Quantitative genetic analysis of ventral midbrain and liver iron in BXD recombinant inbred mice

被引:38
作者
Jones, BC
Reed, CL
Hitzemann, R
Wiesinger, JA
McCarthy, KA
Buwen, JP
Beard, JL
机构
[1] Penn State Univ, Dept Biobehav Hlth, University Pk, PA 16802 USA
[2] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland, OR 97201 USA
[3] Penn State Univ, Dept Nutr, University Pk, PA 16802 USA
关键词
iron; dopamine; brain; genetics; liver; QTL;
D O I
10.1080/10284150310001624192
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Male and female mice from 15 of the BXD/Ty recombinant inbred strain panel were examined for regional brain and liver iron content. Brain regions included medial prefrontal cortex, nucleus accumbens, caudate-putamen and ventral midbrain. Our focal tissue was the ventral midbrain, containing the ventral tegmentum and substantia nigra. This area contains the perikarya of the dopamine neurons that project to nucleus accumbens and caudate-putamen. Genetic correlations between ventral midbrain and liver iron content were not statistically significant, suggesting that peripheral and central iron regulatory systems are largely independent. Correlations between ventral midbrain iron and iron in the caudate-putamen and nucleus accumbens, but not the prefrontal cortex were moderately high and significant. Ventral midbrain and liver iron contents were subjected to quantitative trait loci analysis to identify associated chromosomal locations. This analysis revealed several suggestive loci for iron content in ventral midbrain but fewer loci for liver. Genetic correlations between ventral midbrain iron and published dopamine functional indices were significant, suggesting a link between ventral midbrain iron status and central dopamine neurobiology. This work shows the value of quantitative genetic analysis in the neurobiology of iron and in showing the close association between ventral midbrain iron and nigrostriatal/mesolimbic dopamine function.
引用
收藏
页码:369 / 377
页数:9
相关论文
共 43 条
[1]   MRI measurement of brain iron in patients with restless legs syndrome [J].
Allen, RP ;
Barker, PB ;
Wehrl, F ;
Song, HK ;
Earley, CJ .
NEUROLOGY, 2001, 56 (02) :263-265
[2]   Neonatal iron deficiency results in irreversible changes in dopamine function in rats [J].
Beard, J ;
Erikson, KM ;
Jones, BC .
JOURNAL OF NUTRITION, 2003, 133 (04) :1174-1179
[3]   Neurobehavioral analysis of developmental iron deficiency in rats [J].
Beard, JL ;
Erikson, KM ;
Jones, BC .
BEHAVIOURAL BRAIN RESEARCH, 2002, 134 (1-2) :517-524
[4]   Type I and Type II error rates for quantitative trait loci (QTL) mapping studies using recombinant inbred mouse strains [J].
Belknap, JK ;
Mitchell, SR ;
OToole, LA ;
Helms, ML ;
Crabbe, JC .
BEHAVIOR GENETICS, 1996, 26 (02) :149-160
[5]   GENETIC CORRELATION BETWEEN OPEN-FIELD ACTIVITY AND DEFECATION - ANALYSIS WITH THE CXB RECOMBINANT-INBRED STRAINS [J].
BLIZARD, DA ;
BAILEY, DW .
BEHAVIOR GENETICS, 1979, 9 (05) :349-357
[6]   Sex and strain influence the effect of ethanol on central monoamines [J].
Boone, EM ;
Cook, MN ;
Hou, X ;
Jones, BC .
JOURNAL OF STUDIES ON ALCOHOL, 1997, 58 (06) :590-599
[7]  
BOTHWELL TH, 1979, IRON METABOLISM MAN, P576
[8]  
Buck K, 2000, AM J MED GENET, V96, P696, DOI 10.1002/1096-8628(20001009)96:5<696::AID-AJMG17>3.0.CO
[9]  
2-6
[10]   Mapping murine loci for physical dependence on ethanol [J].
Buck, KJ ;
Rademacher, BLS ;
Metten, P ;
Crabbe, JC .
PSYCHOPHARMACOLOGY, 2002, 160 (04) :398-407