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Temporary Modification of Salivary Protein Profile and Individual Responses to Repeated Phenolic Astringent Stimuli

机译:唾液蛋白谱的临时修改和个人对重复的酚类涩味刺激的反应。

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The extent of the change in salivary protein characteristics after repeated stimulations was shown to be correlated to differences in perceived astringency. Salivary characteristics of 77 subjects were compared after masticatory (S1) and taste/masticatory (S2) stimulations. The variations (S2 minus S1) of protein concentration and saliva haze-forming capacity (HFC) were used to define 3 subject groups: low responding (LR, n = 20), medium responding (MR, n = 37), and high responding (HR, n = 20). Salivary protein concentration did not change in LR subjects; decreased a little, but significantly, in MR subjects; and strongly decreased in HR subjects. After S2, HFC increased in LR subjects, slightly decreased in MR subjects, and strongly decreased in HR subjects. Salivary protein electrophoresis patterns for HR and LR subjects were analyzed. No significant modifications of glycosylated proline-rich proteins (PRPs), PRPs, and amylases and a slight decrease in cystatins and histatins were found when S2 and S1 samples were compared in LR subjects, whereas HR subjects showed a strong decrease in all the above proteins after S2. Significant modifications of mucins were not found. Tannic acid (TA, 3 g/L) astringency ratings after S1 from HR subjects were significantly higher than those from the other 2 groups, whereas no differences were found comparing LR and MR ratings. The “carryover” effect due to 4 sequential exposures to TA samples (1.4 g/L) was observed in both HR and MR groups, whereas no significant astringency rating variation was found in the LR group. The results support the inhibiting role of proteins with strong phenol-binding activity on astringency elicitation. Individual physiological variations of parotid gland functionality might account for differences in sensitivity to astringent phenolic stimuli.
机译:反复刺激后唾液蛋白质特性的变化程度显示与感觉到的涩味差异有关。在咀嚼(S1)和味觉/咀嚼(S2)刺激后比较了77位受试者的唾液特征。使用蛋白质浓度和唾液雾形成能力(HFC)的变化(S2减去S1)来定义3个受试者组:低应答(LR,n = 20),中应答(MR,n = 37)和高应答(HR,n = 20)。 LR受试者的唾液蛋白浓度没有变化;在MR受试者中有所降低,但显着降低;并在HR受试者中大大降低。在S2之后,LR受试者的HFC升高,MR受试者的HFC略有降低,而HR受试者的HFC显着降低。分析了HR和LR受试者的唾液蛋白电泳图谱。当在LR受试者中比较S2和S1样品时,未发现糖基化富含脯氨酸的蛋白(PRP),PRP和淀粉酶的显着修饰,并且胱抑素和组蛋白的含量略有下降,而HR受试者的上述所有蛋白均表现出明显的下降在S2之后。未发现粘蛋白的显着修饰。 HR受试者S1后的单宁酸(TA,3 g / L)涩味等级显着高于其他两组,但比较LR和MR等级时没有发现差异。在HR和MR组均观察到4次连续暴露于TA样品(1.4 g / L)引起的“残留”效应,而LR组未发现明显的涩味等级变化。结果支持具有强酚结合活性的蛋白质对涩味诱发的抑制作用。腮腺功能的个体生理变化可能解释了对涩味酚类刺激物敏感性的差异。

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  • 来源
    《Chemical Senses》 |2010年第1期|p.75-85|共11页
  • 作者单位

    Dipartimento di Biotecnologie Agrarie, Università degli Studi di Firenze, Via Donizetti 6, Firenze 50144, Italy;

    Dipartimento di Biotecnologie Agrarie, Università degli Studi di Firenze, Via Donizetti 6, Firenze 50144, Italy;

    Centro Interdipartimentale per la Ricerca in Viticoltura ed Enologia, Università di Padova, Via XXVIII Aprile, 1431015 Conegliano (TV), Italy;

    Department of Food Technology, University of Helsinki, P.O. Box 66 (Agnes Sjöbergin katu 2) FI-00014, Finland;

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