INHIBITION OF HAMSTER CHORDA TYMPANI NEURAL RESPONSE BY COPPER CHLORIDE

Citation
We. Myers et al., INHIBITION OF HAMSTER CHORDA TYMPANI NEURAL RESPONSE BY COPPER CHLORIDE, Chemical senses, 18(5), 1993, pp. 495-507
Citations number
29
Categorie Soggetti
Physiology,Neurosciences,Chemistry
Journal title
ISSN journal
0379864X
Volume
18
Issue
5
Year of publication
1993
Pages
495 - 507
Database
ISI
SICI code
0379-864X(1993)18:5<495:IOHCTN>2.0.ZU;2-F
Abstract
Copper chloride was evaluated as a specific inhibitor of neural respon ses to sweet taste stimuli in the golden hamster (Mesocricetus auratus ). The chorda tympani whole-nerve response to taste stimuli was record ed before and after the tongue was treated 30 S with 0.01, 0.1 and 1 m M CuCl2. Sweet stimuli [sucrose, fructose, saccharin (calcium salt), D -phenylalanine], which primarily stimulate chorda tympani S fibers, an d non-sweet stimuli (NaCl, NH4Cl) were used. At 0.01 mM, copper chlori de had little effect. At 0.10 mM it partially inhibited responses to s ucrose and saccharin, but had little effect on responses to D-Phe, fru ctose, NaCl, NH4Cl, or a mixture of sucrose plus L-Phe. L-Phe, which h as the same chelating properties as D-Phe, is not an S-fiber stimulus and likely reduced sucrose inhibiton by chelating the cupric ion. Anal ysis of concentration - response functions revealed that 0.1 mM copper chloride inhibited the neural response to low concentrations of sucro se by about 25%, but did not significantly inhibit high concentrations of sucrose, suggesting competitive inhibition. In contrast, 0.1 mM Cu Cl2 reduced saccharin responses by 25% throughout the effective range, suggesting non-competitive inhibition. Occupation of a saccharide rec eptor site by copper may interfere with dimer but not monomer receptio n and distort the saccharin receptor site. At 1 mM, CuCl2 non-competit ively inhibited responses to sucrose, fructose, saccharin and the non- sweet NaCl (an N-fiber stimulus), but not NH4Cl (an H-fiber stimulus). The mechanisms of copper chloride inhibition are difficult to establi sh because its effects are weak at concentrations where they are speci fic.