Morita Masahiko, Sakurada Masami, Watanabe Fumiko, Yamasaki Tetsuo, Doi Hiroshi, Ezaki Hirotaka, Morishita Koji, Miyakex Takayuki
Function Research Group, Healthcare Products Development Center, KYOWA HAKKO BIO CO., LTD., 2, Miyukigao-ka, Tsukuba, Ibaraki 305-0841, Japan.
Tokorozawa Heart Center, 2-61-11, Kamiarai, Tokorozawa, Saitama 359-1142, Japan.
Immunol Endocr Metab Agents Med Chem. 2013 Sep;13(3):214-220. doi: 10.2174/18715222113139990008.
Decreased nitric oxide (NO) bioavailability and increased lipid oxidation are associated with progressive endothelial dysfunction. L-Citrulline, the effective precursor of L-arginine which is essential as a substrate for endothelial NO synthase (eNOS), is effective in enhancing NO-dependent signaling. However, little is known about the efficacy of L-citrulline supplementation on lipoprotein oxidation and endothelial dysfunction.
Twenty-two patients (aged 41 - 64 years old) diagnosed with vasospastic angina with flow-mediated dilation (FMD) of the brachial artery (< 5.5 %) received 800 mg/day of L-citrulline for 8 weeks. FMD (%), blood NOx, asymmetric dimethylarginine (ADMA), small dense LDL, oxidized lipids, amino acids concentrations were measured before and after supplementation.
Compared with baseline values, FMD (%) was significantly improved at 4 and 8 weeks as well as at 4 weeks after the end of intake. L-Citrulline supplementation caused a significant lowering of plasma ADMA levels. Plasma L-arginine/ADMA ratio and NOx levels rose markedly throughout the study period. Moreover, significant reductions of serum oxidized LDL and lectin-like oxidized LDL receptor 1 (LOX-1) ligand containing ApoB (LAB), an indicator of the biological activity of oxidized lipoprotein binding to LOX-1, were observed after L-citrulline intake.
L-Citrulline supplementation improves endothelial dysfunction, probably due to potentiating NO-dependent reactions and decreasing the state of lipoprotein oxidation in humans.
一氧化氮(NO)生物利用度降低和脂质氧化增加与进行性内皮功能障碍相关。L-瓜氨酸是L-精氨酸的有效前体,而L-精氨酸作为内皮型一氧化氮合酶(eNOS)的底物至关重要,L-瓜氨酸在增强NO依赖性信号传导方面有效。然而,关于补充L-瓜氨酸对脂蛋白氧化和内皮功能障碍的疗效知之甚少。
22例诊断为血管痉挛性心绞痛且肱动脉血流介导的舒张功能(FMD)<5.5%的患者(年龄41 - 64岁),接受800毫克/天的L-瓜氨酸治疗8周。在补充前后测量FMD(%)、血NOx、不对称二甲基精氨酸(ADMA)、小而密低密度脂蛋白、氧化脂质、氨基酸浓度。
与基线值相比,在第4周和第8周以及摄入结束后4周时FMD(%)显著改善。补充L-瓜氨酸导致血浆ADMA水平显著降低。在整个研究期间,血浆L-精氨酸/ADMA比值和NOx水平显著升高。此外,在摄入L-瓜氨酸后,观察到血清氧化型低密度脂蛋白和凝集素样氧化型低密度脂蛋白受体1(LOX-1)配体含载脂蛋白B(LAB,氧化脂蛋白与LOX-1结合的生物活性指标)显著降低。
补充L-瓜氨酸可改善内皮功能障碍,可能是由于增强了人体中NO依赖性反应并降低了脂蛋白氧化状态。