期刊论文详细信息
Journal of Biomedical Science
Changes in microRNA expression profile in hippocampus during the acquisition and extinction of cocaine-induced conditioned place preference in rats
Xiaowei Guan3  Hailin Liu2  Chun-Lin Chen1 
[1] Department of Biological Science, National Sun Yat-Sen University, Kaohsiung 80424, Taiwan;Department of Anesthesiology, Huai’an First People’s Hospital, Nanjing Medical University, Huaian 223300, China;Department of Human Anatomy, Nanjing Medical University, 140 Hanzhong Road, Nanjing 210029, China
关键词: Conditioned place preference;    Microarray;    microRNA;    Hippocampus;    Cocaine;   
Others  :  821526
DOI  :  10.1186/1423-0127-20-96
 received in 2013-10-18, accepted in 2013-12-16,  发布年份 2013
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【 摘 要 】

Background

MicroRNA (miRNA) emerges as important player in drug abuse. Yet, their expression profile in neurological disorder of cocaine abuse has not been well characterized. Here, we explored the changes of miRNA expression in rat hippocampus following repeated cocaine exposure and subsequent abstinence from cocaine treatment.

Results

Conditioned place preference (CPP) procedure was used to assess the acquisition and extinction of cocaine-seeking behavior in rats. MiRNA microarray was performed to examine miRNAs levels in rat hippocampus. Quantitative RT-PCR was conducted to further confirm results in microarray study. Finally, bioinformatic predictions were made to suggest potential target genes of cocaine-responsive miRNA in this study. MiRNA array found that 34 miRNA levels were changed in rat hippocampus while acquiring cocaine CPP and 42 miRNAs levels were altered after the cocaine-induced CPP were extinguished, as compared to normal controls. The findings from qRT-PCR study support results from microarray analysis.

Conclusions

The current study demonstrated dynamic changes in miRNA expression in rat hippocampus during the acquisition and extinction of cocaine-induced CPP. Some miRNAs which have been previously reported to be involved in brain disorders and drug abuse, including miR-133b, miR-134, miR-181c, miR-191, miR-22, miR-26b, miR-382, miR-409-3p and miR-504, were found to be changed in their expression following repeated cocaine exposure and subsequent abstinence from cocaine treatment. These findings may extend our understanding of the regulatory network underlying cocaine abuse and may provide new targets for the future treatment of drug abuse.

【 授权许可】

   
2013 Chen et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Freeman WM, Brebner K, Lynch WJ, Robertson DJ, Roberts DC, Vrana KE: Cocaine-responsive gene expression changes in rat hippocampus. Neuroscience 2001, 108:371-380.
  • [2]Nestler EJ: Molecular basis of long-term plasticity underlying addiction. Nat Rev Neurosci 2001, 2:119-128.
  • [3]Nestler EJ: The neurobiology of cocaine addiction. Sci Pract Perspect 2005, 3:4-10.
  • [4]Lu H, Cheng PL, Lim BK, Khoshnevisrad N, Poo MM: Elevated BDNF after cocaine withdrawal facilitates LTP in medial prefrontal cortex by suppressing GABA inhibition. Neuron 2010, 67:821-833.
  • [5]Bannon M, Kapatos G, Albertson D: Gene expression profiling in the brains of human cocaine abusers. Addict Biol 2005, 10:119-126.
  • [6]Shruti K, Shrey K, Vibha R: Micro RNAs: tiny sequences with enormous potential. Biochem Biophys Res Commun 2011, 407:445-449.
  • [7]Chandrasekar V, Dreyer JL: MicroRNAs miR-124, let-7d and miR-181a regulate cocaine-induced plasticity. Mol Cell Neurosci 2009, 42:350-362.
  • [8]Chandrasekar V, Dreyer JL: Regulation of MiR-124, Let-7d, and MiR-181a in the accumbens affects the expression, extinction, and reinstatement of cocaine-induced conditioned place preference. Neuropsychopharmacology 2011, 36:1149-1164.
  • [9]Hollander JA, Im HI, Amelio AL, Kocerha J, Bali P, Lu Q, Willoughby D, Wahlestedt C, Conkright MD, Kenny PJ: Striatal microRNA controls cocaine intake through CREB signalling. Nature 2010, 466:197-202.
  • [10]Im HI, Hollander JA, Bali P, Kenny PJ: MeCP2 controls BDNF expression and cocaine intake through homeostatic interactions with microRNA-212. Nat Neurosci 2010, 13:1120-1127.
  • [11]Schaefer A, Im HI, Venø MT, Fowler CD, Min A, Intrator A, Kjems J, Kenny PJ, O’Carroll D, Greengard P: Argonaute 2 in dopamine 2 receptor-expressing neurons regulates cocaine addiction. J Exp Med 2010, 207:1843-1851.
  • [12]Eipper-Mains JE, Kiraly DD, Palakodeti D, Mains RE, Eipper BA, Graveley BR: MicroRNA-Seq reveals cocaine-regulated expression of striatal microRNAs. RNA 2011, 17:1529-1543.
  • [13]Zhai HF, Zhang ZY, Zhao M, Qiu Y, Ghitza UE, Lu L: Conditioned drug reward enhances subsequent spatial learning and memory in rats. Psychopharmacology (Berl) 2007, 195:193-201.
  • [14]Del Olmo N, Higuera-Matas A, Miguéns M, García-Lecumberri C, Borcel E, Solís JM, Ambrosio E: Hippocampal synaptic plasticity and water maze learning in cocaine self-administered. Ann N Y Acad Sci 2006, 1074:427-437.
  • [15]Meyers RA, Zavala AR, Neisewander JL: Dorsal, but not ventral, hippocampal lesions disrupt cocaine place conditioning. Neuroreport 2003, 14:2127-2131.
  • [16]Lippi G, Steinert JR, Marczylo EL, D’Oro S, Fiore R, Forsythe ID, Schratt G, Zoli M, Nicotera P, Young KW: Targeting of the Arpc3 actin nucleation factor by miR-29a/b regulates dendritic spine morphology. J Cell Biol 2011, 194:889-904.
  • [17]Nudelman AS, DiRocco DP, Lambert TJ, Garelick MG, Le J, Nathanson NM, Storm DR: Neuronal activity rapidly induces transcription of the CREB-regulated microRNA-132, in vivo. Hippocampus 2010, 20:492-498.
  • [18]Saba R, Störchel PH, Aksoy-Aksel A, Kepura F, Lippi G, Plant TD, Schratt GM: Dopamine-regulated microRNA MiR-181a controls GluA2 surface expression in hippocampal neurons. Mol Cell Biol 2012, 32:619-632.
  • [19]Schratt GM, Tuebing F, Nigh EA, Kane CG, Sabatini ME, Kiebler M, Greenberg ME: A brain-specific microRNA regulates dendritic spine development. Nature 2006, 439:283-289.
  • [20]Jimenez-Mateos EM, Engel T, Merino-Serrais P, McKiernan RC, Tanaka K, Mouri G, Sano T, O’Tuathaigh C, Waddington JL, Prenter S, Delanty N, Farrell MA, O’Brien DF, Conroy RM, Stallings RL, DeFelipe J, Henshall DC: Silencing microRNA-134 produces neuroprotective and prolonged seizure-suppressive effects. Nat Med 2012, 18:1087-1094.
  • [21]Hu K, Zhang C, Long L, Long X, Feng L, Li Y, Xiao B: Expression profile of microRNAs in rat hippocampus following lithium-pilocarpine-induced status epilepticus. Neurosci Lett 2011, 488:252-257.
  • [22]Risbud RM, Porter BE: Changes in MicroRNA expression in the whole hippocampus and Hippocampal synaptoneurosome fraction following pilocarpine induced status epilepticus. PLoS One 2013, 8:e53464.
  • [23]Zovoilis A, Agbemenyah HY, Agis-Balboa RC, Stilling RM, Edbauer D, Rao P, Farinelli L, Delalle I, Schmitt A, Falkai P, Bahari-Javan S, Burkhardt S, Sananbenesi F, Fischer A: microRNA-34c is a novel target to treat dementias. EMBO J 2011, 30:4299-4308.
  • [24]Sanchez-Simon FM, Zhang XX, Loh HH, Law PY, Rodriguez RE: Morphine regulates dopaminergic neuron differentiation via miR-133b. Mol Pharmacol 2010, 78:935-942.
  • [25]Barreto-Valer K, López-Bellido R, Macho Sánchez-Simón F, Rodríguez RE: Modulation by cocaine of dopamine receptors through miRNA-133b in Zebrafish Embryos. PLoS One 2012, 7:e52701.
  • [26]Huang W, Li MD: Differential allelic expression of dopamine D1 receptor gene (DRD1) is modulated by microRNA miR-504. Biol Psychiatry 2009, 65:702-705.
  • [27]Caputo V, Sinibaldi L, Fiorentino A, Parisi C, Catalanotto C, Pasini A, Cogoni C, Pizzuti A: Brain derived neurotrophic factor (BDNF) expression is regulated by microRNAs miR-26a and miR-26b allele-specific binding. PLoS One 2011, 6:e28656.
  • [28]Schroeder FA, Penta KL, Matevossian A, Jones SR, Konradi C, Tapper AR, Akbarian S: Drug-induced activation of dopamine D(1) receptor signaling and inhibition of class I/II histone deacetylase induce chromatin remodeling in reward circuitry and modulate cocaine-related behaviors. Neuropsychopharmacology 2008, 33:2981-2992.
  • [29]Tropea TF, Kabir ZD, Kaur G, Rajadhyaksha AM, Kosofsky BE: Enhanced dopamine D1 and BDNF signaling in the adult dorsal striatum but not nucleus accumbens of prenatal cocaine treated mice. Front Psychiatry 2011, 2:67.
  • [30]Yao L, McFarland K, Fan P, Jiang Z, Inoue Y, Diamond I: Activator of G protein signaling 3 regulates opiate activation of protein kinase A signaling and relapse of heroin-seeking behavior. Proc Natl Acad Sci USA 2005, 102:8746-8751.
  • [31]Mannoury la Cour C, El Mestikawy S, Hanoun N, Hamon M, Lanfumey L: Regional differences in the coupling of 5-hydroxytryptamine-1A receptors to G proteins in the rat brain. Mol Pharmacol 2006, 70:1013-1021.
  • [32]Straiker AJ, Borden CR, Sullivan JM: G-protein alpha subunit isoforms couple differentially to receptors that mediate presynaptic inhibition at rat hippocampal synapses. J Neurosci 2002, 22:2460-2468.
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