{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/101824"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/101824","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Potential metabolic effect of sucralose following an oral glucose load in subjects with obesity and normal-weight subjects","abstract":"Objective: Whether sucralose, the most commonly used non-nutritive sweetener (NNS), affects glucose metabolism in people is unclear. It has been reported that, when consumed acutely before an oral glucose tolerance test (OGTT), sucralose enhances insulinemic responses and decreases insulin sensitivity in subjects with obesity who are not regular consumers of NNS. However, studies in normal-weight adults, none of which control for use of NNS, found sucralose does not affect insulin responses to the ingestion of glucose or other carbohydrates. The objectives of the current study are to determine if those effects of sucralose can be replicated in subjects with obesity, are generalizable to normal-weight subjects when controlling for history of NNS use, and are caused merely by the sweet taste of sucralose (i.e., sham-feeding). In addition, with the aim of identifying potential mechanisms by which sucralose may decrease postprandial insulin sensitivity, we here investigated whole-body glucose kinetics by using a dual-tracer approach. Finally, we tested the hypothesis that, due to the compromised intestinal permeability associated with obesity, sucralose consumption is associated with higher plasma sucralose concentrations in people with obesity. Research Design and Methods: Ten normal-weight subjects (BMI: 22.8 ± 0.9 kg/m2) and nine subjects with obesity (BMI: 37.7 ± 6.1 kg/m2), all non-regular users of NNS, non-diabetic, and without significant insulin resistance (based on a homeostatic model assessment of insulin resistance score < 3), underwent a 5-hour modified OGTT in which ingested glucose was labeled with one tracer while a second glucose tracer was infused intravenously at a constant rate on three separate testing days. Each testing day differed only by which pre-load solution (water ingestion (control condition), sucralose ingestion (experimental condition), or sucralose sham-fed (taste condition)) was administered 10 minutes prior to the OGTT in a randomized crossover design. Blood samples were taken throughout observation to determine plasma glucose, insulin, C-peptide, glucose-dependent insulinotropic polypeptide (GIP), glucose tracer-to-tracee ratio, and sucralose concentrations. Results: In subjects with obesity, compared to the control condition, sucralose sham-feeding reduced insulin and C-peptide concentrations within the first hour of the OGTT (both p-values ≤ 0.05), whereas sucralose ingestion increased plasma C-peptide incremental area under the curve (iAUC) by 22 ± 10% (p < 0.05) and tended to increase plasma insulin iAUC by 16 ± 9% (p = 0.09) and plasma glucose iAUC by 34 ± 12% (p = 0.06). No condition affected GIP. There were no differences among conditions in the degree of suppression of endogenous glucose production (EGP) after the glucose load, but both sucralose conditions affected the pattern of oral glucose rate of appearance (Ra) and glucose rate of disappearance (Rd). Compared to the water condition, sucralose affected the pattern of change with time including i) a greater decline (50-60 min) and subsequently a reduced decline (120-140 min) in oral glucose Ra (p = 0.03), and ii) a reduced glucose Rd (50-80 min) and subsequently an increased glucose Rd (140-160 min) after the glucose load (p < 0.05). While the reduction in glucose Rd during the taste condition and the increase in Rd 140-160 min after the glucose load could be explained by prevailing plasma insulin concentrations, the reduction in glucose Rd 50-80 min after the glucose load on the experimental condition cannot. During this time period, plasma insulin concentrations after sucralose ingestion were similar or higher than after water ingestion, which is in agreement with previous results of a decreased insulin sensitivity in subjects with obesity when sucralose ingestion preceded an OGTT. In normal-weight subjects, there were no significant differences among conditions in plasma glucose, C-peptide, GIP, or plasma glucose or hormones iAUCs, but both sucralose conditions tended to equally lower mean plasma insulin concentrations following the OGTT (p = 0.09) and suppressed EGP to a greater degree (p = 0.09) compared to water. There were no significant differences between groups for peak sucralose concentrations, the time to reach peak sucralose concentration, and plasma sucralose iAUCs (all p-values > 0.19). Conclusions: These data demonstrate that sucralose differentially affects hormonal responses to an oral glucose load in subjects with obesity and normal weight subjects. Sucralose ingestion (not merely its taste) increases insulin secretion to an oral glucose load and transiently reduces glucose Rd in people with obesity, but not in normal-weight subjects. These findings support the hypothesis that sucralose may have adverse effects on glucose metabolism in people with obesity, which is the group that most frequently consumes NNS to facilitate weight management. These data also underscore a physiological role for sweetness perception in glucose homeostasis, which supports the notion that sweetness, regardless of an associated caloric contribution, should be consumed in moderation.","abstract_html":"Objective: Whether sucralose, the most commonly used non-nutritive sweetener (NNS), affects glucose metabolism in people is unclear. It has been reported that, when consumed acutely before an oral glucose tolerance test (OGTT), sucralose enhances insulinemic responses and decreases insulin sensitivity in subjects with obesity who are not regular consumers of NNS. However, studies in normal-weight adults, none of which control for use of NNS, found sucralose does not affect insulin responses to the ingestion of glucose or other carbohydrates. The objectives of the current study are to determine if those effects of sucralose can be replicated in subjects with obesity, are generalizable to normal-weight subjects when controlling for history of NNS use, and are caused merely by the sweet taste of sucralose (i.e., sham-feeding). In addition, with the aim of identifying potential mechanisms by which sucralose may decrease postprandial insulin sensitivity, we here investigated whole-body glucose kinetics by using a dual-tracer approach. Finally, we tested the hypothesis that, due to the compromised intestinal permeability associated with obesity, sucralose consumption is associated with higher plasma sucralose concentrations in people with obesity. Research Design and Methods: Ten normal-weight subjects (BMI: 22.8 ± 0.9 kg/m2) and nine subjects with obesity (BMI: 37.7 ± 6.1 kg/m2), all non-regular users of NNS, non-diabetic, and without significant insulin resistance (based on a homeostatic model assessment of insulin resistance score &lt; 3), underwent a 5-hour modified OGTT in which ingested glucose was labeled with one tracer while a second glucose tracer was infused intravenously at a constant rate on three separate testing days. Each testing day differed only by which pre-load solution (water ingestion (control condition), sucralose ingestion (experimental condition), or sucralose sham-fed (taste condition)) was administered 10 minutes prior to the OGTT in a randomized crossover design. Blood samples were taken throughout observation to determine plasma glucose, insulin, C-peptide, glucose-dependent insulinotropic polypeptide (GIP), glucose tracer-to-tracee ratio, and sucralose concentrations. Results: In subjects with obesity, compared to the control condition, sucralose sham-feeding reduced insulin and C-peptide concentrations within the first hour of the OGTT (both p-values ≤ 0.05), whereas sucralose ingestion increased plasma C-peptide incremental area under the curve (iAUC) by 22 ± 10% (p &lt; 0.05) and tended to increase plasma insulin iAUC by 16 ± 9% (p = 0.09) and plasma glucose iAUC by 34 ± 12% (p = 0.06). No condition affected GIP. There were no differences among conditions in the degree of suppression of endogenous glucose production (EGP) after the glucose load, but both sucralose conditions affected the pattern of oral glucose rate of appearance (Ra) and glucose rate of disappearance (Rd). Compared to the water condition, sucralose affected the pattern of change with time including i) a greater decline (50-60 min) and subsequently a reduced decline (120-140 min) in oral glucose Ra (p = 0.03), and ii) a reduced glucose Rd (50-80 min) and subsequently an increased glucose Rd (140-160 min) after the glucose load (p &lt; 0.05). While the reduction in glucose Rd during the taste condition and the increase in Rd 140-160 min after the glucose load could be explained by prevailing plasma insulin concentrations, the reduction in glucose Rd 50-80 min after the glucose load on the experimental condition cannot. During this time period, plasma insulin concentrations after sucralose ingestion were similar or higher than after water ingestion, which is in agreement with previous results of a decreased insulin sensitivity in subjects with obesity when sucralose ingestion preceded an OGTT. In normal-weight subjects, there were no significant differences among conditions in plasma glucose, C-peptide, GIP, or plasma glucose or hormones iAUCs, but both sucralose conditions tended to equally lower mean plasma insulin concentrations following the OGTT (p = 0.09) and suppressed EGP to a greater degree (p = 0.09) compared to water. There were no significant differences between groups for peak sucralose concentrations, the time to reach peak sucralose concentration, and plasma sucralose iAUCs (all p-values &gt; 0.19). Conclusions: These data demonstrate that sucralose differentially affects hormonal responses to an oral glucose load in subjects with obesity and normal weight subjects. Sucralose ingestion (not merely its taste) increases insulin secretion to an oral glucose load and transiently reduces glucose Rd in people with obesity, but not in normal-weight subjects. These findings support the hypothesis that sucralose may have adverse effects on glucose metabolism in people with obesity, which is the group that most frequently consumes NNS to facilitate weight management. These data also underscore a physiological role for sweetness perception in glucose homeostasis, which supports the notion that sweetness, regardless of an associated caloric contribution, should be consumed in moderation.","abstract_has_math":false,"creators":["Nichol, Alexander Daniel"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"M.S.","degree_level":"Thesis","degree_discipline":"Food Science & Human Nutrition","degree_department":null,"school":null,"contributors":["Pepino, Yanina","Dailey, Megan J.","Erdman, John W."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2018,"date_issued":"2018-09-27T16:47:35Z","date_published":"2018-09-27T16:47:35Z","updated_at":"2026-07-22T22:24:40Z","subjects":["sucralose","glucose","insulin","C-peptide","GIP","glucose kinetics","glucose tracer","obesity"],"languages":["en"],"rights":["Copyright 2018 Alexander Nichol"],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2142/101824","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Pepino, Yanina","Dailey, Megan J.","Erdman, John W."]},{"key":"dc:creator","label":"Author","values":["Nichol, Alexander Daniel"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2018-09-27T16:47:35Z","2020-09-28T09:15:25Z","2018-07-16","2018-08"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Food Science & Human Nutrition"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M.S."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["sucralose","glucose","insulin","C-peptide","GIP","glucose kinetics","glucose tracer","obesity"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["en"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 2018 Alexander Nichol"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/101824"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Objective: Whether sucralose, the most commonly used non-nutritive sweetener (NNS), affects glucose metabolism in people is unclear. It has been reported that, when consumed acutely before an oral glucose tolerance test (OGTT), sucralose enhances insulinemic responses and decreases insulin sensitivity in subjects with obesity who are not regular consumers of NNS. However, studies in normal-weight adults, none of which control for use of NNS, found sucralose does not affect insulin responses to the ingestion of glucose or other carbohydrates. The objectives of the current study are to determine if those effects of sucralose can be replicated in subjects with obesity, are generalizable to normal-weight subjects when controlling for history of NNS use, and are caused merely by the sweet taste of sucralose (i.e., sham-feeding). In addition, with the aim of identifying potential mechanisms by which sucralose may decrease postprandial insulin sensitivity, we here investigated whole-body glucose kinetics by using a dual-tracer approach. Finally, we tested the hypothesis that, due to the compromised intestinal permeability associated with obesity, sucralose consumption is associated with higher plasma sucralose concentrations in people with obesity. Research Design and Methods: Ten normal-weight subjects (BMI: 22.8 ± 0.9 kg/m2) and nine subjects with obesity (BMI: 37.7 ± 6.1 kg/m2), all non-regular users of NNS, non-diabetic, and without significant insulin resistance (based on a homeostatic model assessment of insulin resistance score < 3), underwent a 5-hour modified OGTT in which ingested glucose was labeled with one tracer while a second glucose tracer was infused intravenously at a constant rate on three separate testing days. Each testing day differed only by which pre-load solution (water ingestion (control condition), sucralose ingestion (experimental condition), or sucralose sham-fed (taste condition)) was administered 10 minutes prior to the OGTT in a randomized crossover design. Blood samples were taken throughout observation to determine plasma glucose, insulin, C-peptide, glucose-dependent insulinotropic polypeptide (GIP), glucose tracer-to-tracee ratio, and sucralose concentrations. Results: In subjects with obesity, compared to the control condition, sucralose sham-feeding reduced insulin and C-peptide concentrations within the first hour of the OGTT (both p-values ≤ 0.05), whereas sucralose ingestion increased plasma C-peptide incremental area under the curve (iAUC) by 22 ± 10% (p < 0.05) and tended to increase plasma insulin iAUC by 16 ± 9% (p = 0.09) and plasma glucose iAUC by 34 ± 12% (p = 0.06). No condition affected GIP. There were no differences among conditions in the degree of suppression of endogenous glucose production (EGP) after the glucose load, but both sucralose conditions affected the pattern of oral glucose rate of appearance (Ra) and glucose rate of disappearance (Rd). Compared to the water condition, sucralose affected the pattern of change with time including i) a greater decline (50-60 min) and subsequently a reduced decline (120-140 min) in oral glucose Ra (p = 0.03), and ii) a reduced glucose Rd (50-80 min) and subsequently an increased glucose Rd (140-160 min) after the glucose load (p < 0.05). While the reduction in glucose Rd during the taste condition and the increase in Rd 140-160 min after the glucose load could be explained by prevailing plasma insulin concentrations, the reduction in glucose Rd 50-80 min after the glucose load on the experimental condition cannot. During this time period, plasma insulin concentrations after sucralose ingestion were similar or higher than after water ingestion, which is in agreement with previous results of a decreased insulin sensitivity in subjects with obesity when sucralose ingestion preceded an OGTT. In normal-weight subjects, there were no significant differences among conditions in plasma glucose, C-peptide, GIP, or plasma glucose or hormones iAUCs, but both sucralose conditions tended to equally lower mean plasma insulin concentrations following the OGTT (p = 0.09) and suppressed EGP to a greater degree (p = 0.09) compared to water. There were no significant differences between groups for peak sucralose concentrations, the time to reach peak sucralose concentration, and plasma sucralose iAUCs (all p-values > 0.19). Conclusions: These data demonstrate that sucralose differentially affects hormonal responses to an oral glucose load in subjects with obesity and normal weight subjects. Sucralose ingestion (not merely its taste) increases insulin secretion to an oral glucose load and transiently reduces glucose Rd in people with obesity, but not in normal-weight subjects. These findings support the hypothesis that sucralose may have adverse effects on glucose metabolism in people with obesity, which is the group that most frequently consumes NNS to facilitate weight management. These data also underscore a physiological role for sweetness perception in glucose homeostasis, which supports the notion that sweetness, regardless of an associated caloric contribution, should be consumed in moderation.","Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2020-08-01","The student, Alexander Nichol, accepted the attached license on 2018-07-16 at 09:34.","The student, Alexander Nichol, submitted this Thesis for approval on 2018-07-16 at 09:46.","This Thesis was approved for publication on 2018-07-16 at 16:35.","DSpace SAF Submission Ingestion Package generated from Vireo submission #12884 on 2018-09-27 at 11:37:22","Made available in DSpace on 2018-09-27T16:47:35Z (GMT). No. of bitstreams: 2 NICHOL-THESIS-2018.pdf: 554779 bytes, checksum: 04ec270f4966836db59cdf46be87edd3 (MD5) LICENSE.txt: 4213 bytes, checksum: 9bd1a32e633e5e1fdb07422c7de0d7c8 (MD5) Previous issue date: 2018-07-16","Embargo set by: Seth Robbins for item 107925 Lift date: 2020-09-27T16:47:41Z Reason: Author requested closed access (OA after 2yrs) in Vireo ETD system","Limited Restriction Lifted for Item 107925 on 2020-09-28T09:15:25Z."]},{"key":"dc:format","label":"Dc Format","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Potential metabolic effect of sucralose following an oral glucose load in subjects with obesity and normal-weight subjects"]}]}],"canonical_facts":{"dc:contributor":["Pepino, Yanina","Dailey, Megan J.","Erdman, John W."],"dc:creator":["Nichol, Alexander Daniel"],"dc:date":["2018-09-27T16:47:35Z","2020-09-28T09:15:25Z","2018-07-16","2018-08"],"dc:description":["Objective: Whether sucralose, the most commonly used non-nutritive sweetener (NNS), affects glucose metabolism in people is unclear. It has been reported that, when consumed acutely before an oral glucose tolerance test (OGTT), sucralose enhances insulinemic responses and decreases insulin sensitivity in subjects with obesity who are not regular consumers of NNS. However, studies in normal-weight adults, none of which control for use of NNS, found sucralose does not affect insulin responses to the ingestion of glucose or other carbohydrates. The objectives of the current study are to determine if those effects of sucralose can be replicated in subjects with obesity, are generalizable to normal-weight subjects when controlling for history of NNS use, and are caused merely by the sweet taste of sucralose (i.e., sham-feeding). In addition, with the aim of identifying potential mechanisms by which sucralose may decrease postprandial insulin sensitivity, we here investigated whole-body glucose kinetics by using a dual-tracer approach. Finally, we tested the hypothesis that, due to the compromised intestinal permeability associated with obesity, sucralose consumption is associated with higher plasma sucralose concentrations in people with obesity. Research Design and Methods: Ten normal-weight subjects (BMI: 22.8 ± 0.9 kg/m2) and nine subjects with obesity (BMI: 37.7 ± 6.1 kg/m2), all non-regular users of NNS, non-diabetic, and without significant insulin resistance (based on a homeostatic model assessment of insulin resistance score < 3), underwent a 5-hour modified OGTT in which ingested glucose was labeled with one tracer while a second glucose tracer was infused intravenously at a constant rate on three separate testing days. Each testing day differed only by which pre-load solution (water ingestion (control condition), sucralose ingestion (experimental condition), or sucralose sham-fed (taste condition)) was administered 10 minutes prior to the OGTT in a randomized crossover design. Blood samples were taken throughout observation to determine plasma glucose, insulin, C-peptide, glucose-dependent insulinotropic polypeptide (GIP), glucose tracer-to-tracee ratio, and sucralose concentrations. Results: In subjects with obesity, compared to the control condition, sucralose sham-feeding reduced insulin and C-peptide concentrations within the first hour of the OGTT (both p-values ≤ 0.05), whereas sucralose ingestion increased plasma C-peptide incremental area under the curve (iAUC) by 22 ± 10% (p < 0.05) and tended to increase plasma insulin iAUC by 16 ± 9% (p = 0.09) and plasma glucose iAUC by 34 ± 12% (p = 0.06). No condition affected GIP. There were no differences among conditions in the degree of suppression of endogenous glucose production (EGP) after the glucose load, but both sucralose conditions affected the pattern of oral glucose rate of appearance (Ra) and glucose rate of disappearance (Rd). Compared to the water condition, sucralose affected the pattern of change with time including i) a greater decline (50-60 min) and subsequently a reduced decline (120-140 min) in oral glucose Ra (p = 0.03), and ii) a reduced glucose Rd (50-80 min) and subsequently an increased glucose Rd (140-160 min) after the glucose load (p < 0.05). While the reduction in glucose Rd during the taste condition and the increase in Rd 140-160 min after the glucose load could be explained by prevailing plasma insulin concentrations, the reduction in glucose Rd 50-80 min after the glucose load on the experimental condition cannot. During this time period, plasma insulin concentrations after sucralose ingestion were similar or higher than after water ingestion, which is in agreement with previous results of a decreased insulin sensitivity in subjects with obesity when sucralose ingestion preceded an OGTT. In normal-weight subjects, there were no significant differences among conditions in plasma glucose, C-peptide, GIP, or plasma glucose or hormones iAUCs, but both sucralose conditions tended to equally lower mean plasma insulin concentrations following the OGTT (p = 0.09) and suppressed EGP to a greater degree (p = 0.09) compared to water. There were no significant differences between groups for peak sucralose concentrations, the time to reach peak sucralose concentration, and plasma sucralose iAUCs (all p-values > 0.19). Conclusions: These data demonstrate that sucralose differentially affects hormonal responses to an oral glucose load in subjects with obesity and normal weight subjects. Sucralose ingestion (not merely its taste) increases insulin secretion to an oral glucose load and transiently reduces glucose Rd in people with obesity, but not in normal-weight subjects. These findings support the hypothesis that sucralose may have adverse effects on glucose metabolism in people with obesity, which is the group that most frequently consumes NNS to facilitate weight management. These data also underscore a physiological role for sweetness perception in glucose homeostasis, which supports the notion that sweetness, regardless of an associated caloric contribution, should be consumed in moderation.","Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2020-08-01","The student, Alexander Nichol, accepted the attached license on 2018-07-16 at 09:34.","The student, Alexander Nichol, submitted this Thesis for approval on 2018-07-16 at 09:46.","This Thesis was approved for publication on 2018-07-16 at 16:35.","DSpace SAF Submission Ingestion Package generated from Vireo submission #12884 on 2018-09-27 at 11:37:22","Made available in DSpace on 2018-09-27T16:47:35Z (GMT). No. of bitstreams: 2 NICHOL-THESIS-2018.pdf: 554779 bytes, checksum: 04ec270f4966836db59cdf46be87edd3 (MD5) LICENSE.txt: 4213 bytes, checksum: 9bd1a32e633e5e1fdb07422c7de0d7c8 (MD5) Previous issue date: 2018-07-16","Embargo set by: Seth Robbins for item 107925 Lift date: 2020-09-27T16:47:41Z Reason: Author requested closed access (OA after 2yrs) in Vireo ETD system","Limited Restriction Lifted for Item 107925 on 2020-09-28T09:15:25Z."],"dc:format":["application/pdf"],"dc:identifier":["http://hdl.handle.net/2142/101824"],"dc:language":["en"],"dc:rights":["Copyright 2018 Alexander Nichol"],"dc:subject":["sucralose","glucose","insulin","C-peptide","GIP","glucose kinetics","glucose tracer","obesity"],"dc:title":["Potential metabolic effect of sucralose following an oral glucose load in subjects with obesity and normal-weight subjects"],"dc:type":["text"],"thesis:degree_discipline":["Food Science & Human Nutrition"],"thesis:degree_level":["Thesis"],"thesis:degree_name":["M.S."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:24:40Z"}