首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Morphine and opioid peptides reduce paraventricular neuronal activity: studies on the rat hypothalamic slice preparation.
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Morphine and opioid peptides reduce paraventricular neuronal activity: studies on the rat hypothalamic slice preparation.

机译:吗啡和阿片样物质肽会降低心室旁神经元活动:对大鼠下丘脑切片制备的研究。

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摘要

Extracellular discharges of neurons in the paraventricular nucleus (PVN) were recorded from slices of rat hypothalamus in vitro. PVN neurons (n = 14) were identified by the criteria of (i) phasic activity patterns and (ii) antidromic invasion from the neurohypophysial tract. Neurons not displaying either of these features were considered unidentified with respect to physiological function (n = 85). The majority of unidentified neurons responded to bath application of morphine (1 microM), [D-Ala2,Met5]enkephalin (1 microM) or beta-endorphin (0.01-1 microM) with a prompt, reversible, dose-related reduction in spike discharge frequency. Naloxone (1 microM) antagonized the opioid-induced depressions in some, but not all, cases. At the concentrations tested, no tachyphylaxis to the effects of the opioids was observed. The opioid effects on putative neurohypophysial neurons were less pronounced; while 2 were depressed, the remaining 12 displayed no change in frequency or pattern of discharge to micromolar concentrations of morphine, [D-Ala2,Met5]enkephalin, or beta-endorphin. Our results indicate that opioids depress neuronal activity in the rat PVN via an interaction with a specific opiate receptor but that this effect is more pronounced on unidentified neurons than on putative neurohypophysial neurons in the slice.
机译:体外从大鼠下丘脑切片中记录了室旁核(PVN)中神经元的细胞外放电。 PVN神经元(n = 14)通过(i)阶段性活动模式和(ii)来自神经垂体道的抗皮层侵入的标准进行鉴定。没有表现出这些特征的神经元在生理功能方面被认为是未知的(n = 85)。大多数未鉴定的神经元对浴液中吗啡(1 microM),[D-Ala2,Met5]脑啡肽(1 microM)或β-内啡肽(0.01-1 microM)的入浴反应迅速,可逆,剂量相关的峰值降低放电频率。纳洛酮(1 microM)在某些(但不是全部)病例中拮抗阿片类药物引起的抑郁症。在所测试的浓度下,未观察到对阿片样物质作用的速激肽抑制作用。阿片类药物对假定的神经垂体神经元的作用不太明显。压抑2例时,其余12例的放电频率或放电模式与吗啡,[D-Ala2,Met5]脑啡肽或β-内啡肽的微摩尔浓度无变化。我们的结果表明,阿片类药物通过与特定阿片受体的相互作用降低大鼠PVN的神经元活性,但这种作用在未识别的神经元上比在切片中假定的神经下垂神经元上更为明显。

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