Heart Center, First Hospital, Tsinghua University, Beijing, China.
Pharm Biol. 2013 Apr;51(4):463-73. doi: 10.3109/13880209.2012.740052. Epub 2013 Jan 22.
Peroxynitrite (ONOO(-)) formation triggers oxidative/nitrative stress and contributes to exacerbated myocardial ischemia/reperfusion (MI/R) injury. Catalpol, an iridoid glycoside, abundantly found in the roots of Rehmannia glutinosa L. that is included in the family Phrymaceae in the order Lamiales, endemic to China, was found to have neuroprotective effects. However, the effect of catalpol on MI/R injury has not been identified.
This study investigated whether catalpol attenuates oxidative/nitrative stress in acute MI/R.
Adult male rats were subjected to 30 min of myocardial ischemia and 3 h of reperfusion and were treated with saline, catalpol (5 mg/kg, i.p., 5 min before reperfusion) or catalpol plus wortmannin (15 µg/kg intraperitoneally injected 15 min before reperfusion).
Pretreatment with catalpol significantly improved cardiac functions, reduced myocardial infarction, apoptosis and necrosis of cardiomyocytes after MI/R (all p < 0.05). Meanwhile, ONOO(-) formation was markedly reduced after catalpol treatment (3.01 ± 0.22 vs. 4.66 ± 0.53 pmol/mg protein in vehicle, p < 0.05). In addition, catalpol increased Akt and endothelial nitric oxide synthase phosphorylation, nitric oxide (NO) production, anti-oxidant capacity and reduced MI/R-induced inducible nitric oxide synthase expression and superoxide anion (·O(2)(-)) production in I/R hearts. PI3K inhibitor wortmannin not only blocked catalpol-induced Akt activation, but also attenuated all the beneficial effects of catalpol. Suppression of ONOO(-) formation by either catalpol or an ONOO(-) scavenger uric acid (5 mg/kg) reduced myocardial infarct size in MI/R rats.
In conclusion, catalpol affords cardioprotection against MI/R insult by attenuating ONOO(-) formation, which is attributable to increased physiological NO and decreased ·O(2)(-) production.
过氧亚硝酸盐(ONOO(-))的形成会引发氧化/硝化应激,并导致心肌缺血/再灌注(MI/R)损伤加剧。梓醇是玄参科列当目列当属植物地黄的根茎中大量存在的环烯醚萜苷,具有神经保护作用。然而,梓醇对 MI/R 损伤的影响尚未确定。
本研究旨在探讨梓醇是否能减轻急性 MI/R 中的氧化/硝化应激。
成年雄性大鼠进行 30 分钟心肌缺血和 3 小时再灌注,并给予生理盐水、梓醇(再灌注前 5 分钟腹腔内 5mg/kg)或梓醇加渥曼青霉素(再灌注前 15 分钟腹腔内 15μg/kg)处理。
梓醇预处理显著改善了心脏功能,减少了 MI/R 后心肌梗死、心肌细胞凋亡和坏死(均 p<0.05)。同时,梓醇处理后 ONOO(-)的形成明显减少(药物组 3.01±0.22 比对照组 4.66±0.53 pmol/mg 蛋白,p<0.05)。此外,梓醇增加了 Akt 和内皮型一氧化氮合酶的磷酸化、一氧化氮(NO)的产生、抗氧化能力,并减少了 MI/R 诱导的诱导型一氧化氮合酶表达和超氧阴离子(·O(2)(-))的产生。PI3K 抑制剂渥曼青霉素不仅阻断了梓醇诱导的 Akt 激活,而且还减弱了梓醇的所有有益作用。梓醇或 ONOO(-)清除剂尿酸(5mg/kg)抑制 ONOO(-)的形成,均减少了 MI/R 大鼠的心肌梗死面积。
综上所述,梓醇通过减轻 ONOO(-)的形成提供了对 MI/R 损伤的心脏保护作用,这归因于生理 NO 的增加和·O(2)(-)的产生减少。