Liu Jun, Song Nana, Guardiola Juan, Roman Jesse, Yu Jerry
Pulmonary Division, Department of Medicine, University of Louisville; and Robley Rex VA Medical Center Louisville, KY, USA.
Front Physiol. 2016 Dec 9;7:588. doi: 10.3389/fphys.2016.00588. eCollection 2016.
Sensory units of pulmonary slowly adapting receptors (SARs) are more active in large airways than in small airways. However, there is no explanation for this phenomenon. Although sensory structures in large airways resemble those in small airways, they are bigger and more complex. Possibly, a larger receptor provides greater surface area for depolarization, and thus has a lower activating threshold and/or a higher sensitivity to stretch, leading to more nerve electrical activities. Recently, a single sensory unit has been reported to contain multiple receptors. Therefore, sensory units in large airways may contain more SARs, which may contribute to high activities. To test this hypothesis, we used a double staining technique to identify sensory receptor sizes. We labeled the sensory structure with Na/K-ATPase antibodies and the myelin sheath with myelin basic protein (MBP) antibodies. A SAR can be defined as the end formation beyond MBP labeling. Thus, we are able to compare sizes of sensory structures and SARs in large (trachea and bronchi) vs. small (bronchioles <500 μm in diameter) airways in the rabbit. We found that even though the sensory structure was bigger in large airways than in small airways (3340 ± 223 vs. 1168 ± 103 μm; < 0.0001), there was no difference in receptor sizes (349 ± 14 vs. 326 ± 16 μm; > 0.05). However, the sensory structure contains more SARs in large airways than in small airways (9.6 ± 0.6 vs. 3.6 ± 0.3; < 0.0001). Thus, our data support the hypothesis that greater numbers of SARs in sensory units of large airways may contribute to higher activities.
肺慢适应性感受器(SARs)的感觉单元在大气道中比在小气道中更活跃。然而,对于这种现象尚无解释。尽管大气道中的感觉结构与小气道中的相似,但它们更大且更复杂。可能,更大的感受器为去极化提供了更大的表面积,因此具有更低的激活阈值和/或对拉伸更高的敏感性,导致更多的神经电活动。最近,有报道称单个感觉单元包含多个感受器。因此,大气道中的感觉单元可能包含更多的SARs,这可能导致高活性。为了验证这一假设,我们使用双染色技术来识别感觉感受器的大小。我们用Na/K-ATP酶抗体标记感觉结构,用髓鞘碱性蛋白(MBP)抗体标记髓鞘。一个SAR可以定义为超过MBP标记的终末结构。因此,我们能够比较兔的大(气管和支气管)气道与小(直径<500μm的细支气管)气道中感觉结构和SARs的大小。我们发现,尽管大气道中的感觉结构比小气道中的大(3340±223 vs. 1168±103μm;<0.0001),但感受器大小没有差异(349±14 vs. 326±16μm;>0.05)。然而,大气道中感觉结构所含的SARs比小气道中的多(9.6±0.6 vs. 3.6±0.3;<0.0001)。因此,我们的数据支持这一假设,即大气道感觉单元中更多数量的SARs可能导致更高的活性。