Nicotine modifies in vivo and in vitro rat hippocampal amyloid precursor protein processing in young but not old rats

被引:4
作者
Scerri, Charles [1 ]
Stewart, Caroline A. [1 ]
Balfour, David J. K. [1 ]
Breen, Kieran C. [1 ]
机构
[1] Univ Dundee, Ninewells Hosp & Med Sch, Med Res Inst, Div Neurosci, Dundee DD1 9SY, Scotland
关键词
Alzheimer's disease; Nicotine; Amyloid precursor protein; Hippocampus; Age; DENTATE GYRUS; PC12; CELLS; ALZHEIMERS; RECEPTORS; SECRETION; NEUROGENESIS; DISEASE; BRAIN; NEUROPROTECTION; ACTIVATION;
D O I
10.1016/j.neulet.2012.02.042
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies have shown that administration of nicotine modifies the expression and secretion of amyloid precursor protein (APP) in various cell lines. The present study investigated the extent to which chronic subcutaneous nicotine administration influences APP levels and processing in cerebral cortex, striatum and hippocampus of young and old rat brains. The results showed that constant nicotine infusion (0.25 or 4.00 mg/kg/day) increased the levels of particulate APP (APPp) but not secreted APP (APPs) in the hippocampus of young rats in vivo. This response to nicotine was not observed in the striatum or cerebral cortex of young rats or in any of the brain regions examined in old animals. Subsequent in vitro analysis demonstrated that nicotine enhanced the release of APPs from hippocampal slice preparations and that this increase was attenuated by mecamylamine, a non-selective nicotinic acetylcholine receptor (nAChR) antagonist. The in vitro effect of nicotine on APPs was age-related, being only detected from hippocampal slices derived from the young but not the older animals. These results suggest that nicotine modulates APP expression and secretion in the hippocampus and that the responses observed to the drug are age-dependent being only detected in younger rats. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:22 / 26
页数:5
相关论文
共 30 条
[1]   Differential regulation of nicotinic acetylcholine receptors in PC12 cells by nicotine and nerve growth factor (Reprinted from Soc Neurosci Abstr, vol 26, pg 373, 2000) [J].
Avila, AM ;
Dávila-García, MI ;
Ascarrunz, VS ;
Xiao, YX ;
Kellar, KJ .
MOLECULAR PHARMACOLOGY, 2003, 64 (04) :974-986
[2]   DESENSITIZATION OF THE NICOTINE-INDUCED MESOLIMBIC DOPAMINE RESPONSES DURING CONSTANT INFUSION WITH NICOTINE [J].
BENWELL, MEM ;
BALFOUR, DJK ;
BIRRELL, CE .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (02) :454-460
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]  
BREEN KC, 1998, MOL NEUROBIOL, V16, P163
[5]   Soluble form of amyloid precursor protein regulates proliferation of progenitors in the adult subventricular zone [J].
Caillé, I ;
Allinquant, B ;
Dupont, E ;
Bouillot, C ;
Langer, A ;
Müller, U ;
Prochiantz, A .
DEVELOPMENT, 2004, 131 (09) :2173-2181
[6]   Cholinergic agonists stimulate secretion of soluble full-length amyloid precursor protein in neuroendocrine cells [J].
Efthimiopoulos, S ;
Vassilacopoulou, D ;
Ripellino, JA ;
Tezapsidis, N ;
Robakis, NK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :8046-8050
[7]   Mouse models of Alzheimeir's disease: Insight into treatment [J].
German, DC ;
Eisch, AJ .
REVIEWS IN THE NEUROSCIENCES, 2004, 15 (05) :353-369
[8]   Nicotine modulates expression of amyloid precursor protein and amyloid precursor-like protein 2 in mouse brain and in SH-SY5Y neuroblastoma cells [J].
Gutala, Ramana ;
Wang, Ju ;
Hwang, Yoon Y. ;
Haq, Riaz ;
Li, Ming D. .
BRAIN RESEARCH, 2006, 1093 :12-19
[9]   EFFECTS OF CHOLINERGIC-RICH NEURAL GRAFTS ON RADIAL MAZE PERFORMANCE OF RATS AFTER EXCITOTOXIC LESIONS OF THE FOREBRAIN CHOLINERGIC PROJECTION SYSTEM .2. CHOLINERGIC DRUGS AS PROBES TO INVESTIGATE LESION-INDUCED DEFICITS AND TRANSPLANT-INDUCED FUNCTIONAL RECOVERY [J].
HODGES, H ;
ALLEN, Y ;
SINDEN, J ;
LANTOS, PL ;
GRAY, JA .
NEUROSCIENCE, 1991, 45 (03) :609-623
[10]   Enhanced neurogenesis in Alzheimer's disease transgenic (PDGF-APPsw,lnd)mice [J].
Jin, KL ;
Galvan, V ;
Xie, L ;
Mao, XO ;
Gorostiza, OF ;
Bredesen, DE ;
Greenberg, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (36) :13363-13367