Literature DB >> 7675196

Suppression of ponto-geniculo-occipital waves by neurotoxic lesions of pontine caudo-lateral peribrachial cells.

S Datta1, J A Hobson.   

Abstract

Ponto-geniculo-occipital waves precede rapid eye movement sleep and play an important role in triggering and maintaining rapid eye movement sleep. Ponto-geniculo-occipital waves have been implicated in several important functions such as sensorimotor integration, learning, cognition, development of the visual system, visual hallucination, and startle response. Peribrachial area neurons have long been thought to play a key role in the triggering of ponto-geniculo-occipital wave. However, the exact location within the peribrachial area for triggering pontine ponto-geniculo-occipital wave has not been unequivocally demonstrated. In an attempt to address this issue, kainic acid was microinjected (1.0 micrograms) unilaterally into the caudo-lateral peribrachial area of four cats in order to destroy the cell bodies located in that region and thus to study the effects of their destruction upon waking-sleep states and ponto-geniculo-occipital waves. The kainic acid produced a small spherical area of nerve cell loss and/or gliosis centered on the stereotaxic coordinates of P: 4.0, L: 4.5, and H: -2.5. The maximum diameter of that spherical area of cell loss was 0.9 mm. Unilateral lesioning of the caudo-lateral peribrachial area decreased ponto-geniculo-occipital waves during rapid eye movement sleep by 85% ipsi-laterally and 15% contralaterally in the lateral geniculate body without significantly changing the amounts of time spent in wake, slow-wave sleep, and rapid eye movement sleep. These results suggest that the caudo-lateral peribrachial area cells are critical to the genesis of ponto-geniculo-occipital waves, and provide compelling evidence that the different parts of the peribrachial area have quite different roles in the generation of discrete rapid eye movement sleep signs. We propose that caudo-lateral peribrachial cells exert an excitatory influence on rostral peribrachial cells, which then directly activate the ponto-geniculo-occipital waves that are recorded in the lateral geniculate body. Results of this study are not only important to understand the mechanisms generating ponto-geniculo-occipital waves but also could be used as an experimental tool to study the functions of this wave.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7675196     DOI: 10.1016/0306-4522(95)00081-s

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  12 in total

1.  Reassessment of the structural basis of the ascending arousal system.

Authors:  Patrick M Fuller; Patrick Fuller; David Sherman; Nigel P Pedersen; Clifford B Saper; Jun Lu
Journal:  J Comp Neurol       Date:  2011-04-01       Impact factor: 3.215

Review 2.  Neurobiological mechanisms for the regulation of mammalian sleep-wake behavior: reinterpretation of historical evidence and inclusion of contemporary cellular and molecular evidence.

Authors:  Subimal Datta; Robert Ross Maclean
Journal:  Neurosci Biobehav Rev       Date:  2007-03-12       Impact factor: 8.989

Review 3.  Cellular basis of pontine ponto-geniculo-occipital wave generation and modulation.

Authors:  S Datta
Journal:  Cell Mol Neurobiol       Date:  1997-06       Impact factor: 5.046

Review 4.  Control of sleep and wakefulness.

Authors:  Ritchie E Brown; Radhika Basheer; James T McKenna; Robert E Strecker; Robert W McCarley
Journal:  Physiol Rev       Date:  2012-07       Impact factor: 37.312

5.  A restricted parabrachial pontine region is active during non-rapid eye movement sleep.

Authors:  P Torterolo; S Sampogna; M H Chase
Journal:  Neuroscience       Date:  2011-06-15       Impact factor: 3.590

6.  Pontine-wave generator activation-dependent memory processing of avoidance learning involves the dorsal hippocampus in the rat.

Authors:  Subimal Datta; Subhash Saha; Sarah L Prutzman; Olivia J Mullins; Vijayakumar Mavanji
Journal:  J Neurosci Res       Date:  2005-06-01       Impact factor: 4.164

7.  Phasic motor activity reduction occurring with horizontal rapid eye movements during active sleep in human.

Authors:  J Kohyama; M Shimohira; T Hasegawa; T Kouji; Y Iwakawa
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

8.  Avoidance task training potentiates phasic pontine-wave density in the rat: A mechanism for sleep-dependent plasticity.

Authors:  S Datta
Journal:  J Neurosci       Date:  2000-11-15       Impact factor: 6.167

9.  Activation of phasic pontine-wave generator in the rat: a mechanism for expression of plasticity-related genes and proteins in the dorsal hippocampus and amygdala.

Authors:  Subimal Datta; Guangmu Li; Sanford Auerbach
Journal:  Eur J Neurosci       Date:  2008-03-26       Impact factor: 3.386

10.  Fear extinction memory consolidation requires potentiation of pontine-wave activity during REM sleep.

Authors:  Subimal Datta; Matthew W O'Malley
Journal:  J Neurosci       Date:  2013-03-06       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.