l-精氨酸/一氧化氮途径与成人多动症的氧化应激:哌甲酯治疗的效果。

IF 3.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kathrin Sinningen , Barbara Emons , Pierre Böhme , Georg Juckel , Beatrice Hanusch , Bibiana Beckmann , Dimitrios Tsikas , Thomas Lücke
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引用次数: 1

摘要

引言:注意力缺陷多动障碍(ADHD)是一种曾经被认为只发生在儿童身上的精神障碍。同时,众所周知,成年人也会受到影响。儿童和成人治疗注意力不集中、冲动、缺乏自我调节和多动症状的一线药物是哌甲酯(MPH)。已知的MPH的不良反应包括心血管问题,如血压和心率升高。因此,需要生物标志物来监测MPH潜在的心血管副作用。l-精氨酸/一氧化氮(Arg/NO)途径参与去甲肾上腺素和多巴胺的释放以及正常的心血管功能,因此是寻找生物标志物的主要候选途径。本研究的目的是研究成人ADHD患者血浆和尿液中的Arg/NO通路以及氧化应激,以及MPH药物的潜在影响。方法:在29例ADHD成人(39.2±10.9岁)和32例健康对照(CO)(38.0±11.6岁)的血浆和尿液中,用气相色谱-质谱法测定了NO合成抑制剂不对称二甲基精氨酸(ADMA)及其主要尿代谢产物二甲胺(DMA)和丙二醛(MDA)。结果:在29例ADHD患者中,14例目前未接受MPH治疗(-MPH),15例接受MPH(+MPH)治疗。未接受MPH治疗的患者的血浆硝酸盐浓度显著高于CO(-MPH 60.3μM[46.2-76.0]vs.CO 44.4μM[35.0-52.7];p=0.002),而-MPH患者的血浆亚硝酸盐浓度往往更高(2.77μM[2.26-3.27])vs.CO(2.13μM[1.50-2.93];p=0.053)。此外,血浆肌酸酐浓度存在显著差异,其中-MPH的浓度明显高于其他两组(-MPH 141μM[128-159];+MPH 96.2μM[702-140];Co 75.9μM[620-94.7];p结论:未接受MPH(-MPH)治疗的成人ADHD患者显示出不同的Arg/NO途径,但Arg的生物利用度在各组之间似乎是一致的。我们的研究结果表明,ADHD患者的尿液重吸收可能增加和/或亚硝酸盐和硝酸盐的排泄可能减少,导致血浆亚硝酸盐浓度增加。MPH似乎通过尚不清楚的机制部分逆转了这些作用,并且不影响氧化应激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
l-Arginine/nitric oxide pathway and oxidative stress in adults with ADHD: Effects of methylphenidate treatment

Introduction

Attention deficit hyperactivity disorder (ADHD) is a mental disorder that was once thought to occur only in children. Meanwhile, it is known that adults can also be affected. The first-line drug in children and adults to treat symptoms of inattention, impulsivity, lack of self-regulation, and hyperactivity is methylphenidate (MPH). Known adverse effects of MPH include cardiovascular problems, such as elevated blood pressure and heart rate. Therefore, biomarkers to monitor potential cardiovascular side effects of MPH are needed. The l-Arginine/Nitric oxide (Arg/NO) pathway is involved in noradrenaline and dopamine release as well as in normal cardiovascular functioning and is therefore a prime candidate for the search of biomarkers. The aim of the present study was to investigate the Arg/NO pathway as well as oxidative stress in adult ADHD patients in plasma and urine and the potential influence of MPH medication.

Methods

In plasma and urine samples of 29 adults with ADHD (39.2 ± 10.9 years) and 32 healthy adults serving as controls (CO) (38.0 ± 11.6 years) the major NO metabolites nitrite and nitrate, Arg, the NO synthesis inhibitor asymmetric dimethylarginine (ADMA) and its major urinary metabolite dimethylamine (DMA) as well as malondialdehyde (MDA) were measured by gas chromatography–mass spectrometry.

Results

Of the 29 patients with ADHD 14 were currently without MPH treatment (-MPH) and 15 were treated with MPH (+MPH). Plasma nitrate concentrations were significantly higher in patients not treated with MPH vs. CO (-MPH 60.3 μM [46.2–76.0] vs. CO 44.4 μM [35.0–52.7]; p = 0.002), while plasma nitrite tended to be higher in -MPH patients (2.77 μM [2.26–3.27]) vs. CO (2.13 μM [1.50–2.93]; p = 0.053). Additionally, plasma creatinine concentrations were significantly different, with -MPH showing significantly higher concentrations than the other two groups (-MPH 141 μM [128–159]; +MPH 96.2 μM [70.2–140]; Co 75.9 μM [62.0–94.7]; p < 0.001). Urinary creatinine excretion tended to be lowest in -MPH group vs. +MPH and CO (-MPH 11.4 ± 8.88 mM; +MPH 20.7 ± 9.82 mM; 16.6 ± 7.82 mM; p = 0.076). None of the other metabolites, including MDA, a marker of oxidative stress, showed a difference between the groups.

Conclusion

Adult patients with ADHD, who are not treated with MPH (-MPH), showed varied Arg/NO pathway, but Arg bioavailability seemed to be consistent over the groups. Our findings imply that urinary reabsorption may be increase and/or excretion of nitrite and nitrate may be decreased in ADHD, resulting in an increase in the plasma concentration of nitrite. MPH seems to partially reverse these effects by not yet known mechanisms, and does not affect oxidative 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.
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