Peregud Danil I, Yakovlev Alexander A, Stepanichev Mikhail Yu, Onufriev Mikhail V, Panchenko Leonid F, Gulyaeva Natalia V
Federal State Budgetary Institution "V. Serbsky Federal Medical Research Centre for Psychiatry and Drug Addiction", of the Ministry of Health of the Russian Federation, Moscow, Russia, 119002.
Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, 5a Butlerov Str., Moscow, Russia, 117485.
Cell Mol Neurobiol. 2016 Aug;36(6):839-849. doi: 10.1007/s10571-015-0267-6. Epub 2015 Sep 7.
Nitric oxide (NO) mediates pharmacological effects of opiates including dependence and abstinence. Modulation of NO synthesis during the induction phase of morphine dependence affects manifestations of morphine withdrawal syndrome, though little is known about mechanisms underlying this phenomenon. Neurotrophic and growth factors are involved in neuronal adaptation during opiate dependence. NO-dependent modulation of morphine dependence may be mediated by changes in expression and activity of neurotrophic and/or growth factors in the brain. Here, we studied the effects of NO synthesis inhibition during the induction phase of morphine dependence on the expression of brain-derived neurotrophic factor (BDNF), glial-derived neurotrophic factor (GDNF), nerve growth factor (NGF), and insulin-like growth factor 1 (IGF1) as well as their receptors in rat brain regions after spontaneous morphine withdrawal in dependent animals. Morphine dependence in rats was induced within 6 days by 12 injections of morphine in increasing doses (10-100 mg/kg), and NO synthase inhibitor L-N(G)-nitroarginine methyl ester (L-NAME) (10 mg/kg) was given 1 h before each morphine injection. The expression of the BDNF, GDNF, NGF, IGF1, and their receptors in the frontal cortex, striatum, hippocampus, and midbrain was assessed 40 h after morphine withdrawal. L-NAME treatment during morphine intoxication resulted in an aggravation of the spontaneous morphine withdrawal severity. Morphine withdrawal was accompanied by upregulation of BDNF, IGF1, and their receptors TrkB and IGF1R, respectively, on the mRNA level in the frontal cortex, and only BDNF in hippocampus and midbrain. L-NAME administration during morphine intoxication decreased abstinence-induced upregulation of these mRNAs in the frontal cortex, hippocampus and midbrain. L-NAME prevented from abstinence-induced elevation of mature but not pro-form of BDNF polypeptide in the frontal cortex. While morphine abstinence did not affect TrkB protein levels as well as its phosphorylation status, inhibition of NO synthesis decreased levels of phosphorylated TrkB after withdrawal. Thus, NO signaling during induction of dependence may be involved in the mechanisms of BDNF expression and processing at abstinence, thereby affecting signaling through TrkB in the frontal cortex.
一氧化氮(NO)介导阿片类药物的药理作用,包括依赖性和戒断反应。吗啡依赖诱导期内NO合成的调节会影响吗啡戒断综合征的表现,不过对于这一现象背后的机制知之甚少。神经营养因子和生长因子参与阿片类药物依赖期间的神经元适应过程。NO依赖性的吗啡依赖调节可能是由大脑中神经营养因子和/或生长因子的表达及活性变化介导的。在此,我们研究了在吗啡依赖诱导期抑制NO合成对依赖动物自发吗啡戒断后大鼠脑区中脑源性神经营养因子(BDNF)、胶质细胞源性神经营养因子(GDNF)、神经生长因子(NGF)和胰岛素样生长因子1(IGF1)及其受体表达的影响。通过12次注射递增剂量(10 - 100mg/kg)的吗啡在6天内诱导大鼠产生吗啡依赖,并且在每次吗啡注射前1小时给予NO合酶抑制剂L - N(G)-硝基精氨酸甲酯(L - NAME)(10mg/kg)。在吗啡戒断40小时后评估额叶皮质、纹状体、海马体和中脑BDNF、GDNF、NGF、IGF1及其受体的表达。吗啡中毒期间L - NAME处理导致自发吗啡戒断严重程度加重。吗啡戒断分别伴随着额叶皮质、海马体和中脑mRNA水平上BDNF、IGF1及其受体TrkB和IGF1R的上调,海马体和中脑仅BDNF上调。吗啡中毒期间给予L - NAME可降低额叶皮质、海马体和中脑这些mRNA的戒断诱导上调。L - NAME可防止额叶皮质中成熟形式而非前体形式的BDNF多肽因戒断而升高。虽然吗啡戒断不影响TrkB蛋白水平及其磷酸化状态,但抑制NO合成会降低戒断后磷酸化TrkB的水平。因此,依赖诱导期间的NO信号传导可能参与戒断时BDNF表达和加工的机制,从而影响额叶皮质中通过TrkB的信号传导。