3-Nitropropionic acid-induced neurotoxicity - assessed by ultra high resolution positron emission tomography with comparison to magnetic resonance spectroscopy

被引:22
作者
Brownell, AL
Chen, YI
Yu, MX
Wang, XK
Dedeoglu, A
Cicchetti, F
Jenkins, BG
Beal, MF
机构
[1] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
[2] Vet Adm Med Ctr, Bedford, MA USA
[3] CHUL, Unite Neurosci, Quebec City, PQ, Canada
[4] Cornell Univ, New York Presbyterian Hosp, Weill Med Coll, Dept Neurol & Neurosci, New York, NY USA
关键词
glucose utilization; Huntington's disease; magnetic resonance spectroscopy; neurodegeneration; 3-nitropropionic acid; positron emission tomography;
D O I
10.1111/j.1471-4159.2004.02408.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To explore acute and long-term effects of 3-nitropropionic acid (3-NP)-induced neurotoxicity, longitudinal positron emission tomography (PET) studies of energy metabolism and magnetic resonance spectroscopic (MRS) studies of neurochemicals were conducted in a rat model. The first injection of 3-NP (20 mg/kg i.p.) was followed by MRS study of neurochemicals and PET study of glucose utilization using [F-18]2-fluorodeoxy-D-glucose (F-18-FDG). After that, 3-NP administration was done two times a day with a dose of 10 mg/kg i.p. until animals were symptomatic or for a maximum of 5 days combined with daily PET studies. Long-term effects were investigated 4 weeks and 4 months after cessation of 3-NP. These studies showed a significant inter-animal variation in response of 3-NP toxicity. Animals that developed large striatal lesions had decreased glucose utilization in the striatum and cortex 1 day after starting 3-NP injections. Similarly succinate and lactate/macromolecule levels were enhanced; these changes being, however, reversible. Progressive degeneration was observed by decreasing striatal glucose utilization and N-acetylaspartate (NAA) and increasing choline. These observations paralleled with weight loss and deficits in behavior. Animals that did not develop lesions showed reversible enhancement in cortical glucose utilization and no change in striatal glucose utilization or neurochemicals or locomotor activity.
引用
收藏
页码:1206 / 1214
页数:9
相关论文
共 43 条
[1]   ALTERNATIVE EXCITOTOXIC HYPOTHESES [J].
ALBIN, RL ;
GREENAMYRE, JT .
NEUROLOGY, 1992, 42 (04) :733-738
[2]   3-NITROPROPIONATE, TOXIC SUBSTANCE OF INDIGOFERA, IS A SUICIDE INACTIVATOR OF SUCCINATE-DEHYDROGENASE - (RAT-LIVER MITOCHONDRIA CARBANION-N-5 FLAVIN ADDUCTS 2-PROTON ABSTRACTION MECHANISM) [J].
ALSTON, TA ;
MELA, L ;
BRIGHT, HJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (09) :3767-3771
[3]   Differential diagnosis of parkinsonism with [18F]fluorodeoxyglucose and PET [J].
Antonini, A ;
Kazumata, K ;
Feigin, A ;
Mandel, F ;
Dhawan, V ;
Margouleff, C ;
Eidelberg, D .
MOVEMENT DISORDERS, 1998, 13 (02) :268-274
[4]   DOES IMPAIRMENT OF ENERGY-METABOLISM RESULT IN EXCITOTOXIC NEURONAL DEATH IN NEURODEGENERATIVE ILLNESSES [J].
BEAL, MF .
ANNALS OF NEUROLOGY, 1992, 31 (02) :119-130
[5]   Mitochondrial Dysfunction in Neurodegenerative Diseases [J].
Johri, Ashu ;
Beal, M. Flint .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2012, 342 (03) :619-630
[6]  
BEAL MF, 1993, J NEUROSCI, V13, P4181
[7]   Chronic systemic pesticide exposure reproduces features of Parkinson's disease [J].
Betarbet, R ;
Sherer, TB ;
MacKenzie, G ;
Garcia-Osuna, M ;
Panov, AV ;
Greenamyre, JT .
NATURE NEUROSCIENCE, 2000, 3 (12) :1301-1306
[8]   Topological analysis of striatal lesions induced by 3-nitropropionic acid in the Lewis rat [J].
Blum, D ;
Gall, D ;
Cuvelier, L ;
Schiffmann, SN .
NEUROREPORT, 2001, 12 (08) :1769-1772
[9]   Hyperactivity and hypoactivity in a rat model of Huntington's disease: the systemic 3-nitropropionic acid model [J].
Borlongan, CV ;
Koutouzis, TK ;
Freeman, TB ;
Hauser, RA ;
Cahill, DW ;
Sanberg, PR .
BRAIN RESEARCH PROTOCOLS, 1997, 1 (03) :253-257
[10]   REGIONAL MITOCHONDRIAL RESPIRATORY ACTIVITY IN HUNTINGTONS-DISEASE BRAIN [J].
BRENNAN, WA ;
BIRD, ED ;
APRILLE, JR .
JOURNAL OF NEUROCHEMISTRY, 1985, 44 (06) :1948-1950