层次复杂性和老化——迈向老化物理学

T. Witten
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引用次数: 0

摘要

在本文中,我们扩展了Witten和她的团队之前的工作,定义了一个经典的物理驱动的老龄化人口生存模型(Eakin, 1994;Eakin and Witten, 1995;Eakin and Witten, 1995;Witten和Eakin, 1997)通过重新审视老化力的概念,并引入老化动量、动能和势能的概念。作为使用这些结构的一个例子,我们随后在(Yu et al., 1982)饮食限制实验中探讨了这些概念的含义。人口老龄化的历史与生存分析领域紧密相连(Witten, 1981;Elandt-Johnson and Johnson, 1999)。然而,生存分析是从早期的可靠性理论学科中出现的(Abdel-Hameed et al., 1984;安塞尔和菲利普斯,1994)。可靠性理论的构建源于计算机科学家约翰·冯·诺伊曼(John Von Neumann)在20世纪50年代进行的gedankt实验。他的兴趣(Neumann, 1956)在于如何用不可靠的部件构建一个可靠的生物有机体。在冯·诺伊曼的思想实验之前,可靠性的概念并没有得到明确的定义。冯·诺伊曼的论点如下。他首先定义了条件瞬时故障率的概念,用λ(t)表示。我们对此的解释如下。失败的条件是,并没有发生在时间t的有机体幸存了下来,直到时间t。考虑到这一点,我们可以定义一个有机体的可靠度R (t)的概率没有失败的生物在时间t。如果我们让f (t)时间(第一个)失败(这是一样的故障密度函数),然后可靠性R (t)是由R (t) = 1−(t), f (t) =∫t 0 f(τ)dτ((Abdel-Hameed et al ., 1984;Deshpande and Purohit, 2005;Elandt-Johnson and Johnson, 1999;Kalbfleish and Prentice, 2002;无法无天,2003))。我们如何得到可靠性R(t)的方程?我们这样做。假设我们问可靠性R(t +∆t)是什么,其中∆t是一个小的时间增量。换句话说,假设我们知道生物体在时刻t的可靠性,并且我们想知道生物体在时间t之后的一个小时间增量∆t的可靠性。为了使生物体在时刻t+∆t能够工作,生物体必须至少在时刻t之前处于工作状态,然后在时间间隔(t, t+∆t)内没有发生故障。我们可以用数学方法表示如下。可靠性R(t +∆t)由R(t +∆t) = R(t)−λ(t)R(t)∆t(1)给出。阅读方程[1],我们看到,要在t+∆t时刻具有功能(可操作),生物体必须在t时刻具有功能(用方程右侧的可靠性项R(t)表示)。接下来,我们必须减去所有在时间间隔(t, t +∆t)内失败的项目(由等式[1]右侧的第二项给出)。减去后剩下的是在时间t +∆t时仍具有功能的所有生物体或物品。稍微重排一下代数我们得到R(t +∆t) - R(t)∆t = - λ(t)R(t)(2)因此,让∆t→0(记住微积分),方程[1]变成了简单的微分方程
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hierarchical Complexity and Aging - Towards a Physics of Aging
In this paper we extend the previous work of Witten and her team on defining a classical physics driven model of survival in aging populations (Eakin, 1994; Eakin and Witten, 1995a; Eakin and Witten, 1995b; Witten and Eakin, 1997) by revisiting the concept of a force of aging and introducing the concepts of a momentum of aging, a kinetic energy and a potential energy of an aging. As an example of the use of these constructs, we then explore the implications of these concepts with respect to the (Yu et al., 1982) diet restriction experiments. 1 HISTORY OF RELIABILITY The history of the demographics of aging is tightly bound to the field of survival analysis (Witten, 1981; Elandt-Johnson and Johnson, 1999). Survival analysis, however, emerged from the earlier discipline of reliability theory (Abdel-Hameed et al., 1984; Ansell and Phillips, 1994). The constructs of reliability theory emerged from the 1950’s gedankt experiments of the computer scientist John Von Neumann. His interest (Neumann, 1956) was in how one would go about building a reliable biological organism out of unreliable parts. Until the thought experiments of von Neumann, the concept of reliability had not been well-defined. Von Neumann’s argument proceeded as follows. He began by defining the concept of the conditional instantaneous failure rate, denoted by λ(t). We interpret this as follows. The condition is that the failure has not occurred at time t given that the organism has survived until time t. With this in mind, we may then define the reliability R(t) of an organism as the probability of no failure of the organism before time t. If we let f (t) be the time to (first) failure (this is the same as the failure density function), then the reliability R(t) is given by R(t) = 1−F(t) where F(t) = ∫ t 0 f (τ)dτ ((Abdel-Hameed et al., 1984; Deshpande and Purohit, 2005; Elandt-Johnson and Johnson, 1999; Kalbfleish and Prentice, 2002; Lawless, 2003)). How do we actually obtain an equation for the reliability R(t)? We do this as follows. Suppose we ask what is the reliability R(t +∆t) where ∆t is a small time increment. In other words, suppose that we know the reliability of the organism at time t and we want to know the organism’s reliability at a small time increment ∆t later than time t. In order for the organism to be operational at time t+∆t, the organism must have been operational until at least time t and then not have failed in the time interval (t, t +∆t). We can express this mathematically as follows. The reliability R(t +∆t) is given by R(t +∆t) = R(t)−λ(t)R(t)∆t (1) Reading equation [1], we see that to be functional (operational) at time t+∆t, the organisms had to be functional at time t (denoted by the reliability term R(t) on the right hand side of the equation). Next, we have to subtract out all of the items that failed in the time interval (t, t +∆t) (given by the second term on the right hand side of equation [1]). What remains after this subtraction is all of the organisms or items that remain functional at time t +∆t. A bit of algebraic rearrangement and we have R(t +∆t)−R(t) ∆t =−λ(t)R(t) (2) It follows that letting ∆t → 0 (remembering our calculus), Equation [1] becomes the simple differential equation given by
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