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1 c counterparts, generally termed 'artificial sweeteners'.
2 sugar, but due to the caloric nature of the sweetener.
3 tense sweetness and is used as a non-caloric sweetener.
4 idely used as non-caloric intense artificial sweetener.
5 ogical activities and functional low-calorie sweetener.
6 has been used as herbal medicine and natural sweetener.
7 n be inhibited by simply changing the liquid sweetener.
8 syrups are gaining popularity as new natural sweeteners.
9 s for commercial-scale production of natural sweeteners.
10 derived, natural low-calorie or zero-calorie sweeteners.
11 r sensation for example by using flavours or sweeteners.
12 sing of sucrose more than that of artificial sweeteners.
13 the consequences of consuming high-intensity sweeteners.
14 of glycosidases and low-calorie carbohydrate sweeteners.
15 her of which dispensed natural or artificial sweeteners.
16 arin and acesulfame K, two common artificial sweeteners.
17 sweet taste receptor and a panel of selected sweeteners.
18 reflect consumption of corn- and cane-based sweeteners.
19 tor and for the design of new noncalorigenic sweeteners.
20 ructose and glucose are not commonly used as sweeteners.
21 y content and large amounts of high-fructose sweeteners.
22 f sugars, protein sweeteners, and artificial sweeteners.
23 de guidance for the design of new artificial sweeteners.
24 and the functionally different groups of the sweeteners.
25 bility of the protein to form dimers or bind sweeteners.
26 1R3 recognizes diverse natural and synthetic sweeteners.
27 sponsiveness to saccharin, sucrose and other sweeteners.
28 dily detected when embedded in mixtures with sweeteners.
29 an sugar and are used as natural, noncaloric sweeteners.
30 ollowed by rebaudioside A and the artificial sweeteners.
31 ed countries, necessitate use of low-calorie sweeteners.
32 tness potency is comparable to known natural sweeteners.
33 and chemosensory analysis of new low-calorie sweeteners.
34 aloric sweeteners and 2% contain low-calorie sweeteners.
35 es diterpene glycosides that are low calorie sweeteners, about 300 times sweeter than saccharose.
37 t correlation between SRP and the artificial sweetener acesulfame, a promising wastewater indicator,
38 sweetened with an alternative high-intensity sweetener (acesulfame potassium; AceK) as well as in ani
42 rn syrup (HFCS) is a fructose-glucose liquid sweetener alternative to sucrose (common table sugar) fi
45 % over 5 years without the use of artificial sweeteners and assessed the effect of the proposed strat
46 rebaudioside A and stevioside in samples of sweeteners and beverages prepared from extracts of the p
47 of both beverages sweetened with low-calorie sweeteners and beverages sweetened with caloric sweetene
48 ent trends in the availability of sugars and sweeteners and changes in intakes of total sugars, added
49 n engineering to design improved low-calorie sweeteners and excipients for food and pharmaceutical pr
50 relation of beverages containing low-calorie sweeteners and fruit juices with cardiometabolic outcome
51 ing T1r3 showed no preference for artificial sweeteners and had diminished but not abolished behavior
52 ifted their preferences away from artificial sweeteners and in favour of glucose after experiencing g
53 the detection of various sugars, artificial sweeteners and L-amino acids is exclusively mediated by
55 assess anthropogenically derived artificial sweeteners and per- and polyfluoroalkyl substances (PFAS
61 categories included visible fats, nutritive sweeteners and sweetened beverages, desserts, and snacks
63 strain variation in consumption of sodium or sweeteners and therefore are attributed to mechanisms sp
64 ases of fruit, processed meat, salty snacks, sweeteners and toppings, SSBs, and total calories, fiber
66 ated in response to sugar but not artificial sweeteners, and are activated by direct delivery of suga
68 ed on development of low-calorie alternative sweeteners, and novel sweeteners-based solutions are evo
71 ccurately predict two Fab structures of anti-sweetener antibodies prior to crystallographic determina
76 s, which are promoted as non-caloric natural sweeteners, are now incorporated into dietary supplement
77 rence for sucralose, treated this artificial sweetener as qualitatively different-compared to sucralo
78 e results suggest that B6 mice perceive some sweeteners as more intense, but NaSaccharin as sweeter a
79 the zwitterionic, trisubstituted guanidinium sweeteners as well as TES, specific differences exist an
80 d whether the addition of the high-intensity sweetener aspartame to a multidisciplinary weight-contro
83 s of mammalian species toward the artificial sweeteners aspartame and neotame are determined by the s
86 shell nanoparticles stabilized with a common sweetener, aspartame (AuNP@Ag@Asm), combine the antimicr
88 few studies describe the fate of artificial sweeteners (ASWs) in wastewater treatment plants (WWTPs)
89 identify 14 different natural and artificial sweeteners at millimolar concentrations, as well as comm
95 h a hydrogen bonded water network, while the sweeteners bind with high affinity directly to the recep
96 consumption of tea sweetened with nutritive sweetener, but not with non-nutritive sweetener, has cal
97 cies-dependent sweet taste toward artificial sweeteners, but also provide guidance for designing nove
98 ought to influence gustatory transduction of sweeteners, but studies have provided conflicting result
99 Steviol glycosides are natural zero-calorie sweeteners, but the most desirable ones are biosynthesiz
100 creases the yield and purity level of stevia sweeteners by the use of environmentally friendly method
103 health and performance, alternative beverage sweeteners, capturing the natural goodness of fruits and
105 indicates that the structure of most potent sweeteners combines a hydrophobic scaffold functionalize
107 analyses targeting the alcohol, caffeine and sweetener components of beverages yielded additional loc
108 6.8 Fab fragment complexed with high-potency sweetener compound SC45647 and nontasting high-affinity
110 he majority of the predicted natural intense sweeteners comprise saponin or stevioside scaffolds.
112 e domain of T1R3 is required for recognizing sweetener cyclamate and sweet taste inhibitor lactisole.
114 ingestive rewarding effect, which artificial sweeteners do not have, signals the nutrient value of su
116 ures composed of blackberry leaf and natural sweeteners (dried apples, prunes, figs, raisins, apricot
117 ence that maternal consumption of artificial sweeteners during pregnancy may influence infant BMI.
124 ing their potential use as safe low-calories sweeteners for individuals who need to control sugar int
125 gnificant difference was shown between the 3 sweeteners for triglyceride and glucose concentrations a
126 ular docking) based for identifying possible sweeteners from a vast database of natural molecules.
128 ood obesity and widespread use of artificial sweeteners, further research is warranted to confirm our
134 eteners and beverages sweetened with caloric sweeteners had poorer dietary quality, exhibited higher
139 The consumption of added sugars (caloric sweeteners) has been linked to obesity, diabetes, and he
140 ritive sweetener, but not with non-nutritive sweetener, has calming effect on consumers with acute st
141 ing the activation of the receptors by these sweeteners have been identified, the molecular mechanism
142 These results suggest that some artificial sweeteners have previously uncharacterized metabolic eff
144 shellfish" (for Li, Co, Cu, Zn, Se and Mo), "sweeteners, honey and confectionery" particularly dark c
145 including the use of alternative low-calorie sweeteners, honey, fruit preparations, novel cultures, l
147 ls of dopamine efflux compared to artificial sweetener in dorsal striatum, whereas disrupting glucose
148 Organic brown rice syrup (OBRS) is used as a sweetener in organic food products as an alternative to
149 saccharide, is increasingly used as an added sweetener in processed foods in the form of high fructos
153 precise role of sodas containing artificial sweeteners in bladder sensations and urological function
155 fect of increased consumption of low-calorie sweeteners in diet beverages on dietary patterns and ene
157 ed AS and SS beverages and use of artificial sweeteners in hot drinks were assessed by a self-reporte
159 he caloric content of foods using artificial sweeteners in rats resulted in increased caloric intake,
160 alysis of the physico-chemical properties of sweeteners in the database indicates that the structure
161 dsorption-desorption properties of different sweeteners in the oral cavity were evaluated using high
163 reasingly replacing sugar with non-nutritive sweeteners in their sweetened products to control or red
164 studies suggest that exposure to artificial sweeteners in utero may predispose offspring to develop
170 tterness associated with the two sulfonamide sweeteners, indicating that hTAS2R antagonists are activ
171 of a 3% solution of saccharin, a noncaloric sweetener, induced synaptic GluA1 similarly to 25% sucro
172 bacterial plasma membrane receptor underlies sweetener-induced growth of a health promoting gut bacte
174 tevia rebaudiana is used commercially in the sweetener industry due to the high content of steviol gl
176 an enduring inhibitory effect on artificial sweetener intake, an effect that did not depend on sweet
178 e to assess whether intake of high-intensity sweeteners is associated with increased food intake and
180 ened beverages without the use of artificial sweeteners is predicted to reduce the prevalence of over
183 however, past research examining low-calorie sweeteners (LCSs) and body weight has produced mixed res
188 suggest that the p-cyanophenyl moiety on the sweetener ligand acts as a molecular pointer in the CD s
189 o the superpotent trisubstituted guanidinium sweetener ligand N-(p-cyanophenyl)-N'-(diphenylmethyl)gu
190 on or metabolism from other fructose-glucose sweeteners like sucrose, honey, and fruit juice concentr
191 aive animals resulted in reduced, artificial sweetener-like intake of glucose during subsequent gluco
193 onsumption of products containing artificial sweeteners may lead to increased body weight and obesity
194 ive consequences of consuming high-intensity sweeteners may occur in those most likely to use them fo
195 h versus low intakes of corn- and cane-based sweeteners (measured as sweetened beverage intake).
197 male rats suggests that consumption of such sweeteners might contribute to, rather than ameliorate,
200 de anion, and the binding of the superpotent sweetener N-(p-cyanophenyl)-N'-(diphenylmethyl)-guanidin
201 12) or similar amounts containing artificial sweeteners (n = 10) were given single-blind in a 10-wk p
203 re of NC6.8 complexed with the super-potency sweetener NC174 reveals that although the same residues
205 rs (glucose and fructose) and 2 high-potency sweeteners (neohesperidin dihydrochalcone and aspartame)
208 reduction is substitution with non-nutritive sweeteners (NNS - artificial sweeteners and stevia).
212 nd metabolism and that effects of artificial sweeteners on adipose tissue biology may be largely inde
213 ng the effect of nutritive and non-nutritive sweeteners on emotional state of participants exposed to
214 determined and the effect of added milk and sweeteners on the antioxidant activity of Kenyan teas wa
215 ng Stevia leaves depends on their final use (sweetener or antioxidant), although, hot air at 180 degr
217 crose, are generally preferred to artificial sweeteners owing to their post-ingestive rewarding effec
219 e receptors by natural sugars and artificial sweeteners, paracrine and endocrine hormones, especially
225 onses of cultured cells expressing the human sweetener receptor directly parallel the psychophysical
226 cetic acids have been synthesized for use as sweetener receptor photoaffinity labeling reagents.
227 es remove the inhibitor from the heteromeric sweetener receptor TAS1R2-TAS1R3, which activates cells
228 This assay measured the reward value of sweeteners relative to lick-induced optogenetic activati
233 se and human precursor cells with artificial sweeteners, saccharin and acesulfame potassium, enhanced
234 s and showed that preference for a synthetic sweetener, SC-45647, was abolished following i.p. inject
235 for the production of a high-potency natural sweetener, sensitive to low temperature during the devel
243 nd sugar alcohols, small molecule artificial sweeteners such as saccharin and acesulfame K, and prote
245 red with sucrose, the more commonly consumed sweetener, such differences are not apparent, and appeti
247 e glycosylation of other naturally occurring sweeteners, such as the mogrosides from monk fruit, and
249 MCH) neurons during intake of the artificial sweetener sucralose increases striatal dopamine levels a
250 ls was promoted by sugars and the noncaloric sweetener sucralose, and blocked by the sweet receptor a
252 tritive sweetener (sugar) or a non-nutritive sweetener (sucralose or stevia) on emotional state, in t
253 t peptide secretion stimulated by artificial sweetener (sucralose), dipeptide (glycylsarcosine), lipi
255 n previously that inclusion of an artificial sweetener, SUCRAM, included in the diet of weaning pigle
257 , with a 5 s evoked period, responses to the sweeteners sucrose, maltose, acesulfame-K, SC-45647, and
258 ry puree supplemented with different natural sweeteners (sucrose, palm sugar, erythritol, xylitol, st
259 inking tea sweetened with either a nutritive sweetener (sugar) or a non-nutritive sweetener (sucralos
260 number of hand luggage items like detergent, sweetener, sugar, acetylsalicylic acid (aspirin), and pa
263 ely recovered from a household detergent and sweetener that can be used as camouflage for the analyte
264 dioside (Reb) D is a high intensity, natural sweetener that shows great potential for substituting su
266 concerns about the consumption of artificial sweeteners, the demand for natural sweeteners has recent
267 st in further Glycyrrhiza spp. to be used as sweeteners, the roots of G. triphylla have been investig
268 the major receptor for sugars and noncaloric sweeteners, there is also evidence of T1r-independent sw
269 ins serves as the primary taste receptor for sweeteners, there is growing evidence that responses to
270 trial sectors, from flavours, fragrances and sweeteners through to natural pesticides and pharmaceuti
272 compare intra-gastric sugar and non-caloric sweetener to investigate how post-ingestive effects can
275 hibition in electrophysiological response to sweeteners upon exposure of the monkey tongue to a combi
281 or differences in the behavioural effects of sweeteners versus sugar, and uncover an essential circui
282 velocity values for aqueous solutions of two sweeteners viz., maltose monohydrate and acesulfame-K ha
285 availability of added or refined sugars and sweeteners was shown to have fallen 16% from 152 g/d in
286 ization evoked by focally applied artificial sweeteners was significantly enhanced by adenosine (50 m
292 alcohols, dietary fibers, syrups and natural sweeteners were used as sucrose alternatives in the prod
293 e purchases of caloric-sweetened desserts or sweeteners, which accounted for a substantial proportion
294 pidly up-regulated by glucose and artificial sweeteners, which act through T1R2 + T1R3/alpha-gustduci
295 discriminator for super- versus high-potency sweeteners, which can be exploited in the design of new,
297 rages sweetened with caloric and low-calorie sweeteners with dietary quality and food-purchasing patt
298 Based on the most exhaustive database of sweeteners with known sweetness values, a new quantitati