Sessler F M, Cheng J T, Waterhouse B D
Department of Cell Biology and Anatomy, University of Texas Health Science Center, Dallas 75235.
Brain Res. 1988 Apr 12;446(1):77-89. doi: 10.1016/0006-8993(88)91298-x.
The present studies were conducted as part of an ongoing investigation of the effects of norepinephrine (NE) in neuronal circuits of the mammalian brain. In this report, we describe noradrenergic actions in the lateral hypothalamus (LH), an area which has been implicated in the central integration of cardiovascular regulatory mechanisms, fluid balance and ingestive behaviors. Microiontophoretically applied NE was interacted with extracellularly recorded responses of LH neurons to iontophoretically applied putative neurotransmitters gamma-aminobutyric acid (GABA), acetylcholine (ACh) and glutamate (Glu); and activation of known input pathways from the reticular thalamus (RT) and the lateral preoptic area (LPO). Peri-event histograms of cell responses were computed before, during and after NE microiontophoresis (5-50 nA) and used to quantitatively evaluate monoamine-induced effects on spontaneous and stimulus evoked activity of LH neurons. In 16 of 23 LH neurons, RT-stimulus-induced inhibition was markedly prolonged from a mean of 28.3 +/- 4.8 ms to 44.7 +/- 5.2 ms, during iontophoretic application of NE. In 22 of 38 LH cells, LPO-stimulus-induced excitatory responses were enhanced above control levels during NE administration. In further tests, inhibitory responses of LH cells to iontophoretic pulses of GABA were potentiated during NE administration in 69% (24 of 35) of the cases tested. ACh-induced excitation was potentiated in 9 of 21 cells. In 4 of these cases, otherwise subthreshold doses of ACh caused marked increases in cell firing during the period of NE administration. By contrast, Glu-evoked excitation was antagonized by NE iontophoresis in 65.5% (17 of 26) of LH cells tested. These findings indicate that, as in other noradrenergic target regions of the CNS, NE can facilitate synaptically mediated responses of LH neurons. Taken together these observations suggest that NE may play an important regulatory role in the synaptic transfer of information within LH circuits, and consequently exert considerable influence over the homeostatic functions mediated by this structure.
本研究是对去甲肾上腺素(NE)在哺乳动物大脑神经回路中作用的一项正在进行的调查的一部分。在本报告中,我们描述了去甲肾上腺素能在下丘脑外侧区(LH)的作用,该区域与心血管调节机制、体液平衡和摄食行为的中枢整合有关。通过微离子电泳施加的NE与细胞外记录的LH神经元对微离子电泳施加的假定神经递质γ-氨基丁酸(GABA)、乙酰胆碱(ACh)和谷氨酸(Glu)的反应相互作用;以及来自丘脑网状核(RT)和外侧视前区(LPO)的已知输入通路的激活。在NE微离子电泳(5-50 nA)之前、期间和之后计算细胞反应的事件周围直方图,并用于定量评估单胺对LH神经元自发和刺激诱发活动的影响。在23个LH神经元中的16个中,在离子电泳施加NE期间,RT刺激诱导的抑制从平均28.3±4.8毫秒显著延长至44.7±5.2毫秒。在38个LH细胞中的22个中,在给予NE期间,LPO刺激诱导的兴奋性反应增强至对照水平以上。在进一步的测试中,在69%(35个中的24个)测试病例中,在给予NE期间,LH细胞对GABA微离子电泳脉冲的抑制反应增强。21个细胞中的9个中,ACh诱导的兴奋增强。在其中4个病例中,否则亚阈值剂量的ACh在给予NE期间导致细胞放电显著增加。相比之下,在65.5%(26个中的17个)测试的LH细胞中,NE离子电泳拮抗Glu诱发的兴奋。这些发现表明,与中枢神经系统的其他去甲肾上腺素能靶点区域一样,NE可以促进LH神经元的突触介导反应。综合这些观察结果表明,NE可能在LH回路内的信息突触传递中起重要调节作用,因此对该结构介导的稳态功能施加相当大的影响。