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皮肤电穿孔理论:连接相邻角质形成细胞的直通水性通道段的意义。

Theory of skin electroporation: implications of straight-through aqueous pathway segments that connect adjacent corneocytes.

作者信息

Weaver J C, Vaughan T E, Chizmadzhev Y

机构信息

Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

J Investig Dermatol Symp Proc. 1998 Aug;3(2):143-7. doi: 10.1038/jidsymp.1998.29.

Abstract

Previous in vitro experiments have shown that transdermal high-voltage pulses (Uskin approximately 100 V; duration approximately 1 ms) create local transport regions (LTR) away from appendages in human skin. Quantitative interpretation of the associated ionic and molecular transport led to the view that a large number of aqueous pathways were created, and these connect the corneocytes within an LTR. Here we use the "brick wall" model of the stratum corneum, modified so that morphology important to understanding electrical behavior is emphasized. In this model a minimum-size LTR is regarded as an idealized stack of corneocytes in which the 5-6 multilamellar lipid bilayer membranes between adjacent corneocytes are electroporated. As in artificial planar bilayer and cell membrane electroporation, a distribution of pathway sizes is expected during pulsing, and during recovery after pulsing individual pathway segments are expected to shrink and close randomly, with a time constant tau(seg) that depends on temperature and on lipid composition. Numerical simulations based on stochastic closure of individual segments were used to predict the electrical conductance G(LTR)(t) of a minimum-size LTR after pulsing stops. These theoretical results show that simple exponential decay, G(LTR)(t) = G(LTR)(0)exp(-t/tau(seg)), occurs with minimal fluctuations if the number of pathways is large (np > 10(2)), but for much smaller values the conduction decreases erratically. A "stochastic bottleneck" leading to complete closure is reached only at about np < 3. Thus, for the same number of electrically created pathways, the stratum corneum will remain "open" longer if the pathways are located within an LTR than if the same number of pathways are distributed sparsely over the skin. These predictions are relevant to postpulse transport, including the trapping of linear macromolecules that can hold pathway segments open for prolonged intervals.

摘要

先前的体外实验表明,经皮高压脉冲(皮肤表面电压Us约为100 V;持续时间约为1 ms)可在人体皮肤中形成远离附属器的局部转运区域(LTR)。对相关离子和分子转运的定量解释表明,形成了大量的水性通道,这些通道连接了LTR内的角质形成细胞。在此,我们使用角质层的“砖墙”模型,并进行了修改,以便强调对理解电行为至关重要的形态学特征。在该模型中,最小尺寸的LTR被视为角质形成细胞的理想化堆叠,其中相邻角质形成细胞之间的5 - 6个多层脂质双分子层膜被电穿孔。与人工平面双分子层和细胞膜电穿孔一样,在脉冲期间预计会出现通道尺寸分布,并且在脉冲后的恢复过程中,预计各个通道段会随机收缩和关闭,其时间常数τ(seg)取决于温度和脂质组成。基于单个段的随机关闭的数值模拟用于预测脉冲停止后最小尺寸LTR的电导G(LTR)(t)。这些理论结果表明,如果通道数量较多(np > 10²),则会发生简单的指数衰减,即G(LTR)(t) = G(LTR)(0)exp(-t/τ(seg)),波动最小,但对于小得多的值,传导会不稳定地下降。只有在np < 3左右时才会达到导致完全关闭的“随机瓶颈”。因此,对于相同数量的电形成通道,如果通道位于LTR内,角质层保持“开放”的时间将比相同数量的通道稀疏分布在皮肤上的情况更长。这些预测与脉冲后转运相关,包括线性大分子的捕获,这些大分子可使通道段长时间保持开放。

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