Aboitiz F
Departamento de Morfología Experimental, Facultad de Medicina, Universidad de Chile, Santiago, Chile.
J Hirnforsch. 1995;36(4):461-72.
The present paper reviews some issues related to the evolutionary origin of distinct components of the cerebral hemispheres in vertebrates, which entails the problem of biological homology between anatomical structures. Considering that the term homology is essentially a comparative concept, making emphasis on structural correspondences between organs or body parts, I use the term evolutionary, or phylogenetic homology to denote a common evolutionary origin of two characters. In particular, the controversy of a possible phylogenetic homology between reptilian dorsal ventricular ridge (DVR) and parts of mammalian neocortex is analyzed in some detail. Although it is likely that DVR is a derived character of reptiles while neocortex is a derived character of mammals, the two structures might still originate from the same primordial anlage in the common ancestor. One main problem in the comparison of telencephalic components between reptiles and mammals is that the protrusion of reptilian DVR into the lateral ventricle causes a distortion of the topographic relations in the hemisphere. In order to determine possible homologues of DVR, it is necessary to establish clear-cut telencephalic landmarks. Since lateral cortex is similarly localized in reptiles and mammals, it is suggested that the embryonic position and timing of development of reptilian DVR in relation to lateral cortex may give special insight on the phylogenetic origins of the former. If, as implied by the work of early authors, DVR arose in evolution through an extension of the embryonic period of neuronal proliferation and migration, it may be considered as a genuine novelty in brain evolution. It is also proposed that, regardless of whether DVR and extrastriate neocortex can or cannot be considered phylogenetic homologues, some of the integrative functions performed by them might have a common evolutionary origin, that became localized in reptilian DVR and in mammalian extrastriate neocortex.
本文回顾了一些与脊椎动物大脑半球不同组成部分的进化起源相关的问题,这涉及到解剖结构之间的生物学同源性问题。鉴于同源性这个术语本质上是一个比较概念,强调器官或身体部位之间的结构对应关系,我使用进化同源性或系统发育同源性这个术语来表示两个特征的共同进化起源。特别详细分析了爬行动物背侧脑室嵴(DVR)与哺乳动物新皮层部分之间可能存在的系统发育同源性的争议。尽管DVR可能是爬行动物的衍生特征,而新皮层是哺乳动物的衍生特征,但这两种结构仍可能起源于共同祖先的同一原始原基。爬行动物和哺乳动物端脑组成部分比较中的一个主要问题是,爬行动物DVR向侧脑室的突出导致了半球地形关系的扭曲。为了确定DVR可能的同源物,有必要建立明确的端脑地标。由于侧皮层在爬行动物和哺乳动物中的定位相似,有人提出,爬行动物DVR相对于侧皮层的胚胎位置和发育时间可能会为前者的系统发育起源提供特殊见解。如果正如早期作者的研究暗示的那样,DVR在进化过程中是通过神经元增殖和迁移的胚胎期延长而出现的,那么它可能被视为大脑进化中的一个真正新奇之处。还提出,无论DVR和纹外新皮层能否被视为系统发育同源物,它们执行的一些整合功能可能有共同的进化起源,这种起源在爬行动物DVR和哺乳动物纹外新皮层中定位。