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[气体交换系统的系统发育]

[Phylogeny of gas exchange systems].

作者信息

Jürgens K D, Gros G

机构信息

Abteilung Vegetative Physiologie, Medzinische Hochschule, Hannover.

出版信息

Anasthesiol Intensivmed Notfallmed Schmerzther. 2002 Apr;37(4):185-98. doi: 10.1055/s-2002-25080.

Abstract

Several systems of gas transport have developed during evolution, all of which are able to sufficiently supply oxygen to the tissues and eliminate the CO2 produced by the metabolism, in spite of great distances between the environment and the individual cells of the tissues. Almost all these systems utilize a combination of convection and diffusion steps. Convection achieves an efficient transport of gas over large distances, but requires energy and cannot occur across tissue barriers. Diffusion, on the other hand, achieves gas transport across barriers, but requires optimization of diffusion paths and diffusion areas. When two convectional gas flows are linked via a diffusional barrier (gas/fluid in the case of the avian lung, fluid/fluid in the case of gills), the directions in which the respective convectional movements pass each other are important determinants of gas exchange efficiency (concurrent, countercurrent and cross-current systems). The tracheal respiration found in insects has the advantage of circumventing the convective gas transport step in the blood, thereby avoiding the high energy expenditure of circulatory systems. This is made possible by a system of tracheae, ending in tracheoles, that reaches from the body surface to every cell within the body. The last step of gas transfer in these animals occurs by diffusion from the tracheoles ("air capillaries") to the mitochondria of cells. The disadvantage is that the tracheal system occupies a substantial fraction of body volume and that, due to limited mechanical stability of tracheal walls, this system would not be able to operate under conditions of high hydrostatic pressures, i. e. in large animals. Respiration in an "open" system, i. e. direct exposure of the diffusional barrier to the environmental air, eliminates the problem of bringing the oxygen to the barrier by convection, as is necessary in the avian and mammalian lung, in the insects' tracheal system and in the gills. An open system is found in the respiration via the skin, which is of significance in some amphibians, but is limited by the thickness of the skin that constitutes a substantial diffusion path for O2 and CO2. The thick skin, on the other hand, provides mechanical protection as well as flexibility for the animals' body and helps avoid massive water loss via the body surface. The gills of fishes, in contrast, exhibit rather short diffusion distances, are located in a mechanically protected space, and the problem of water loss does not exist. The flows of blood and water occur in opposite direction (countercurrent flow) and this situation makes an arterial PO2 approaching the environmental PO2 possible. A major disadvantage is constituted by the environmental medium since water contains little O2 compared to air and, to compensate this, much energy is expended to maintain a high flow rate of water through the gills. In the mammalian lung ("pool system"), the presence of a dead space and the rhythmic ventilation that replaces only a small fraction of the gas volume of the lung per breath, are responsible for an arterial PO2 (2/3 of the atmospheric PO2) that cannot reach the expiratory PO2. However, an advantage of this feature is the constantly high alveolar and arterial PCO2, which provides a highly effective H(+) buffer system in the entire body. The apparent disadvantage of the mammalian lung is avoided by the avian lung, which uses an extended system of airways to establish continuous equilibration of a part of the capillary blood with fresh air (cross current system), during inspiration as well as during expiration. In this system, arterial PO2 can significantly exceed expiratory PO2. A disadvantage here is the enormous amount of space taken up by the avian lung, in animals of 1 kg body weight three times as much as taken up by the mammalian lung. All respiratory exchange systems considered here exhibit high degrees of optimization - yet follow highly diverse construction principles. There is no such thing as an ideal gas exchange system. The system that has evolved in each species depends to an impressive extent on environmental conditions, on body build and size, on the animal's patterns of movement and on its energy consumption.

摘要

在进化过程中发展出了几种气体运输系统,尽管环境与组织的单个细胞之间距离很远,但所有这些系统都能够为组织充分供应氧气并清除新陈代谢产生的二氧化碳。几乎所有这些系统都利用了对流和扩散步骤的组合。对流实现了气体在大距离上的高效运输,但需要能量且不能跨越组织屏障。另一方面,扩散实现了气体跨屏障的运输,但需要优化扩散路径和扩散面积。当两个对流气流通过扩散屏障相连时(鸟类肺部的气体/液体情况,鳃的液体/液体情况),各自对流运动相互通过的方向是气体交换效率的重要决定因素(顺流、逆流和错流系统)。昆虫的气管呼吸具有绕过血液中对流气体运输步骤的优点,从而避免了循环系统的高能量消耗。这是通过一个气管系统实现的,该系统以气管末端终止,从体表延伸到体内的每个细胞。这些动物中气体转移的最后一步是通过从气管末端(“气毛细血管”)向细胞线粒体的扩散来完成的。缺点是气管系统占据了相当大的身体体积,并且由于气管壁的机械稳定性有限,该系统在高静水压力条件下(即大型动物中)无法运行。“开放”系统中的呼吸,即扩散屏障直接暴露于环境空气中,消除了像鸟类和哺乳动物肺部、昆虫气管系统和鳃那样通过对流将氧气带到屏障的问题。通过皮肤进行的呼吸就是一种开放系统,这在一些两栖动物中具有重要意义,但受到皮肤厚度的限制,皮肤构成了氧气和二氧化碳的重要扩散路径。另一方面,厚厚的皮肤为动物身体提供了机械保护和灵活性,并有助于避免通过体表大量失水。相比之下,鱼类的鳃具有相当短的扩散距离,位于机械保护的空间内,并且不存在失水问题。血液和水流以相反方向流动(逆流),这种情况使得动脉血氧分压接近环境血氧分压成为可能。一个主要缺点是环境介质造成的,因为与空气相比,水中含氧量很少,为了弥补这一点,需要消耗大量能量来维持水通过鳃的高流速。在哺乳动物肺部(“池系统”),存在死腔以及每次呼吸仅替换肺部气体体积一小部分的节律性通气,导致动脉血氧分压(大气血氧分压的2/3)无法达到呼气血氧分压。然而,这一特征的一个优点是肺泡和动脉血二氧化碳分压持续保持较高水平,这在整个身体中提供了一个高效的H⁺缓冲系统。鸟类肺部避免了哺乳动物肺部明显的缺点,它利用一个扩展的气道系统在吸气和呼气期间都能使一部分毛细血管血液与新鲜空气持续平衡(错流系统)。在这个系统中,动脉血氧分压可以显著超过呼气血氧分压。这里的一个缺点是鸟类肺部占据的空间巨大,对于体重1千克的动物来说,其占据的空间是哺乳动物肺部的三倍。这里考虑的所有呼吸交换系统都表现出高度的优化——但遵循高度不同的构建原则。不存在理想的气体交换系统。在每个物种中进化出的系统在很大程度上取决于环境条件、身体结构和大小、动物的运动模式及其能量消耗。

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