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白蛋白与天然肺表面活性剂及提取的肺脂质相互作用引起的表面性质变化。

Surface property changes from interactions of albumin with natural lung surfactant and extracted lung lipids.

作者信息

Holm B A, Notter R H, Finkelstein J N

出版信息

Chem Phys Lipids. 1985 Sep;38(3):287-98. doi: 10.1016/0009-3084(85)90022-2.

Abstract

These experiments characterize the effects of albumin on the dynamic surface activity of natural lung surfactant (LS), and an extracted mixed lipid fraction (CLL), at physiologic temperature, humidity, and film cycling rate on an oscillating bubble apparatus. Measurements of albumin effects on the surface pressure-time (pi-t) adsorption isotherms of CLL and LS are also reported. Results show that albumin in concentrations greater than or equal to 20 mg/ml increased the minimum dynamic surface tension of LS suspensions (0.4 mg phospholipid/ml) from less than 1 dyne/cm to 21 dynes/cm at 37 degrees C. Albumin in low concentrations (2 mg/ml) had a similar detrimental effect on the dynamic surface activity of extracted surfactant lipids, CLL. In addition, albumin also inhibited the isolated adsorption facility of LS and CLL; instead of adsorbing rapidly to their maximum spreading pressures of 45 dynes/cm, both surfactant mixtures (at 0.063 and 0.125 mg phospholipid/ml) adsorbed more slowly or reached lower final surface pressures in the presence of plasma protein. A striking finding was that albumin inhibition of surface activity was moderated or abolished at high lipid concentrations. For example, minimum dynamic surface tensions less than 1 dyne/cm were reached on the oscillating bubble for natural LS at concentrations greater than 0.75 mg/ml and CLL at concentrations greater than 1.5 mg/ml, even in the presence of very large amounts of albumin (100 mg/ml). Similarly, LS and CLL adsorption facility was protected from albumin inhibition at sufficiently high phospholipid concentrations. Albumin inhibition of natural LS adsorption was also moderated by the presence of 1.4 mM Ca2+ ions. These results show that albumin in plasma transudates has the potential to seriously impair alveolar surfactant activity in vivo. However, the detrimental effect will be mitigated if a critical threshold of phospholipid is present.

摘要

这些实验表征了白蛋白在生理温度、湿度和振荡气泡装置上的薄膜循环速率条件下,对天然肺表面活性剂(LS)以及提取的混合脂质组分(CLL)动态表面活性的影响。还报告了白蛋白对CLL和LS表面压力-时间(π-t)吸附等温线的影响测量结果。结果表明,浓度大于或等于20mg/ml的白蛋白在37℃时将LS悬浮液(0.4mg磷脂/ml)的最小动态表面张力从小于1达因/厘米提高到21达因/厘米。低浓度(2mg/ml)的白蛋白对提取的表面活性剂脂质CLL的动态表面活性也有类似的有害影响。此外,白蛋白还抑制了LS和CLL的孤立吸附功能;在血浆蛋白存在的情况下,两种表面活性剂混合物(0.063和0.125mg磷脂/ml)不是迅速吸附到其45达因/厘米的最大铺展压力,而是吸附得更慢或达到更低的最终表面压力。一个显著的发现是,在高脂质浓度下,白蛋白对表面活性的抑制作用会减弱或消除。例如,即使存在大量白蛋白(100mg/ml),当天然LS浓度大于0.75mg/ml且CLL浓度大于1.5mg/ml时,振荡气泡上的最小动态表面张力也会低于1达因/厘米。同样,在足够高的磷脂浓度下,LS和CLL的吸附功能可免受白蛋白抑制。1.4mM Ca2+离子的存在也减轻了白蛋白对天然LS吸附的抑制作用。这些结果表明,血浆渗出液中的白蛋白有可能在体内严重损害肺泡表面活性剂活性。然而,如果存在磷脂的临界阈值,有害影响将得到缓解。

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