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Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice

In patients with irritable bowel syndrome, visceral pain is evoked more readily following distension of the colorectum. However, the identity of extrinsic afferent nerve pathway that detects and transmits visceral pain from the colorectum to the spinal cord is unclear. In this study, we identified w...

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Autores principales: Kyloh, Melinda, Nicholas, Sarah, Zagorodnyuk, Vladimir P., Brookes, Simon J., Spencer, Nick J.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046361/
https://www.ncbi.nlm.nih.gov/pubmed/21390285
http://dx.doi.org/10.3389/fnins.2011.00016
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author Kyloh, Melinda
Nicholas, Sarah
Zagorodnyuk, Vladimir P.
Brookes, Simon J.
Spencer, Nick J.
author_facet Kyloh, Melinda
Nicholas, Sarah
Zagorodnyuk, Vladimir P.
Brookes, Simon J.
Spencer, Nick J.
author_sort Kyloh, Melinda
collection PubMed
description In patients with irritable bowel syndrome, visceral pain is evoked more readily following distension of the colorectum. However, the identity of extrinsic afferent nerve pathway that detects and transmits visceral pain from the colorectum to the spinal cord is unclear. In this study, we identified which extrinsic nerve pathway(s) underlies nociception from the colorectum to the spinal cord of rodents. Electromyogram recordings were made from the transverse oblique abdominal muscles in anesthetized wild type (C57BL/6) mice and acute noxious intraluminal distension stimuli (100–120 mmHg) were applied to the terminal 15 mm of colorectum to activate visceromotor responses (VMRs). Lesioning the lumbar colonic nerves in vivo had no detectable effect on the VMRs evoked by colorectal distension. Also, lesions applied to the right or left hypogastric nerves failed to reduce VMRs. However, lesions applied to both left and right branches of the rectal nerves abolished VMRs, regardless of whether the lumbar colonic or hypogastric nerves were severed. Electrical stimulation applied to either the lumbar colonic or hypogastric nerves in vivo, failed to elicit a VMR. In contrast, electrical stimulation (2–5 Hz, 0.4 ms, 60 V) applied to the rectum reliably elicited VMRs, which were abolished by selective lesioning of the rectal nerves. DiI retrograde labeling from the colorectum (injection sites 9–15 mm from the anus, measured in unstretched preparations) labeled sensory neurons primarily in dorsal root ganglia (DRG) of the lumbosacral region of the spinal cord (L6-S1). In contrast, injection of DiI into the mid to proximal colon (injection sites 30–75 mm from the anus, measured in unstretched preparations) labeled sensory neurons in DRG primarily of the lower thoracic level (T6-L2) of the spinal cord. The visceral pain pathway activated by acute noxious distension of the terminal 15 mm of mouse colorectum is transmitted predominantly, if not solely, through rectal/pelvic afferent nerve fibers to the spinal cord. The sensory neurons of this spinal afferent pathway lie primarily in the lumbosacral region of the spinal cord, between L6 and S1.
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spelling pubmed-30463612011-03-09 Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice Kyloh, Melinda Nicholas, Sarah Zagorodnyuk, Vladimir P. Brookes, Simon J. Spencer, Nick J. Front Neurosci Neuroscience In patients with irritable bowel syndrome, visceral pain is evoked more readily following distension of the colorectum. However, the identity of extrinsic afferent nerve pathway that detects and transmits visceral pain from the colorectum to the spinal cord is unclear. In this study, we identified which extrinsic nerve pathway(s) underlies nociception from the colorectum to the spinal cord of rodents. Electromyogram recordings were made from the transverse oblique abdominal muscles in anesthetized wild type (C57BL/6) mice and acute noxious intraluminal distension stimuli (100–120 mmHg) were applied to the terminal 15 mm of colorectum to activate visceromotor responses (VMRs). Lesioning the lumbar colonic nerves in vivo had no detectable effect on the VMRs evoked by colorectal distension. Also, lesions applied to the right or left hypogastric nerves failed to reduce VMRs. However, lesions applied to both left and right branches of the rectal nerves abolished VMRs, regardless of whether the lumbar colonic or hypogastric nerves were severed. Electrical stimulation applied to either the lumbar colonic or hypogastric nerves in vivo, failed to elicit a VMR. In contrast, electrical stimulation (2–5 Hz, 0.4 ms, 60 V) applied to the rectum reliably elicited VMRs, which were abolished by selective lesioning of the rectal nerves. DiI retrograde labeling from the colorectum (injection sites 9–15 mm from the anus, measured in unstretched preparations) labeled sensory neurons primarily in dorsal root ganglia (DRG) of the lumbosacral region of the spinal cord (L6-S1). In contrast, injection of DiI into the mid to proximal colon (injection sites 30–75 mm from the anus, measured in unstretched preparations) labeled sensory neurons in DRG primarily of the lower thoracic level (T6-L2) of the spinal cord. The visceral pain pathway activated by acute noxious distension of the terminal 15 mm of mouse colorectum is transmitted predominantly, if not solely, through rectal/pelvic afferent nerve fibers to the spinal cord. The sensory neurons of this spinal afferent pathway lie primarily in the lumbosacral region of the spinal cord, between L6 and S1. Frontiers Research Foundation 2011-02-22 /pmc/articles/PMC3046361/ /pubmed/21390285 http://dx.doi.org/10.3389/fnins.2011.00016 Text en Copyright © 2011 Kyloh, Nicholas, Zagorodnyuk, Brookes and Spencer. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Neuroscience
Kyloh, Melinda
Nicholas, Sarah
Zagorodnyuk, Vladimir P.
Brookes, Simon J.
Spencer, Nick J.
Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice
title Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice
title_full Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice
title_fullStr Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice
title_full_unstemmed Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice
title_short Identification of the Visceral Pain Pathway Activated by Noxious Colorectal Distension in Mice
title_sort identification of the visceral pain pathway activated by noxious colorectal distension in mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046361/
https://www.ncbi.nlm.nih.gov/pubmed/21390285
http://dx.doi.org/10.3389/fnins.2011.00016
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