首页> 美国卫生研究院文献>Taylor Francis Open Select >Nitroxidergic modulation of behavioural cardiovascular and immune responses and brain NADPH diaphorase activity upon morphine tolerance/dependence in rats
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Nitroxidergic modulation of behavioural cardiovascular and immune responses and brain NADPH diaphorase activity upon morphine tolerance/dependence in rats

机译:大鼠对吗啡耐受/依赖性的行为心血管和免疫反应以及脑NADPH心肌黄递酶活性的硝化能调节

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摘要

Opioid and non-opioid effects of acute and chronic morphine administration on behaviour, cardiovascular responses, cell proliferation and apoptosis and nitric-oxide synthase (NOS) activity were studied in rats. A novel score-point scale was introduced to quantify the signs of opioid withdrawal syndrome. NOS inhibitor L-NAME (NG-nitro-L-arginine methyl ester) was applied to reveal the role of NOS/NO pathway in the modulation of morphine-induced in vivo and in vitro responses. The obtained data showed that chronic co-administration of L-NAME drastically attenuated naloxone-precipitated withdrawal syndrome and prevented the development of morphine tolerance to cardiovascular action of morphine. The apoptotic process was very much restricted by L-NAME supplementation of chronic morphine treatment, which resulted in few apoptotic cells, less low molecular weight genomic DNA and preservation of high molecular weight non-fragmented genomic DNA. The study provides new data for nitroxidergic modulation of opioid tolerance and dependence.
机译:在大鼠中研究了急性和慢性吗啡给药对阿片类药物和非阿片类药物的行为,心血管反应,细胞增殖和凋亡以及一氧化氮合酶(NOS)活性的影响。引入了一种新的得分点量表来量化阿片类戒断综合征的体征。使用NOS抑制剂L-NAME(N G -硝基-L-精氨酸甲酯)来揭示NOS / NO途径在吗啡诱导的体内和体外应答调节中的作用。获得的数据表明,长期联合服用L-NAME可以大大减轻纳洛酮沉淀的戒断综合征,并阻止了吗啡对吗啡心血管作用的耐受性。慢性吗啡治疗的补充L-NAME极大地限制了凋亡过程,导致凋亡细胞少,低分子量基因组DNA少,高分子量非片段化基因组DNA的保存。该研究为阿片样物质耐受性和依赖性的氮氧化调节提供了新数据。

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