Moretto A, Dallaire M, Romero P, Ludwig M
Meakins-Christie Laboratories, Royal Victoria Hospital, McGill University, Montreal, Quebec, Canada.
J Appl Physiol (1985). 1994 Oct;77(4):1623-9. doi: 10.1152/jappl.1994.77.4.1623.
Using isolated parenchymal strips from degassed rat lungs, we studied the contribution of the collagen-elastin network to lung tissue hysteretic behavior. Strips were suspended in an organ bath filled with Krebs solution (37 degrees C, pH 7.4) continuously bubbled with 95% O2-5% CO2. One end of the strip was attached to a force transducer and the other to a servo-controlled lever arm. Sinusoidal oscillations of 2.5% of resting length were applied at 1 Hz. Measurements were sampled under baseline conditions at different levels of stress (sigma = 10-26 g/cm). Porcine pancreatic elastase (0.05 IU.mg tissue-1.ml Krebs solution-1) was then added to the bath, and tension and length were measured continuously for 15 min at sigma = 15 g/cm. After washout, measurements were repeated at sigma = 10-26 g/cm. Elastance (E) and resistance (R) were calculated using the equation of motion. Hysteresivity (eta), the structural damping coefficient, was obtained using the following equation: eta = (R/E) pi 2f, where f is frequency. At baseline, we found that E and R were significantly dependent on sigma (P < 0.01), whereas eta was unchanged. During enzymatic digestion with elastase, there were significant decreases of tension, E, and R and no change in eta. Significant increases in E and R were found when these parameters were compared at the same sigma before and after treatment. Again, eta did not change. The constancy of eta after elastase suggests that disruption of the elastin-collagen network does not alter the coupling between elastic and dissipative processes in lung tissue.
我们使用从脱气大鼠肺中分离出的实质组织条带,研究了胶原蛋白 - 弹性蛋白网络对肺组织滞后行为的作用。将组织条带悬浮于充满Krebs溶液(37℃,pH 7.4)的器官浴中,该溶液持续通入95% O₂ - 5% CO₂。组织条带的一端连接到力传感器,另一端连接到伺服控制的杠杆臂。以1 Hz的频率施加静息长度2.5%的正弦振荡。在基线条件下,于不同应力水平(σ = 10 - 26 g/cm)下进行测量采样。然后向浴中加入猪胰弹性蛋白酶(0.05 IU·mg组织⁻¹·ml Krebs溶液⁻¹),并在σ = 15 g/cm下连续测量15分钟的张力和长度。冲洗后,在σ = 10 - 26 g/cm下重复测量。使用运动方程计算弹性(E)和阻力(R)。通过以下方程获得结构阻尼系数滞后率(η):η = (R/E)π²f,其中f为频率。在基线时,我们发现E和R显著依赖于σ(P < 0.01),而η不变。在用弹性蛋白酶进行酶消化期间,张力、E和R显著降低,而η没有变化。当在处理前后相同的σ下比较这些参数时,发现E和R显著增加。同样,η没有变化。弹性蛋白酶处理后η的恒定表明弹性蛋白 - 胶原蛋白网络的破坏不会改变肺组织中弹性和耗散过程之间的耦合。