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豚鼠支气管中的非肾上腺素能、非胆碱能神经激活:对张力具有强大且频率依赖性的稳定作用。

Non-adrenergic, non-cholinergic neural activation in guinea-pig bronchi: powerful and frequency-dependent stabilizing effect on tone.

作者信息

Lindén A, Ullman A, Löfdahl C G, Skoogh B E

机构信息

Division of Pulmonary Medicine, Renströmska Hospital, University of Göteborg, Sweden.

出版信息

Br J Pharmacol. 1993 Jul;109(3):845-51. doi: 10.1111/j.1476-5381.1993.tb13652.x.

Abstract
  1. We examined non-adrenergic, non-cholinergic (NANC) stimulation for its stabilizing effect on bronchial smooth-muscle tone with respect to its regulatory power and the effect of variations in neural impulse frequency. 2. The guinea-pig isolated main bronchus (n = 4-12) was pretreated with indomethacin (10 microM) and incubated with atropine (1 microM) and guanethidine (10 microM). Electrical field stimulation (EFS: 1200 mA, 0.5 ms, 240 s) was applied at various levels of tone prior to EFS: first without tone, then at a moderate tone induced by histamine (0.3 microM) and, finally, at a high tone induced by histamine (6 microM). Three different stimulation frequencies (1, 3 or 10 Hz) were used in order to produce moderate to near-maximum contractile and relaxant NANC neural responses. Both the contractile and the relaxant NANC responses were tetrodotoxin-sensitive in the guinea-pig isolated main bronchus (3 Hz). 3. Without tone prior to EFS, NANC activation (1, 3 or 10 Hz) induced a pronounced contractile response. At a moderate level of tone prior to EFS, NANC activation induced a less pronounced contractile response. At the highest level of tone prior to EFS, NANC activation induced a relaxant response. All these NANC responses adjusted the tone towards a similar level and this 'stabilization level' was 56(6)% at 1 Hz, 65(3)% at 3 Hz and 56(5)% at 10 Hz, expressed as a percentage of the maximum histamine-induced (0.1 mM) tone in each airway preparation. 4. There was a difference of approximately 90% of maximum between the highest and the lowest tone level prior to NANC activation. This difference was reduced by the converging contractile and relaxantNANC responses and the magnitude of this 'convergence effect' was 40(8)% at 1 Hz, 72(4)% at 3 Hz and 90(2)% at 10 Hz.5. These findings indicate that NANC neural activation stabilizes bronchial smooth-muscle tone via a contraction when the tone is low prior to activation and via a relaxation when the tone is high prior to activation. The NANC stabilizing effect on tone appears to be powerful and its magnitude can be controlled by the neural impulse frequency. The level of tone towards which the NANC responses converge does not appear to be markedly altered by variations in the impulse frequency. Our findings are consistent with a regulatory role for NANC responses in the control of bronchial smooth-muscle tone.
摘要
  1. 我们研究了非肾上腺素能、非胆碱能(NANC)刺激对支气管平滑肌张力的稳定作用,涉及到其调节能力以及神经冲动频率变化的影响。2. 将豚鼠离体主支气管(n = 4 - 12)用吲哚美辛(10微摩尔)预处理,并用阿托品(1微摩尔)和胍乙啶(10微摩尔)孵育。在电场刺激(EFS:1200毫安,0.5毫秒,240秒)之前,在不同张力水平下施加电场刺激:首先是无张力状态,然后是由组胺(0.3微摩尔)诱导的中等张力状态,最后是由组胺(6微摩尔)诱导的高张力状态。使用三种不同的刺激频率(1、3或10赫兹),以产生中等至接近最大的收缩性和舒张性NANC神经反应。在豚鼠离体主支气管(3赫兹)中,收缩性和舒张性NANC反应均对河豚毒素敏感。3. 在EFS之前无张力时,NANC激活(1、3或10赫兹)诱导出明显的收缩反应。在EFS之前处于中等张力水平时, NANC激活诱导出不太明显的收缩反应。在EFS之前处于最高张力水平时,NANC激活诱导出舒张反应。所有这些NANC反应都将张力调节至相似水平,这种“稳定水平”在1赫兹时为56(6)%,在3赫兹时为65(3)%,在10赫兹时为56(5)%,以每种气道制剂中组胺诱导的最大(0.1毫摩尔)张力的百分比表示。4. 在NANC激活之前,最高和最低张力水平之间的差异约为最大值的90%。这种差异通过收缩性和舒张性NANC反应的趋同而减小,这种“趋同效应”的幅度在1赫兹时为40(8)%,在3赫兹时为72(4)%,在10赫兹时为90(2)%。5. 这些发现表明,NANC神经激活在激活前张力较低时通过收缩来稳定支气管平滑肌张力,而在激活前张力较高时通过舒张来稳定。NANC对张力的稳定作用似乎很强,其幅度可由神经冲动频率控制。NANC反应趋同的张力水平似乎不会因冲动频率的变化而明显改变。我们的发现与NANC反应在控制支气管平滑肌张力中的调节作用一致。

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本文引用的文献

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Cholinergic and nonadrenergic mechanisms in human and guinea pig airways.人和豚鼠气道中的胆碱能和非肾上腺素能机制。
J Appl Physiol Respir Environ Exerc Physiol. 1984 Apr;56(4):958-65. doi: 10.1152/jappl.1984.56.4.958.
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Inhibitory innervation to the guinea pig trachealis muscle.豚鼠气管平滑肌的抑制性神经支配。
J Appl Physiol Respir Environ Exerc Physiol. 1981 Feb;50(2):374-82. doi: 10.1152/jappl.1981.50.2.374.
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Substance P and capsaicin-induced contraction of human bronchi.P物质和辣椒素引起的人支气管收缩。
Acta Physiol Scand. 1983 Sep;119(1):49-53. doi: 10.1111/j.1748-1716.1983.tb07304.x.

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