Striatal 6-OHDA lesion in mice: Investigating early neurochemical changes underlying Parkinson's disease

被引:38
作者
Branchi, Igor [1 ]
D'Andrea, Ivana [1 ]
Armida, Monica [2 ]
Carnevale, Danieta [3 ]
Ajmone-Cat, Maria Antonietta [3 ]
Pezzola, Antonella [2 ]
Potenza, Rosa Luisa [2 ]
Morgese, Maria Grazia [4 ]
Cassano, Tommaso [4 ]
Minghetti, Luisa [3 ]
Popoli, Patrizia [2 ]
Alleva, Enrico [1 ]
机构
[1] Ist Super Sanita, Sect Behav Neurosci, Dept Cell Biol & Neurosci, I-00161 Rome, Italy
[2] Ist Super Sanita, Sect Cent Nervous Syst Pharmacol, Dept Therapeut Res & Med Evaluat, I-00161 Rome, Italy
[3] Ist Super Sanita, Expt Neurol Sect, Dept Cell Biol & Neurosci, I-00161 Rome, Italy
[4] Univ Foggia, Dept Biomed Sci, I-71100 Foggia, Italy
关键词
BDNF; Oxidative stress; F2-isoprostane; Prostaglandin E2; Anxiety; Emotional; EARLY SOCIAL ENRICHMENT; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; BASAL GANGLIA CIRCUITRY; DOPAMINERGIC-NEURONS; NONMOTOR SYMPTOMS; ANXIETY-LIKE; L-DOPA; 6-HYDROXYDOPAMINE LESIONS; NEUROTROPHIC FACTOR; SUBSTANTIA-NIGRA;
D O I
10.1016/j.bbr.2009.11.020
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Early phases of Parkinson's disease (PD) are characterized by a mild reduction of dopamine (DA) in striatum and by emergence of psychiatric disturbances that precede overt motor symptoms. in order to characterize the neurochemical re-arrangements induced by such striatal impairment, we used a mouse model in which a low dose of 6-hydroxydopamine (6-OHDA) was bilaterally injected into the dorsal striatum. These mice showed a DA reduction of about 40% that remained stable up to 12 weeks after injection. This reduction was accompanied by changes in DA metabolite levels, such as HVA, transiently reduced at 4 weeks, and DOPAC, decreased at 12 weeks. No change in the 5-hydroxytryptamine (5-HT) levels was found but the 5-hydroxyindoleacetic acid (5-HIAA)/5-HT ratio was increased at 4 weeks. In addition, at the same time-point, the levels of 15-F-2t-IsoP, an index of oxidative stress, and of PGE2, a major product of cyclooxygenase-2, were decreased in different brain areas while BDNF levels were increased. These neurochemical changes were accompanied by altered behavioral responses concerning the emotional reactivity. Overall, the present findings suggest that a change of 5-HT metabolism and a modification of oxidative stress levels may play a role in the early PD degeneration phases. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:137 / 143
页数:7
相关论文
共 68 条
  • [1] Depression in Parkinson's disease - Must be properly diagnosis and treated to avoid serious morbidity
    Allain, H
    Schuck, S
    Mauduit, N
    [J]. BRITISH MEDICAL JOURNAL, 2000, 320 (7245) : 1287 - 1288
  • [2] Characterization of the striatal 6-OHDA model of Parkinson's disease in wild type and α-synuclein-deleted mice
    Alvarez-Fischer, Daniel
    Henze, Carmen
    Strenzke, Corinna
    Westrich, Jan
    Ferger, Boris
    Hoeglinger, Guenter U.
    Oertel, Wolfgang H.
    Hartmann, Andreas
    [J]. EXPERIMENTAL NEUROLOGY, 2008, 210 (01) : 182 - 193
  • [3] COMPLEX DEFICITS ON REACTION-TIME PERFORMANCE FOLLOWING BILATERAL INTRASTRIATAL 6-OHDA INFUSION IN THE RAT
    AMALRIC, M
    MOUKHLES, H
    NIEOULLON, A
    DASZUTA, A
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1995, 7 (05) : 972 - 980
  • [4] Enriched environment protects the nigrostriatal dopaminergic system and induces astroglial reaction in the 6-OHDA rat model of Parkinson's disease
    Anastasia, Agustin
    Torre, Luciana
    de Erausquin, Gabriel A.
    Masco, Daniel H.
    [J]. JOURNAL OF NEUROCHEMISTRY, 2009, 109 (03) : 755 - 765
  • [5] Nonsteroidal anti-inflammatory drugs in experimental parkinsonian models and Parkinson's disease
    Asanuma, Masato
    Miyazaki, Ikuko
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2008, 14 (14) : 1428 - 1434
  • [6] BANKIEWICZ KS, 1999, CURR PROTOC NEUROSCI, V2
  • [7] Brain-derived neurotrophic factor is required for the establishment of the proper number of dopaminergic neurons in the substantia nigra pars compacta
    Baquet, ZC
    Bickford, PC
    Jones, KR
    [J]. JOURNAL OF NEUROSCIENCE, 2005, 25 (26) : 6251 - 6259
  • [8] Belzung C., 1999, TEC BEHAV N, V13, P738
  • [9] Functional changes of the basal ganglia circuitry in Parkinson's disease
    Blandini, F
    Nappi, G
    Tassorelli, C
    Martignoni, E
    [J]. PROGRESS IN NEUROBIOLOGY, 2000, 62 (01) : 63 - 88
  • [10] Toxin-induced models of Parkinson's disease
    Bové J.
    Prou D.
    Perier C.
    Przedborski S.
    [J]. NeuroRX, 2005, 2 (3): : 484 - 494