Horn L W
Respir Physiol. 1978 Sep;34(3):345-57. doi: 10.1016/0034-5687(78)90133-0.
Lung surfactant might exchange reversibly between the alveolar gas-liquid interface and the liquid lining layer. This solubilization process could then contribute to time-dependent pulmonary mechanical phenomena. Theoretical analysis of a model alveolus shows how solubilization can produce recoil pressure relaxation of the lung. The analysis shows that for most experimental observations reported the solubilization kinetics probably could not have been determined by the actual fitting in, or squeezing out, of surfactant in the surface film. Most data are consistent with a solubilization rate controlled by diffusion in the liquid sublayer. However, in order for a diffusion-controlled mechanism to be significant the diffusing substance should be large, such as a micelle, and the alveolar liquid layer should be at least 1 micrometer thick. These conditions are quite realistic for slightly edematous lungs and thus might apply to many experimental, or pathological, situations.
肺表面活性剂可能在肺泡气液界面和液体衬里层之间进行可逆交换。然后,这种溶解过程可能导致与时间相关的肺力学现象。对模型肺泡的理论分析表明溶解如何产生肺的回缩压力松弛。分析表明,对于所报道的大多数实验观察结果,溶解动力学可能无法通过表面膜中表面活性剂的实际融入或挤出测定。大多数数据与液体亚层中扩散控制的溶解速率一致。然而,为了使扩散控制机制显著,扩散物质应该很大,如胶束,并且肺泡液体层应该至少1微米厚。这些条件对于轻度水肿的肺相当现实,因此可能适用于许多实验或病理情况。