Sumners C, Shalit S L, Kalberg C J, Raizada M K
Am J Physiol. 1987 Jun;252(6 Pt 1):C650-6. doi: 10.1152/ajpcell.1987.252.6.C650.
In this study we have examined the actions of angiotensin II (ANG II) on catecholamine metabolism in neuronal brain cell cultures prepared from the hypothalamus and brain stem. Neuronal cultures prepared from the brains of 1-day-old Sprague-Dawley rats exhibit specific neuronal uptake mechanisms for both norepinephrine (NE) and dopamine (DA), and also monoamine oxidase (MAO) and catechol O-methyltransferase (COMT) activity. Separate neuronal uptake sites for NE and DA were identified by using specific neuronal uptake inhibitors for each amine. In previous studies, we determined that ANG II (10 nM-1 microM) stimulates increased neuronal [3H]NE uptake by acting at specific receptors. We have confirmed these results here and in addition have shown that ANG II (1 nM-10 microM, 10-120 min) has no significant effects on neuronal [3H]DA uptake. These results suggest that the actions of ANG II are restricted to the NE transporter in neuronal cultures. It is possible that ANG II stimulates the intraneuronal metabolism of at least part of the NE that is taken up, because the peptide stimulates MAO activity, an effect mediated by specific ANG II receptors. ANG II had no effect on COMT activity in neuronal cultures. Therefore, the use of neuronal cultures of hypothalamus and brain stem we have determined that ANG II can specifically alter NE metabolism in these areas, while apparently not altering DA metabolism.
在本研究中,我们检测了血管紧张素II(ANG II)对从下丘脑和脑干制备的神经元脑细胞培养物中儿茶酚胺代谢的作用。从1日龄Sprague-Dawley大鼠大脑制备的神经元培养物对去甲肾上腺素(NE)和多巴胺(DA)均表现出特异性神经元摄取机制,同时还具有单胺氧化酶(MAO)和儿茶酚-O-甲基转移酶(COMT)活性。通过使用针对每种胺的特异性神经元摄取抑制剂,确定了NE和DA各自独立的神经元摄取位点。在先前的研究中,我们确定ANG II(10 nM - 1 μM)通过作用于特定受体刺激神经元[3H]NE摄取增加。我们在此证实了这些结果,此外还表明ANG II(1 nM - 10 μM,10 - 120分钟)对神经元[3H]DA摄取没有显著影响。这些结果表明,ANG II的作用仅限于神经元培养物中的NE转运体。ANG II可能刺激了至少部分摄取的NE的神经元内代谢,因为该肽刺激了MAO活性,这是一种由特定ANG II受体介导的效应。ANG II对神经元培养物中的COMT活性没有影响。因此,通过使用下丘脑和脑干的神经元培养物,我们确定ANG II可以特异性改变这些区域的NE代谢,而显然不会改变DA代谢。