Nishida T, Hayashi T, Inamoto T, Kato R, Ibuki N, Takahara K, Takai T, Yoshikawa Y, Uchimoto T, Saito K, Tanda N, Kouno J, Minami K, Uehara H, Hirano H, Nomi H, Okada Y, Azuma H
Department of Urology, Osaka Medical College, Osaka, Japan; Department of Urology, Matsubara Tokushukai Hospital, Osaka, Japan.
Laboratory of Cardiovascular Pharmacotherapy and Toxicology, Osaka University of Pharmaceutical Sciences, Osaka, Japan.
Transplant Proc. 2018 Jan-Feb;50(1):250-258. doi: 10.1016/j.transproceed.2017.12.014.
Hydrogen (H) and carbon monoxide (CO) gas are both reported to reduce reactive oxygen species and alleviate tissue ischemia-reperfusion (I-R) injury. The present study was conducted to evaluate the effects of a mixture of H gas and CO gas (dual gas) in comparison with hydrogen gas (H: 2%) alone on I-R renal injury (composition of dual gas; N: 77.8%; O: 20.9%; H: 1.30%; CO: 250 parts per million).
Adult male Sprague-Dawley rats (body weight 250-280 g) were divided into 5 groups: (1) sham operation control, (2) dual gas inhalation (dual treatment) without I-R treatment, (3) I-R renal injury, (4) H gas alone inhalation (H treatment) with I-R renal injury, and (5) dual treatment with I-R renal injury. I-R renal injury was induced by clamping the left renal artery and vein for 45 minutes followed by reperfusion, and then contralateral nephrectomy was performed 2 weeks later. Renal function was markedly decreased at 24 hours after reperfusion, and thereafter the effects of dual gas were assessed by histologic examination and determination of the superoxide radical, together with functional and molecular analyses.
Pathologic examination of the kidney of I-R rats revealed severe renal damage. Importantly, cytoprotective effects of the dual treatment in comparison with H treatment and I-R renal injury were observed in terms of superoxide radical scavenging activity and histochemical features. Rats given dual treatment and I-R renal injury showed significant decreases in blood urea nitrogen. Increased expression of several inflammatory cytokines (tumor necrosis factor-α, interleukin-6, intracellular adhesion molecule-1, nuclear factor-κB, hypoxia inducible factor-1α, and heme oxygenase-1) was attenuated by the dual treatment.
Dual gas inhalation decreases oxidative stress and markedly improves I-R-induced renal injury.
据报道,氢气(H)和一氧化碳(CO)气体均可减少活性氧并减轻组织缺血再灌注(I-R)损伤。本研究旨在评估氢气和一氧化碳气体混合物(双气体)与单独使用氢气(H:2%)相比对I-R肾损伤的影响(双气体组成;N:77.8%;O:20.9%;H:1.30%;CO:百万分之250)。
成年雄性Sprague-Dawley大鼠(体重250-280g)分为5组:(1)假手术对照组,(2)吸入双气体(双治疗)但未进行I-R处理,(3)I-R肾损伤组,(4)单独吸入氢气(H治疗)并伴有I-R肾损伤,(5)双治疗并伴有I-R肾损伤。通过夹闭左肾动脉和静脉45分钟后再灌注诱导I-R肾损伤,然后在2周后进行对侧肾切除术。再灌注后24小时肾功能显著下降,此后通过组织学检查、超氧阴离子测定以及功能和分子分析评估双气体的作用。
I-R大鼠肾脏的病理检查显示严重肾损伤。重要的是,在超氧阴离子清除活性和组织化学特征方面,观察到双治疗与H治疗及I-R肾损伤相比具有细胞保护作用。接受双治疗并伴有I-R肾损伤的大鼠血尿素氮显著降低。双治疗减弱了几种炎性细胞因子(肿瘤坏死因子-α、白细胞介素-6、细胞间黏附分子-1、核因子-κB、缺氧诱导因子-1α和血红素加氧酶-1)的表达增加。
吸入双气体可降低氧化应激并显著改善I-R诱导的肾损伤。