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通过向去大脑猫的脑桥背侧被盖微注射α1-肾上腺素能拮抗剂来调节前庭脊髓反射。

Modulation of vestibulospinal reflexes through microinjection of an alpha 1-adrenergic antagonist in the dorsal pontine tegmentum of decerebrate cats.

作者信息

Cirelli C, D'Ascanio P, Horn E, Pompeiano O, Stampacchia G

机构信息

Dipartimento di Fisiologia e Biochimica, Università di Pisa, Italy.

出版信息

Arch Ital Biol. 1993 Sep;131(4):275-302.

PMID:7902697
Abstract
  1. The possibility that the norepinephrine (NE)-containing locus coeruleus (LC) neurons produce changes in posture as well as in gain of the vestibulospinal (VS) reflexes by acting on the dorsolateral pontine tegmentum (DPT) and the related medullary inhibitory reticulospinal (RS) system through alpha 1-adrenoceptors has been investigated in decerebrate cats. 2. Injection of the alpha 1-adrenergic antagonist prazosin PRZ (0.25 microliter at 0.1-1 microgram/microliter solvent) into the DPT, namely in the dorsal pontine reticular formation (pRF), as well as in the peribrachial nucleus of one side, decreased the postural activity in the ipsilateral limbs while increasing that of the contralateral limbs. In addition, the amplitude of modulation and thus the gain of the multiunit EMG responses of the ipsilateral and to a lesser extent of the contralateral triceps brachii to roll tilt of the animal at 0.15 Hz, +/- 10 degrees, increased. These effects appeared 5-10 min after the injection, reached the highest values in about 40-60 min and persisted for additional 1.5-2 h before disappearing. 3. The effects were site-specific and to some extent dose-dependent. However, neither changes in posture nor in gain of the VS reflexes were obtained after injection in the effective area of an equal volume of solvent. 4. In order to account for these findings it was postulated that the alpha 1-antagonist blocks the tonic inhibitory influence that the NE-containing LC neurons exert on ipsilateral DPT either by exciting through alpha 1-receptors interposed inhibitory interneurons, or by inhibiting presynaptically excitatory afferents to the same pontine tegmental structures. The increased discharge of these neurons and the related medullary inhibitory RS neurons would reduce the postural activity in the ipsilateral limbs. However, since the inhibitory RS neurons show a response pattern to tilt opposite in sign to that elicited by the excitatory VS neurons, we could expect that for a given labyrinth signal, the increased discharge of the RS neurons in the animal at rest would lead to a greater disinhibition of limb extensor motoneurons during ipsilateral tilt. These motoneurons would then respond more efficiently to the same excitatory volleys elicited by given parameters of stimulation, thus leading to an increased gain of the EMG responses of forelimb extensors to labyrinth stimulation. The possibility that the DPT of one side activates inhibitory RS neurons of both sides explains why PRZ increases the gain of the VS reflexes not only ipsilaterally but also contralaterally to the side of the injection.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 去甲肾上腺素(NE)能蓝斑(LC)神经元通过α1肾上腺素能受体作用于脑桥背外侧被盖区(DPT)及相关的延髓抑制性网状脊髓(RS)系统,从而改变姿势以及前庭脊髓(VS)反射增益的可能性,已在去大脑猫中进行了研究。2. 将α1肾上腺素能拮抗剂哌唑嗪(PRZ,0.25微升,浓度为0.1 - 1微克/微升溶剂)注射到DPT,即脑桥背侧网状结构(pRF)以及一侧的臂周核,会降低同侧肢体的姿势活动,同时增加对侧肢体的姿势活动。此外,同侧肱三头肌多单位肌电图(EMG)对动物以0.15赫兹、±10度滚动倾斜的调制幅度以及增益增加,对侧肱三头肌的增益增加幅度较小。这些效应在注射后5 - 10分钟出现,约40 - 60分钟达到最大值,并在消失前持续1.5 - 2小时。3. 这些效应具有部位特异性且在一定程度上呈剂量依赖性。然而,在有效区域注射等体积溶剂后,姿势或VS反射增益均未出现变化。4. 为了解释这些发现,推测α1拮抗剂阻断了含NE的LC神经元对同侧DPT的紧张性抑制作用,这种抑制作用要么是通过α1受体兴奋中间抑制性神经元来实现,要么是通过突触前抑制到相同脑桥被盖结构的兴奋性传入神经来实现。这些神经元以及相关延髓抑制性RS神经元放电增加会降低同侧肢体的姿势活动。然而,由于抑制性RS神经元对倾斜的反应模式与兴奋性VS神经元引发的反应模式相反,我们可以预期,对于给定的迷路信号,动物静止时RS神经元放电增加会导致同侧倾斜期间肢体伸肌运动神经元的去抑制作用增强。然后,这些运动神经元会对给定刺激参数引发的相同兴奋性冲动做出更有效的反应,从而导致前肢伸肌对迷路刺激的EMG反应增益增加。一侧的DPT激活两侧抑制性RS神经元的可能性解释了为什么PRZ不仅增加同侧VS反射的增益,也增加注射侧对侧VS反射的增益。(摘要截断于400字)

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