Davies B L, Brundage C M, Harris M B, Taylor B E
Institute of Arctic Biology, University of Alaska Fairbanks, Rm 311 Irving I, 902 N Koyukuk Drive, Fairbanks, AK 99775, USA.
J Comp Physiol B. 2009 Jul;179(5):579-92. doi: 10.1007/s00360-009-0339-3. Epub 2009 Jan 30.
Location of the lung respiratory rhythm generator (RRG) in the bullfrog brainstem was investigated by examining neurokinin-1 and mu-opioid receptor (NK1R, muOR) colocalization by immunohistochemistry and characterizing the role of these receptors in lung rhythm and episodic pattern generation. NK1R and muOR occurred in brainstems from all developmental stages. In juvenile bullfrogs a distinct area of colocalization was coincident with high-intensity fluorescent labeling of muOR; high-intensity labeling of muOR was not distinctly and consistently localized in tadpole brainstems. NK1R labeling intensity did not change with development. Similarity in colocalization is consistent with similarity in responses to substance P (SP, NK1R agonist) and DAMGO (muOR agonist) when bath applied to bullfrog brainstems of different developmental stages. In early stage tadpoles and juvenile bullfrogs, SP increased and DAMGO decreased lung burst frequency. In juvenile bullfrogs, SP increased lung burst frequency, episode frequency, but decreased number of lung bursts per episode and lung burst duration. In contrast, DAMGO decreased lung burst frequency and burst cycle frequency, episode frequency, and number of lung bursts per episode but increased all other lung burst parameters. Based on these results, we hypothesize that NK1R and muOR colocalization together with a metamorphosis-related increase in muOR intensity marks the location of the lung RRG but not necessarily the lung episodic pattern generator.
通过免疫组织化学检查神经激肽-1和μ-阿片受体(NK1R、μOR)的共定位,并确定这些受体在肺节律和发作模式产生中的作用,研究了牛蛙脑干中肺呼吸节律发生器(RRG)的位置。NK1R和μOR存在于所有发育阶段的脑干中。在幼年牛蛙中,一个明显的共定位区域与μOR的高强度荧光标记重合;μOR的高强度标记在蝌蚪脑干中没有明显且一致的定位。NK1R标记强度不随发育而变化。当将P物质(SP,NK1R激动剂)和DAMGO(μOR激动剂)浴应用于不同发育阶段的牛蛙脑干时,共定位的相似性与反应的相似性一致。在早期蝌蚪和幼年牛蛙中,SP增加而DAMGO降低肺爆发频率。在幼年牛蛙中,SP增加肺爆发频率、发作频率,但减少每次发作的肺爆发次数和肺爆发持续时间。相反,DAMGO降低肺爆发频率和爆发周期频率、发作频率以及每次发作的肺爆发次数,但增加所有其他肺爆发参数。基于这些结果,我们假设NK1R和μOR的共定位以及与变态相关的μOR强度增加标志着肺RRG的位置,但不一定是肺发作模式发生器的位置。