Pelaia P, Rocco M, De Blasi R A, Spadetta G, Alampi D, Araimo F S, Nicolucci S
Istituto di Anestesiologia e Rianimazione, Università degli Studi di Roma, La Sapienza.
Minerva Anestesiol. 1995 Apr;61(4):133-9.
To verify and quantify lipidic peroxidation by means of tiobarbituric-acid reactive substance (TBARS) dosage in patients treated daily with HBO. To verify if a potentiated glutathione enzymatic system, with N-acetylcisteine (NAC) treatment, may determine higher HBO tolerance and reduced lipidic peroxidation.
Randomised study on patients treated with 20 HBO 2.2 ATA (90' oxygen) sessions.
Hyperbaric Medical Centre.
Seventeen patients divided, at random, into two groups; group A: 10 patients treated with only HBO; group B: 7 patients treated with NAC antioxidant therapy (Fluimucil, Zambon Group, Italy) 1800 mg/day in addition to HBO.
None.
TBARS on blood sample at T0 (basal) T1 (at the end of the 1st HBO session) T2 (at the beginning of the 20th HBO session) T3 (at the end of the 20th). The group A TBARS analysis at the different study time has shown significant data (p < 0.01) as the difference between TBARS values of the two groups at T2 (p < 0.01).
HBO induces a lipidic peroxidation even if the therapeutical protocol cannot determine lung or cerebral oxygen toxicity symptoms. The NAC administration, during HBO treatment, determines a protection against the HBO radicalic stress.
通过对每日接受高压氧治疗(HBO)的患者进行硫代巴比妥酸反应性物质(TBARS)定量检测,以验证并量化脂质过氧化情况。验证经N - 乙酰半胱氨酸(NAC)治疗增强的谷胱甘肽酶系统是否可提高HBO耐受性并减少脂质过氧化。
对接受20次2.2ATA(90分钟吸氧)HBO治疗的患者进行随机研究。
高压氧医学中心。
17名患者随机分为两组;A组:10名患者仅接受HBO治疗;B组:7名患者除接受HBO治疗外,还接受NAC抗氧化治疗(意大利赞邦集团的福路米可,1800毫克/天)。
无。
在T0(基础值)、T1(第1次HBO治疗结束时)、T2(第20次HBO治疗开始时)、T3(第20次HBO治疗结束时)采集血样检测TBARS。A组在不同研究时间的TBARS分析显示有显著数据(p < 0.01),T2时两组TBARS值差异也有统计学意义(p < 0.01)。
即使治疗方案未引发肺部或脑部氧中毒症状,HBO仍会诱导脂质过氧化。在HBO治疗期间给予NAC可对HBO自由基应激起到保护作用。