Selective inhibition of sweetness by the sodium salt of ±2-(4-methoxyphenoxy)propanoic acid

被引:57
作者
Schiffman, SS
Booth, BJ
Sattely-Miller, EA
Graham, BG
Gibes, KM
机构
[1] Duke Univ, Sch Med, Dept Psychiat, Durham, NC 27710 USA
[2] Nutrasweet Co, Mt Prospect, IL 60056 USA
关键词
D O I
10.1093/chemse/24.4.439
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The purpose of this study was to determine the degree to which the sodium salt of +/-2-(4-methoxyphenoxy)propanoic acid (Na-PMP) reduced sweet intensity ratings of 15 sweeteners in mixtures, Na-PMP has been approved for use in confectionary/ frostings, soft candy and snack products in the USA at concentrations up to 150 p.p.m. A trained panel evaluated the effect of Na-PMP on the intensity of the following 15 sweeteners: three sugars (fructose, glucose, sucrose), three terpenoid glycosides (monoammonium glycyrrhizinate, rebaudioside-A, stevioside), two dipeptide derivatives (alitame, aspartame), two N-sulfonylamides (acesulfame-K, sodium saccharin), two polyhydric alcohols (mannitol, sorbitol), 1 dihydrochalcone (neohesperidin dihydrochalcone), one protein (thaumatin) and one sulfamate (sodium cyclamate). Sweeteners were tested at concentrations isosweet with 2.5, 5, 7.5 and 10% sucrose in mixtures with two levels of Na-PMP: 250 and 500 p.p.m. in addition, the 15 sweeteners were tested either immediately or 30 s after a pre-rinse with 500 p.p.m. Na-PMP. in mixtures, Na-PMP at both the 250 and 500 p.p.m. levels significantly blocked sweetness intensity for 12 of the 15 sweeteners. However, when Na-PMP was mixed with three of the 15 sweeteners (monoammonium glycyrrhizinate, neohesperidin dihydrochalcone and thaumatin), there was little reduction in sweetness intensity. Pre-rinsing with Na-PMP both inhibited and enhanced sweetness with the greatest enhancements found for monoammonium glycyrrhizinate, neohesperidin dihydrochalcone and thaumatin, which were not suppressed by Na-PMP in mixtures. The mixture data suggest that Na-PMP is a selective competitive inhibitor of. sweet taste. The finding that pre-treatment can produce enhancement may be due to sensitization of sweetener receptors by Na-PMP.
引用
收藏
页码:439 / 447
页数:9
相关论文
共 27 条
[1]  
[Anonymous], 1992, P229 SAS I INC
[2]   TRANSDUCTION IN TASTE RECEPTOR-CELLS REQUIRES CAMP-DEPENDENT PROTEIN-KINASE [J].
AVENET, P ;
HOFMANN, F ;
LINDEMANN, B .
NATURE, 1988, 331 (6154) :351-354
[3]   THE CHEMICAL BASIS OF SWEETNESS PERCEPTION IN BEVERAGES [J].
BIRCH, GG .
FOOD CHEMISTRY, 1994, 51 (04) :359-364
[4]   Monogeusia for fructose, glucose, sucrose, and maltose [J].
Breslin, PAS ;
Beauchamp, GK ;
Pugh, EN .
PERCEPTION & PSYCHOPHYSICS, 1996, 58 (03) :327-341
[5]   THE ACTIVE ION-TRANSPORT PROPERTIES OF CANINE LINGUAL EPITHELIA INVITRO - IMPLICATIONS FOR GUSTATORY TRANSDUCTION [J].
DESIMONE, JA ;
HECK, GL ;
MIERSON, S ;
DESIMONE, SK .
JOURNAL OF GENERAL PHYSIOLOGY, 1984, 83 (05) :633-656
[6]  
DUBOIS GE, 1991, ACS SYM SER, V450, P261
[7]  
DUBOIS GE, 1997, OLFACTION TASTE CENT, P32
[8]   PHARMACOLOGICAL EVALUATION OF N-METHYL-ACTINODAPHNINE, A NEW VASCULAR ALPHA-ADRENOCEPTOR ANTAGONIST, ISOLATED FROM ILLIGERA-LUZONENSIS [J].
GUH, JH ;
KO, FN ;
YU, SM ;
WU, YC ;
TENG, CM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 279 (01) :33-41
[9]   RS-39604 - A POTENT, SELECTIVE AND ORALLY-ACTIVE 5-HT4 RECEPTOR ANTAGONIST [J].
HEGDE, SS ;
BONHAUS, DW ;
JOHNSON, LG ;
LEUNG, E ;
CLARK, RD ;
EGLEN, RM .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 115 (06) :1087-1095