scholarly journals Effects of a dairy product (pecorino cheese) naturally rich in cis-9, trans-11 conjugated linoleic acid on lipid, inflammatory and haemorheological variables: A dietary intervention study

2010 ◽  
Vol 20 (2) ◽  
pp. 117-124 ◽  
Author(s):  
F. Sofi ◽  
A. Buccioni ◽  
F. Cesari ◽  
A.M. Gori ◽  
S. Minieri ◽  
...  
2007 ◽  
Vol 107 (4) ◽  
pp. 586-594 ◽  
Author(s):  
Lisa Aronson Friedman ◽  
Linda Snetselaar ◽  
Phyllis Stumbo ◽  
Linda Van Horn ◽  
Baljinder Singh ◽  
...  

2015 ◽  
Vol 55 (2) ◽  
pp. 793-798 ◽  
Author(s):  
Faith I. Umoh ◽  
Ikuko Kato ◽  
Jianwei Ren ◽  
Phillip L. Wachowiak ◽  
Mack T. Ruffin ◽  
...  

The Lancet ◽  
2009 ◽  
Vol 373 (9666) ◽  
pp. 829-835 ◽  
Author(s):  
Jing Chen ◽  
Dongfeng Gu ◽  
Jianfeng Huang ◽  
Dabeeru C Rao ◽  
Cashell E Jaquish ◽  
...  

BMC Nutrition ◽  
2015 ◽  
Vol 1 (1) ◽  
Author(s):  
Courtney Rose Davis ◽  
Janet Bryan ◽  
Jonathan Marcus Hodgson ◽  
Carlene Wilson ◽  
Karen Joy Murphy

2009 ◽  
Vol 103 (2) ◽  
pp. 249-255 ◽  
Author(s):  
Jie Cao ◽  
Ying Zhang ◽  
Wei Chen ◽  
Xiujuan Zhao

Epidemiological studies suggest that a diet high in flavonoids protects against chronic diseases such as CVD and cancer. The objective of the present study was to evaluate the relationship between the intake of quercetin, kaempferol, isorhamnetin, apigenin and luteolin and their corresponding plasma concentrations, and further to explore whether these flavonoids can serve as biomarkers of their intake. Flavonoid intake and their plasma concentrations were analysed in ninety-two subjects consuming their habitual diet. Flavonoid intake was estimated with 7-d dietary records using available data on the flavonoid content of food. Plasma flavonoid concentrations were quantified by HPLC. In addition, we undertook a dietary intervention study to investigate plasma apigenin concentration after the consumption of celery leaf. The mean intake estimates of quercetin, kaempferol, isorhamnetin, apigenin and luteolin amounted to 13·58, 14·97, 12·31, 4·23 and 8·08 mg/d, respectively. The corresponding mean plasma concentrations were 80·23, 57·86, 39·94, 10·62 and 99·90 nmol/l. The mean 7 d intake of five flavonoids was positively correlated to their corresponding plasma concentrations, with correlation coefficients ranging from 0·33 to 0·51 (P < 0·05). In the dietary intervention study, the plasma apigenin concentration rose after celery leaf ingestion, and fell within 28 h to below the limit of detection (2·32 nmol/l). The present results suggest that quercetin, kaempferol, isorhamnetin, apigenin and luteolin are bioavailable from the diet. The levels of fasting plasma flavonoids seem to be suitable biomarkers of short-term intake. The combination of plasma flavonoids with their intake may prove useful when the possible health-protective effects of flavonoids are studied.


2010 ◽  
Vol 21 (9) ◽  
pp. 1379-1386 ◽  
Author(s):  
Elizabeth H. Ruder ◽  
Terryl J. Hartman ◽  
Michael J. Rovine ◽  
Joanne F. Dorgan

1993 ◽  
Vol 76 (3) ◽  
pp. 644-649 ◽  
Author(s):  
Nalur Chandrasekaran Shantha ◽  
Eric Andrew Decker ◽  
Bernhard Hennig

Abstract Four methylation methods were evaluated for use in the gas chromatographic (GC) quantitation of conjugated linoleic acid (CLA) isomers, which are potential anticarcinogen. The methods were (1) sodium methoxide in methanol (NaOMe-MeOH), (2) American Oil Chemists' Society (AOCS) procedure Ce 2-66, which involves methanolic sodium hydroxide followed by boron trifluoride in methanol, (3) tetramethylguanidine in methanol (TMG-MeOH), and (4) direct transesterification with methanolbenzene- acetyl chloride (DAC). Purified methyl esters of isomerized linoleic acid containing 86% CLA isomers were methylated and analyzed by GC. The AOCS and DAC methods resulted in 3 and 50% losses in cis-9,trans-11-octadecadienoic acid (9c, 111 CLA isomer) and trans-10,cis-12 octadecadienoic acid (10t, 12c CLA isomers), respectively. Compared with the control, the AOCS and DAC methods increased the yield of the trans,trans CLA isomers (trans-9,trans-11- and trans-10, trans-12-octadecadienoic acid) by 1.07-fold and a 10-fold, respectively. A non-CLA artifact that eluted close to CLA peaks was formed during methylation by the AOCS and DAC methods. Thus, the DAC and AOCS methods are not suitable for quantitation of CLA isomers. The NaOMe-MeOH and TMG-MeOH methods, however, are suitable for quantitation of CLA isomers in fats containing low concentrations of free fatty acids.


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