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味觉受体2型(TAS2R)基因的变异解释了两种常见抗生素苦味的差异。

Variation in TAS2R receptor genes explains differential bitterness of two common antibiotics.

作者信息

Nolden Alissa A, Hayes John E, Feeney Emma L

机构信息

Department of Food Science, University of Massachusetts, Amherst, MA, United States.

Department of Food Science, The Pennsylvania State University, University Park, PA, United States.

出版信息

Front Genet. 2022 Jul 28;13:960154. doi: 10.3389/fgene.2022.960154. eCollection 2022.

DOI:10.3389/fgene.2022.960154
PMID:35967977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9366911/
Abstract

For pharmaceuticals to deliver their full benefits with maximum efficacy, patients need to follow recommended dosing schedules, in terms of amount and frequency. Unfortunately, the aversive taste of many drugs, especially bitterness, can reduce patient compliance in oral liquid formulations. Given common genetic differences in bitter taste receptor genes (), some individuals may be at increased risk for poor compliance due to heightened bitterness that becomes a barrier to proper use. Here we report on the sensory profile of two antibiotics, chloramphenicol and ofloxacin, investigating whether bitterness intensity associates with nominally functional variants. Participants ( = 143) rated suprathreshold intensity on a general Labeled Magnitude Scale (gLMS) for chloramphenicol and ofloxacin; propylthiouracil (PROP) was included as a control, given robust prior associations with variants. The dominant sensation from chloramphenicol and ofloxacin was bitterness, falling just below "moderate" on a gLMS. diplotype associated with variable bitterness of chloramphenicol and PROP, but not ofloxacin. The bitterness of ofloxacin associated with a SNP (V187A). This pilot study provides novel evidence on differences in the bitterness from two antibiotics, which are associated with variants. Improved understanding of individualized barriers to patient compliance, especially for oral formulations, can guide future efforts to optimize delivery systems for improved compliance.

摘要

为了使药物发挥最大疗效并充分展现其益处,患者需要按照推荐的剂量和频次服用。不幸的是,许多药物的不良味道,尤其是苦味,会降低患者对口服液体制剂的依从性。鉴于苦味受体基因存在常见的遗传差异,一些个体可能因苦味增强而导致依从性差的风险增加,苦味成为正确用药的障碍。在此,我们报告了两种抗生素(氯霉素和氧氟沙星)的感官特征,研究苦味强度是否与名义上有功能的变体相关。参与者(n = 143)使用通用标记量值量表(gLMS)对氯霉素和氧氟沙星的阈上强度进行评分;丙硫氧嘧啶(PROP)作为对照纳入,因为之前已有其与变体的有力关联。氯霉素和氧氟沙星的主要感觉是苦味,在gLMS上略低于“中度”。双倍型与氯霉素和PROP的可变苦味相关,但与氧氟沙星无关。氧氟沙星的苦味与一个单核苷酸多态性(V187A)相关。这项初步研究提供了关于两种抗生素苦味差异的新证据,这些差异与变体相关。更好地理解影响患者依从性的个体障碍,尤其是口服制剂方面的障碍,可为未来优化给药系统以提高依从性的努力提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/9366911/9110f64cf2db/fgene-13-960154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/9366911/1f3e24342921/fgene-13-960154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/9366911/7e384d636529/fgene-13-960154-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/9366911/9110f64cf2db/fgene-13-960154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/9366911/1f3e24342921/fgene-13-960154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/9366911/7e384d636529/fgene-13-960154-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9b/9366911/9110f64cf2db/fgene-13-960154-g003.jpg

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