Clinical Associations of Bitter Taste Perception and Bitter Taste Receptor Variants and the Potential for Personalized Healthcare

被引:3
|
作者
Mao, Ziwen [1 ,2 ]
Cheng, Weyland [1 ,2 ,3 ]
Li, Zhenwei [2 ]
Yao, Manye [2 ]
Sun, Keming [2 ]
机构
[1] Zhengzhou Univ, Henan Childrens Hosp, Zhengzhou Childrens Hosp, Henan Prov Key Lab Childrens Genet & Metab Dis,Chi, Zhengzhou, Henan, Peoples R China
[2] Zhengzhou Univ, Henan Childrens Hosp, Zhengzhou Childrens Hosp, Dept Orthopaed Surg,Childrens Hosp, Zhengzhou, Henan, Peoples R China
[3] Zhengzhou Univ, Henan Childrens Hosp, Zhengzhou Childrens Hosp, Henan Prov Key Lab Childrens Genet & Metab Dis,Chi, 33 Longhu Waihuan East Rd, Zhengzhou, Henan, Peoples R China
关键词
bitter taste receptors; chronic rhinosinusitis; obesity; oral health; cancer; MENTHOL CIGARETTE PREFERENCE; BODY-MASS INDEX; GENE TAS2R38; 6-N-PROPYLTHIOURACIL PROP; ALCOHOL-CONSUMPTION; THERAPEUTIC TARGET; FOOD PREFERENCES; DENTAL-CARIES; SENSITIVITY; POLYMORPHISMS;
D O I
10.2147/PGPM.S390201
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bitter taste receptors (T2Rs) consist of 25 functional receptors that can be found in various types of cells throughout the human body with responses ranging from detecting bitter taste to suppressing pathogen-induced inflammation upon activation. Numerous studies have observed clinical associations with genetic or phenotypic variants in bitter taste receptors, most notably that of the receptor isoform T2R38. With genetic variants playing a role in the response of the body to bacterial quorum-sensing molecules, bacterial metabolites, medicinal agonists and nutrients, we examine how T2R polymorphisms, expression levels and bitter taste perception can lead to varying clinical associations. From these genetic and phenotypic differences, healthcare management can potentially be individualized through appropriately administering drugs with bitter masking to increase compliance; optimizing nutritional strategies and diets; avoiding the use of T2R agonists if this pathway is already activated from bacterial infections; adjusting drug regimens based on differing prognoses; or adjusting drug regimens based on T2R expression levels in the target cell type and bodily region.
引用
收藏
页码:121 / 132
页数:12
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