Loss of interstitial cells of Cajal and inhibitory innervation in insulin-dependent diabetes

被引:268
作者
He, CL
Soffer, EE
Ferris, CD
Walsh, RM
Szurszewski, JH
Farrugia, G
机构
[1] Mayo Clin, Dept Physiol & Biophys, Div Gastroenterol & Hepatol, Enter Neurosci Program, Rochester, MN 55905 USA
[2] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[3] Vanderbilt Univ, Med Ctr, Nashville, TN USA
关键词
D O I
10.1053/gast.2001.26264
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Gastrointestinal complications of long-standing diabetes include nausea, vomiting, abdominal pain, diarrhea, and constipation. The pathophysiology underlying these symptoms is poorly understood. Recent evidence suggests an important role for interstitial cells of Cajal in controlling gastrointestinal motility. The aim of this study was to determine changes in interstitial cells of Cajal and enteric innervation in a patient with insulin-dependent diabetes. Methods: A full thickness jejunal biopsy was obtained from a 38-year-old insulin-dependent diabetic with evidence for diabetic gastroenteropathy. Immunohistochemistry, confocal microscopy, and 3-dimensional reconstruction techniques were used to quantify changes in the volume of interstitial cells of Cajal and enteric innervation. Results: Interstitial cells of Cajal were markedly decreased throughout the entire thickness of the jejunum. A decrease in neuronal nitric oxide synthase, vasoactive intestinal peptide, PACAP, and tyrosine hydroxylase immunopositive nerve fibers was observed in circular muscle layer while substance P immunoreactivity was increased. Conclusions: The data suggest that long-standing diabetes is associated with a decrease in interstitial cells of Cajal volume and a decrease in inhibitory innervation, associated with an increase in excitatory innervation. The changes in interstitial cells of Cajal volume and enteric nerves may underlie the pathophysiology of gastrointestinal complications associated with diabetes and suggest future therapeutic targets.
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收藏
页码:427 / 434
页数:8
相关论文
共 40 条
[1]   LACK OF RELEASE OF VASOACTIVE INTESTINAL POLYPEPTIDE AND CALCITONIN GENE-RELATED PEPTIDE DURING ELECTRICAL-STIMULATION OF ENTERIC NERVES IN STREPTOZOTOCIN-DIABETIC RATS [J].
BELAI, A ;
LINCOLN, J ;
BURNSTOCK, G .
GASTROENTEROLOGY, 1987, 93 (05) :1034-1040
[2]   PROGRESSIVE CHANGES IN ADRENERGIC, SEROTONERGIC, AND PEPTIDERGIC NERVES IN PROXIMAL COLON OF STREPTOZOTOCIN-DIABETIC RATS [J].
BELAI, A ;
LINCOLN, J ;
MILNER, P ;
BURNSTOCK, G .
GASTROENTEROLOGY, 1988, 95 (05) :1234-1241
[3]   DIFFERENTIAL EFFECT OF STREPTOZOTOCIN-INDUCED DIABETES ON THE INNERVATION OF THE ILEUM AND DISTAL COLON [J].
BELAI, A ;
LINCOLN, J ;
MILNER, P ;
BURNSTOCK, G .
GASTROENTEROLOGY, 1991, 100 (04) :1024-1032
[4]   EFFECT OF STREPTOZOTOCIN-DIABETES ON THE LEVEL OF VIP MESSENGER-RNA IN MYENTERIC NEURONS [J].
BELAI, A ;
FACER, P ;
BISHOP, A ;
POLAK, JM ;
BURNSTOCK, G .
NEUROREPORT, 1993, 4 (03) :291-294
[5]   SELECTIVE DAMAGE OF INTRINSIC CALCITONIN GENE-RELATED PEPTIDE-LIKE IMMUNOREACTIVE ENTERIC NERVE-FIBERS IN STREPTOZOTOCIN-INDUCED DIABETIC RATS [J].
BELAI, A ;
BURNSTOCK, G .
GASTROENTEROLOGY, 1987, 92 (03) :730-734
[6]   CHANGES IN ADRENERGIC AND PEPTIDERGIC NERVES IN THE SUBMUCOUS PLEXUS OF STREPTOZOCIN-DIABETIC RAT ILEUM [J].
BELAI, A ;
BURNSTOCK, G .
GASTROENTEROLOGY, 1990, 98 (06) :1427-1436
[7]   ENTERIC NERVES IN DIABETIC RATS - INCREASE IN VASOACTIVE INTESTINAL POLYPEPTIDE BUT NOT SUBSTANCE-P [J].
BELAI, A ;
LINCOLN, J ;
MILNER, P ;
CROWE, R ;
LOESCH, A ;
BURNSTOCK, G .
GASTROENTEROLOGY, 1985, 89 (05) :967-976
[8]   EFFECT OF DIABETES IN THE BB WISTAR RAT ON THE PEPTIDERGIC COMPONENT OF THE ENTERIC INNERVATION [J].
BUCHAN, AMJ .
DIGESTION, 1990, 46 :142-147
[9]   ABNORMAL INTESTINAL MOTILITY IN DIABETICS WITH THE GASTROPARESIS SYNDROME [J].
CAMILLERI, M ;
MALAGELADA, JR .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1984, 14 (06) :420-427
[10]   Interstitial cells of Cajal direct normal propulsive contractile activity in the mouse small intestine [J].
Der-Silaphet, T ;
Malysz, J ;
Hagel, S ;
Arsenault, AL ;
Huizinga, JD .
GASTROENTEROLOGY, 1998, 114 (04) :724-736