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大鼠大脑皮质神经元中神经肽Y免疫反应性表达的抑制性多巴胺能调节。

An inhibitory dopaminergic regulation of the neuropeptide Y immunoreactivity expression in the rat cerebral cortex neurons.

作者信息

Smiałowska M

机构信息

Laboratory of Neurobiology, Polish Academy of Sciences, Kraków.

出版信息

Neuroscience. 1995 Jun;66(3):589-95. doi: 10.1016/0306-4522(95)00028-h.

Abstract

The effect of catecholamine depletion or blockade of dopaminergic or noradrenergic receptors on the neuropeptide Y immunoreactivity was studied in the rat brain cortex using immunohistochemical methods. Neuropeptide Y immunoreactive neurons were counted and the mean density of stained neurons per microscopic field was calculated. It was found that monoamine depletion by reserpine, the blockade of dopaminergic receptors by haloperidol or the specific D1 receptor blockade by SCH23390 caused a significant increase in the neuropeptide Y immunoreactivity in the cortex studied, after 24 h, evaluated as the density of immunoreactive neurons. No significant changes were observed after the blockade of alpha or beta adrenergic receptors (by phenoxybenzamine or propranolol, respectively). Specific D2 receptor blockade by sulpiride induced an insignificant increase only. The results suggest the existence of an inhibitory dopaminergic control of the neuropeptide Y content, mainly via D1 receptors, in neurons of the rat brain cortex.

摘要

利用免疫组织化学方法,在大鼠大脑皮层中研究了儿茶酚胺耗竭或多巴胺能或去甲肾上腺素能受体阻断对神经肽Y免疫反应性的影响。对神经肽Y免疫反应性神经元进行计数,并计算每个显微镜视野中染色神经元的平均密度。结果发现,利血平导致单胺耗竭、氟哌啶醇阻断多巴胺能受体或SCH23390特异性阻断D1受体后,在24小时后,所研究的皮层中神经肽Y免疫反应性显著增加,以免疫反应性神经元的密度来评估。α或β肾上腺素能受体阻断后(分别用酚苄明或普萘洛尔)未观察到显著变化。舒必利特异性阻断D2受体仅引起不显著的增加。结果表明,在大鼠大脑皮层神经元中,主要通过D1受体存在对神经肽Y含量的抑制性多巴胺能控制。

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