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首页> 外文期刊>Korean Circulation Journal >The Effect of L-arginine on Neointima Formation in a Rat Vascular Injury Model
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The Effect of L-arginine on Neointima Formation in a Rat Vascular Injury Model

机译:L-精氨酸对大鼠血管损伤模型新内膜形成的影响

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Background The inhibitory effects of nitric oxide(NO) on platelet adhesion and vascular smooth muscle cell(VSMC) proliferation may have a possible role inhibiting development of neointima following balloon catheter induced injury. We tested the hypothesis that L-arginine, the precursor of NO, would attenuate neointima formation following balloon catheter induced injury via regulation of antagonistic balance between proliferation and apoptosis of VSMC. Methods Adult, male Sprague-Dawley rats(300 to 400g) were anesthetized with ketamine (100mg/kg intraperitoneally). The left common and external carotid artery were exposed. For endothelial denudation, 2mm angioplasty catheter was introduced through the left external carotid artery into the left common carotid artery. The catheter was inflated at I atm. and withdrawn three times. Animals were randomized to receive 2.25% L-arginine in their drinking water(n=14) or placebo(n=16) from 2 days prior to and 9 days following denudation. VSMC proliferation was quantified by immunohistochemical staining with an antibody to the proliferating cell nuclear antigen(PCNA). The cells undergoing apoptosis were identified by terminal nucleotidyl transferase-mediated nick end labeling(TUNEL) method and morphologic changes by computerized planimetry and transmission electron microscopy. Results 1) The neointimal area in injured arteries were significantly reduced in L-arginine supplemented animals compared with placebo group(p Conclusion These results suggested that the inhibitory effect of L-arginine on neointima formation is due to reduced VSMC proliferation, but is not due to increased VSMC apoptosis at the early time period after initmal injur.
机译:背景一氧化氮(NO)对血小板粘附和血管平滑肌细胞(VSMC)增殖的抑制作用可能具有抑制球囊导管诱发的损伤后新内膜发展的可能作用。我们测试了以下假设:NO的前体L-精氨酸会通过调节VSMC增殖与凋亡之间的拮抗平衡来减轻球囊导管诱发的损伤后新内膜的形成。方法用氯胺酮(100mg / kg)腹膜内麻醉成年雄性Sprague-Dawley大鼠(300至400g)。暴露左颈总动脉和颈外动脉。对于内皮剥脱术,将2mm血管成形导管通过左颈外动脉插入左颈总动脉。导管在1 atm充气。然后撤了三遍从剥脱前2天和剥脱后9天开始,将动物随机接受饮用水(n = 14)或安慰剂(n = 16)中的2.25%L-精氨酸。 VSMC增殖通过免疫组织化学染色对增殖细胞核抗原(PCNA)的抗体进行定量。通过末端核苷酸转移酶介导的缺口末端标记法(TUNEL)鉴定经历凋亡的细胞,并通过计算机化平面仪和透射电镜观察形态学变化。结果1)与安慰剂组相比,补充L-精氨酸的动物受伤动脉的新内膜面积明显减少(p结论)这些结果表明,L-精氨酸对新内膜形成的抑制作用是由于VSMC增殖减少,而不是原因损伤后早期的VSMC凋亡增加。

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