Hippocampal-cortical interaction during periods of subcortical silence.

Hippocampal ripples, episodic high-frequency field-potential oscillations primarily occurring during sleep and calmness, have been described in mice, rats, rabbits, monkeys and humans, and so far they have been associated with retention of previously acquired awake experience. Although hippocampal ripples have been studied in detail using neurophysiological methods, the global effects of ripples on the entire brain remain elusive, primarily owing to a lack of methodologies permitting concurrent hippocampal recordings and whole-brain activity mapping. By combining electrophysiological recordings in hippocampus with ripple-triggered functional magnetic resonance imaging, here we show that most of the cerebral cortex is selectively activated during the ripples, whereas most diencephalic, midbrain and brainstem regions are strongly and consistently inhibited. Analysis of regional temporal response patterns indicates that thalamic activity suppression precedes the hippocampal population burst, which itself is temporally bounded by massive activations of association and primary cortical areas. These findings suggest that during off-line memory consolidation, synergistic thalamocortical activity may be orchestrating a privileged interaction state between hippocampus and cortex by silencing the output of subcortical centres involved in sensory processing or potentially mediating procedural learning. Such a mechanism would cause minimal interference, enabling consolidation of hippocampus-dependent memory.

Localization of oestrogen receptors in the sensory and motor areas of the spinal cord in Japanese quail (Coturnix japonica).

In Japanese quail, the presence of aromatase (oestrogen synthase) in the dorsal horn of the spinal cord suggests that spinal sensory processes might be controlled by local actions of oestrogens. This is supported by the presence of oestrogen receptors and aromatase in the dorsal horn of the spinal cord in rats, and by the alteration of sensitivity by oestrogens in various mammalian species and also in canaries. We investigated whether oestrogens that are locally produced in the quail spinal cord can bind to specific receptors in the vicinity of their site of synthesis. We demonstrate the presence of numerous oestrogen receptor alpha-immunoreactive (ERalpha-ir) cell nuclei, predominantly in laminae II and, to a lesser extent, I and III of the dorsal horn of the spinal cord (i.e. in the area where aromatase was previously identified). ERalpha-ir cells were also seen in various parts of the intermediate zone (laminae V-VII). This presence of ERalpha-ir cells in the dorsal horn and intermediate zone fits in well with the distribution of ERalpha-ir cells in homologous areas in mammals, including rats. Only a few labelled cells were found in the ventral horn in the cervical, brachial, thoracic and first lumbar segments, but a conspicuous dense group of large ERalpha-ir cells was identified in lamina IX of the ventral horn in synsacral segments 8-10, which contain the motoneurones innervating the muscles of the cloacal gland. The presence of ERalpha-ir cells in lamina IX of these synsacral segments in quail contrasts with the finding that motoneurones innervating penile muscles in rats contain androgen, but not oestrogen receptors, and are influenced by androgens rather than by oestrogens. Together, these data suggest that spinal actions of oestrogens may modulate the sensory and motor systems that participate in reproduction, as well as other nonreproductive functions in quail.

The assessment of nociceptive and non-nociceptive skin sensitivity in the Japanese quail (Coturnix japonica).

We evaluated the efficacy of two nociceptive tests, the hot water (HWT) and the foot pressure tests (FPT), and one non-nociceptive test (Semmes-Weinstein test, SWT) in assessing skin sensitivity in conscious Japanese quail. All stimuli elicited a reflex-like, strongly reproducible response. Responses in the HWT and FPT were identified as typical nocifensive flight-fight behavior. In untreated birds, these responses occurred at temperatures and forces described previously as noxious. In the SWT, two responses were observed: a slight ruffling of the cloacal gland feathers due to the stimulation of the cloacal gland, and a brief extension of the limbs due to the stimulation of the ilium or pectoral apterium. These reactions occurred at intensities recognized as innocuous. Morphine significantly altered the response latency and threshold in the HWT and FPT, but had no effect in the SWT. However, the SWT response threshold was significantly increased by local application of xylocaine. Taken together, the pattern of the responses, the intensities and the effects of morphine and xylocaine allowed to distinguish between nociceptive and non-nociceptive tests. They also demonstrate the efficacy of these tests to evaluate skin sensitivity in quail and to assess its modulation by chemical factors that affect somatosensory processes.

Aromatization of androgens into estrogens reduces response latency to a noxious thermal stimulus in male quail.

We recently demonstrated the presence of estrogen synthase (aromatase) and of estrogen receptors in the dorsal horn (laminae I-II) throughout the rostrocaudal extent of the spinal cord in male and female Japanese quail. The spinal laminae I-II receive and process abundant sensory information elicited, among others, by acute noxious stimulation of the skin and resulting in rapid, reflex-like withdrawal behavior. In the present study, we demonstrate that systemic treatment with estradiol or testosterone markedly decreases the latency of the foot withdrawal in the hot water test. A simultaneous treatment with an aromatase inhibitor blocks the effects of testosterone demonstrating, hence, that they are mediated by a conversion of testosterone into an estrogen by aromatase. Furthermore, the testosterone- or estradiol-induced decrease in foot withdrawal latency is blocked by a treatment with the estradiol receptor antagonist, tamoxifen, indicating that the effects are largely mediated by the interaction of estradiol with estrogen receptors. Together, these data suggest that sex steroids modulate sensitivity to noxious stimuli possibly by a direct action at the level of the dorsal horn of the spinal cord.