Division of Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic College of Medicine, Rochester, MN, USA.
Respir Physiol Neurobiol. 2012 Aug 15;183(2):159-65. doi: 10.1016/j.resp.2012.06.004. Epub 2012 Jul 3.
Previous studies have demonstrated an important role for beta-2 adrenergic receptors (β(2)AR) in lung fluid clearance. The purpose of this investigation was to examine the relationship between β(2)AR density on lymphocytes and indices of lung water in healthy humans exposed to ≈ 17 h of hypoxia (FIO2 = 12.5% in a hypoxia tent).
Thirteen adults (mean ± SEM; age=31 ± 3 years, BMI=24 ± 1 kg/m(2), VO2 Peak = 40 ± 2 ml/kg/min ) participated. Pulmonary function, CT derived lung tissue volume (V(tis)-tissue, blood and water), lung diffusing capacity for carbon monoxide (D(CO)) and nitric oxide (D(NO)), alveolar-capillary conductance (D(M)), pulmonary capillary blood volume (V(c)) and lung water (CT V(tis)-V(c)) were assessed before and after ≈ 17 h normobaric hypoxia (FIO2 = 12.5%). β(2)AR density on lymphocytes was measured via radioligand binding. Arterial oxygen saturation (SaO2), cardiac output (Q), right ventricular systolic pressure (RVSP) and blood pressure (BP) were also assessed.
After 17 h hypoxia, SaO2 decreased from 97 ± 1 (normoxia) to 82 ± 4% and RVSP increased from 14 ± 3 (normoxia) to 29 ± 2 mmHg (p<0.05) with little change in Q or BP. V(c) and D(M) both increased with hypoxia with a small increase in D(M)/V(c) ratio (p>0.05). CT V(tis) decreased and lung water was estimated to decline 7 ± 13%, respectively. β(2)AR density averaged 1497 ± 187 receptors/lymphocyte and increased 21 ± 34% with hypoxia (range -31 to +86%). The post-hypoxia increase in β(2)AR density was significantly related to the reduction in lung water (r=-0.64, p<0.05), with the subjects with the greatest increase in density demonstrating the largest decline in lung water.
Lung water decreases with 17 h normobaric hypoxia are associated with changes in beta adrenergic receptor density on lymphocytes in healthy adults.
先前的研究表明β-2 肾上腺素能受体(β(2)AR)在肺液清除中起重要作用。本研究的目的是检查健康人暴露于 ≈ 17 小时低氧(在低氧帐篷中 FIO2 = 12.5%)时淋巴细胞上的 β(2)AR 密度与肺水指数之间的关系。
13 名成年人(平均 ± SEM;年龄=31 ± 3 岁,BMI=24 ± 1 kg/m(2),峰值 VO2 = 40 ± 2 ml/kg/min)参与了研究。在 ≈ 17 小时常压低氧(FIO2 = 12.5%)前后评估了肺功能、CT 衍生的肺组织体积(V(tis)-组织、血液和水)、一氧化碳弥散量(D(CO))和一氧化氮(D(NO))、肺泡毛细血管传导率(D(M))、肺毛细血管血容量(V(c))和肺水(CT V(tis)-V(c))。通过放射性配体结合测量淋巴细胞上的 β(2)AR 密度。还评估了动脉血氧饱和度(SaO2)、心输出量(Q)、右心室收缩压(RVSP)和血压(BP)。
低氧 17 小时后,SaO2 从 97 ± 1(常氧)降至 82 ± 4%,RVSP 从 14 ± 3(常氧)升至 29 ± 2 mmHg(p<0.05),Q 或 BP 无明显变化。V(c)和 D(M)均随低氧增加,D(M)/V(c)比值略有增加(p>0.05)。CT V(tis)下降,肺水估计分别下降 7 ± 13%。β(2)AR 密度平均为 1497 ± 187 个/淋巴细胞,低氧时增加 21 ± 34%(范围 -31 至 +86%)。低氧后β(2)AR 密度的增加与肺水的减少呈显著相关(r=-0.64,p<0.05),密度增加最大的受试者肺水下降最大。
健康成年人在 17 小时常压低氧时肺水减少与淋巴细胞上β肾上腺素能受体密度的变化有关。