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蓝斑中的阿片类物质抑制作用。

Opioid inhibition in locus coeruleus.

作者信息

Travagli R A, Dunwiddie T V, Williams J T

机构信息

Vollum Institute, Oregon Health Sciences University, Portland 97201, USA.

出版信息

J Neurophysiol. 1995 Aug;74(2):519-28. doi: 10.1152/jn.1995.74.2.519.

Abstract
  1. Inhibition of locus coeruleus (LC) neurons by opioids is mediated by hyperpolarization associated with an increase in potassium conductance. However, opioids caused an outward current even at potentials more negative than the potassium equilibrium potential in the majority of LC neurons recorded in brain slices cut in the horizontal plane. 2. Whole cell and intracellular recording were made from LC neurons in the slice preparation and currents were measured with a switch clamp amplifier. 3. Local application of [Met]5enkephalin (ME) by iontophoresis resulted in two different effects depending on the site of application. Iontophoresis of ME close to the cell caused an outward current that reversed polarity near the potassium equilibrium potential. Whereas application at a distance > 200 microns resulted in an outward current that did not reverse polarity even at strongly negative potentials. 4. When potassium conductances were blocked with internal Cs and/or external Ba, the opioid current was reduced to < 15% of control. 5. Low sodium solutions were used to reduce sodium-dependent conductances. These solutions hyperpolarized LC neurons themselves, decreased outward currents caused by ME, and shifted the reversal potential of the ME induced current to less negative values. 6. Electrotonic coupling of LC neurons in neonatal animals is thought to synchronize spontaneous activity. In this study, synchronous activity in cells from adult animals also was observed, suggesting that electrotonic coupling in the LC persists into adulthood. 7. Carbenoxolone, an agent thought to block electrotonic coupling, had no effect on the action potential, spontaneous activity, or the resting conductance but blocked electrotonic coupling between LC neurons in neonates, blocked synchronous activity in LC neurons from adult animals, and shifted the reversal potential of the opioid current to the potassium equilibrium potential. 8. All results are consistent with the hypothesis that LC cells are electrotonically coupled. Such electrotonic coupling at the level of the nucleus locus coeruleus would mediate synchronous regulation of noradrenaline in widespread areas of the brain.
摘要
  1. 阿片类药物对蓝斑(LC)神经元的抑制作用是由与钾电导增加相关的超极化介导的。然而,在水平平面切割的脑片中记录的大多数LC神经元中,即使在比钾平衡电位更负的电位下,阿片类药物也会引起外向电流。2. 采用全细胞和细胞内记录技术,从脑片制备中的LC神经元记录电流,并使用开关钳放大器进行测量。3. 通过离子电渗法局部应用[甲硫氨酸]5脑啡肽(ME)会产生两种不同的效应,这取决于应用部位。在细胞附近进行ME离子电渗会引起外向电流,该电流在钾平衡电位附近反转极性。而在距离>200微米处应用则会导致外向电流,即使在强负电位下也不会反转极性。4. 当用内部铯和/或外部钡阻断钾电导时,阿片类药物电流降低至对照的<15%。5. 低钠溶液用于降低钠依赖性电导。这些溶液使LC神经元自身超极化,减少了ME引起的外向电流,并将ME诱导电流的反转电位向较不负的值移动。6. 新生动物中LC神经元的电紧张耦联被认为可使自发活动同步。在本研究中,也观察到了成年动物细胞中的同步活动,这表明LC中的电紧张耦联持续到成年期。7. 羧苄青霉素,一种被认为可阻断电紧张耦联的药物,对动作电位、自发活动或静息电导没有影响,但可阻断新生动物LC神经元之间的电紧张耦联,阻断成年动物LC神经元中的同步活动,并将阿片类药物电流的反转电位移至钾平衡电位。8. 所有结果都与LC细胞存在电紧张耦联的假设一致。在蓝斑核水平的这种电紧张耦联将介导大脑广泛区域去甲肾上腺素的同步调节。

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