Meal cysteine improves postprandial glucose control in rats fed a high-sucrose meal

被引:45
作者
Blouet, Clemence
Mariotti, Francois
Mikogami, Takashi
Tome, Daniel
Huneau, Jean-Francois [2 ]
机构
[1] Armor Proteines SAS, F-35460 St Brice En Cogles, France
[2] Inst Natl Agronom, INAPG, INRA, UMR 914, F-75005 Paris, France
关键词
alpha-lactalbumin; cysteine; N-acetylcysteine; glutathione; glucose homeostasis;
D O I
10.1016/j.jnutbio.2006.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Whey protein, particularly the alpha-lactalbumin fraction, are rich in cysteine (cys) and could therefore favor postprandial glucose homeostasis by a glutathione-mediated effect. This work investigates the effects of the ingestion of an alpha-lactalbumin-rich whey concentrate (alpha-LAC) during a high-sucrose (HS) meal on postprandial glucose homeostasis in healthy rats. In the first experiment, rats received an HS meal containing 14% protein, in which the protein source was either alpha-LAC (HSa) or total milk proteins, alone (HS0) or supplemented with 17 mg (HS1) or 59 mg (HS2) of N-acetylcysteine (NAC). This resulted in a total cys content 3.6-fold higher in the HS1 and HSa meals and 12-fold higher in the HS2 meal, when compared to the HS0 meal. Postprandial parameters were monitored for 3 h after ingestion of the meal. The same measurements were performed on rats injected with 4 mmol/kg of buthionine sulfoximine (BSO), a specific inhibitor of glutathione synthesis. Increasing the meal's cys content dose-dependently reduced both postprandial glucose and insulin (P<.05). The inhibition of glutathione synthesis with BSO injection abrogated the beneficial effects of NAC supplementation on postprandial glucose response but did not affect those of alpha-LAC. These results show that (1) the substitution of alpha-LAC for total milk protein reduces glucose response, as does the addition of a cys donor to the meal, (2) but contrary to those of a simple cys donor, the beneficial effects of alpha-LAC are not entirely mediated by glutathione synthesis, suggesting additional mechanisms. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:519 / 524
页数:6
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