A cytoarchitectonic analysis is presented of a configuration of cells which extends through the medial preoptic and rostral part of the anterior hypothalamus of the guinea pig, rat, hamster, and mouse. Within that configuration, called here the sexually dimorphic nuclear complex of the medial preoptic-anterior hypothalamic area (SDNC-MPAH), there is nearly continuous variation in cellular distribution or packing density as one proceeds rostrocaudally, as well as variations between females and males at corresponding levels. The major cell groups comprising SDNC-MPAH are the medial preoptic nucleus (MP) and the preventricular portion of the periventricular nucleus (Pep) rostrally, and the anterior hypothalamic nucleus (AH), anterior portion of periventricular nucleus, (Pea), and bed nucleus of stria terminalis (ST) caudally. The most striking cytoarchitectonic dimorphisms usually involve MP and AH. In all four species examined, MP is larger and, except for the mouse, appears to be more densely cellular in the female than in the male. Most prominently in the rat and guinea pig, AH is densely cellular throughout in the female, including the subependymal zone, whereas in the male AH lies at a distance from the third ventricle, separated from the ependyma by a cell-poor zone. The significance of these findings may lie in the fact that the region exhibiting the sexual dimorphisms has been shown to be involved in the regulation of reproductive functions which are sexually differentiated and developmentally influenced by the fetal or perinatal hormonal milieu in some species.

Neurogenesis was studied in the medial preoptic area of the guinea pig by the method of tritiated thymidine autoradiography. Eight cytoarchitectonic divisions were examined, 4 of which display sexual dimorphism and 4 that do not. Neurogenesis in the nonsexually dimorphic divisions was found to end at embryonic day (E) 27, while in each of the sexually dimorphic divisions neurogenesis continued after this and persisted until at least E31 in the central compact and principal portions of the medial preoptic nucleus. Since the testes become active at E25 in the guinea pig (Resko, 1970), it is possible that gonadal secretions influence the proliferation and subsequent developmental processes of neurons destined for the sexually dimorphic nuclei.

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An intraventricular neuronal complex has been identified with scanning and transmission electron microscopy at the base of the lamina terminalis of the mouse. The raspberry-shaped complex protrudes from a thickened bulge on the ependymal surface of the lamina terminalis or adjacent rostral floor of the third ventricle. Neurons and occasional ependymal cells cover the surface of the complex. Its core is made up of neurons, ependymal cells, and neuronal processes, which are usually compactly arranged. The core is continuous, through a breach in the ependymal layers, with the subependymal neuropil of the lamina terminalis. Within the core of the complex are large numbers of axodendritic synapses. Axonal varicosities and synaptic terminals are filled with vesicles and mitochondria. Synaptic endings have one of two populations of vesicles: exclusively clear, small, round or flattened vesicles. In view of the known structural and functional characteristics of the lamina terminalis, it is possible that the neuronal complex may participate in neurohormonal regulatory systems of the hypothalamus and hypophysis or in the network of circumventricular organs mediating angiotensin effects.