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新生大鼠体外脑干脊髓中呼吸神经元的微环境

Microenvironment of respiratory neurons in the in vitro brainstem-spinal cord of neonatal rats.

作者信息

Brockhaus J, Ballanyi K, Smith J C, Richter D W

机构信息

II. Physiologisches Institut, Universität Göttingen, Germany.

出版信息

J Physiol. 1993 Mar;462:421-45. doi: 10.1113/jphysiol.1993.sp019562.

DOI:10.1113/jphysiol.1993.sp019562
PMID:8331589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1175308/
Abstract
  1. O2-, K(+)- and pH-sensitive microelectrodes were used to measure extracellular oxygen pressure (PO2), K+ activity (aKo) and pH (pHo) in ventral regions of the medulla oblongata containing respiratory neurons in the in vitro brainstem-spinal cord preparation from 0 to 4-day-old rats. 2. The location of respiratory neurons was mapped by extracellular recordings with conventional microelectrodes, or with the reference barrel of ion-sensitive microelectrodes. The major populations of respiratory neurons were distributed in the ventrolateral reticular formation near the nucleus ambiguus at depths of 300-600 microns. In this area, aKo baseline increased from 3.2 to 3.8 mM whereas steady-state values of PO2 and pHo fell from 120 to 7 mmHg and from 6.9 to 6.7, respectively. 3. During rhythmic inspiratory discharges recorded with suction electrodes from ventral roots of spinal (C3-C5) and cranial (IX, X, XII) nerves, aKo transiently increased by up to 100 microM, and PO2 fell maximally by 0.4 mmHg. During episodes of non-rhythmic neuronal discharge, aKo increased by as much as 0.4 mM and PO2 decreased by about 10 mmHg. In contrast, no variations in pHo could be detected during such activities. 4. Activation of medullary neurons by tetanic electrical stimulation of axonal tracts in the ventrolateral column of the spinal cord at the level of the phrenic motoneuron pool produced aKo elevations of up to 5 mM, decreases of PO2 by up to 50 mmHg, and pHo increases by a maximum of 0.07 pH units. These aKo and PO2 transients were reduced by more than 80% during blockade of synaptic transmission with 5 mM manganese (Mn2+) and completely blocked by 1 microM tetrodotoxin (TTX). 5. The tissue PO2 gradient as well as activity-related decreases of PO2 were completely abolished after block of oxidative cellular metabolism by addition of 2-10 mM cyanide (CN-) to the bathing solution. 6. Inhibition of the Na(+)-K+ pump by addition of 3-50 microM ouabain (3-10 min) caused a reversible increase of aKo by 0.8-3 mM, a delayed recovery of stimulus-induced aKo elevations, and produced a disturbance of the respiratory rhythm. 7. The sensitivity of the respiratory network to oxygen depletion was tested by superfusing the neuraxis with hypoxic solutions gassed with N2 instead of O2 (5-20 min).(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 使用对O₂⁻、K⁺和pH敏感的微电极,在0至4日龄大鼠的离体脑干 - 脊髓标本中,测量含有呼吸神经元的延髓腹侧区域的细胞外氧分压(PO₂)、K⁺活性(aKo)和pH(pHo)。2. 通过使用传统微电极或离子敏感微电极的参考电极进行细胞外记录,绘制呼吸神经元的位置。呼吸神经元的主要群体分布在疑核附近腹外侧网状结构中,深度为300 - 600微米。在该区域,aKo基线从3.2 mM增加到3.8 mM,而PO₂和pHo的稳态值分别从120 mmHg降至7 mmHg和从6.9降至6.7。3. 在使用吸力电极从脊髓(C3 - C5)腹根和脑神经(IX、X、XII)记录的节律性吸气放电期间,aKo瞬时增加高达100 μM,PO₂最大下降0.4 mmHg。在非节律性神经元放电期间,aKo增加多达0.4 mM,PO₂下降约10 mmHg。相比之下,在此类活动期间未检测到pHo的变化。4. 通过在膈运动神经元池水平对脊髓腹外侧柱的轴突束进行强直电刺激来激活延髓神经元,可使aKo升高高达5 mM,PO₂降低高达50 mmHg,pHo最多增加0.07个pH单位。在用5 mM锰(Mn²⁺)阻断突触传递期间,这些aKo和PO₂瞬变减少超过80%,并被1 μM河豚毒素(TTX)完全阻断。5. 通过向浴液中添加2 - 10 mM氰化物(CN⁻)阻断细胞氧化代谢后,组织PO₂梯度以及与活动相关的PO₂降低完全消失。6. 添加3 - 50 μM哇巴因(3 - 10分钟)抑制Na⁺ - K⁺泵,导致aKo可逆性增加0.8 - 3 mM,刺激诱导的aKo升高延迟恢复,并产生呼吸节律紊乱。7. 通过用氮气而不是氧气充气的低氧溶液灌注神经轴(5 - 20分钟)来测试呼吸网络对缺氧的敏感性。(摘要截短至400字)

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