Alteration of dopaminergic markers in gastrointestinal tract of different rodent models of Parkinson's disease

被引:89
作者
Tian, Y. -M. [1 ]
Chen, X. [1 ]
Luo, D. -Z. [1 ]
Zhang, X. -H. [1 ]
Xue, H. [1 ]
Zheng, L. -F. [1 ]
Yang, N. [1 ]
Wang, X. -M. [1 ]
Zhu, J. -X. [1 ]
机构
[1] Capital Med Univ, Dept Physiol, Sch Basic Med Sci, Beijing 100069, Peoples R China
基金
中国国家自然科学基金;
关键词
tyrosine hydroxylase; dopamine transporter; 6-hydroxydopamine; 1-methyl-4-phenyl-1; 2; 3; 6-tetrahydropyridine; dopamine;
D O I
10.1016/j.neuroscience.2008.02.033
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Parkinson's disease (PD) is a progressive neurological disorder that is often associated with various gastrointestinal (GI) symptoms. The link between the alteration of dopaminergic system and the symptoms of the GI tract in PD is complicated. To determine the changes in the dopaminergic system in the GI tract in PD, two kinds of rodent PD models were used in the present study. One was 6-hydroxydopamine (6-OHDA) -treated rats in which 6-OHDA was microinjected in the bilateral substantia nigra (SN). The other was 1 -methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) -treated mice in which MPTP was injected intraperitoneally. Immunofluorescence, reverse transcription (RT)-real time polymerase chain reaction (PCR) and Western blot were used to evaluate and compare the levels of mRNA and protein expression of tyrosine hydroxylase (TH) and dopamine transporter (DAT) in the GI tract between normal and rodent PD models, as well as between 6-OHDA-treated rats and MPTP-treated mice. The results indicated that TH- and DAT-positive cells were widely distributed in the GI tract. There were significant differences in TH and DAT expression in the GI tract between normal and PD models, as well as between 6-OHDA-treated rats and MPTP-treated mice. The protein levels of TH and DAT in the GI tract were significantly increased in 6-OHDA-treated rats, but the protein level of TH was significantly decreased in MPTP-treated mice. In addition, there was visible atrophy of gastric epithelial parietal cells in MPTP-treated mice, although the protein level of DAT was not significantly changed. The different alterations of dopaminergic system in the GI tract of the two kinds of PD models might underline the differences in GI symptoms in PD patients and might be correlated with the disease severity and disease process affecting the GI tract. (c) 2008 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:634 / 644
页数:11
相关论文
共 30 条
[1]
Loss of enteric dopaminergic neurons and associated changes in colon motility in an MPTP mouse model of Parkinson's disease [J].
Anderson, Grant ;
Noorian, All Reza ;
Taylor, Georgia ;
Anitha, Mallappa ;
Bernhard, Doug ;
Srinivasan, Shanthi ;
Greene, James G. .
EXPERIMENTAL NEUROLOGY, 2007, 207 (01) :4-12
[2]
Gastric α-synuclein immunoreactive inclusions in Meissner's and Auerbach's plexuses in cases staged for Parkinson's disease-related brain pathology [J].
Braak, H ;
de Vos, RAI ;
Bohl, J ;
Del Tredici, K .
NEUROSCIENCE LETTERS, 2006, 396 (01) :67-72
[3]
EISENHOFER G, 1993, MOVEMENT DISORD, V8, P83
[4]
CENTRAL AND PERIPHERAL DOPAMINE D-1/DA(1) RECEPTOR MODULATION OF GASTRIC-SECRETION AND EXPERIMENTAL GASTRIC-MUCOSAL INJURY [J].
GLAVIN, GB ;
HALL, AM .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1995, 26 (06) :1277-1279
[5]
Neural regulation of in vitro giant contractions in the rat colon [J].
Gonzalez, A ;
Sarna, SK .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 281 (01) :G275-G282
[6]
Gastric emptying time and gastric motility in patients with Parkinson's disease [J].
Hardoff, R ;
Sula, M ;
Tamir, A ;
Soil, A ;
Front, A ;
Badarna, S ;
Honigman, S ;
Giladi, N .
MOVEMENT DISORDERS, 2001, 16 (06) :1041-1047
[7]
INHIBITION OF GASTROINTESTINAL MOTILITY BY MPTP VIA ADRENERGIC AND DOPAMINERGIC MECHANISMS [J].
HASKEL, Y ;
HANANI, M .
DIGESTIVE DISEASES AND SCIENCES, 1994, 39 (11) :2364-2367
[9]
Gastrointestinal motility problems in patients with Parkinson's disease - Effects of antiparkinsonian treatment and guidelines for management [J].
Jost, WH .
DRUGS & AGING, 1997, 10 (04) :249-258
[10]
Li MS, 1999, GASTROENTEROLOGY, V116, pA1029