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相似性原理与内在几何学:跨物种尺度缩放的对比方法

Similarity principles and intrinsic geometries: contrasting approaches to interspecies scaling.

作者信息

Yates F E, Kugler P N

出版信息

J Pharm Sci. 1986 Nov;75(11):1019-27. doi: 10.1002/jps.2600751103.

Abstract

We criticize standard allometric approaches on the grounds that they emphasize scaling to one variable at a time, whereas chemically reactive hydrodynamic systems involved in pharmacokinetic phenomena are of higher dimension. We show that attempts based on mechanical similitude to set a dosage that would be equivalent across species (for example, from mouse to humans) lead to ambiguous results. Another failing of standard allometry may be its incapability to accommodate the neoteny of Homo sapiens, even though it helped discover the phenomenon. The retarded development in our species implied by neoteny can most clearly be seen in the evidence that both our brain size and our lifespan lie well above the allometric curve for Class Mammalia for these features. In contrast to allometry, which proposes a search for scaling coefficients through invariant external measurement reference frames, we propose a search for transformations of coordinate space coefficients in an intrinsic geometry for the mammalian body plan.

摘要

我们批评标准的异速生长方法,理由是它们强调一次仅按一个变量进行缩放,而药代动力学现象中涉及的化学反应流体动力学系统具有更高维度。我们表明,基于力学相似性来设定跨物种(例如从小鼠到人类)等效剂量的尝试会导致模糊的结果。标准异速生长法的另一个缺陷可能是它无法适应智人的幼态持续现象,尽管它有助于发现这一现象。幼态持续所暗示的我们物种发育迟缓,最明显地体现在这样的证据中:我们的脑容量和寿命都远高于哺乳动物类在这些特征上的异速生长曲线。与通过不变的外部测量参考系来寻找缩放系数的异速生长法不同,我们建议在哺乳动物身体结构的内在几何中寻找坐标空间系数的变换。

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