Immersing lungs in hydrogen-rich saline attenuates lung ischaemia-reperfusion injury

被引:21
作者
Takahashi, Mamoru [1 ]
Chen-Yoshikawa, Toyofumi F. [1 ]
Saito, Masao [1 ]
Tanaka, Satona [1 ]
Miyamoto, Ei [1 ]
Ohata, Keiji [1 ]
Kondo, Takeshi [1 ]
Motoyama, Hideki [1 ]
Hijiya, Kyoko [1 ]
Aoyama, Akihiro [1 ]
Date, Hiroshi [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Thorac Surg, Kyoto, Japan
关键词
Lung ischaemia-reperfusion injury; Lung preservation; Hydrogen-rich solution; RATS; TRANSPLANTATION; GRAFT; DYSFUNCTION; PROTECTION; MODEL;
D O I
10.1093/ejcts/ezw342
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES: Anti-oxidant effects of hydrogen have been reported in studies examining ischaemia-reperfusion injury (IRI). In this study, we evaluated the therapeutic efficacy of immersing lungs in hydrogen-rich saline on lung IRI. METHODS: Lewis rats were divided into three groups: (i) sham, (ii) normal saline and (iii) hydrogen-rich saline. In the first experiment, the left thoracic cavity was filled with either normal saline or hydrogen-rich saline for 1 h. Then, we measured the hydrogen concentration in the left lung using a sensor gas chromatograph (N = 3 per group). In the second experiment, lung IRI was induced by occlusion of the left pulmonary hilum for 1 h, followed by reperfusion for 3 h. During the ischaemic period, the left thoracic cavity was filled with either normal saline or hydrogen-rich saline. After reperfusion, we assessed lung function, histological changes and cytokine production (N = 5-7 per group). RESULTS: Immersing lungs in hydrogen-rich saline resulted in an elevated hydrogen concentration in the lung (6.9 +/- 2.9 mu mol/1 g lung). After IRI, pulmonary function (pulmonary compliance and oxygenation levels) was significantly higher in the hydrogen-rich saline group than in the normal saline group (P < 0.05). Similarly, pro-inflammatory cytokine levels (interleukin-1 beta and interleukin-6) in the left lung were significantly lower in the hydrogen-rich saline group than in the normal saline group (P < 0.05). CONCLUSIONS: Immersing lungs in hydrogen-rich saline delivered hydrogen into the lung and consequently attenuated lung IRI. Hydrogen-rich solution appears to be a promising approach to managing lung IRI.
引用
收藏
页码:442 / 448
页数:7
相关论文
共 26 条
[1]   Hydrogen-Rich University of Wisconsin Solution Attenuates Renal Cold Ischemia-Reperfusion Injury [J].
Abe, Toyofumi ;
Li, Xiao-Kang ;
Yazawa, Koji ;
Hatayama, Naoyuki ;
Xie, Lin ;
Sato, Bunpei ;
Kakuta, Yoichi ;
Tsutahara, Koichi ;
Okumi, Masayoshi ;
Tsuda, Hidetoshi ;
Kaimori, Jun-ya ;
Isaka, Yoshitaka ;
Natori, Michiya ;
Takahara, Shiro ;
Nonomura, Norio .
TRANSPLANTATION, 2012, 94 (01) :14-21
[2]   Protection by 20-5,14-HEDGE Against Surgically Induced Ischemia Reperfusion Lung Injury in Rats [J].
Ali, Irshad ;
Gruenloh, Stephanie ;
Gao, Ying ;
Clough, Anne ;
Falck, John R. ;
Medhora, Meetha ;
Jacobs, Elizabeth R. .
ANNALS OF THORACIC SURGERY, 2012, 93 (01) :282-289
[3]   Treating myocardial ischemia-reperfusion injury by targeting endothelial cell transcription [J].
Boyle, EM ;
Canty, TG ;
Morgan, EN ;
Yun, W ;
Pohlman, TH ;
Verrier, ED .
ANNALS OF THORACIC SURGERY, 1999, 68 (05) :1949-1953
[4]   Hydrogen-Enriched Preservation Protects the Isogeneic Intestinal Graft and Amends Recipient Gastric Function During Transplantation [J].
Buchholz, Bettina M. ;
Masutani, Kosuke ;
Kawamura, Tomohiro ;
Peng, Ximei ;
Toyoda, Yoshiya ;
Billiar, Timothy R. ;
Bauer, Anthony J. ;
Nakao, Atsunori .
TRANSPLANTATION, 2011, 92 (09) :985-992
[5]   Neuroprotective effects of hydrogen saline in neonatal hypoxia-ischemia rat model [J].
Cai, Jianmei ;
Kang, Zhimin ;
Liu, Kan ;
Liu, Wenwu ;
Li, RunPing ;
Zhang, John H. ;
Luo, Xu ;
Sun, Xuejun .
BRAIN RESEARCH, 2009, 1256 :129-137
[6]   Update on ischemia-reperfusion injury in lung transplantation [J].
Chen, Fengshi ;
Date, Hiroshi .
CURRENT OPINION IN ORGAN TRANSPLANTATION, 2015, 20 (05) :515-520
[7]   Modulation of electron transport protects cardiac mitochondria and decreases myocardial injury during ischemia and reperfusion [J].
Chen, Qun ;
Camara, Amadou K. S. ;
Stowe, David F. ;
Hoppel, Charles L. ;
Lesnefsky, Edward J. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2007, 292 (01) :C137-C147
[8]   Lung ischemia-reperfusion injury: a molecular and clinical view on a complex pathophysiological process [J].
den Hengst, Willem A. ;
Gielis, Jan F. ;
Lin, Judy Y. ;
Van Schil, Paul E. ;
De Windt, Leon J. ;
Moens, An L. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2010, 299 (05) :H1283-H1299
[9]   OXYGEN-DEPENDENT LIPID-PEROXIDATION DURING LUNG ISCHEMIA [J].
FISHER, AB ;
DODIA, C ;
TAN, ZT ;
AYENE, I ;
ECKENHOFF, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (02) :674-679
[10]   The Poly(Adenosine Diphosphate-Ribose) Polymerase Inhibitor PJ34 Reduces Pulmonary Ischemia-Reperfusion Injury in Rats [J].
Hatachi, Go ;
Tsuchiya, Tomoshi ;
Miyazaki, Takuro ;
Matsumoto, Keitaro ;
Yamasaki, Naoya ;
Okita, Naoyuki ;
Nanashima, Atsushi ;
Higami, Yoshikazu ;
Nagayasu, Takeshi .
TRANSPLANTATION, 2014, 98 (06) :618-624