Ozdulger Ali, Cinel Ismail, Koksel Oguz, Cinel Leyla, Avlan Dincer, Unlu Ali, Okcu Hulya, Dikmengil Murat, Oral Ugur
Department of Thoracic and Cardiovascular Surgery, Mersin University School of Medicine, Mersin, Turkey.
Shock. 2003 Apr;19(4):366-72. doi: 10.1097/00024382-200304000-00012.
Apoptotic loss of parenchymal cells may lead to organ dysfunctions in critically ill patients with septic states. As an antioxidant, the protective effects of N-acetylcysteine (NAC) are documented in many experimental and clinical studies. In this experimental study, we investigated the role of chronically used NAC in septic lung injury on a cecal ligation and puncture (CLP) model. To evaluate this, 30 male Wistar rats were randomly divided into four groups as sham (n = 7), CLP (n = 8), sham + NAC (n = 7) and CLP + NAC (n = 8) groups. NAC was administered 150 mg kg(-1) day through intramuscular route beginning 6 h after the operations and lasting for a period of 1 week. One week later, histopathology and epithelial apoptosis were assessed by hematoxylin-eosin and immunohistochemically by M30 and caspase 3 staining to demonstrate septic lung injury. Additionally, lung tissue myeloperoxidase (MPO) activity, malondialdehyde (MDA), and nitrite/nitrate levels were measured. The MPO activity and MDA levels in lung homogenates were found to be increased in CLP group and the administration of NAC prevented their increase significantly (P < 0.05). However, there were no significant differences among the groups regarding nitrite/nitrate levels. The number of apoptotic cells was significantly lower in CLP+NAC group than CLP group, and this finding was supported by M30 and caspase 3 expression in lung (P < 0.05). Lung histopathology was also protected by NAC in CLP-induced sepsis. In conclusion, the chronic use of NAC inhibited MPO activity and lipid peroxidation, which resulted in reduction of apoptosis in lung in this CLP model. Because lung tissue nitrite/nitrate levels did not change significantly, organs other than the lungs may be responsible for producing the increased nitric oxide during sepsis. The chronic use of NAC needs further investigation for its possible antiapoptotic potential in septic states besides its documented antioxidant and antiinflammatory effects.
在脓毒症状态的重症患者中,实质细胞的凋亡性损失可能导致器官功能障碍。作为一种抗氧化剂,N-乙酰半胱氨酸(NAC)的保护作用在许多实验和临床研究中都有记载。在本实验研究中,我们在盲肠结扎和穿刺(CLP)模型上研究了长期使用NAC在脓毒症肺损伤中的作用。为了评估这一点,将30只雄性Wistar大鼠随机分为四组,即假手术组(n = 7)、CLP组(n = 8)、假手术+NAC组(n = 7)和CLP + NAC组(n = 8)。术后6小时开始通过肌肉注射途径给予NAC,剂量为150 mg kg(-1) 天,持续1周。1周后,通过苏木精-伊红染色评估组织病理学和上皮细胞凋亡,并通过M30和半胱天冬酶3染色进行免疫组织化学检测以证明脓毒症肺损伤。此外,还测量了肺组织髓过氧化物酶(MPO)活性、丙二醛(MDA)以及亚硝酸盐/硝酸盐水平。发现CLP组肺匀浆中的MPO活性和MDA水平升高,而给予NAC可显著阻止其升高(P < 0.05)。然而,各组之间亚硝酸盐/硝酸盐水平没有显著差异。CLP + NAC组的凋亡细胞数量明显低于CLP组,这一发现得到了肺组织中M30和半胱天冬酶3表达的支持(P < 0.05)。在CLP诱导的脓毒症中,NAC也保护了肺组织病理学。总之,在该CLP模型中,长期使用NAC可抑制MPO活性和脂质过氧化,从而减少肺组织中的细胞凋亡。由于肺组织亚硝酸盐/硝酸盐水平没有明显变化,肺部以外的器官可能是脓毒症期间一氧化氮产生增加的原因。除了已记载的抗氧化和抗炎作用外,长期使用NAC在脓毒症状态下可能的抗凋亡潜力还需要进一步研究。