Chlorogenic Acid Moderately Decreases the Quality of Whey Proteins in Rats
详细信息    查看全文
文摘
During processing and storage, phenolic compounds (PCs) may react with food protein bound aminoacids (AAs). Such reactions have been reported to change physicochemical and to decrease in vitrodigestion properties of proteins. A rat growth and nitrogen (N) balance study was conducted to provewhether derivatization with chlorogenic acid (CA) affects the nutritional quality of -lactoglobulin (-LG). Test diets (10% protein level) contained nonderivatized -LG (LG, treated under omission ofCA), low derivatization level -LG (LGL), high derivatization level -LG (LGH), or casein supplementedwith L-methionine (0.3% of diet; C+met) as an internal standard. An additional group received untreated-LG supplemented with pure CA (1.03% of diet; LG+CA). The AA composition of test proteins,plasma AAs, and liver glutathione (GSH) concentrations were determined. Protein digestibility-corrected amino acid score (PDCAAS) was calculated using human or rat AA requirement patternsand rat fecal digestibility values. N excretion was significantly higher in feces and lower in urine ofrats fed with LGH as compared to LG and LGL. Consequently, true N digestibility (TND) wassignificantly lower with LGH as compared to LG and LGL. The lower content of methionine, cysteine,lysine, and tryptophan in LGH corresponded to a reduced TND. Net protein utilization (NPU) was notdifferent between treated -LG fed diet groups but was lower than in LG+CA and C+met fed groups.Only at a relatively high level of derivatization with CA, the otherwise good nutritional quality of -LGis affected so that TND is reduced, while NPU still remains unaffected. Derivatization of -LG withCA does not seem to lead to an additional deficiency in a specific indispensable AA in growing ratsfed with 10% protein.Keywords: Chlorogenic acid; lactoglobulin isolate derivatization; protein quality; nitrogen balance;rats

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700