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PMID: 21300066 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural

Cellular changes in diabetic and idiopathic gastroparesis.

Gastroenterology ·Vol. 140 ·No. 5 ·2011-05-00 ·页码 1575-85.e8

Grover M, Farrugia G, Lurken MS, Bernard CE, Faussone-Pellegrini MS, Smyrk TC, Parkman HP, Abell TL, Snape WJ, Hasler WL, Ünalp-Arida A, Nguyen L, Koch KL, Calles J, Lee L, Tonascia J, Hamilton FA, Pasricha PJ, NIDDK Gastroparesis Clinical Research Consortium

Abstract

Cellular changes associated with diabetic and idiopathic gastroparesis are not well described. The aim of this study was to describe histologic abnormalities in gastroparesis and compare findings in idiopathic versus diabetic gastroparesis. Full-thickness gastric body biopsy specimens were obtained from 40 patients with gastroparesis (20 diabetic) and matched controls. Sections were stained for H&E and trichrome and immunolabeled with antibodies against protein gene product (PGP) 9.5, neuronal nitric oxide synthase (nNOS), vasoactive intestinal peptide, substance P, and tyrosine hydroxylase to quantify nerves, S100β for glia, Kit for interstitial cells of Cajal (ICC), CD45 and CD68 for immune cells, and smoothelin for smooth muscle cells. Tissue was also examined by transmission electron microscopy. Histologic abnormalities were found in 83% of patients. The most common defects were loss of ICC with remaining ICC showing injury, an abnormal immune infiltrate containing macrophages, and decreased nerve fibers. On light microscopy, no significant differences were found between diabetic and idiopathic gastroparesis with the exception of nNOS expression, which was decreased in more patients with idiopathic gastroparesis (40%) compared with diabetic patients (20%) by visual grading. On electron microscopy, a markedly increased connective tissue stroma was present in both disorders. This study suggests that on full-thickness biopsy specimens, cellular abnormalities are found in the majority of patients with gastroparesis. The most common findings were loss of Kit expression, suggesting loss of ICC, and an increase in CD45 and CD68 immunoreactivity. These findings suggest that examination of tissue can lead to valuable insights into the pathophysiology of these disorders and offer hope that new therapeutic targets can be found.

MeSH 主题词
Adult Aged Aged, 80 and over Biopsy Diabetes Mellitus/pathology Female Gastric Emptying/physiology Gastroparesis/pathology,physiopathology Humans Interstitial Cells of Cajal/ultrastructure Male Microscopy, Electron, Transmission Middle Aged Stomach/pathology,physiopathology Young Adult
作者与单位
共 19 位作者,点击展开单位 / ORCID
Grover Madhusudan
Mayo Clinic, Rochester, Minnesota, USA.
Farrugia Gianrico
Lurken Matthew S
Bernard Cheryl E
Faussone-Pellegrini Maria Simonetta
Smyrk Thomas C
Parkman Henry P
Abell Thomas L
Snape William J
Hasler William L
Ünalp-Arida Aynur
Nguyen Linda
Koch Kenneth L
Calles Jorges
Lee Linda
Tonascia James
Hamilton Frank A
Pasricha Pankaj J
NIDDK Gastroparesis Clinical Research Consortium
Article Info
Journal
Gastroenterology
Abbr.
Gastroenterology
ISSN
1528-0012
Published
2011-05-00
电子出版
2011-00-04
页码
1575-85.e8
Language
English
Country/Region
United States
NLM ID
0374630
基金资助
NIDDK NIH HHS · U01DK073975 · United States
NIDDK NIH HHS · U01 DK074008 · United States
NIDDK NIH HHS · P01 DK068055-06A1 · United States
NIDDK NIH HHS · R01 DK057061-12 · United States
NIDDK NIH HHS · U01 DK074007-05 · United States
NIDDK NIH HHS · U01 DK073974-05 · United States
NIDDK NIH HHS · R01 DK057061 · United States
NIDDK NIH HHS · U01 DK073975 · United States
NIDDK NIH HHS · U01 DK074035 · United States
NIDDK NIH HHS · U01 DK073983 · United States
NIDDK NIH HHS · U01DK073985 · United States
NIDDK NIH HHS · U01DK073974 · United States
NIDDK NIH HHS · U01 DK073975-05 · United States
NIDDK NIH HHS · P30 DK084567-02 · United States
NIDDK NIH HHS · P01 DK068055 · United States
NIDDK NIH HHS · U01 DK074007 · United States
NIDDK NIH HHS · P01 DK68055 · United States
NIDDK NIH HHS · U01 DK073985 · United States
NIDDK NIH HHS · U01 DK074008-05 · United States
NIDDK NIH HHS · U01 DK073985-05 · United States
NIDDK NIH HHS · U01DK074008 · United States
NIDDK NIH HHS · U01DK074007 · United States
NIDDK NIH HHS · DK57061 · United States
NIDDK NIH HHS · U01DK073983 · United States
NIDDK NIH HHS · U01 DK073983-05 · United States
NIDDK NIH HHS · U01 DK073974 · United States
NIDDK NIH HHS · P30 DK084567 · United States
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