High Endogenous Salivary Amylase Activity Is Associated with Improved Glycemic Homeostasis following Starch Ingestion in Adults

被引:149
作者
Mandel, Abigail L. [1 ]
Breslin, Paul A. S. [1 ,2 ]
机构
[1] Monell Chem Senses Ctr, Philadelphia, PA 19104 USA
[2] Rutgers State Univ, Dept Nutr Sci, Sch Environm & Biol Sci, New Brunswick, NJ 08903 USA
关键词
POSTPRANDIAL GLYCEMIA; GLUCOSE; DIGESTION; INSULIN; HEALTH; TASTE; FOOD; EVOLUTION; RESPONSES; HUMANS;
D O I
10.3945/jn.111.156984
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
In the current study, we determined whether increased digestion of starch by high salivary amylase concentrations predicted postprandial blood glucose following starch ingestion. Healthy, nonobese individuals were prescreened for salivary amylase activity and classified as high (HA) or low amylase (LA) if their activity levels per minute fell 1 SD higher or lower than the group mean, respectively. Fasting HA (n = 7) and LA In = 7) individuals participated in 2 sessions during which they ingested either a starch (experimental) or glucose solution (control) on separate days. Blood samples were collected before, during, and after the participants drank each solution. The samples were analyzed for plasma glucose and insulin concentrations as well as diploid AMY? gene copy number. HA individuals had significantly more AMY1 gene copies within their genomes than did the EA individuals. We found that following starch ingestion, HA individuals had significantly lower postprandial blood glucose concentrations at 45, 60, and 75 min, as well as significantly lower AUC and peak blood glucose concentrations than the LA individuals. Plasma insulin concentrations in the HA group were significantly higher than baseline early in the testing session, whereas insulin concentrations in the LA group did not increase at this time. Following ingestion of the glucose solution, however, blood glucose and insulin concentrations did not differ between the groups. These observations are interpreted to suggest that HA individuals may be better adapted to ingest starches, whereas LA individuals may be at greater. risk for insulin resistance and diabetes if chronically ingesting starch-rich diets. J. Nutr. 142: 853-858, 2012.
引用
收藏
页码:853 / 858
页数:6
相关论文
共 31 条
[1]   The cephalic insulin response to meal ingestion in humans is dependent on both cholinergic and noncholinergic mechanisms and is important for postprandial glycemia [J].
Ahrén, B ;
Holst, JJ .
DIABETES, 2001, 50 (05) :1030-1038
[2]   Monogeusia for fructose, glucose, sucrose, and maltose [J].
Breslin, PAS ;
Beauchamp, GK ;
Pugh, EN .
PERCEPTION & PSYCHOPHYSICS, 1996, 58 (03) :327-341
[3]   Origins and evolution of the Western diet: health implications for the 21st century [J].
Cordain, L ;
Eaton, SB ;
Sebastian, A ;
Mann, N ;
Lindeberg, S ;
Watkins, BA ;
O'Keefe, JH ;
Brand-Miller, J .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2005, 81 (02) :341-354
[4]   Contributions to the physiology of gastric secretion XIII. The response of the glands to substances applied to the gastric mucosa [J].
Farrell, JI .
AMERICAN JOURNAL OF PHYSIOLOGY, 1928, 85 (03) :672-684
[5]   STARCH HYDROLYSIS IN MAN - INTRALUMINAL PROCESS NOT REQUIRING MEMBRANE DIGESTION [J].
FOGEL, MR ;
GRAY, GM .
JOURNAL OF APPLIED PHYSIOLOGY, 1973, 35 (02) :263-267
[6]   THE HUMAN ALPHA-AMYLASE MULTIGENE FAMILY CONSISTS OF HAPLOTYPES WITH VARIABLE NUMBERS OF GENES [J].
GROOT, PC ;
BLEEKER, MJ ;
PRONK, JC ;
ARWERT, F ;
MAGER, WH ;
PLANTA, RJ ;
ERIKSSON, AW ;
FRANTS, RR .
GENOMICS, 1989, 5 (01) :29-42
[7]   SALIVA - ITS ROLE IN HEALTH AND DISEASE [J].
HERRERA, JL ;
LYONS, MF ;
JOHNSON, LF .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1988, 10 (05) :569-578
[8]   Physical and chemical transformations of cereal food during oral digestion in human subjects [J].
Hoebler, C ;
Karinthi, A ;
Devaux, MF ;
Guillon, F ;
Gallant, DJG ;
Bouchet, B ;
Melegari, C ;
Barry, JL .
BRITISH JOURNAL OF NUTRITION, 1998, 80 (05) :429-436
[9]   SOME PROPERTIES OF SALIVARY AMYLASE - SURVEY OF LITERATURE AND SOME OBSERVATIONS [J].
JACOBSEN, N ;
MELVAER, KL ;
HENSTENP.A .
JOURNAL OF DENTAL RESEARCH, 1972, 51 (02) :381-&
[10]  
Leuchs EF., 1831, Ann. der Phys. und Chemie, V98, P623