Inhalation of hydrogen gas ameliorates glyoxylate-induced calcium oxalate deposition and renal oxidative stress in mice.
Inhalation of hydrogen gas ameliorates glyoxylate-induced calcium oxalate deposition and renal oxidative stress in mice.
复制标题
吸入氢气可改善乙醛酸诱导的草酸钙沉积和小鼠肾脏氧化应激。
DOI:
--
复制
发表时间:
2015-03
期刊:
影响因子:
--
通讯作者:
Guo, Zhiyong
中科院分区:
文献类型:
--
作者:
Ye, Zhouheng;Gao, Songyan;Sun, Xuejun;Guo, Zhiyong
The aim of this study is to evaluate the protective effect and underlying mechanism of hydrogen gas (H2) to glyoxylate induced renal calcium oxalate (CaOx) crystal deposition in mice. In present work, rodent renal CaOx crystal deposition model was introduced by intra-abdominal injection of glyoxylate (100 mg/kg/d) for 5 days. Two days before administration of glyoxylate, inhalation of H2 for 30 min per day was initiated and continued for 7 days. By the end of the study, the samples of 24 hours urine, serum and renal tissue were collected for biochemical and pathological assay. According to levels of urine calcium excretion, renal calcium deposition, a serum excretion of kidney injury molecule-1 (KIM-1) assay and a TUNEL assay, inhalation of H2 could successfully decrease the CaOx crystallizations and protect against renal injury. Crystal deposition in the kidneys is associated with oxidative stress, which was indicated by increased levels of renal malondialdehyde (MDA) and 8-hydroxydeoxyguanosine (8-OHdG) and decreased activities of superoxide dismutase (SOD), glutathione (GSH) and catalase (CAT). These effects were reversed by a high-dose H2 pretreatment. The renal expressions of osteopontin (OPN), CD44, monocyte chemoattractant protein-1 (MCP-1) and interleukin-10 (IL-10) were markedly increased in glyoxylate-treated mice, and H2 significantly attenuated the increase of OPN, CD44 and MCP-1 but upregulated the expression of IL-10. Our findings demonstrate that inhalation of H2 reduces renal crystallization, renal oxidative injury and inflammation and it may be a candidate agent with few adverse effects for prevention of nephrolithiasis.
登录
查看更多内容
DOI:
10.1016/s0022-5347(18)38369-1
发表时间:
2004-04
期刊:
Journal of the American Society of Nephrology : JASN
影响因子:
--
作者:
M. Asselman;A. Verhulst;M. de Broe;C. Verkoelen
通讯作者:
M. Asselman;A. Verhulst;M. de Broe;C. Verkoelen
DOI:
10.1007/s10157-004-0292-0
发表时间:
2004-06
期刊:
Journal of Clinical and Experimental Nephrology
影响因子:
--
作者:
Saeed R. Khan
通讯作者:
Saeed R. Khan
影响因子:
5
作者:
Jin, Yuanmeng;Liu, Ruijie;Chen, Nan
通讯作者:
Chen, Nan
影响因子:
--
作者:
Khan, SR
通讯作者:
Khan, SR
DOI:
10.1016/j.bbrc.2007.07.088
发表时间:
2007-09-28
影响因子:
3.1
作者:
Fukuda, Kei-Ichi;Asoh, Sadamitsu;Ohta, Shigeo
通讯作者:
Ohta, Shigeo