The distinctiveness of ionic and nonionic bitter stimuli

被引:39
作者
Frank, ME
Bouverat, BP
MacKinnon, BI
Hettinger, TP
机构
[1] Univ Connecticut, Ctr Hlth, Program Neurosci, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Div Neurosci, Dept Oral Diag,Sch Dent Med, Farmington, CT 06030 USA
关键词
bitter taste; ionic bitter stimuli; nonionic bitter stimuli; gustation; golden hamster; species variation; denatonium and quinine; caffeine and SOA; magnesium sulfate;
D O I
10.1016/j.physbeh.2003.09.009
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
The diverse chemical structures of stimuli that are bitter to humans suggest a need for multiple bitter receptors. Reactions of golden hamsters (Mesocricetus auratus) to 1 mM quinine hydrochloride, 3 mM denatonium benzoate, 180 mM magnesium sulfate, 30-100 mM caffeine, and 1 - 1.5 mM sucrose oclaacetate (SOA) were studied to address whether there are multiple sensations elicited by bitter stimuli. Methods included behavioral generalization of LiCl-induced conditioned taste aversions (CTAs), intake preference tests, and electrophysiological recordings from the chorda tympani (CT) nerve. The five compounds, all bitter to humans, were all innately aversive to hamsters. CTA for the ionic quinine HCl, denatonium benzoate, and MgSO4 mutually cross-generalized and these ionic compounds were effective CT stimuli. Yet, the hamsters were much less sensitive to denatonium than humans, requiring a 100,000 times higher concentration for detection. CTA for nonionic caffeine and SOA did not cross-generalize to quinine or the other two ionic stimuli and these nonionic compounds were not effective CT stimuli. SOA and caffeine may elicit aversive reflexes or systemic reactions rather than taste sensations in the animals. Thus, the three ionic and two nonionic compounds form separate aversive stimulus classes in hamsters, neither of which appears to be a close homologue of the human bitter taste. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:421 / 431
页数:11
相关论文
共 103 条
[1]   A novel family of mammalian taste receptors [J].
Adler, E ;
Hoon, MA ;
Mueller, KL ;
Chandrashekar, J ;
Ryba, NJP ;
Zuker, CS .
CELL, 2000, 100 (06) :693-702
[2]  
ANDICK B, 1981, CHEM SENSES, V6, P197
[3]   Adenosine and caffeine modulate circadian rhythms in the Syrian hamster [J].
Antle, MC ;
Steen, NM ;
Mistlberger, RE .
NEUROREPORT, 2001, 12 (13) :2901-2905
[4]   Training and characterization of a quinine taste discrimination in rhesus monkeys [J].
Aspen, J ;
Gatch, MB ;
Woods, JH .
PSYCHOPHARMACOLOGY, 1999, 141 (03) :251-257
[5]   High-resolution genetic mapping of the sucrose octaacetate taste aversion (Soa) locus on mouse Chromosome 6 [J].
Bachmanov, AA ;
Li, X ;
Li, SR ;
Neira, M ;
Beauchamp, GK ;
Azen, EA .
MAMMALIAN GENOME, 2001, 12 (09) :695-699
[6]   SPECIES DIFFERENCES IN TASTE RESPONSES [J].
BEIDLER, LM ;
FISHMAN, IY ;
HARDIMAN, CW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1955, 181 (02) :235-239
[7]   THE CHEMISTRY OF DEFENSE - THEORY AND PRACTICE [J].
BERENBAUM, MR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (01) :2-8
[8]  
BLIZARD DA, 2003, UNPUB VARIATION INTA
[9]   NEUROPHYSIOLOGY OF GENICULATE GANGLION (FACIAL-NERVE) TASTE SYSTEMS - SPECIES COMPARISONS [J].
BOUDREAU, JC ;
SIVAKUMAR, L ;
DO, LT ;
WHITE, TD ;
ORAVEC, J ;
HOANG, NK .
CHEMICAL SENSES, 1985, 10 (01) :89-127
[10]   POLYGENIC DETERMINATION OF QUININE AVERSION AMONG MICE [J].
BOUGHTER, JD ;
HARDER, DB ;
CAPELESS, CG ;
WHITNEY, G .
CHEMICAL SENSES, 1992, 17 (04) :427-434