Nelson S, Summer W R, Jakab G J
Am Rev Respir Dis. 1985 Jun;131(6):923-7. doi: 10.1164/arrd.1985.131.6.923.
Respiratory infections are frequently observed in patients with chronic obstructive pulmonary disease, indicating that host defenses are compromised. Antibacterial defenses of the lung against such infections include the alveolar macrophage and polymorphonuclear leukocytes (PMN) that migrate into the lung to provide auxiliary phagocytic defenses. To test the hypothesis that aminophylline acutely impairs pulmonary antibacterial defenses, mice were challenged by aerosol inhalation with Staphylococcus aureus or Proteus mirabilis and injected intraperitoneally with aminophylline (20, 40, or 80 mg/kg). Pulmonary bactericidal activity and total lavaged lung cell and differential counts were determined 4 h after bacterial challenge. The highest dose of aminophylline suppressed the killing of S. aureus so that 55 +/- 5% of the initial viable bacteria remained as compared with 22 +/- 4% in the control animals. In contrast, there was a dose-related suppression of pulmonary antibacterial defenses against gram-negative bacteria. With doses of 40 and 80 mg/kg, lung defenses were ablated, allowing the proliferation of P. mirabilis to 115 +/- 9% and 253 +/- 9%, respectively, the control value being 26 +/- 3%. The number of PMN obtained by lavage after aerosol challenge with P. mirabilis was also inhibited by aminophylline in a dose-dependent manner. From the lungs of untreated animals 5.0 +/- 0.3 X 10(6) PMN were recovered as compared with 3.3 +/- 0.1 X 10(6), 2.5 +/- 0.2 X 10(6), and 1.8 +/- 0.1 X 10(6), respectively, with increasing doses of aminophylline. The bactericidal activity of lavaged PMN from the lungs of aminophylline-treated rats challenged with the gram-negative bacterium in vivo was significantly depressed when compared with that in control animals.(ABSTRACT TRUNCATED AT 250 WORDS)
慢性阻塞性肺疾病患者经常出现呼吸道感染,这表明宿主防御功能受损。肺部针对此类感染的抗菌防御包括肺泡巨噬细胞和迁移至肺部以提供辅助吞噬防御的多形核白细胞(PMN)。为了验证氨茶碱会急性损害肺部抗菌防御这一假说,通过雾化吸入金黄色葡萄球菌或奇异变形杆菌对小鼠进行攻击,并腹腔注射氨茶碱(20、40或80毫克/千克)。在细菌攻击后4小时测定肺部杀菌活性、总灌洗肺细胞数量及分类计数。最高剂量的氨茶碱抑制了金黄色葡萄球菌的杀灭,使得初始活菌的55±5%留存下来,而对照动物中这一比例为22±4%。相比之下,针对革兰氏阴性菌的肺部抗菌防御存在剂量相关的抑制。使用40和80毫克/千克剂量时,肺部防御功能被消除,奇异变形杆菌分别增殖至对照值的115±9%和253±9%,对照值为26±3%。用奇异变形杆菌进行雾化攻击后通过灌洗获得的PMN数量也以剂量依赖方式受到氨茶碱抑制。未处理动物肺部回收5.0±0.3×10⁶个PMN,随着氨茶碱剂量增加,回收数量分别为3.3±0.1×l0⁶个、2.5±0.2×10⁶个和1.8±0.1×10⁶个。与对照动物相比,体内用革兰氏阴性菌攻击的氨茶碱处理大鼠肺部灌洗PMN的杀菌活性显著降低。(摘要截断于250字)