibility was determined for the test and the reference proteins by measuring 15 N and 13C enrichments in the digesta by EA-IRMS. Caecal IAA digestibility of 13C spirulina was determined by measuring the quantity of AA in the caecum by UPLC and the 13C enrichment in AA by GC-C-IRMS. Group effects were tested using one way ANOVA and differences between groups using Bonferroni test. Results Six hours after ingestion, most of the dietary 15 N and 13C were found in the caecum and colon. But there at least twice more 15 N nitrogen in the caecum and colon in the spirulina group than in the two other groups. Therefore, spirulina protein digestibility (86.0 ± 0.7%) was lower (P < 0.001) than sunflower (95.1 ± 0.5%) and goat milk digestibility (97.2 ± 0.2%). 13C spirulina digestibility tended to be different (P = 0.06) when mixed to spirulina (90.6 ± 0.6%), sunflower (88.8 ± 0.5%) or goat milk (89.0 ± 0.5%) isolates. The caecal IAA digestibility of 13C spirulina was lower in the spirulina group than in sunflower and goat milk groups for every IAA tested, and the mean was 91.6 ± 0.2% for sunflower, 91.4 ± 0.4% for goat milk and 85.4 ± 0.6% for spirulina. Conclusions Spirulina protein is of lower digestibility than other animal or plant proteins. Protein and amino digestibility of a tracer dose of 13C spirulina appears to vary depending on the protein component of the meal. These results question the use of spirulina as a reference protein for the dual isotope method. Funding Sources French Research National Agency (ANR), SOFIPROTEOL. Supporting Tables, Images and/or Graphs


1985 ◽  
Vol 115 (1) ◽  
pp. 111-122 ◽  
Author(s):  
Peter R. Flanagan ◽  
James Cluett ◽  
Michael J. Chamberlain ◽  
Leslie S. Valberg

2015 ◽  
Vol 33 (7_suppl) ◽  
pp. 58-58
Author(s):  
Evan Kovac ◽  
Kai-Hsiung Chang ◽  
Eric A. Klein ◽  
Nima Sharifi

58 Background: Previous work has shown that 5α-reductase prefers androstenedione (AD) in favor of testosterone (T) for dihydrotestosterone (DHT) synthesis in castration-resistant prostate cancer. Yet, 5α-reductase substrate preference in the setting of localized prostate tissue has yet to be fully elucidated. We propose a novel ex-vivo method for tracking steroid handling by the prostate and report our preliminary findings. Methods: Prostate tissue from the peripheral and transitional zones of patients who underwent radical prostatectomy (RP) for localized prostate cancer were incubated in media, along with (3H)-labeled AD and (14C)-labeled T. Media was collected after 7, 24 and 48 hours of incubation, treated with glucuronidase and high performance liquid chromatography (HPLC) was used to identify steroids tagged with either 3H or 14C. Results: In total, 11 patients were consented for tissue procurement at the time of RP. Qualitatively, both AD and T are utilized by the prostate to produce DHT. Over time, concentrations of tritiated AD decreased, while concentrations of tritiated T, 5α-androstanedione and DHT rose. Similarly, concentrations of 14C-T decreased over a 48-hour period, while AD, 5α-androstanedione and DHT increased. Conclusions: We describe a dual isotope method for characterizing androgen handling by prostate tissue from patients with localized prostate cancer, using 2-channel radiolabel detection. Preliminary results show that both AD and T can be utilized by localized prostate cancer tissue. Future work will focus on determining if different phenotypes of androgen handling exist among various patient genotypes and cancer risk groups.


1994 ◽  
Vol 15 (4) ◽  
pp. 241
Author(s):  
M. J. Wilson ◽  
C M. Boivin ◽  
M. A. Green ◽  
S. M. Allen

2002 ◽  
Vol 29 (7) ◽  
pp. 863-875 ◽  
Author(s):  
Alejandro Sánchez-Crespo ◽  
Johan Petersson ◽  
Sven Nyren ◽  
Margareta Mure ◽  
Robb W. Glenny ◽  
...  

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