Recently, insulin synthesis and the presence of an insulin receptor have be
en demonstrated in the brain. Intracerebroventricular infusion of insulin c
auses a selective increase in the amount of slow-wave sleep. In the present
study, the sleep-wake cycle of transgenic mice, with or without habenular
neuronal expression of the human insulin gene, was studied to investigate t
he possible role of brain insulin as a sleep modulator. Slow-wave sleep dur
ation was increased in those mice expressing human insulin in the habenula.
However, it is possible that this effect was not due to expression of the
insulin transgene, but to the genetic background of one of the parental str
ains (CBA) used for insertion of the transgene. Users of transgenic mice sh
ould be aware of this possibility and be cautious in interpreting results w
hen hybrid embryos are used as transgene recipients.