Therapeutic effects of concurrent autologous bone marrow cell infusion and metabolic intervention in ischemia-induced angiogenesis in the hypercholesterolemic mouse hindlimb

被引:14
作者
de Nigris, Filomena
Williams-Ignarro, Sharon
Sica, Vincenzo
D'Armiento, Francesco P.
Lerman, Lilach O.
Byrns, Russell E.
Sica, Giacomo
Fiorito, Carmela
Ignarro, Louis J.
Napoli, Claudio [1 ]
机构
[1] Univ Naples Federico II, Sch Med 1, Dept Gen Pathol, Div Clin Pathol & Excellence Res Ctr Cardiovasc D, I-80138 Naples, Italy
[2] Univ Calif Los Angeles, David Geffen Sch Med, Div Anesthesiol, Los Angeles, CA 90095 USA
[3] Univ Naples Federico II, Sch Med 2, Dept Biomorphol Sci, I-80131 Naples, Italy
[4] Mayo Coll Med, Div Hypertens, Rochester, MN USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol Pharmacol, Los Angeles, CA 90095 USA
关键词
bone marrow cell; hypercholesterolemia; ischemic hindlimb; peripheral arterial disease; L-arginine; antioxidants; nitric oxide;
D O I
10.1016/j.ijcard.2006.05.020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lower-limb ischemia is a major health problem especially when associated to hypercholesterolemia. Because of the absence of effective treatment in the advanced stages of the disease, amputation is undertaken to alleviate unbearable symptoms. Since tissue ischemia and hypercholesterolemia are associated with an overwhelming generation of oxygen radicals, metabolic intervention with antioxidants and L-arginine can induce beneficial effects beyond those achieved by a novel therapeutic approach represented by the use of autologous bone marrow cells (BMCs). The protective effect of BMCs and vascular protection by metabolic cotreatment (1.0% vitamin E added to the chow, 0.05% vitamin C and 6% L-arginine added to the drinking water) were examined in ischemia-induced angiogenesis in the hypercholesterolemic mouse hindlimb. Intravenous BMC therapy improved blood flow and increased capillary densities. This beneficial effect was amplified by metabolic cotreatment, an intervention inducing vascular protection, at least in part, through the nitric oxide pathway, reduction of systemic oxidative stress and macrophage activation. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:238 / 243
页数:6
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