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大鼠鼻腔中气味剂摄取的数值模拟。

Numerical modeling of odorant uptake in the rat nasal cavity.

作者信息

Yang Geoffrey C, Scherer Peter W, Zhao Kai, Mozell Maxwell M

机构信息

Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, 240 Skirkanich Hall/6321, 210 South 33rd Street, Philadelphia, PA 19104, USA.

出版信息

Chem Senses. 2007 Mar;32(3):273-84. doi: 10.1093/chemse/bjl056. Epub 2007 Jan 13.

Abstract

An anatomically accurate 3-dimensional numerical model of the right rat nasal cavity was developed and used to compute low, medium, and high flow rate inspiratory and expiratory mucosal odorant uptake (imposed patterning) for 3 odorants with different mucus solubilities. The computed surface mass flux distributions were compared with anatomic receptor gene expression zones identified in the literature. In general, simulations predicted that odorants that were highly soluble in mucus were absorbed dorsally and medially, corresponding roughly to receptors from one of the gene expression zones. Insoluble odorants tended to be absorbed more peripherally in the rat olfactory region corresponding to the other 2 zones. These findings also agreed in general with the electroolfactogram measurements and the voltage-sensitive dye measurements reported in the literature. This numerical approach is the first to predict detailed odorant flux information across the olfactory mucosa in the rat nasal cavity during inspiratory and expiratory flow and to relate it to anatomic olfactory receptor location, physiological function, and biochemical experiment. This numerical technique can allow us to separate the contributions of imposed and inherent patterning mechanisms on the rat olfactory mucosa.

摘要

构建了一个解剖结构精确的大鼠右鼻腔三维数值模型,并用于计算三种具有不同黏液溶解度的气味剂在低、中、高流速吸气和呼气时的黏膜气味剂摄取(施加模式)。将计算得到的表面质量通量分布与文献中确定的解剖学受体基因表达区域进行比较。总体而言,模拟预测在黏液中高度可溶的气味剂在背侧和内侧被吸收,大致对应于一个基因表达区域的受体。不溶性气味剂倾向于在大鼠嗅觉区域更外周被吸收,对应于其他两个区域。这些发现总体上也与文献中报道的嗅觉电图测量和电压敏感染料测量结果一致。这种数值方法首次预测了吸气和呼气过程中大鼠鼻腔嗅觉黏膜上详细的气味剂通量信息,并将其与解剖学嗅觉受体位置、生理功能和生化实验相关联。这种数值技术可以使我们区分施加模式和固有模式机制对大鼠嗅觉黏膜的贡献。

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