Neurons in the guinea pig (Cavia porcellus) lateral lumbosacral spinal cord project to the central part of the lateral periaqueductal gray matter

Rutger Kuipers; Esther Marije Klop

doi:10.1016/j.brainres.2006.05.039

Neurons in the guinea pig (Cavia porcellus) lateral lumbosacral spinal cord project to the central part of the lateral periaqueductal gray matter

Brain Research ◽

10.1016/j.brainres.2006.05.039 ◽

2006 ◽

Vol 1101 (1) ◽

pp. 43-50 ◽

Cited By ~ 5

Author(s):

Rutger Kuipers ◽

Esther Marije Klop

Keyword(s):

Spinal Cord ◽

Guinea Pig ◽

Gray Matter ◽

Periaqueductal Gray ◽

Cavia Porcellus ◽

Periaqueductal Gray Matter ◽

Lumbosacral Spinal Cord

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Involvement of the Cholinergic System and Periaqueductal Gray Matter in the Modulation of Tonic Immobility in the Guinea Pig

Physiology & Behavior ◽

10.1016/s0031-9384(97)00134-0 ◽

1997 ◽

Vol 62 (1) ◽

pp. 53-59 ◽

Cited By ~ 33

Author(s):

Claudia Regina Monassi ◽

Anette Hoffmann ◽

Leda Menescal-de-Oliveira

Keyword(s):

Guinea Pig ◽

Gray Matter ◽

Cholinergic System ◽

Tonic Immobility ◽

Periaqueductal Gray ◽

Periaqueductal Gray Matter

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Serotonin 5-HT2 and 5-HT1A receptors in the periaqueductal gray matter differentially modulate tonic immobility in guinea pig

Brain Research ◽

10.1016/j.brainres.2004.02.061 ◽

2004 ◽

Vol 1009 (1-2) ◽

pp. 169-180 ◽

Cited By ~ 19

Author(s):

Claudia Regina Monassi ◽

Leda Menescal-de-Oliveira

Keyword(s):

Guinea Pig ◽

Gray Matter ◽

Tonic Immobility ◽

Periaqueductal Gray ◽

Periaqueductal Gray Matter

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Barrington's nucleus in the guinea pig (Cavia porcellus): Location in relation to noradrenergic cell groups and connections to the lumbosacral spinal cord

Brain Research Bulletin ◽

10.1016/j.brainresbull.2006.10.026 ◽

2007 ◽

Vol 72 (1) ◽

pp. 49-56 ◽

Cited By ~ 1

Author(s):

Rutger Kuipers ◽

Ellie Eggens-Meijer ◽

Gordon McMurray

Keyword(s):

Spinal Cord ◽

Guinea Pig ◽

Cavia Porcellus ◽

Lumbosacral Spinal Cord ◽

Cell Groups ◽

Noradrenergic Cell Groups

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Analgesia from electrical stimulation of the periaqueductal gray matter in the cat: behavioral observations and inhibitory effects on spinal cord interneurons

Brain Research ◽

10.1016/0006-8993(73)90748-8 ◽

1973 ◽

Vol 50 (2) ◽

pp. 441-446 ◽

Cited By ~ 332

Author(s):

John C. Liebeskind ◽

Gise`le Guilbaud ◽

Jean-Marie Besson ◽

Jean-Louis Oliveras

Keyword(s):

Spinal Cord ◽

Electrical Stimulation ◽

Gray Matter ◽

Periaqueductal Gray ◽

Inhibitory Effects ◽

Periaqueductal Gray Matter ◽

Behavioral Observations ◽

Stimulation Of

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Antinocioceptive Effects of Spinal Cord Stimulation by Activation of Periaqueductal Gray Matter and Rostral Ventromedial Medulla: A Mechanism Beyond the Gate Control Theory

Neuromodulation Technology at the Neural Interface ◽

10.1111/ner.12788 ◽

2018 ◽

Vol 21 (5) ◽

pp. 520-521 ◽

Cited By ~ 2

Author(s):

Mousa Taghipour ◽

Fariborz Ghaffarpasand

Keyword(s):

Spinal Cord ◽

Control Theory ◽

Gray Matter ◽

Spinal Cord Stimulation ◽

Periaqueductal Gray ◽

Rostral Ventromedial Medulla ◽

Periaqueductal Gray Matter ◽

Gate Control Theory ◽

Ventromedial Medulla ◽

Gate Control

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Repeated spinal cord stimulation decreases the extracellular level of γ-aminobutyric acid in the periaqueductal gray matter of freely moving rats

Brain Research ◽

10.1016/0006-8993(95)00911-9 ◽

1995 ◽

Vol 699 (2) ◽

pp. 231-241 ◽

Cited By ~ 58

Author(s):

Carl-Olav Stiller ◽

Bengt Linderoth ◽

William T. O'Connor ◽

Johan Franck ◽

Torkel Falkenberg ◽

...

Keyword(s):

Spinal Cord ◽

Gray Matter ◽

Spinal Cord Stimulation ◽

Periaqueductal Gray ◽

Aminobutyric Acid ◽

Periaqueductal Gray Matter ◽

Freely Moving Rats ◽

Extracellular Level ◽

Freely Moving

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Inhibition of spinal cord interneurons by narcotic microinjection and focal electrical stimulation in the periaqueductal gray matter

Brain Research ◽

10.1016/0006-8993(79)90536-5 ◽

1979 ◽

Vol 172 (2) ◽

pp. 243-257 ◽

Cited By ~ 126

Author(s):

Gary J. Bennett ◽

David J. Mayer

Keyword(s):

Spinal Cord ◽

Electrical Stimulation ◽

Gray Matter ◽

Periaqueductal Gray ◽

Periaqueductal Gray Matter

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Collateral projections of neurons in laminae I, III, and IV of rat spinal cord to thalamus, periaqueductal gray matter, and lateral parabrachial area

The Journal of Comparative Neurology ◽

10.1002/cne.22081 ◽

2009 ◽

Vol 515 (6) ◽

pp. 629-646 ◽

Cited By ~ 61

Author(s):

Khulood M. Al-Khater ◽

Andrew J. Todd

Keyword(s):

Spinal Cord ◽

Gray Matter ◽

Periaqueductal Gray ◽

Rat Spinal Cord ◽

Periaqueductal Gray Matter

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Antinociception induced by intravenous dipyrone (metamizol) upon dorsal horn neurons: Involvement of endogenous opioids at the periaqueductal gray matter, the nucleus raphe magnus, and the spinal cord in rats

Brain Research ◽

10.1016/j.brainres.2005.04.083 ◽

2005 ◽

Vol 1048 (1-2) ◽

pp. 211-217 ◽

Cited By ~ 37

Author(s):

Enrique Vazquez ◽

Norma Hernandez ◽

William Escobar ◽

Horacio Vanegas

Keyword(s):

Spinal Cord ◽

Dorsal Horn ◽

Gray Matter ◽

Periaqueductal Gray ◽

Endogenous Opioids ◽

Periaqueductal Gray Matter ◽

Nucleus Raphe Magnus ◽

Dorsal Horn Neurons ◽

Raphe Magnus

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Faculty Opinions recommendation of Fos activation in hypothalamic neurons during cold or warm exposure: projections to periaqueductal gray matter.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.724120640.793517552 ◽

2016 ◽

Author(s):

Shaun Morrison

Keyword(s):

Gray Matter ◽

Periaqueductal Gray ◽

Hypothalamic Neurons ◽

Periaqueductal Gray Matter

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