Alzheimer's disease:: relationship between muscarinic cholinergic receptors, β-amyloid and tau proteins

被引:46
作者
Pavía, J [1 ]
de Ceballos, ML
de la Cuesta, FS
机构
[1] Univ Malaga, Malaga Sch Med, Dept Pharmacol, E-29071 Malaga, Spain
[2] CSIC, Inst Cajal, E-28002 Madrid, Spain
关键词
Alzheimer's disease; muscarinic receptors; beta-amyloid; tau;
D O I
10.1111/j.1472-8206.1998.tb00975.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Senile dementia is one of the most important health problems in developed countries. The main disease causing dementia is Alzheimer's disease that is characterized by the progressive deterioration of the cholinergic system, beta-amyloid production and deposition, and neurofibrillary tangle formation. Most of the reviewed data, along with data from experiments performed in our laboratory, suggest that there are no changes in the number of muscarinic receptors between Alzheimer and control brains, although the receptors expressed in Alzheimer's disease brains can be anomalous in their function. The muscarinic receptor-G-protein interaction also seems to be impaired in Alzheimer's disease compared with control brains, as well as the G-protein system, with an important decrease in the function of the Gq/11, the most important G-protein stimulating phosphoinositide hydrolysis in human brain; in addition, the second messenger system is also impaired, with a decrease in the synthesis of phosphoinositides and in the number of IP3 receptors. Muscarinic cholinergic receptors are also linked to beta-amyloid production, stimulation of the M-1 subtype with agonists results in the processing of the beta-amyloid precursor protein to non-amyloidogenic products and administration of a fraction of the beta-amyloid (beta-amyloid 25-35) to rats, results in a decrease in the number of muscarinic receptors in brain. M-1 agonists also decrease the phosphorylation of tau proteins, playing again a modulatory role in the pathogenesis of Alzheimer's disease. The existence of a link between beta-amyloid and tau proteins also has been reported; treatment of hippocampal neurones with beta-amyloid, or the 25-35 residue fragment, resulted in an increase in tau protein phosphorylation. The particular contribution of muscarinic receptors, beta-amyloid and tau proteins in the pathogenesis of Alzheimer's disease remains still unclear. Probably Alzheimer's disease could be due to a progressive degeneration in the relationship between the three components covered in this review. (C) Elsevier, Paris.
引用
收藏
页码:473 / 481
页数:9
相关论文
共 100 条
[91]   CHOLINERGIC LESIONS BY 192-IGG-SAPORIN AND SHORT-TERM RECOGNITION MEMORY - ROLE OF THE SEPTOHIPPOCAMPAL PROJECTION [J].
STECKLER, T ;
KEITH, AB ;
WILEY, RG ;
SAHGAL, A .
NEUROSCIENCE, 1995, 66 (01) :101-114
[92]   Nicotinic receptors, muscarinic receptors and choline acetyltransferase activity in the temporal cortex of Alzheimer patients with differing apolipoprotein E genotypes [J].
Svensson, AL ;
Warpman, U ;
HellstromLindahl, E ;
Bogdanovic, N ;
Lannfelt, L ;
Nordberg, A .
NEUROSCIENCE LETTERS, 1997, 232 (01) :37-40
[93]   Exposure of rat hippocampal neurons to amyloid beta peptide (25-35) induces the inactivation of phosphatidyl inositol-3 kinase and the activation of tau protein kinase I glycogen synthase kinase-3 beta [J].
Takashima, A ;
Noguchi, K ;
Michel, G ;
Mercken, M ;
Hoshi, M ;
Ishiguro, K ;
Imahori, K .
NEUROSCIENCE LETTERS, 1996, 203 (01) :33-36
[94]   BEHAVIORAL, HISTOCHEMICAL AND BIOCHEMICAL CONSEQUENCES OF SELECTIVE IMMUNOLESIONS IN DISCRETE REGIONS OF THE BASAL FOREBRAIN CHOLINERGIC SYSTEM [J].
TORRES, EM ;
PERRY, TA ;
BLOKLAND, A ;
WILKINSON, LS ;
WILEY, RG ;
LAPPI, DA ;
DUNNETT, SB .
NEUROSCIENCE, 1994, 63 (01) :95-122
[95]   DIRECT MODULATION OF VOLTAGE-DEPENDENT CALCIUM CHANNELS BY MUSCARINIC ACTIVATION OF A PERTUSSIS TOXIN-SENSITIVE G-PROTEIN IN HIPPOCAMPAL-NEURONS [J].
TOSELLI, M ;
LANG, J ;
COSTA, T ;
LUX, HD .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1989, 415 (03) :255-261
[96]   192-IMMUNOGLOBULIN G-SAPORIN PRODUCES GRADED BEHAVIORAL AND BIOCHEMICAL-CHANGES ACCOMPANYING THE LOSS OF CHOLINERGIC NEURONS OF THE BASAL FOREBRAIN AND CEREBELLAR PURKINJE-CELLS [J].
WAITE, JJ ;
CHEN, AD ;
WARDLOW, ML ;
WILEY, RG ;
LAPPI, DA ;
THAL, LJ .
NEUROSCIENCE, 1995, 65 (02) :463-476
[97]   PROTEIN FACTOR ESSENTIAL FOR MICROTUBULE ASSEMBLY [J].
WEINGARTEN, MD ;
LOCKWOOD, AH ;
HWO, SY ;
KIRSCHNER, MW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (05) :1858-1862
[98]  
WHITE P, 1977, LANCET, V1, P668
[99]   NEUROTROPHIC AND NEUROTOXIC EFFECTS OF AMYLOID BETA-PROTEIN - REVERSAL BY TACHYKININ NEUROPEPTIDES [J].
YANKNER, BA ;
DUFFY, LK ;
KIRSCHNER, DA .
SCIENCE, 1990, 250 (4978) :279-282
[100]   DECREASED BRAIN [H-3]INOSITOL 1,4,5-TRISPHOSPHATE BINDING IN ALZHEIMERS-DISEASE [J].
YOUNG, LT ;
KISH, SJ ;
LI, PP ;
WARSH, JJ .
NEUROSCIENCE LETTERS, 1988, 94 (1-2) :198-202