Brain histamine and behavioral neuroscience

The human histaminergic system contains approximately 64.000 neurons located in a posterior region of the hypothalamus, the tuberomamillary nucleus. Projections of such a relatively small number of neurons are surprisingly widespread throughout the central nervous system. Histaminergic neurons are highly active during wakefulness and contribute to the physiology of arousal state, exploration, pain modulation, nutrition, thermoregulation and brain energy metabolism, learning and memory functioning [1]. The possibility to assess the contribution of brain histamine (HA) to specific behavioral changes is a complex task, taking into consideration the broad modulatory activity exerted by this amine at different levels of cortical and subcortical circuitry. An explanation of the diversity of functions of the histaminergic system may be attributed to the heterogeneous nature of HA neurons that are organized into functionally distinct circuits, impinging on different brain regions, and display selective control mechanisms [2]. From a quantitative perspective, data from genetic models indicate that lack of HA is associated with reduced motor activity reasonably due to impaired arousal state and motivation [3]. Recent findings have unveiled an additional relevant contribution of brain HA on qualitative features of the displayed motor behavior both in humans and animals [4]. Ercan-Sencicek and colleagues [5] have elaborated a histaminergic hypothesis of tic phenomenology on the basis of the identification of a rare autosomal dominant form of Tourette’s syndrome highly correlated with a nonsense mutation, Hdc W317X, on the gene for histidine decarboxylase (HDC) the keyenzyme responsible for HA synthesis. HA and the H3receptor have a strong influence on dopaminergic activity in the Basal Ganglia suggesting an unexpected role of HA in the pathophysiology of movement disorders, not only confined to tic symptomatology. The peculiar distribution of the H3 receptor, mainly confined to the brain, calls for a better understanding of the role of this amine in brain circuitry [6]. The H3 receptor likely represents a selective pharmacological target to modulate brain HA. Albeit a direct involvement of the histaminergic system has been suggested, to our knowledge, only in the Tourette’s syndrome, markers of an altered HA activity have been described in several neuropsychiatric conditions characterized by stereotypical or abnormal motor behavior and thoughts, such as Schizophrenia, Parkinson’s disease, Huntington’s disease or Addiction [3][6]. In view of these results, we have recently described the effect of an acute brain HA depletion on the display of motor sequences of naïve CD1 mice in the open-field [7]. Our approach does not require any previous conditioning and the analysis is carried out following a high-res video recording of the ongoing behavior. HA depletion was obtained by intracerebroventricular administration of the HDC inhibitor alpha-fluoromethylhistidine and motor sequences were detected and analyzed using a multivariate technique known as temporal pattern (t-pattern) analysis. Basically, a t-pattern represents a sequence describing repetitive aspects of a studied behavior [8] and can be formally presented using the following expressions: