Methamphetamine self-administration and voluntary exercise have opposing effects on medial prefrontal cortex gliogenesis

被引:108
作者
Mandyam, Chitra D. [1 ]
Wee, Sunmee
Eisch, Amelia J.
Richardson, Heather N.
Koob, George F.
机构
[1] Scripps Res Inst, Committee Neurobiol Addict Disorders, La Jolla, CA 92037 USA
[2] Univ Texas SW, Med Ctr, Dept Psychiat, Dallas, TX 75390 USA
关键词
medial prefrontal cortex; methamphetamine; self-administration; Ki-67; bromodeoxyuridine; voluntary exercise;
D O I
10.1523/JNEUROSCI.2505-07.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Psychostimulant abuse produces deficits in prefrontal cortex (PFC) function, whereas physical activity improves PFC-dependent cognition and memory. The present study explored the vulnerability of medial PFC (mPFC) precursor proliferation and survival to methamphetamine self-administration and voluntary exercise, factors that may have opposing effects on mPFC plasticity to facilitate functional consequences. Intermittent 1 h access to methamphetamine (I-ShA) increased, but daily 1 and 6 h access decreased, proliferation and survival, with dose-dependent effects on mature cell phenotypes. All groups showed increased cell death. Voluntary exercise enhanced proliferation and survival but, in contrast to methamphetamine exposure, did not alter cell death or mature phenotypes. Furthermore, enhanced cell survival by I-ShA and voluntary exercise had profound effects on gliogenesis with differential regulation of oligodendrocytes versus astrocytes. In addition, new cells in the adult mPFC stain for the neuronal marker neuronal nuclear protein, although enhanced cell survival by I-ShA and voluntary exercise did not result in increased neurogenesis. Our findings demonstrate that mPFC gliogenesis is vulnerable to psychostimulant abuse and physical activity with distinct underlying mechanisms. The susceptibility of mPFC gliogenesis to even modest doses of methamphetamine could account for the pronounced pathology linked to psychostimulant abuse.
引用
收藏
页码:11442 / 11450
页数:9
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