4.7 Article

A Mutation in Hnrnph1 That Decreases Methamphetamine-Induced Reinforcement, Reward, and Dopamine Release and Increases Synaptosomal hnRNP H and Mitochondrial Proteins

期刊

JOURNAL OF NEUROSCIENCE
卷 40, 期 1, 页码 107-130

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1808-19.2019

关键词

addiction; Hnrnph1; methamphetamine; mitochondria; psychostimulants; RNA binding protein

资金

  1. National Institutes of Health/National Institute on Drug Abuse [R00DA029635, R01DA039168, F31DA40324, N01DA-14-7788]
  2. National Institutes of Health/National Institute of General Medical Sciences [T32GM008541]
  3. Burroughs Wellcome Fund Transformative Training Program in Addiction Science Grant [1011479]
  4. Division Of Environmental Biology
  5. Direct For Biological Sciences [1011479] Funding Source: National Science Foundation

向作者/读者索取更多资源

Individual variation in the addiction liability of amphetamines has a heritable genetic component. We previously identified Hnrnph1 (heterogeneous nuclear ribonucleoprotein H1) as a quantitative trait gene underlying decreased methamphetamine-induced locomotor activity in mice. Here, we showed that mice (both females and males) with a heterozygous mutation in the first coding exon of Hnrnph1 (H1(+/-)) showed reduced methamphetamine reinforcement and intake and dose-dependent changes in methamphetamine reward as measured via conditioned place preference. Furthermore, H1(+)(/-) mice showed a robust decrease in methamphetamine-induced dopamine release in the NAc with no change in baseline extracellular dopamine, striatal whole-tissue dopamine, dopamine transporter protein, dopamine uptake, or striatal methamphetamine and amphetamine metabolite levels. Immunohistochemical and immunoblot staining of midbrain dopaminergic neurons and their forebrain projections for TH did not reveal any major changes in staining intensity, cell number, or forebrain puncta counts. Surprisingly, there was a twofold increase in hnRNP H protein in the striatal synaptosome of H1(+)(/-) mice with no change in whole-tissue levels. To gain insight into the mechanisms linking increased synaptic hnRNP H with decreased methamphetamine-induced dopamine release and behaviors, synaptosomal proteomic analysis identified an increased baseline abundance of several mitochondrial complex 1 and V proteins that rapidly decreased at 30 min after methamphetamine administration in H1(+)(/- )mice. In contrast, the much lower level of basal synaptosomal mitochondrial proteins in WT mice showed a rapid increase. We conclude that H1(+)(/-) decreases methamphetamine-induced dopamine release, reward, and reinforcement and induces dynamic changes in basal and methamphetamine-induced synaptic mitochondrial function.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据