Pilot study for in vivo cellular imaging of the muscularis propria and ex vivo molecular imaging of myenteric neurons (with video)

Background It is challenging to optimally sample the muscularis propria endoscopically for the diagnosis of muscle layer diseases, especially for motility disorders resulting from neuroenteric dysfunction. Objectives Ultramagnification in vivo imaging of the muscularis mucosa and ex vivo identificat...

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Veröffentlicht in:Gastrointestinal endoscopy 2009-05, Vol.69 (6), p.1129-1134
Hauptverfasser: Sumiyama, Kazuki, MD, PhD, Tajiri, Hisao, MD, PhD, Kato, Fusao, PhD, Imura, Taiko, PhD, Ono, Kaori, MSc, Ikeda, Keiichi, MD, PhD, Imazu, Hiroo, MD, PhD, Gostout, Christopher J., MD
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container_issue 6
container_start_page 1129
container_title Gastrointestinal endoscopy
container_volume 69
creator Sumiyama, Kazuki, MD, PhD
Tajiri, Hisao, MD, PhD
Kato, Fusao, PhD
Imura, Taiko, PhD
Ono, Kaori, MSc
Ikeda, Keiichi, MD, PhD
Imazu, Hiroo, MD, PhD
Gostout, Christopher J., MD
description Background It is challenging to optimally sample the muscularis propria endoscopically for the diagnosis of muscle layer diseases, especially for motility disorders resulting from neuroenteric dysfunction. Objectives Ultramagnification in vivo imaging of the muscularis mucosa and ex vivo identification of myenteric neuronal elements by confocal microscopy. Design Ex vivo and in vivo porcine animal studies. Setting Short-term study in an animal laboratory. Interventions The muscularis propria in the stomach and esophagus was accessed by resecting the mucosal layer with endoscopic submucosal dissection or cap EMR techniques or by creating a submucosal space by the submucosal endoscopy with mucosal flap technique. The muscularis propria was stained with Nissl stains and 2 types of neuronal molecular stains. The muscular layer was imaged with the endocytoscope in vivo. The muscularis stained with molecular-based stains was also evaluated with a confocal microscope. Results Cellular microstructures resembling spindle-shaped smooth muscle cells were visualized by endocytoscopy in vivo. Confocal endoscopic microscopy demonstrated that in vivo topical application of neuronal molecular stains successfully stained the muscularis and specifically highlighted neuron-like cells. Limitation Animal model pilot study. Conclusions In vivo endoscopic histologic evaluation of the muscularis propria is technically feasible and easy. Minimally invasive advanced endoscopic imaging may be useful for the diagnosis and study of neuroenteric disorders at the level of the muscularis propria, avoiding surgical full-thickness tissue sampling.
doi_str_mv 10.1016/j.gie.2008.08.007
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Objectives Ultramagnification in vivo imaging of the muscularis mucosa and ex vivo identification of myenteric neuronal elements by confocal microscopy. Design Ex vivo and in vivo porcine animal studies. Setting Short-term study in an animal laboratory. Interventions The muscularis propria in the stomach and esophagus was accessed by resecting the mucosal layer with endoscopic submucosal dissection or cap EMR techniques or by creating a submucosal space by the submucosal endoscopy with mucosal flap technique. The muscularis propria was stained with Nissl stains and 2 types of neuronal molecular stains. The muscular layer was imaged with the endocytoscope in vivo. The muscularis stained with molecular-based stains was also evaluated with a confocal microscope. Results Cellular microstructures resembling spindle-shaped smooth muscle cells were visualized by endocytoscopy in vivo. Confocal endoscopic microscopy demonstrated that in vivo topical application of neuronal molecular stains successfully stained the muscularis and specifically highlighted neuron-like cells. Limitation Animal model pilot study. Conclusions In vivo endoscopic histologic evaluation of the muscularis propria is technically feasible and easy. Minimally invasive advanced endoscopic imaging may be useful for the diagnosis and study of neuroenteric disorders at the level of the muscularis propria, avoiding surgical full-thickness tissue sampling.</description><identifier>ISSN: 0016-5107</identifier><identifier>EISSN: 1097-6779</identifier><identifier>DOI: 10.1016/j.gie.2008.08.007</identifier><identifier>PMID: 19215917</identifier><identifier>CODEN: GAENBQ</identifier><language>eng</language><publisher>Maryland heights, MO: Mosby, Inc</publisher><subject>Animals ; Biological and medical sciences ; Cell Nucleus - ultrastructure ; Digestive system. 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Objectives Ultramagnification in vivo imaging of the muscularis mucosa and ex vivo identification of myenteric neuronal elements by confocal microscopy. Design Ex vivo and in vivo porcine animal studies. Setting Short-term study in an animal laboratory. Interventions The muscularis propria in the stomach and esophagus was accessed by resecting the mucosal layer with endoscopic submucosal dissection or cap EMR techniques or by creating a submucosal space by the submucosal endoscopy with mucosal flap technique. The muscularis propria was stained with Nissl stains and 2 types of neuronal molecular stains. The muscular layer was imaged with the endocytoscope in vivo. The muscularis stained with molecular-based stains was also evaluated with a confocal microscope. Results Cellular microstructures resembling spindle-shaped smooth muscle cells were visualized by endocytoscopy in vivo. Confocal endoscopic microscopy demonstrated that in vivo topical application of neuronal molecular stains successfully stained the muscularis and specifically highlighted neuron-like cells. Limitation Animal model pilot study. Conclusions In vivo endoscopic histologic evaluation of the muscularis propria is technically feasible and easy. Minimally invasive advanced endoscopic imaging may be useful for the diagnosis and study of neuroenteric disorders at the level of the muscularis propria, avoiding surgical full-thickness tissue sampling.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Nucleus - ultrastructure</subject><subject>Digestive system. Abdomen</subject><subject>Endoscopy</subject><subject>Equipment Design</subject><subject>Gastric Mucosa - ultrastructure</subject><subject>Gastroenterology and Hepatology</subject><subject>Gastroenterology. Liver. Pancreas. 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Abdomen</topic><topic>Endoscopy</topic><topic>Equipment Design</topic><topic>Gastric Mucosa - ultrastructure</topic><topic>Gastroenterology and Hepatology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gastroscopes</topic><topic>Inclusion Bodies - diagnostic imaging</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Medical sciences</topic><topic>Microscopy, Confocal - instrumentation</topic><topic>Microscopy, Video - instrumentation</topic><topic>Myenteric Plexus - ultrastructure</topic><topic>Myocytes, Smooth Muscle - ultrastructure</topic><topic>Neurons - ultrastructure</topic><topic>Pilot Projects</topic><topic>Sensitivity and Specificity</topic><topic>Swine</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sumiyama, Kazuki, MD, PhD</creatorcontrib><creatorcontrib>Tajiri, Hisao, MD, PhD</creatorcontrib><creatorcontrib>Kato, Fusao, PhD</creatorcontrib><creatorcontrib>Imura, Taiko, PhD</creatorcontrib><creatorcontrib>Ono, Kaori, MSc</creatorcontrib><creatorcontrib>Ikeda, Keiichi, MD, PhD</creatorcontrib><creatorcontrib>Imazu, Hiroo, MD, PhD</creatorcontrib><creatorcontrib>Gostout, Christopher J., MD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gastrointestinal endoscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sumiyama, Kazuki, MD, PhD</au><au>Tajiri, Hisao, MD, PhD</au><au>Kato, Fusao, PhD</au><au>Imura, Taiko, PhD</au><au>Ono, Kaori, MSc</au><au>Ikeda, Keiichi, MD, PhD</au><au>Imazu, Hiroo, MD, PhD</au><au>Gostout, Christopher J., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pilot study for in vivo cellular imaging of the muscularis propria and ex vivo molecular imaging of myenteric neurons (with video)</atitle><jtitle>Gastrointestinal endoscopy</jtitle><addtitle>Gastrointest Endosc</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>69</volume><issue>6</issue><spage>1129</spage><epage>1134</epage><pages>1129-1134</pages><issn>0016-5107</issn><eissn>1097-6779</eissn><coden>GAENBQ</coden><abstract>Background It is challenging to optimally sample the muscularis propria endoscopically for the diagnosis of muscle layer diseases, especially for motility disorders resulting from neuroenteric dysfunction. Objectives Ultramagnification in vivo imaging of the muscularis mucosa and ex vivo identification of myenteric neuronal elements by confocal microscopy. Design Ex vivo and in vivo porcine animal studies. Setting Short-term study in an animal laboratory. Interventions The muscularis propria in the stomach and esophagus was accessed by resecting the mucosal layer with endoscopic submucosal dissection or cap EMR techniques or by creating a submucosal space by the submucosal endoscopy with mucosal flap technique. The muscularis propria was stained with Nissl stains and 2 types of neuronal molecular stains. The muscular layer was imaged with the endocytoscope in vivo. The muscularis stained with molecular-based stains was also evaluated with a confocal microscope. Results Cellular microstructures resembling spindle-shaped smooth muscle cells were visualized by endocytoscopy in vivo. Confocal endoscopic microscopy demonstrated that in vivo topical application of neuronal molecular stains successfully stained the muscularis and specifically highlighted neuron-like cells. Limitation Animal model pilot study. Conclusions In vivo endoscopic histologic evaluation of the muscularis propria is technically feasible and easy. Minimally invasive advanced endoscopic imaging may be useful for the diagnosis and study of neuroenteric disorders at the level of the muscularis propria, avoiding surgical full-thickness tissue sampling.</abstract><cop>Maryland heights, MO</cop><pub>Mosby, Inc</pub><pmid>19215917</pmid><doi>10.1016/j.gie.2008.08.007</doi><tpages>6</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Cell Nucleus - ultrastructure
Digestive system. Abdomen
Endoscopy
Equipment Design
Gastric Mucosa - ultrastructure
Gastroenterology and Hepatology
Gastroenterology. Liver. Pancreas. Abdomen
Gastroscopes
Inclusion Bodies - diagnostic imaging
Investigative techniques, diagnostic techniques (general aspects)
Medical sciences
Microscopy, Confocal - instrumentation
Microscopy, Video - instrumentation
Myenteric Plexus - ultrastructure
Myocytes, Smooth Muscle - ultrastructure
Neurons - ultrastructure
Pilot Projects
Sensitivity and Specificity
Swine
Ultrasonography
title Pilot study for in vivo cellular imaging of the muscularis propria and ex vivo molecular imaging of myenteric neurons (with video)
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