Recirculating bioavailable nicotine metabolite using ascorbic acid: A pragmatic approach for treating nicotine dependence

Murugesan Arumugam , Raman Lakshmi Sundaram , Vishal Jayajothi , Manish Arul , Jerad A Suresh , Sathesh Kumar Kesavan
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Abstract

Nicotine undergoes metabolism, converting into the oxidized metabolite cotinine, which can persist in the body for several weeks and potentially lead to fatal conditions, such as cancer. Conventional nicotine replacement therapy provides additional nicotine to the body, thereby increasing the chance of accumulating the toxic metabolite cotinine. Consequently, we proposed a hypothesis: converting cotinine back into nicotine using a suitable reducing agent, such as ascorbic acid, could be a practical approach. This conversion would allow cotinine to be reutilized for its central nervous system effects before its eventual elimination from the body. In the current study, we examined this hypothesis by using plasma samples from smokers. Volunteers (both non-smokers and smokers) were screened and recruited for this study. In the initial time- and dose-dependent studies, we incubated plasma samples from non-smokers with cotinine and ascorbic acid. Changes in cotinine and nicotine levels were quantified using HPLC-PDA. Based on the findings of these experiments, we selected a concentration of 1 µM ascorbic acid and incubated it with plasma samples from 25 smokers for 10 min. A time-dependent study revealed that nicotine was detected in non-smokers' plasma samples after a 10-minute incubation with 28.38 µM of both cotinine and ascorbic acid. In a subsequent dose-dependent study, the maximum concentration of nicotine was observed at 1 µM ascorbic acid. Among the 25 samples of smokers’ plasma, the mean nicotine concentration increased from 0.565 ± 0.196 to 1.937 ± 0.622 µM (P = 0.0081), while cotinine levels decreased from 1.278 ± 0.253 to 0.754 ± 0.137 µM (P = 0.0087). This study conclusively demonstrated that ascorbic acid, at a specified concentration, effectively converts cotinine back into nicotine in smokers' plasma. Importantly, this conversion did not occur in water or in the absence of ascorbic acid in the plasma, indicating enzyme involvement.

Abstract Image

利用抗坏血酸循环生物可利用的尼古丁代谢物:治疗尼古丁依赖的实用方法
尼古丁经过代谢,转化为氧化的代谢物可替宁,可替宁可以在体内持续数周,并可能导致致命的疾病,如癌症。传统的尼古丁替代疗法为身体提供了额外的尼古丁,从而增加了积累有毒代谢物可替宁的机会。因此,我们提出了一个假设:使用一种合适的还原剂,如抗坏血酸,将可替宁转化为尼古丁可能是一种实用的方法。这种转化将允许可替宁在其最终从体内消除之前被重新利用其中枢神经系统的作用。在目前的研究中,我们通过使用吸烟者的血浆样本来检验这一假设。志愿者(包括不吸烟者和吸烟者)被筛选并招募参加这项研究。在最初的时间和剂量依赖性研究中,我们用可替宁和抗坏血酸培养非吸烟者的血浆样本。采用HPLC-PDA定量测定可替宁和尼古丁水平的变化。基于这些实验结果,我们选择了浓度为1 μ M的抗坏血酸,并将其与25名吸烟者的血浆样品孵育10分钟。一项时间依赖性研究表明,在28.38 μ M的可替宁和抗坏血酸孵育10分钟后,非吸烟者的血浆样品中检测到尼古丁。在随后的剂量依赖性研究中,在1 μ M抗坏血酸时观察到尼古丁的最大浓度。25份吸烟者血浆中尼古丁平均浓度从0.565±0.196上升至1.937±0.622µM (P = 0.0081),可替宁平均浓度从1.278±0.253下降至0.754±0.137µM (P = 0.0087)。本研究最终证明,在特定浓度下,抗坏血酸能有效地将吸烟者血浆中的可替宁转化为尼古丁。重要的是,这种转化不会发生在水中或血浆中缺乏抗坏血酸的情况下,这表明酶的参与。
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CiteScore
2.60
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