Sex Differences in the Brain: A Whole Body Perspective

Most writing on sexual differentiation of the mammalian brain (including our own) considers just two organs: the gonads and the brain. This perspective, which leaves out all other body parts, misleads us in several ways. First, there is accumulating evidence that all organs are sexually differentiated, and that sex differences in peripheral organs affect the brain. We demonstrate this by reviewing examples involving sex differences in muscles, adipose tissue, the liver, immune system, gut, kidneys, bladder, and placenta that affect the nervous system and behavior. The second consequence of ignoring other organs when considering neural sex differences is that we are likely to miss the fact that some brain sex differences develop to compensate for differences in the internal environment (i.e., because male and female brains operate in different bodies, sex differences are required to make output/function more similar in the two sexes). We also consider evidence that sex differences in sensory systems cause male and female brains to perceive different information about the world; the two sexes are also perceived by the world differently and therefore exposed to differences in experience via treatment by others. Although the topic of sex differences in the brain is often seen as much more emotionally charged than studies of sex differences in other organs, the dichotomy is largely false. By putting the brain firmly back in the body, sex differences in the brain are predictable and can be more completely understood

Neuronal growth, atrophy and death in a sexually dimorphic song nucleus in the zebra finch brain

The song control nuclei of the zebra finch brain contain more neurones of larger diameter in the male than in the female. This sexual dimorphism is thought to result from differential growth of neurones in the two sexes. Using neurohistological techniques and radioactive tracers, we have studied the development of several forebrain nuclei involved in the control of song and find that the dimorphism arises from neuronal atrophy and death in the female brain as well as from an increase in cell-body size and afferent terminals from other forebrain nuclei in the male. Although the timing of these events varies from nucleus to nucleus, the sequence is essentially similar in all of them except area X. Here we describe the events in one of these nuclei, the robust nucleus of archistriatum (RA), as an example