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有证据表明,不同的神经通路介导豚鼠气管的副交感神经收缩和舒张。

Evidence that distinct neural pathways mediate parasympathetic contractions and relaxations of guinea-pig trachealis.

作者信息

Canning B J, Undem B J

机构信息

Johns Hopkins Medical Institutions, Asthma and Allergy Center, Baltimore, MD 21224.

出版信息

J Physiol. 1993 Nov;471:25-40. doi: 10.1113/jphysiol.1993.sp019889.

Abstract
  1. The guinea-pig trachea was isolated with its extrinsic innervation intact and pinned to the bottom of a water-jacketed dissecting dish filled with warmed, oxygenated Krebs solution. The trachea was not separated from the oesophagus. Isometric tension was measured in a segment of the rostral portion of the trachea. 2. Stimulation of the vagus nerves caudal to the nodose ganglia elicited contractions of the trachealis that were blocked by the muscarinic receptor antagonist atropine. Following addition of atropine and contraction of the trachealis with prostaglandin F2 alpha (PGF2 alpha), vagus nerve stimulation elicited non-adrenergic, non-cholinergic relaxations. Both responses elicited by stimulation of the vagi were abolished by cutting the recurrent laryngeal nerves and were considered parasympathetic in nature as they were sensitive to the autonomic ganglion blockers trimetaphan and hexamethonium. 3. Experiments were designed in which ganglionic blockers were added to the buffer bathing the entire preparation or, alternatively, added only to the buffer perfusing the tracheal lumen. When given equal access to the trachea and oesophagus, hexamethonium was 56-fold more potent an inhibitor of vagally mediated relaxations of the trachealis than vagally mediated contractions. Selective administration of hexamethonium to the buffer perfusing the tracheal lumen did not decrease the potency of the ganglionic blocker versus vagally mediated contractions. By contrast, even at a concentration of 1 mM, intratracheally administered hexamethonium failed to inhibit vagally mediated relaxations by 50%. Comparable results were obtained using trimetaphan. 4. Consistent with previous observations, removing the portion of the oesophagus contiguous with the region of the trachea at which isometric tension was measured abolished parasympathetic relaxations of the trachealis. Oesophagus removal was without effect on parasympathetic nerve-induced contractions. Removing the dorsal half of the oesophagus or the mucosa and submucosa of the oesophagus did not affect the parasympathetic relaxant innervation. 5. The compound action potential of guinea-pig recurrent laryngeal nerves evoked by vagus nerve stimulation consisted of three distinct peaks representing populations of axons with fast, intermediate and slow conduction velocities. The voltage-response characteristics of vagally mediated contractions were identical to those of the compound action potential peak representing fibres with intermediate (10 m/s) conduction velocities. By contrast, the voltage-response characteristics of the vagally mediated relaxations were best correlated with the compound action potential peak representing fibres with slow (0.4-3 m/s) conduction velocities.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 将豚鼠气管与其外在神经支配完整地分离出来,固定在一个装有温热、充氧的克雷布斯溶液的水套式解剖盘中。气管未与食管分离。在气管头端部分的一段测量等长张力。2. 刺激结状神经节尾侧的迷走神经会引起气管平滑肌收缩,该收缩可被毒蕈碱受体拮抗剂阿托品阻断。加入阿托品并用前列腺素F2α(PGF2α)使气管平滑肌收缩后,迷走神经刺激会引起非肾上腺素能、非胆碱能舒张。刺激迷走神经引发的这两种反应在切断喉返神经后均消失,且由于它们对自主神经节阻滞剂曲美芬和六甲铵敏感,因此被认为本质上是副交感神经介导的。3. 设计了一些实验,将神经节阻滞剂加入到浸泡整个标本的缓冲液中,或者仅加入到灌注气管腔的缓冲液中。当六甲铵对气管和食管有同等作用时,它对迷走神经介导的气管平滑肌舒张的抑制作用比对迷走神经介导的收缩作用强56倍。将六甲铵选择性地加入到灌注气管腔的缓冲液中,并不会降低神经节阻滞剂对迷走神经介导收缩的效力。相比之下,即使在1 mM的浓度下,气管内给予六甲铵也无法使迷走神经介导的舒张作用抑制50%。使用曲美芬也得到了类似的结果。4. 与之前的观察结果一致,切除与测量等长张力的气管区域相邻的食管部分,会消除气管平滑肌的副交感神经介导的舒张。切除食管对副交感神经诱导的收缩没有影响。切除食管的背侧半部分或食管的黏膜和黏膜下层,并不影响副交感神经的舒张性神经支配。5. 迷走神经刺激诱发的豚鼠喉返神经复合动作电位由三个不同的峰组成,分别代表具有快、中、慢传导速度的轴突群。迷走神经介导的收缩的电压 - 反应特性与代表传导速度为中等(10 m/s)的纤维的复合动作电位峰的特性相同。相比之下,迷走神经介导的舒张的电压 - 反应特性与代表传导速度慢(0.4 - 3 m/s)的纤维的复合动作电位峰的相关性最好。(摘要截选至400字)

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