Is smooth muscle growth in primate arteries regulated by endothelial nitric oxide synthase?

被引:15
作者
Mattsson, EJR
Geary, RL
Kraiss, LW
Vergel, S
Liao, JK
Corson, MA
Au, T
Hanson, SR
Clowes, AW
机构
[1] Univ Washington, Sch Med, Dept Surg, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[3] Sahlgrens Univ Hosp, Dept Surg, S-41345 Gothenburg, Sweden
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Surg, Winston Salem, NC 27103 USA
[5] Univ Utah, Sch Med, Dept Surg, Salt Lake City, UT USA
[6] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[7] Emory Univ, Sch Med, Dept Med, Atlanta, GA USA
关键词
D O I
10.1016/S0741-5214(98)70138-7
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose: We investigated whether control of constitutive endothelial cell nitric oxide synthase (cNOS) and nitric oxide (NO) by changes in shear stress might be important for the regulation of smooth muscle cell (SMC) growth and vascular diameter. Methods: Bilateral femoral arteriovenous fistulas were placed in baboons to increase the blood flow in the external iliac arteries. At 2 months, the fistula was ligated on one side to restore normal flow (flow switch). Results: In response to flow switch and a decrease in shear stress, iliac artery lumenal area decreased and SMC proliferation was induced. A decline in NO production, cNOS messenger RNA (mRNA), and protein were associated with these biological effects. In a subset of animals with iliac arteries under high flow infusion of No-nitro-L-arginine, an inhibitor of cNOS, did not induce proliferation. Conclusion: Shear stress can regulate cNOS, vasoconstriction, and SMC proliferation. A decrease in nitric oxide may be necessary, but is not sufficient to induce SMC proliferation in response to a decrease in blood flow.
引用
收藏
页码:514 / 521
页数:8
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