Endothelial nitric oxide synthase mediates cutaneous vasodilation during local heating and is attenuated in middle-aged human skin

被引:101
作者
Bruning, Rebecca S.
Santhanam, Lakshmi [2 ,3 ]
Stanhewicz, Anna E.
Smith, Caroline J.
Berkowitz, Dan E. [2 ,3 ]
Kenney, W. Larry
Holowatz, Lacy A. [1 ]
机构
[1] Penn State Univ, Dept Kinesiol, Noll Lab 113, University Pk, PA 16802 USA
[2] Johns Hopkins Univ, Sch Med, Dept Anesthesia & Crit Care Med, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Bioengn, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
inducible nitric oxide synthase; neuronal nitric oxide synthase; skin blood flow; vascular aging; MICROVASCULAR FUNCTION; HYPERCHOLESTEROLEMIC HUMANS; BLOOD-FLOW; IN-VIVO; MECHANISMS; ACETYLCHOLINE; CIRCULATION; DYSFUNCTION; INHIBITION;
D O I
10.1152/japplphysiol.01354.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Bruning RS, Santhanam L, Stanhewicz AE, Smith CJ, Berkowitz DE, Kenney WL, Holowatz LA. Endothelial nitric oxide synthase mediates cutaneous vasodilation during local heating and is attenuated in middle-aged human skin. J Appl Physiol 112: 2019-2026, 2012. First published April 12, 2012; doi:10.1152/japplphysiol.01354.2011.-Local skin heating is used to assess microvascular function in clinical populations because NO is required for full expression of the response; however, controversy exists as to the precise NO synthase (NOS) isoform producing NO. Human aging is associated with attenuated cutaneous vasodilation but little is known about the middle aged, an age cohort used for comparison with clinical populations. We hypothesized that endothelial NOS (eNOS) is the primary isoform mediating NO production during local heating, and eNOS-dependent vasodilation would be reduced in middle-aged skin. Vasodilation was induced by local heating (42 degrees C) and during acetylcholine dose-response (ACh-DR: 0.01, 0.1, 1.0, 5.0, 10.0, 50.0, 100.0 mmol/l) protocols. Four microdialysis fibers were placed in the skin of 24 men and women; age cohorts were 12 middle-aged (53 +/- 1 yr) and 12 young (23 +/- 1 yr). Sites served as control, nonselective NOS inhibited [N-G-nitro-L-arginine methyl ester (L-NAME)], inducible NOS (iNOS) inhibited (1400W), and neuronal NOS (nNOS) inhibited (N-omega-propyl-L-arginine). After full expression of the local heating response, L-NAME was perfused at all sites. Cutaneous vascular conductance was measured and normalized to maximum (%CVCmax: Nitropress). L-NAME reduced %CVCmax at baseline, all phases of the local heating response, and at all ACh concentrations compared with all other sites. iNOS inhibition reduced the initial peak (53 +/- 2 vs. 60 +/- 2%CVCmax; P < 0.001); however, there were no other differences between control, nNOS-, and iNOS-inhibited sites during the phases of local heating or ACh-DR. When age cohorts were compared, NO-dependent vasodilation during local heating (52 +/- 6 vs. 68 +/- 4%CVCmax; P = 0.013) and ACh perfusion (50 mmol/l: 83 +/- 3 vs. 93 +/- 2%CVCmax; 100 mmol/l: 83 +/- 4 vs. 92 +/- 3%CVCmax; both P = 0.03) were reduced in middle-aged skin. There were no differences in NOS isoform expression obtained from skin biopsy samples between groups (all P > 0.05). These data suggest that eNOS mediates the production of NO during local heating and that cutaneous vasodilation is attenuated in middle-aged skin.
引用
收藏
页码:2019 / 2026
页数:8
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