Tanoue Y, Morita S, Ochiai Y, Haraguchi N, Tominaga R, Kawachi Y, Yasui H
The Department of Cardiovascular Surgery, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
J Thorac Cardiovasc Surg. 1999 Sep;118(3):547-56. doi: 10.1016/S0022-5223(99)70195-9.
Nitric oxide has cardioprotective effects through several mechanisms. However, nitric oxide may have deleterious effects in the presence of superoxide because it is converted to peroxynitrite, which then initiates lipid peroxidation. Using a canine model of orthotopic heart transplantation, we examined whether adding an organic nitric oxide donor, nitroglycerin, to preservation solution elicits lipid peroxidation after reperfusion and causes deleterious effects on coronary endothelial function and left ventricular function.
The donor heart was preserved for 24 hours in cold University of Wisconsin solution with nitroglycerin (0.1 mg/mL) supplementation (group NTG, n = 8) or in standard University of Wisconsin solution (group C, n = 8). After reperfusion, changes of coronary resistance were measured during the infusion of acetylcholine (0.1 mg/min) and of sodium nitroprusside (1 mg/min), and percent coronary relaxation was calculated. Left ventricular function was evaluated by pressure-volume relations with the use of a conductance catheter, thereby deriving the slopes of end-systolic pressure-volume relation, stroke work-end-diastolic volume relation, and maximum rate of change of left ventricular pressure-end-diastolic volume relation. Serum lipid peroxide level was measured. Percent coronary relaxation was similar for the 2 groups. The slopes of end-systolic pressure-volume relation, stroke work-end-diastolic volume relation, and maximum rate of change of left ventricular pressure-end-diastolic volume relation in group NTG were significantly higher than those in group C. On the other side, serum lipid peroxide level in group NTG was significantly higher than that in group C.
Nitroglycerin may have detrimental effects evidenced by the increase in lipid peroxidation, which implied peroxynitrite formation. However, the overall effect of nitroglycerin was cardioprotective. Although the exact mechanism is yet to be clarified, the superb cardioprotective effect of nitroglycerin overwhelms the exaggeration of lipid peroxidation.
一氧化氮通过多种机制发挥心脏保护作用。然而,在超氧化物存在的情况下,一氧化氮可能产生有害影响,因为它会转化为过氧亚硝酸盐,进而引发脂质过氧化。我们使用犬原位心脏移植模型,研究在保存液中添加有机一氧化氮供体硝酸甘油是否会在再灌注后引发脂质过氧化,并对冠状动脉内皮功能和左心室功能产生有害影响。
供体心脏在含硝酸甘油(0.1mg/mL)补充剂的冷威斯康星大学溶液中保存24小时(NTG组,n = 8),或在标准威斯康星大学溶液中保存(C组,n = 8)。再灌注后,在输注乙酰胆碱(0.1mg/min)和硝普钠(1mg/min)期间测量冠状动脉阻力变化,并计算冠状动脉舒张百分比。使用电导导管通过压力-容积关系评估左心室功能,从而得出收缩末期压力-容积关系、每搏功-舒张末期容积关系以及左心室压力-舒张末期容积关系的最大变化率。测量血清脂质过氧化物水平。两组的冠状动脉舒张百分比相似。NTG组的收缩末期压力-容积关系、每搏功-舒张末期容积关系以及左心室压力-舒张末期容积关系的最大变化率均显著高于C组。另一方面,NTG组的血清脂质过氧化物水平显著高于C组。
硝酸甘油可能产生有害影响,脂质过氧化增加证明了这一点,这意味着过氧亚硝酸盐的形成。然而,硝酸甘油的总体作用是心脏保护作用。尽管确切机制尚待阐明,但硝酸甘油卓越的心脏保护作用超过了脂质过氧化的加剧。