Quantification and interpretation of nitric oxide-dependent cutaneous vasodilation during local heating.

IF 3.3 3区 医学 Q1 PHYSIOLOGY Journal of applied physiology Pub Date : 2024-11-01 Epub Date: 2024-10-17 DOI:10.1152/japplphysiol.00558.2024
S Tony Wolf, Gabrielle A Dillon, Lacy M Alexander, W Larry Kenney, Anna E Stanhewicz
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Abstract

Human cutaneous microdialysis approaches for assessing nitric oxide (NO)-dependent blood flow include local heating (LH) of the skin until a plateau is reached, followed by infusion of a NO synthase inhibitor such as NG-nitro-l-arginine methyl ester (l-NAME); however, varied methods of quantifying and expressing NO-dependent vasodilation can obfuscate data interpretation and reproducibility. We retrospectively assessed NO-dependent vasodilation during LH to 39°C or 42°C, calculated as the 1) absolute contribution of the NO-dependent component (along with baseline and the non-NO-dependent component) to the total cutaneous vascular conductance (CVC) response to LH, normalized to maximal CVC (%CVCmax); 2) difference in %CVCmax (Δ%CVCmax) between the LH plateau and post-NO synthase inhibition (l-NAME plateau; Δ%CVCmax = LH plateau - l-NAME plateau); 3) percentage of the LH plateau attributable to Δ%CVCmax (%plateau = Δ%CVCmax/LH plateau × 100); and 4) %plateau when correcting for baseline. The LH plateaus during 39°C and 42°C were 48 ± 17%CVCmax (9 ± 5% baseline; 2 ± 4% non-NO dependent; 36 ± 15% NO dependent) and 88 ± 10%CVCmax (15 ± 8% baseline; 9 ± 10% non-NO dependent; 64 ± 13% NO dependent), respectively. The absolute contributions of the non-NO-dependent and NO-dependent components of the response (P < 0.0001) and the Δ%CVCmax (66 ± 14 vs. 38 ± 15%) were greater during 42°C compared with 39°C (all P ≤ 0.02); however, there were no differences between the two protocols in %plateau (75 ± 13 vs. 80 ± 10%; P = 0.57) or %plateauBL (88 ± 14 vs. 95 ± 8%; P = 0.31). For both protocols, the values were greater for %plateauBL versus Δ%CVCmax and %plateau (P ≤ 0.0001), and for %plateau versus Δ%CVCmax (P ≤ 0.05). Quantification of NO-dependent skin vasodilation responses to LH is dependent upon the mathematical approach and verbal description, which can meaningfully impact data interpretation and reproducibility.NEW & NOTEWORTHY Local heating protocols are commonly used in conjunction with intradermal microdialysis for assessing nitric oxide (NO)-dependent microvascular function in humans, but various methods used to quantify and describe NO-dependent vasodilation may impact data interpretation. We compared four approaches for quantifying NO-dependent cutaneous vasodilation during local heating at 39°C and 42°C. We identify discrepancies in calculated NO-dependent dilation responses that are dependent upon the mathematical approach and meaningfully impact data interpretation and reproducibility.

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局部加热时一氧化氮依赖性皮肤血管扩张的定量与解读
评估一氧化氮(NO)依赖性血流的人体皮肤微透析方法包括局部加热(LH)皮肤直至达到高原,然后注入一氧化氮合酶抑制剂(如 L-NAME);然而,量化和表达一氧化氮依赖性血管扩张的方法各不相同,可能会混淆数据解释和可重复性。我们回顾性地评估了 LH 升至 39°C 或 42°C 时的 NO 依赖性血管舒张,计算方法如下:(1) NO 依赖性成分(连同基线和非 NO 依赖性成分)对 LH 的总皮肤血管传导(CVC)反应的绝对贡献,归一化为最大 CVC(%CVCmax);(2) LH 高原与 NO 抑制后(L-NAME 高原;∆%CVCmax=LH 高原-L-NAME 高原)之间的 %CVCmax 差值(∆%CVCmax);(3) ∆%CVCmax 所占 LH 高原的百分比(%Plateau = ∆%CVCmax/LH 高原*100);以及 (4) 校正基线后的 %Plateau。39°C和42°C时的LH高原分别为48±17%CVCmax(9±5%基线;2±4%非NO依赖;36±15%NO依赖)和88±10%CVCmax(15±8%基线;9±10%非NO依赖;64±13%NO依赖)。42°C与39°C相比,非NO依赖性和NO依赖性反应成分(pmax(66±14% vs. 38±15%))的绝对贡献更大(所有p均≤0.02);然而,两种方案的Plateau%(75±13% vs. 80±10%;p=0.57)或PlateauBL%(88±14% vs. 95±8%;p=0.31)没有差异。在两种方案中,%PlateauBL 相对于 ∆%CVCmax 和 %Plateau 的数值更大(p≤0.0001),%Plateau 相对于 ∆%CVCmax 的数值更大(p≤0.05)。NO依赖性皮肤血管扩张对LH反应的量化取决于数学方法和口头描述,这可能会对数据解释和可重复性产生有意义的影响。
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来源期刊
CiteScore
6.00
自引率
9.10%
发文量
296
审稿时长
2-4 weeks
期刊介绍: The Journal of Applied Physiology publishes the highest quality original research and reviews that examine novel adaptive and integrative physiological mechanisms in humans and animals that advance the field. The journal encourages the submission of manuscripts that examine the acute and adaptive responses of various organs, tissues, cells and/or molecular pathways to environmental, physiological and/or pathophysiological stressors. As an applied physiology journal, topics of interest are not limited to a particular organ system. The journal, therefore, considers a wide array of integrative and translational research topics examining the mechanisms involved in disease processes and mitigation strategies, as well as the promotion of health and well-being throughout the lifespan. Priority is given to manuscripts that provide mechanistic insight deemed to exert an impact on the field.
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