Effects of Lead Exposure on Nitric Oxide-associated Gene Expression in the Olfactory Bulb of Mice

被引:23
作者
Kim, Samki [1 ]
Hyun, Jiyoung [1 ]
Kim, Hyunji [1 ]
Kim, Younghee [1 ]
Kim, Eunju [1 ]
Jang, Jungae [1 ]
Kim, Kisok [1 ]
机构
[1] Keimyung Univ, Dept Publ Hlth, Taegu 704701, South Korea
关键词
Lead; Neurotoxicity; Neurotransmitter; Nitric oxide; Olfactory bulb; RAT-BRAIN; SYNTHASE; NEUROTOXICITY; CONSEQUENCES; HYPERTENSION; MECHANISMS; GENERATION; PREGNANCY;
D O I
10.1007/s12011-010-8791-1
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
Lead (Pb) is known to have toxic effects on the brain; however, data regarding its specific toxic effects on the olfactory bulb are lacking. Therefore, we investigated the relationship between acute Pb exposure and alterations in gene expression associated with the nitric oxide signaling pathway in the olfactory bulb of mice. After administration of Pb (intraperitoneal injections of 1 or 10 mg/kg Pb(CH3CO2)(2) center dot 3H(2)O once per day for 4 days), body weight, motor activity, and gene expression in the olfactory bulb of mice were examined. High doses of Pb resulted in significant decreases in body weight, but motor coordination was not significantly altered until 11 days after the end of Pb treatment. The expression patterns of dimethylarginine dimethylaminohydrolase 1 (Ddah1), superoxide dismutase 1 (Sod1), and superoxide dismutase (Ccs) were increased, whereas expression of the Stratifin (Sfn) gene was significantly decreased following treatment with 10 mg/kg Pb. The expression patterns of nitric oxide synthases at the mRNA and protein levels, however, were not significantly altered by treatment with 10 mg/kg Pb. These findings indicate that Pb-induced neurotoxicity may be modulated in part by the expression of Ddah1, Sod1, Ccs, and Sfn in the olfactory bulb.
引用
收藏
页码:683 / 692
页数:10
相关论文
共 31 条
[1]   Teratogen update: Lead and pregnancy [J].
Bellinger, DC .
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2005, 73 (06) :409-420
[2]   Novel neural modulators [J].
Boehning, D ;
Snyder, SH .
ANNUAL REVIEW OF NEUROSCIENCE, 2003, 26 :105-131
[3]   Lead-induced increase in antioxidant enzymes and lipid peroxidation products in developing rat brain [J].
Bokara, Kiran Kumar ;
Brown, Erika ;
McCormick, Rashidi ;
Yallapragada, Prabhakara Rao ;
Rajanna, Sharada ;
Bettaiya, Rajanna .
BIOMETALS, 2008, 21 (01) :9-16
[4]  
BRIDGES D, 2005, SCI STKE, V296, pRE10, DOI DOI 10.1126/STKE.2962005RE10
[5]   Odorant-Dependent Generation of Nitric Oxide in Mammalian Olfactory Sensory Neurons [J].
Brunert, Daniela ;
Kurtenbach, Stefan ;
Isik, Sonnur ;
Benecke, Heike ;
Gisselmann, Guenter ;
Schuhmann, Wolfgang ;
Hatt, Hanns ;
Wetzel, Christian H. .
PLOS ONE, 2009, 4 (05)
[6]   Perinatal lead exposure alters the expression of neuronal nitric oxide synthase in rat brain [J].
Chetty, CS ;
Reddy, GR ;
Murthy, KS ;
Johnson, J ;
Sajwan, K ;
Desaiah, D .
INTERNATIONAL JOURNAL OF TOXICOLOGY, 2001, 20 (03) :113-120
[7]   Odorant-evoked nitric oxide signals in the antennal lobe of Manduca sexta [J].
Collmann, C ;
Carlsson, MA ;
Hansson, BS ;
Nighorn, A .
JOURNAL OF NEUROSCIENCE, 2004, 24 (27) :6070-6077
[8]   DEVELOPMENTAL DELAYS IN EXPLORATION AND LOCOMOTOR-ACTIVITY IN MALE-RATS EXPOSED TO LOW-LEVEL LEAD [J].
CROFTON, KM ;
TAYLOR, DH ;
BULL, RJ ;
SIVULKA, DJ ;
LUTKENHOFF, SD .
LIFE SCIENCES, 1980, 26 (10) :823-831
[9]   Lead and immune function [J].
Dietert, RR ;
Piepenbrink, MS .
CRITICAL REVIEWS IN TOXICOLOGY, 2006, 36 (04) :359-385
[10]   Lead, renal disease and hypertension [J].
Gonick, HC .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2002, 40 (01) :202-204