Titre : |
Artificial sweeteners in US-marketed oral nicotine pouch products : correlation with nicotine contents and effects on product preference |
Type de document : |
document électronique |
Auteurs : |
Sairam, V. Jabba, Auteur ; Peter Silinski, Auteur ; Alicia, Y. Yang, Auteur ; Wenyi Ouyang, Auteur ; Sven, E. Jordt, Auteur |
Editeur : |
National Institutes of Health (NIH) |
Année de publication : |
2024-01 |
Importance : |
p. 263-367 |
Présentation : |
tab., graph |
Langues : |
Anglais (eng) |
Catégories : |
[DIVERS] géographie:Amérique:Amérique du Nord:Etats-Unis [TABAC] chimie du tabac:constituant:alcaloïde:nicotine
|
Mots-clés : |
édulcorant - choix du produit (préférence) |
Index. décimale : |
TA 1.2 Tabac non fumé |
Résumé : |
Introduction:
Artificial sweeteners are listed as ingredients of oral nicotine pouches (ONPs), a new product category with rapidly growing market share. The exact sweetener contents of ONPs remain unknown. Artificial sweeteners in ONPs may facilitate initiation and encourage consumption behavior.
Aims and Methods:
Artificial sweetener contents in major US-marketed ONP brands (Zyn, on!, Velo) were determined by Liquid Chromatography-Mass Spectrometry (LC-MS). Sweetener effects during the initiation of ONP consumption were modeled in single- and two-bottle tests, offering mice ONP extracts calibrated to contain nicotine levels similar to saliva of people who use smokeless tobacco. To examine the contribution of sweet taste perception, consumption behavior was compared between wild-type mice and mice deficient in the sweet taste receptor (Tas1r2-/-).
Results:
Acesulfame-K was detected in on!, Zyn and Velo ONPs (~0.3-0.9 mg/pouch), including products marketed as “Unflavored” or “Flavor ban approved”. In Velo ONPs, sweetened with sucralose (0.6-1.2 mg/pouch), higher nicotine strength products contained higher sucralose levels. Tas1r2-/- mice consumed less ONP extracts than wild-type mice in both sexes. ONP extracts with both higher nicotine and sweetener strengths were tolerated by wildtype mice, but produced stronger aversion in Tas1r2-/- mice.
Conclusions:
ONPs contain significant amounts of artificial sweeteners, with some brands adding more sweetener to ONPs with higher nicotine strengths. Artificial sweeteners, at levels present in ONPs, increase nicotine consumption. Increasing sweetener contents facilitates consumption of ONPs with higher nicotine strengths. Sweetness is a key determinant of ONP use initiation, likely reducing the aversive sensory effects of nicotine and other ONP constituents.
Implications:
Artificial sweeteners such as acesulfame-K or sucralose reduce aversion and facilitate initiation and continued consumption of ONPs. The marketing of some artificially sweetened ONPs as
“Unflavored” of “Flavor ban-approved” suggests that the tobacco industry rejects sweet taste as a determinant for the presence of a characterizing flavor. Sweetness as imparted by artificial
sweeteners in tobacco products needs to be addressed by regulators as a component of a characterizing flavor, with the aim to reduce product appeal and initiation by never users, and
especially youth attracted to sweet flavors. |
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