Giannotti Giuseppe, Caffino Lucia, Malpighi Chiara, Melfi Simona, Racagni Giorgio, Fumagalli Fabio
Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Via Balzaretti 9, 20133, Milano, Italy.
Psychopharmacology (Berl). 2015 Feb;232(4):713-9. doi: 10.1007/s00213-014-3708-x. Epub 2014 Aug 16.
During adolescence, the brain is maturing and more sensitive to drugs of abuse that can influence its developmental trajectory. Recently, attention has been focused on basic fibroblast growth factor (FGF-2) given that its administration early in life enhances the acquisition of cocaine self-administration and sensitization at adulthood (Turner et al. (Pharmacol Biochem Behav 92:100-4, 2009), Clinton et al. (Pharmacol Biochem Behav103:6-17, 2012)). Additionally, we found that abstinence from adolescent cocaine exposure long lastingly dysregulates FGF-2 transcription (Giannotti et al. (Psychopharmacology (Berl) 225:553-60, 2013 ).
The objectives of the study are to evaluate if (1) a single injection of cocaine (20 mg/kg) at postnatal day 35 alters FGF-2 messenger RNA (mRNA) levels and (2) the first injection influences the trophic response to a second injection (10 mg/kg) provided 24 h or 7 days later.
We found regional differences in the FGF-2 expression pattern as either the first or the second injection of cocaine by themselves upregulated FGF-2 mRNA in the medial prefrontal cortex and nucleus accumbens while downregulating it in the hippocampus. The first injection influences the trophic response of the second. Of note, 24 h after the first injection, accumbal and hippocampal FGF-2 changes produced by cocaine in saline-pretreated rats were prevented in cocaine-pretreated rats. Conversely, in the medial prefrontal cortex and hippocampus 7 days after the first injection, the cocaine-induced FGF-2 changes were modified by the subsequent exposure to the psychostimulant.
These findings show that a single cocaine injection is sufficient to produce enduring changes in the adolescent brain and indicate that early cocaine priming alters the mechanisms regulating the trophic response in a brain region-specific fashion.
在青春期,大脑正在发育,对可影响其发育轨迹的滥用药物更为敏感。最近,人们的注意力集中在碱性成纤维细胞生长因子(FGF - 2)上,因为在生命早期给予该因子会增强成年后可卡因自我给药的习得和敏感性(特纳等人(《药理学与生物化学行为》92:100 - 4,2009年),克林顿等人(《药理学与生物化学行为》103:6 - 17,2012年))。此外,我们发现青春期接触可卡因后长期禁欲会导致FGF - 2转录失调(詹诺蒂等人(《精神药理学(柏林)》225:553 - 60,2013年))。
本研究的目的是评估(1)出生后第35天单次注射可卡因(20毫克/千克)是否会改变FGF - 2信使核糖核酸(mRNA)水平,以及(2)首次注射是否会影响24小时或7天后第二次注射(10毫克/千克)的营养反应。
我们发现FGF - 2表达模式存在区域差异,因为首次或第二次注射可卡因本身都会上调内侧前额叶皮质和伏隔核中的FGF - 2 mRNA,同时下调海马体中的FGF - 2 mRNA。首次注射会影响第二次注射的营养反应。值得注意的是,首次注射24小时后,在生理盐水预处理的大鼠中,可卡因引起的伏隔核和海马体FGF - 2变化在可卡因预处理的大鼠中得到了预防。相反,在首次注射7天后的内侧前额叶皮质和海马体中,可卡因诱导的FGF - 2变化会因随后接触精神兴奋剂而改变。
这些发现表明单次注射可卡因足以在青春期大脑中产生持久变化,并表明早期可卡因引发会以脑区特异性方式改变调节营养反应的机制。