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Thiazolidinediones are partially effective bitter blockers

PURPOSE. The bad bitter taste of some medicines is a barrier to overcoming non-compliance with medication use, especially life-saving drugs given to children and the elderly. Here we evaluated a new class of bitter blockers (thiazolidinediones; TZDs). METHODS. In this study, two TZDs were tested, ro...

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Autores principales: Nguyen, Ha, Lin, Cailu, Sasimovich, Ivona, Bell, Katherine, Huang, Amy, Leszkowicz, Emilia, Rawson, Nancy E., Reed, Danielle R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441302/
https://www.ncbi.nlm.nih.gov/pubmed/37609224
http://dx.doi.org/10.1101/2023.08.08.552460
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author Nguyen, Ha
Lin, Cailu
Sasimovich, Ivona
Bell, Katherine
Huang, Amy
Leszkowicz, Emilia
Rawson, Nancy E.
Reed, Danielle R.
author_facet Nguyen, Ha
Lin, Cailu
Sasimovich, Ivona
Bell, Katherine
Huang, Amy
Leszkowicz, Emilia
Rawson, Nancy E.
Reed, Danielle R.
author_sort Nguyen, Ha
collection PubMed
description PURPOSE. The bad bitter taste of some medicines is a barrier to overcoming non-compliance with medication use, especially life-saving drugs given to children and the elderly. Here we evaluated a new class of bitter blockers (thiazolidinediones; TZDs). METHODS. In this study, two TZDs were tested, rosiglitazone (ROSI) and a simpler form of TZD, using a high-potency sweetener as a positive control (neohesperidin dihydrochalcone, NHDC). We tested bitter-blocking effects using the bitter drugs tenofovir alafenamide fumarate (TAF), a treatment for HIV and hepatitis B infection, and praziquantel (PRAZ), a treatment for schistosomiasis, by conducting taste testing with two separate taste panels: a general panel (N=97, 20–23 yrs, 82.5% female, all Eastern European) and a genetically informative panel (N=158, including 68 twin pairs, 18–82 yrs, 76% female, 87% European ancestry). Participants rated the bitterness intensity of the solutions on a 100-point generalized visual analog scale. FINDINGS. Participants in both taste panels rated the bitter drugs TAF and PRAZ as less bitter on average when mixed with NHDC than when sampled alone. ROSI partially suppressed the bitterness of TAF and PRAZ, but effectiveness differed between the two panels: bitterness was significantly reduced for PRAZ but not TAF in the general panel and for TAF but not PRAZ in the genetically informative panel. ROSI was a more effective blocker than the other TZD. IMPLICATIONS. These results suggest that TZDs are partially effective bitter blockers, suggesting other TZDs should be designed and tested with more drugs and on diverse populations to define which ones work best with which drugs and for whom. The discovery of bitter receptor blockers can improve compliance with medication use.
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spelling pubmed-104413022023-08-22 Thiazolidinediones are partially effective bitter blockers Nguyen, Ha Lin, Cailu Sasimovich, Ivona Bell, Katherine Huang, Amy Leszkowicz, Emilia Rawson, Nancy E. Reed, Danielle R. bioRxiv Article PURPOSE. The bad bitter taste of some medicines is a barrier to overcoming non-compliance with medication use, especially life-saving drugs given to children and the elderly. Here we evaluated a new class of bitter blockers (thiazolidinediones; TZDs). METHODS. In this study, two TZDs were tested, rosiglitazone (ROSI) and a simpler form of TZD, using a high-potency sweetener as a positive control (neohesperidin dihydrochalcone, NHDC). We tested bitter-blocking effects using the bitter drugs tenofovir alafenamide fumarate (TAF), a treatment for HIV and hepatitis B infection, and praziquantel (PRAZ), a treatment for schistosomiasis, by conducting taste testing with two separate taste panels: a general panel (N=97, 20–23 yrs, 82.5% female, all Eastern European) and a genetically informative panel (N=158, including 68 twin pairs, 18–82 yrs, 76% female, 87% European ancestry). Participants rated the bitterness intensity of the solutions on a 100-point generalized visual analog scale. FINDINGS. Participants in both taste panels rated the bitter drugs TAF and PRAZ as less bitter on average when mixed with NHDC than when sampled alone. ROSI partially suppressed the bitterness of TAF and PRAZ, but effectiveness differed between the two panels: bitterness was significantly reduced for PRAZ but not TAF in the general panel and for TAF but not PRAZ in the genetically informative panel. ROSI was a more effective blocker than the other TZD. IMPLICATIONS. These results suggest that TZDs are partially effective bitter blockers, suggesting other TZDs should be designed and tested with more drugs and on diverse populations to define which ones work best with which drugs and for whom. The discovery of bitter receptor blockers can improve compliance with medication use. Cold Spring Harbor Laboratory 2023-08-10 /pmc/articles/PMC10441302/ /pubmed/37609224 http://dx.doi.org/10.1101/2023.08.08.552460 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Nguyen, Ha
Lin, Cailu
Sasimovich, Ivona
Bell, Katherine
Huang, Amy
Leszkowicz, Emilia
Rawson, Nancy E.
Reed, Danielle R.
Thiazolidinediones are partially effective bitter blockers
title Thiazolidinediones are partially effective bitter blockers
title_full Thiazolidinediones are partially effective bitter blockers
title_fullStr Thiazolidinediones are partially effective bitter blockers
title_full_unstemmed Thiazolidinediones are partially effective bitter blockers
title_short Thiazolidinediones are partially effective bitter blockers
title_sort thiazolidinediones are partially effective bitter blockers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441302/
https://www.ncbi.nlm.nih.gov/pubmed/37609224
http://dx.doi.org/10.1101/2023.08.08.552460
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