Department of Surgery, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.
Mol Med. 2012 May 9;18(1):676-84. doi: 10.2119/molmed.2011.00103.
Nitric oxide (NO) derived from endothelial nitric oxide synthase (eNOS) is a potent vasodilator and signaling molecule that plays an essential role in vascular remodeling of collateral arteries and perfusion recovery in response to hindlimb ischemia. In ischemic conditions, decreased NO bioavailability was observed because of increased oxidative stress, decreased L-arginine and tetrahydrobiopterin. This study tested the hypothesis that dietary cosupplementation with tetrahydrobiopterin (BH4), L-arginine, and vitamin C acts synergistically to decrease oxidative stress, increase nitric oxide and improve blood flow in response to acute hindlimb ischemia. Rats were fed normal chow, chow supplemented with BH4 or L-arginine (alone or in combination) or chow supplemented with BH4 + L-arginine + vitamin C for 1 wk before induction of unilateral hindlimb ischemia. Cosupplementation with BH4 + L-arginine resulted in greater eNOS expression, Ca²⁺-dependent NOS activity and NO concentration in gastrocnemius from the ischemic hindlimb, as well as greater recovery of foot perfusion and more collateral artery enlargement than did rats receiving either agent separately. The addition of vitamin C to the BH4 + L-arginine regimen did further increase these dependent variables, although only the increase in eNOS expression reached statistical significances. In addition, rats given all three supplements demonstrated significantly less Ca²⁺-independent activity, less nitrotyrosine accumulation, greater glutathione:glutathione disulfide (GSH:GSSG) ratio and less gastrocnemius muscle necrosis, on both macroscopic and microscopic levels. In conclusion, cosupplementation with BH4 + L-arginine + vitamin C significantly increased vascular perfusion after hindlimb ischemia by increasing eNOS activity and reducing oxidative stress and tissue necrosis. Oral cosupplementation of L-arginine, BH4 and vitamin C holds promise as a biological therapy to induce collateral artery enlargement.
一氧化氮(NO)来源于内皮型一氧化氮合酶(eNOS),是一种强效的血管舒张因子和信号分子,在侧支动脉血管重塑和对后肢缺血的灌流恢复中发挥着重要作用。在缺血条件下,由于氧化应激增加、L-精氨酸和四氢生物蝶呤减少,导致 NO 的生物利用度降低。本研究旨在检验如下假设,即联合补充四氢生物蝶呤(BH4)、L-精氨酸和维生素 C 可协同作用,降低氧化应激、增加一氧化氮并改善急性后肢缺血后的血流。在诱导单侧后肢缺血前,大鼠连续 1 周分别喂食正常饲料、补充 BH4 或 L-精氨酸(单独或联合)的饲料、补充 BH4+L-精氨酸+维生素 C 的饲料。联合补充 BH4+L-精氨酸可使缺血后肢比目鱼肌中的 eNOS 表达、Ca²⁺依赖性 NOS 活性和 NO 浓度增加,以及足部灌流恢复更好,侧支动脉扩张更明显,而单独给予任何一种药物的大鼠则没有上述效果。将维生素 C 加入 BH4+L-精氨酸方案中,可进一步增加这些依赖变量,尽管只有 eNOS 表达的增加具有统计学意义。此外,在宏观和微观水平上,所有三种补充剂均可显著降低 Ca²⁺非依赖性活性、硝基酪氨酸积累、增加谷胱甘肽:谷胱甘肽二硫化物(GSH:GSSG)比值、减少比目鱼肌坏死。综上所述,联合补充 BH4+L-精氨酸+维生素 C 可通过增加 eNOS 活性、降低氧化应激和组织坏死,显著增加后肢缺血后的血管灌注。联合补充 L-精氨酸、BH4 和维生素 C 具有作为诱导侧支动脉扩张的生物治疗的潜力。