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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Cocaine increases the intracellular calcium concentration in brain independently of its cerebrovascular effects.
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Cocaine increases the intracellular calcium concentration in brain independently of its cerebrovascular effects.

机译:可卡因不依赖于脑血管作用而增加了脑内细胞内钙的浓度。

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Cocaine abuse increases the risk of life-threatening neurological complications such as strokes and seizures. Although the vasoconstricting properties of cocaine underlie its cerebrovascular effects, the mechanisms underlying its neurotoxicity remain incompletely understood. Here, we use optical techniques to measure cerebral blood volume, hemoglobin oxygenation (S(t)O(2)), and intracellular calcium ([Ca(2+)](i)) to test the hypothesis that cocaine increases [Ca(2+)](i) in the brain. The effects of cocaine were compared with those of methylphenidate, which has similar catecholaminergic effects as cocaine (except for serotonin increases) but no local anesthetic properties, and of lidocaine, which has similar local anesthetic effects as cocaine but is devoid of catecholaminergic actions. To control for the hemodynamic effects of cocaine, we assessed the effects of cocaine in animals in which normal blood pressure was maintained by infusion of phenylephrine, and we also measured the effects of transient hypotension (mimicking that induced by cocaine). We show that cocaine induced significant increases ( approximately 10-15%) in [Ca(2+)](i) that were independent of its hemodynamic effects and of the anesthetic used (isofluorance or alpha-chloralose). Lidocaine but not methylphenidate also induced significant [Ca(2+)](i) increases ( approximately 10-13%). This indicates that cocaine at a dose within the range used by drug users significantly increases the [Ca(2+)](i) in the brain and its local anesthetic, but neither its catecholaminergic nor its hemodynamic actions, underlies this effect. Cocaine-induced [Ca(2+)](i) increases are likely to accentuate the neurotoxic effects from cocaine-induced vasoconstriction and to facilitate the occurrence of seizures from the catecholaminergic effects of cocaine. These findings support the use of calcium channel blockers as a strategy to minimize the neurotoxic effects of cocaine.
机译:滥用可卡因会增加危及生命的神经系统并发症(如中风和癫痫发作)的风险。尽管可卡因的血管收缩特性是其脑血管作用的基础,但其神经毒性的机制尚不完全清楚。在这里,我们使用光学技术来测量脑血容量,血红蛋白氧合(S(t)O(2))和细胞内钙([Ca(2 +)](i)),以测试可卡因增加[Ca( 2 +)](i)在大脑中。将可卡因的作用与哌醋甲酯的作用进行了比较,哌醋甲酯具有与可卡因类似的儿茶酚胺能作用(5-羟色胺增加除外),但无局部麻醉作用,而利多卡因具有与可卡因相似的局部麻醉作用,但没有儿茶酚胺能作用。为了控制可卡因的血液动力学作用,我们评估了可卡因对通过输注去氧肾上腺素维持正常血压的动物的作用,并且还测量了短暂性低血压的影响(模仿可卡因引起的血压降低)。我们显示,可卡因在[Ca(2 +)](i)中引起显着增加(大约10-15%),这与它的血液动力学效应和所用麻醉剂(等荧光或α-氯醛糖)无关。利多卡因而不是哌醋甲酯也诱导了显着的[Ca(2 +)](i)增加(约10-13%)。这表明可卡因的剂量在吸毒者使用的范围内会显着增加大脑及其局部麻醉剂中的[Ca(2 +)](i),但其儿茶酚胺能及其血液动力学作用均不能成为这种作用的基础。可卡因诱导的[Ca(2 +)](i)的增加可能会加剧可卡因诱导的血管收缩的神经毒性作用,并促进可卡因的儿茶酚胺能引起癫痫发作。这些发现支持使用钙通道阻滞剂作为最小化可卡因神经毒性作用的策略。

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