l-NAME的透皮离子电渗应用可用于年轻健康成年人热应激诱发的出汗研究。

IF 3.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Nitric oxide : biology and chemistry Pub Date : 2023-09-01 DOI:10.1016/j.niox.2023.08.001
Yumi Okamoto, Junto Otsuka, Mao Aoki, Tatsuro Amano
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引用次数: 0

摘要

离子电渗透皮给药N-硝基-1-精氨酸甲酯盐酸盐[l-NAME,一种一氧化氮合酶(NOS)抑制剂]已被用作对人类皮肤中NOS依赖性机制的非侵入性评估。然而,在出汗研究中,其可用性尚待调查。先前使用侵入性技术(如皮内微透析技术)给药l-NAME的观察表明,NOS减少了热应激诱导的出汗,但很少影响胆碱能毒蕈碱受体激动剂给药诱导的反应。因此,我们研究了l-NAME的透皮离子电渗给药是否与先前的观察结果类似地调节出汗。20名年轻健康成年人(10名男性,10名女性)在不同的日子参与了两项实验方案。在每个方案之前,通过透皮离子电渗法向前臂皮肤双侧施用生理盐水(对照)和1%l-NAME。在方案1中,0.001%和1%毛果芸香碱在l-NAME处理和未处理部位进行离子电渗给药。在方案2中,通过将下肢浸入热水(43°C)中进行被动加热,直到直肠温度比基线升高0.8°C。在两个方案中都持续测量出汗率。在两种毛果芸香碱浓度下,对照和l-NAME处理部位毛果芸香碱诱导的出汗率没有显著差异(治疗效果和治疗与毛果芸香碱浓度的相互作用P≥0.316)。与对照组相比,被动加热过程中l-NAME处理部位的出汗率有所降低(治疗效果,P=0.020)。值得注意的是,这些观察结果与之前使用皮内微透析技术将l-NAME注入人体皮肤的出汗研究一致。基于我们的结果与已知观察结果的相似性,我们得出结论,l-NAME的透皮离子电渗是一种有效的非侵入性技术,可用于研究热应激期间与NOS相关的出汗机制。
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Transdermal iontophoretic application of l-NAME is available in sweating research induced by heat stress in young healthy adults

Iontophoretic transdermal administration of NG-nitro-l-arginine methyl ester hydrochloride [l-NAME, a nitric oxide synthase (NOS) inhibitor] has been used as a non-invasive evaluation of NOS-dependent mechanisms in human skin. However, the availability has yet to be investigated in sweating research. Prior observations using invasive techniques (e.g., intradermal microdialysis technique) to administer l-NAME have implicated that NOS reduces sweating induced by heat stress but rarely influences the response induced by the administration of cholinergic muscarinic receptor agonists. Therefore, we investigated whether the transdermal iontophoretic administration of l-NAME modulates sweating similar to those prior observations. Twenty young healthy adults (10 males, 10 females) participated in two experimental protocols on separate days. Before each protocol, saline (control) and 1% l-NAME were bilaterally administered to the forearm skin via transdermal iontophoresis. In protocol 1, 0.001% and 1% pilocarpine were iontophoretically administered at l-NAME-treated and untreated sites. In protocol 2, passive heating was applied by immersing the lower limbs in hot water (43 °C) until the rectal temperature increased by 0.8 °C above baseline. The sweat rate was continuously measured throughout both protocols. Pilocarpine-induced sweat rate was not significantly different between the control and l-NAME-treated sites in both pilocarpine concentrations (P ≥ 0.316 for the treatment effect and interaction of treatment and pilocarpine concentration). The sweat rate during passive heating was attenuated at the l-NAME-treated site relative to the control (treatment effect, P = 0.020). Notably, these observations are consistent with prior sweating studies administrating l-NAME into human skin using intradermal microdialysis techniques. Based on the similarity of our results with already known observations, we conclude that transdermal iontophoresis of l-NAME is a valid non-invasive technique for the investigation of the mechanisms of sweating related to NOS during heat stress.

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来源期刊
Nitric oxide : biology and chemistry
Nitric oxide : biology and chemistry 生物-生化与分子生物学
CiteScore
7.50
自引率
7.70%
发文量
74
审稿时长
52 days
期刊介绍: Nitric Oxide includes original research, methodology papers and reviews relating to nitric oxide and other gasotransmitters such as hydrogen sulfide and carbon monoxide. Special emphasis is placed on the biological chemistry, physiology, pharmacology, enzymology and pathological significance of these molecules in human health and disease. The journal also accepts manuscripts relating to plant and microbial studies involving these molecules.
期刊最新文献
Editorial Board The relationship of nitric oxide synthase 3(NOS3) gene polymorphism in the risk of pulmonary arterial hypertension: A systematic review and meta-analysis Critical role of hydrogen sulfide in the management of neurodegenerative disease Nitric oxide and mitochondrial function in cardiovascular diseases Enhancing S-nitrosoglutathione reductase decreases S-nitrosylation of ERO1α and reduces neuronal death in secondary traumatic brain injury
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