TY - JOUR
T1 - Oral intake of hydrogen-rich water inhibits intimal hyperplasia in arterialized vein grafts in rats
AU - Sun, Qiang
AU - Kawamura, Tomohiro
AU - Masutani, Kosuke
AU - Peng, Ximei
AU - Sun, Qing
AU - Stolz, Donna B.
AU - Pribis, John P.
AU - Billiar, Timothy R.
AU - Sun, Xuejun
AU - Bermudez, Christian A.
AU - Toyoda, Yoshiya
AU - Nakao, Atsunori
N1 - Funding Information:
This work was supported by the China Scholarship Council (Q.S.), Daimaru Research Foundation (Q.S.), National Institutes of Health (R21 HL102528-01 to A.N.) and research funds of the Department of Cardiothoracic Surgery. T.K. is a recipient of the Thomas E. Starzl Postdoctoral fellowship.
PY - 2012/4/1
Y1 - 2012/4/1
N2 - Aims: Arterialized vein grafts often fail due to intimal hyperplasia. Hydrogen potently protects organs and cells from many insults via its anti-inflammatory and antioxidant properties. We investigated the efficacy of oral administration of hydrogen-rich water (HW) for prevention of intimal hyperplasia. Methods and results: The inferior vena cava was excised, stored in cold Ringer solution for 2 h, and placed as an interposition graft in the abdominal aorta of syngeneic Lewis rats. HW was generated by immersing a magnesium stick in tap water (Mg 2H2O → Mg (OH)2 H2). Beginning on the day of graft implantation, recipients were given tap water [regular water (RW)], HW or HW that had been subsequently degassed water (DW). Six weeks after grafting, the grafts in the rats given RW or DW had developed intimal hyperplasia, accompanied by increased oxidative injury. HW significantly suppressed intimal hyperplasia. One week after grafting, the grafts in HW-treated rats exhibited improved endothelial integrity with less platelet and white blood cell aggregation. Up-regulation of the mRNAs for intracellular adhesion molecules was attenuated in the vein grafts of the rats receiving HW. Activation of p38 mitogen-activated protein kinase, matrix metalloproteinase (MMP)-2, and MMP-9 was also significantly inhibited in grafts receiving HW. In rat smooth muscle cell (A7r5) cultures, hydrogen treatment for 24 h reduced smooth muscle cell migration. Conclusion: Drinking HW significantly reduced neointima formation after vein grafting in rats. Drinking HW may have therapeutic value as a novel therapy for intimal hyperplasia and could easily be incorporated into daily life. Published on behalf of the European Society of Cardiology. All rights reserved.
AB - Aims: Arterialized vein grafts often fail due to intimal hyperplasia. Hydrogen potently protects organs and cells from many insults via its anti-inflammatory and antioxidant properties. We investigated the efficacy of oral administration of hydrogen-rich water (HW) for prevention of intimal hyperplasia. Methods and results: The inferior vena cava was excised, stored in cold Ringer solution for 2 h, and placed as an interposition graft in the abdominal aorta of syngeneic Lewis rats. HW was generated by immersing a magnesium stick in tap water (Mg 2H2O → Mg (OH)2 H2). Beginning on the day of graft implantation, recipients were given tap water [regular water (RW)], HW or HW that had been subsequently degassed water (DW). Six weeks after grafting, the grafts in the rats given RW or DW had developed intimal hyperplasia, accompanied by increased oxidative injury. HW significantly suppressed intimal hyperplasia. One week after grafting, the grafts in HW-treated rats exhibited improved endothelial integrity with less platelet and white blood cell aggregation. Up-regulation of the mRNAs for intracellular adhesion molecules was attenuated in the vein grafts of the rats receiving HW. Activation of p38 mitogen-activated protein kinase, matrix metalloproteinase (MMP)-2, and MMP-9 was also significantly inhibited in grafts receiving HW. In rat smooth muscle cell (A7r5) cultures, hydrogen treatment for 24 h reduced smooth muscle cell migration. Conclusion: Drinking HW significantly reduced neointima formation after vein grafting in rats. Drinking HW may have therapeutic value as a novel therapy for intimal hyperplasia and could easily be incorporated into daily life. Published on behalf of the European Society of Cardiology. All rights reserved.
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U2 - 10.1093/cvr/cvs024
DO - 10.1093/cvr/cvs024
M3 - Article
C2 - 22287575
AN - SCOPUS:84859088927
SN - 0008-6363
VL - 94
SP - 144
EP - 153
JO - Cardiovascular research
JF - Cardiovascular research
IS - 1
ER -