Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1997 Dec;17(6):565-601.
doi: 10.1023/a:1022529918810.

Ontogeny of sex differences in the mammalian hypothalamus and preoptic area

Affiliations
Review

Ontogeny of sex differences in the mammalian hypothalamus and preoptic area

S A Tobet et al. Cell Mol Neurobiol. 1997 Dec.

Abstract

1. There are numerous sites in the nervous system where steroid hormones dramatically influence development. Increasing interest in mechanisms in neural development is providing avenues for understanding how gonadal steroids alter the ontogeny of these regions during sexual differentiation. 2. An increasing number of researchers are examining effects of gonadal steroids on neurite outgrowth, cell differentiation, cell death, cell migration, and synaptogenesis. The interrelated timing of these events may be a key aspect influenced by gonadal steroids throughout development. 3. The preoptic area and hypothalamus are characteristically heterogeneous in terms of cell type (e.g., different neuropeptides) and cell derivation. Perhaps a major reason for the ontogeny of sexual differences in the preoptic area and hypothalamus lies in the convergence of many different cell types from diverse sources (i.e., proliferative zones surrounding the lateral and third ventricles, and the olfactory placodes) that can be influenced in an interactive manner by gonadal steroid mechanisms. 4. The characterization of multiple mechanisms (e.g., trophic, migratory, apoptotic, fate, etc.,) that contribute to permanent changes in brain structure and ultimately function is essential for unraveling the process of sexual differentiation.

PubMed Disclaimer

References

    1. Allen, L. S., Hines, M., Shryne, J. E., and Gorski, R. A. (1989). Two sexually dimorphic cell groups in the human brain. J. Neurosci.9:497–506. - PMC - PubMed
    1. Al-Shamma, H. A., and DeVries, G. J. (1996). Neurogenesis of the sexually dimorphic vasopressin cells of the bed nucleus of the stria terminalis and amygdala of rats. J. Neurobiol.29:91–98. - PubMed
    1. Altman, J., and Bayer, S. A. (1978). Development of the diencephalon in the rat II. Correlation of the embryonic development of the hypothalamus with the time of origin of its neurons. J. Comp. Neurol.182:973–994. - PubMed
    1. Altman, J., and Bayer, S. A. (1986). The development of the rat hypothalamus. Adv. Anat. Embryol. Cell Biol.100:1–177. - PubMed
    1. Angelbeck, J. H., and DuBrul, E. F. (1983). The effect of neonatal testosterone on specific male and female patterns of phosphorylated cytosolic proteins in the rat preoptic-hypothalamus, cortex and amygdala. Brain Res.264:277–283. - PubMed

Publication types

LinkOut - more resources