Global and local processing of musical sequences: an event-related brain potential study.

Musical processing can be decomposed into the appreciation of global/holistic and local elements. Here, we investigated the pattern of neural activity associated with the processing of contour-violated (CV) and contour-preserved (CP) melodies. The CV and CP musical sequences were obtained by altering the pitch value of one note within the musical phrase, while keeping both the scale and the key constant. In the unadulterated melody, there was a sustained negativity that was larger over the right than left fronto-central regions. Participants were equally accurate in detecting CV and CP trials, but were slower in detecting CP than CV trials. Globally altered melodies (i.e. CV) generated an early, negative waveform (N2) and a P3b deflection, whereas the CP target only generated a P3b wave. This suggests that global precedence may occur at an early perceptual stage and argues in favor of fractionating musical processing into global and local components.

Somesthetic discrimination thresholds in the absence of the corpus callosum.

The aim of this study was to investigate how the absence of the corpus callosum affects somesthetic sensation on the axial midline and in proximal and distal body regions. For this purpose, two-point discrimination ability was evaluated in four acallosal subjects, four callosotomized subjects, six IQ-matched subjects and 10 control subjects with average and above average IQ. Sensory thresholds were established in the distal (index, palm), proximal (forearm), cranio-axial (forehead) and axial (dorsal trunk) body regions. The threshold was defined as the smallest separation at which the two points were perceived at a 70% accuracy level. Results showed that the thresholds of the acallosal and the callosotomized subjects were not significantly different from those of the IQ-matched control groups in the distal, proximal and cranio-axial body regions. However, thresholds in the dorsal trunk were significantly higher in the two experimental groups. It thus appears that the axial regions of the body that are normally densely represented in the corpus callosum function abnormally when this structure is absent or transected. Moreover, compensatory mechanisms normally seen in cases of early brain injury do not seem to apply in the present case since the acallosals showed the same impairments as the callosotomized subjects.

Injection of prostaglandin E2 into the anterior hypothalamic preoptic area activates brown adipose tissue thermogenesis in the rat.

E series prostaglandins (PGE) are known to elicit potent hyperthermia when injected into the anterior hypothalamic preoptic area (POAH) in rats, but the effector mechanisms mediating the rise in temperature are not well defined. In the present study, microinjection of PGE2 into the POAH dose-dependently increased non-shivering thermogenesis in brown adipose tissue (BAT) in urethananesthetized rats, bringing about a marked and sustained rise in interscapular BAT (IBAT) and core temperatures. The effect of intra-POAH PGE2 injection on IBAT and core temperatures could be blocked by systemic pretreatment with the sympathetic ganglionic blocker chlorisondamine chloride or the beta-adrenergic receptor blocker propranolol, thus implicating the involvement of the sympathetic system. Furthermore, the increase in IBAT and core temperatures induced by intra-POAH PGE2 could be blocked by prior injection of the local anesthetic procaine or the GABA receptor agonist muscimol into the ipsilateral ventromedial hypothalamic nucleus (VMH). Taken together, the results suggest that PGE2 increases body temperature by acting in the POAH to stimulate heat production in BAT via a sympathetic efferent mechanism located in the VMH.

Insulin co-injection suppresses the thermogenic response to glutamate microinjection into the VMH in rats.

Selective stimulation of ventromedial hypothalamic nucleus (VMH) neurons by microinjection of the excitatory amino acid glutamate sharply increased interscapular brown adipose tissue (IBAT) and core temperatures in urethane-anaesthetized rats. This effect was blocked by co-injection of insulin (0.1-1 microgram) though not an inactive insulin analog, TNB3 insulin. Injection of insulin (1 microgram) into the contralateral VMH or systemic administration of insulin (1 microgram) had no effect on the thermogenic response to intra-VMH glutamate. These results complement those showing that intra-VMH insulin suppresses the basal firing rate of sympathetic nerves to IBAT and diminishes cold-induced nonshivering thermogenesis in BAT and add support to the view that insulin functions as an inhibitory signal on VMH neurons controlling thermogenesis in BAT.