Serotonergic neurons play a major role in the modulation of emotion and behaviour.
Especially knockout studies have revealed a role for the serotonin1A (5-HT1A) receptor in anxiety related behaviour. Mutant animals exhibit enhanced anxiety like
responses, possibly resulting from impaired autoinhibitory control of midbrain serotonergic
neurons.
To further elucidate the role of the 5-HT1A receptors in affective behaviour, an inverse approach has been used and transgenic
mice overexpressing this receptor subtype have been generated. The expression of the
active 5-HT1A receptor protein as indicated by autoradiography was transiently increased during
the early postnatal development (P1.5) as compared to wildtype mice. Within the next
2 weeks the increase in receptor binding vanished and was also not apparent in adult
animals indicating adaptive changes in the regulation of 5-HT1A receptor expression. Although no evidence for increased receptor binding in the brains
of adult homozygous mice was found by autoradiography, typical phenotypic changes
indicative for overactivity of 5-HT1A receptors were apparent. Transgenic mice revealed a reduced molar ratio of 5-hydroxyindoleacetic
acid to serotonin in several brain areas and elevated serotonin values in the hippocampus
and striatum. Moreover, anxiety-like behaviour was decreased in male and female transgenic
mice and body temperature was lowered in male transgenic mice as compared to heterozygous
and wildtype mice. These findings further underline the pivotal role of 5-HT1A receptors in the homeostasis of anxiety-like behaviour and the crucial importance
of stimulation of the 5-HT1A receptor during the early postnatal development for normal anxiety-like behaviour
throughout life.