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褪黑素可减轻安非他命诱导的幼鼠纹状体囊泡单胺转运体-2 表达的降低。

Melatonin attenuates the amphetamine-induced decrease in vesicular monoamine transporter-2 expression in postnatal rat striatum.

机构信息

Research Center for Neuroscience, Institute of Molecular Biosciences, Mahidol University, Salaya, Nakornpathom 73170, Thailand.

出版信息

Neurosci Lett. 2011 Jan 20;488(2):154-7. doi: 10.1016/j.neulet.2010.11.019. Epub 2010 Nov 13.

Abstract

The vesicular monoamine transporter-2 (VMAT-2) is responsible for packaging intraneuronal dopamine into synaptic vesicles in preparation for synaptic release and is a critical regulator of cytoplasmic dopamine levels and dopaminergic function. It has long been recognized that VMAT-2 is also a critical mediator of amphetamine-induced dopamine release. Amphetamine-induced lesions during development have the potential to produce numerous permanent abnormalities in neural circuitry and function. Therefore, in the present study, we investigated the effects of amphetamine on the levels of VMAT-2, α-synuclein and phosphorylated tyrosine hydroxylase in the striatum of neonatal rats. We found that chronic amphetamine administration in postnatal rats produces dopaminergic deficits in the striatum, including decreases in the levels of VMAT-2 and phosphorylated tyrosine hydroxylase. In addition, an increase in α-synuclein expression was observed in the striatum of postnatal rats following chronic amphetamine treatment. Furthermore, we identified a role of (10mg/kg) melatonin, a methoxyindole released from the pineal gland, in attenuating the detrimental effects of amphetamine on dopaminergic neurons.

摘要

囊泡单胺转运体-2(VMAT-2)负责将多巴胺包装到突触小泡中,为突触释放做准备,是细胞质多巴胺水平和多巴胺能功能的关键调节剂。长期以来,人们一直认为 VMAT-2 也是安非他命诱导多巴胺释放的关键介质。发育过程中的安非他命诱导损伤有可能产生许多神经回路和功能的永久性异常。因此,在本研究中,我们研究了安非他命对新生大鼠纹状体中 VMAT-2、α-突触核蛋白和磷酸化酪氨酸羟化酶水平的影响。我们发现,新生大鼠的慢性安非他命给药会导致纹状体中的多巴胺能缺陷,包括 VMAT-2 和磷酸化酪氨酸羟化酶水平的降低。此外,在慢性安非他命处理后,新生大鼠的纹状体中观察到α-突触核蛋白表达增加。此外,我们发现(10mg/kg)褪黑素,一种从松果腺释放的甲氧基吲哚,在减轻安非他命对多巴胺能神经元的有害作用方面发挥作用。

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