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B Rusak

Publications and source records attributed to B Rusak.

86 records · Page 5Linked to original sources
PubMed1985

Horizontal knife cuts in the suprachiasmatic area prevent hamster gonadal responses to photoperiod.

We used horizontal knife cuts near the suprachiasmatic nucleus (SCN) to investigate the route for day-length information transmission from the SCN to the paraventricular nucleus (PVN). Testicular regression was blocked in animals with knife cuts dorsal to the SCN that spanned its entire rostrocaudal extent, and in PVN-ablated animals. Misplaced cuts in the ventral preoptic area also prevented gonadal regression. These neural insults did not systematically affect the circadian control of activity rhythms. The pathway from the SCN to the pineal runs from the dorsal border of the SCN and travels through the periventricular area toward the PVN.

Animals↗
PubMed1985

Neuropeptide Y immunoreactivity in the hamster geniculo-suprachiasmatic tract.

The distributions of neuropeptide Y (NPY) and avian pancreatic polypeptide (APP) immunoreactivity were examined in the suprachiasmatic nucleus and the geniculate area of male golden hamster brains. In some cases, colchicine was injected intraventricularly to aid in visualization of immunoreactive cell bodies. A group of hamsters were given bilateral or unilateral radiofrequency lesions of the geniculate area and neuropeptide Y immunoreactivity was examined in the suprachiasmatic nucleus after survival times varying between 8 and 300 days. Another group of hamsters received unilateral intraocular injections of anterograde tracers and the overlap of NPY-immunoreactive cells in the geniculate area and labeled retinal afferents was assessed. It was found that NPY- and APP-immunoreactive fibers formed a dense plexus in the ventro-lateral suprachiasmatic nucleus. NPY-immunoreactive cell bodies were observed in the intergeniculate leaflet as well as in the external lamina of the anterior portion of the ventral lateral geniculate nucleus. Unilateral lesions of the geniculate produced a relative reduction in neuropeptide Y immunoreactivity in the ipsilateral suprachiasmatic nucleus whereas bilateral lesions produced a reduction of neuropeptide Y immunoreactivity in both suprachiasmatic nuclei. All NPY-immunoreactive cells in the intergeniculate leaflet were overlapped by bilateral retinal afferents. In the ventral lateral geniculate nucleus, all NPY-immunoreactive cells were overlapped by contralateral retinal afferents; however, not all such cells were in areas receiving ipsilateral retinal afferents. These results indicate that the hamster geniculo-suprachiasmatic tract originates in part from NPY-immunoreactive cell bodies and that these cells lie in areas receiving direct retinal afferents.

Animals↗
PubMed1984

Periventricular and suprachiasmatic lesion effects on photoperiodic responses of the hamster hypophyseal-gonadal axis.

We examined the involvement of neural mechanisms within the suprachiasmatic nucleus (SCN) and periventricular area (PVA), and the role of prolactin (Prl) in control of endocrine function in short day-exposed Syrian hamsters. Hamsters bearing lesions of the SCN or PVA, hamsters implanted with an anterior pituitary under the kidney capsule to provide sustained Prl levels, and sham-operated hamsters were exposed to either 14L:10D or 8L:16D. After 9 wk, hamsters were sacrificed, and their testes and pituitaries were studied in vitro to assess their secretory capacity. SCN lesions and large periventricular lesions impinging on the paraventricular nucleus prevented testicular regression during short-day exposure. Small periventricular lesions and pituitary implants did not prevent gonadal regression in hamsters exposed to short days. Testis weights were positively correlated with basal and luteinizing hormone (LH)-stimulated androgen production in the control and lesioned groups; pituitary implants prevented the decline in androgen production in vitro in gonadally regressed animals. The relative in vitro pituitary response to gonadotropin-releasing hormone (GnRH) stimulation in control and lesioned groups was not reduced by short-day exposure. These data indicate that either axons coursing dorsally from the SCN or extra-SCN structures in the periventricular/paraventricular area are necessary for testicular regression in short photoperiods.

Androgens↗
PubMed1982

Suprachiasmatic stimulation phase shifts rodent circadian rhythms.

The integrity of the suprachiasmatic nuclei (SCN) of the hypothalamus is essential to the expression of normal circadian rhythms in rodents. Electrical stimulation of the SCN caused phase shifts and period changes in the freerunning feeding rhythms of rats and activity rhythms of hamsters. The phase response curve for SCN stimulation appears to parallel that for light pulses. These findings strengthen the hypothesis derived from lesion studies that the SCN are the dominant light-entrained oscillators in the rodent circadian system.

Action Potentials↗
PubMed1979

Neural mechanisms for entrainment and generation of mammalian circadian rhythms.

The identification of a direct retinohypothalamic tract (RHT) terminating in the supra-chiasmatic nuclei (SCN) has focused attention on the role of these structures in the entrainment and generation of circadian rhythms in mammals. Light effects on circadian rhythms are mediated by both the RHT and portions of the classical visual system. The complex interactions of these systems are reflected both in their direct anatomical connections and in the functional changes in entrainment produced by interruption of either set of projections. Destruction of the RHT/SCN eliminated both normal entrainment and normal free-running circadian rhythms. No circadian rhythms has survived SCN ablation in rodents, but a variety of non-circadian cycles can be generated by lesioned animals. The complex behavioral patterns produced by SCN-lesioned hamsters suggest that circadian oscillators continue to function in these animals, but that their activity is no longer integrated into a single circadian framework. The available evidence indicates that the mammalian pacemaking system comprises a set of independent oscillators normally regulated by the SCN and by light information that is transmitted via several retinofugal pathways.

Animals↗