Aβ peptides as one of the crucial volume transmission signals in the trophic units and their interactions with homocysteine.: Physiological implications and relevance for Alzheimer's disease

被引:35
作者
Agnati, L. F.
Genedani, S.
Leo, G.
Forni, A.
Woods, A. S.
Filaferro, M.
Franco, R.
Fuxe, K.
机构
[1] Univ Modena & Reggio Emilia, Physiol Sect, Dept Biomed Sci, I-41100 Modena, Italy
[2] Univ Modena & Reggio Emilia, Pharmacol Sect, Dept Biomed Sci, I-41100 Modena, Italy
[3] Univ Modena & Reggio Emilia, Dept Chem, I-41100 Modena, Italy
[4] IRCCS San Camillo, Venice, Italy
[5] Natl Inst Drug Abuse, Dept Hlth & Human Serv, Baltimore, MD USA
[6] Univ Barcelona, Dept Biochem & Mol Biol, Barcelona, Spain
[7] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
关键词
beta-amyloid peptides; homocysteine; volume transmission; pain threshold; Alzheimer's disease;
D O I
10.1007/s00702-006-0564-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Amyloid peptides (A beta) can operate as volume transmission (VT) signals since they are continuously released from cells of the central nervous system and diffuse in the extra-cellular space of the brain. They have both regulatory and trophic functions on cellular networks. In agreement with A beta regulatory actions on glial-neuronal networks, the present paper reports new findings demonstrating that intrastriatal injections of A beta peptides reduce striatal tyrosine hydroxylase, increase striatal GFAP immunoreactivities and lower pain threshold in experimental rats. Furthermore, it has been demonstrated that exogenous homocysteine (Hcy) binds A beta(1-40) favouring its beta-sheet conformation both in vitro and in vivo and hence the formation of beta-fibrils and development of neurotoxicity. Thus, the hypothesis is discussed that A beta peptides represent crucial VT-signals in the brain and their action is altered by dysmetabolic signals such as high Hcy extra-cellular levels, known to be an important risk factor for Alzheimer's disease.
引用
收藏
页码:21 / 31
页数:11
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[11]   Soluble form of amyloid precursor protein regulates proliferation of progenitors in the adult subventricular zone [J].
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[20]   Homocysteine potentiates β-amyloid neurotoxicity:: role of oxidative stress [J].
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