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控制麻醉猫缺氧呼吸反应的神经递质和神经调质。

Neurotransmitters and neuromodulators controlling the hypoxic respiratory response in anaesthetized cats.

作者信息

Richter D W, Schmidt-Garcon P, Pierrefiche O, Bischoff A M, Lalley P M

机构信息

II. Department of Physiology, University of Gottingen, Humboldtallee 23, 37073 Gottingen, Germany.

出版信息

J Physiol. 1999 Jan 15;514 ( Pt 2)(Pt 2):567-78. doi: 10.1111/j.1469-7793.1999.567ae.x.

Abstract
  1. The contributions of neurotransmitters and neuromodulators to the responses of the respiratory network to acute hypoxia were analysed in anaesthetized cats. 2. Samples of extracellular fluid were collected at 1-1.5 min time intervals by microdialysis in the medullary region of ventral respiratory group neurones and analysed for their content of glutamate, gamma-aminobutyric acid (GABA), serotonin and adenosine by high performance liquid chromatography. Phrenic nerve activity was correlated with these measurements. 3. Levels of glutamate and GABA increased transiently during early periods of hypoxia, coinciding with augmented phrenic nerve activity and then fell below control during central apnoea. Serotonin and adenosine increased slowly and steadily with onset of hypoxic depression of phrenic nerve activity. 4. The possibility that serotonin contributes to hypoxic respiratory depression was tested by microinjecting the 5-HT-1A receptor agonist 8-OH-DPAT into the medullary region that is important for rhythmogenesis. Hypoxic activation of respiratory neurones and phrenic nerve activity were suppressed. Microinjections of NAN-190, a 5-HT-1A receptor blocker, enhanced hypoxic augmentation resulting in apneustic prolongation of inspiratory bursts. 5. The results reveal a temporal sequence in the release of neurotransmitters and neuromodulators and suggest a specific role for each of them in the sequential development of hypoxic respiratory disturbances.
摘要
  1. 在麻醉猫身上分析了神经递质和神经调质对呼吸网络急性缺氧反应的作用。2. 通过微透析以1 - 1.5分钟的时间间隔在腹侧呼吸组神经元的髓质区域采集细胞外液样本,并采用高效液相色谱法分析其谷氨酸、γ-氨基丁酸(GABA)、5-羟色胺和腺苷的含量。膈神经活动与这些测量结果相关联。3. 在缺氧早期,谷氨酸和GABA水平短暂升高,同时膈神经活动增强,随后在中枢性呼吸暂停期间降至对照水平以下。5-羟色胺和腺苷随着膈神经活动的缺氧性抑制开始而缓慢稳定地增加。4. 通过将5-HT-1A受体激动剂8-OH-DPAT微量注射到对节律产生重要的髓质区域,来测试5-羟色胺是否导致缺氧性呼吸抑制。呼吸神经元的缺氧激活和膈神经活动受到抑制。微量注射5-HT-1A受体阻滞剂NAN-190增强了缺氧增强作用,导致吸气爆发的长吸延长。5. 结果揭示了神经递质和神经调质释放的时间顺序,并表明它们各自在缺氧性呼吸紊乱的相继发展中具有特定作用。

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