Unravelling the origin of isoprene in the human body - a forty year odyssey.

IF 3.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS Journal of breath research Pub Date : 2024-04-25 DOI:10.1088/1752-7163/ad4388
P. Mochalski, J. King, K. Unterkofler, Christopher A. Mayhew
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Abstract

In the breath research community's search for volatile organic compounds that can act as non-invasive biomarkers for various diseases, hundreds of endogenous volatiles have been discovered. Whilst these systemic chemicals result from normal and abnormal metabolic activities or pathological disorders, to date very few are of any use for the development of clinical breath tests that could be used for disease diagnosis or to monitor therapeutic treatments. The reasons for this lack of application are manifold and complex, and these complications either limit or ultimately inhibit the analytical application of endogenous volatiles for use in the medical sciences. One such complication is a lack of knowledge on the biological origins of the endogenous volatiles. A major exception to this is isoprene. Since 1984, i.e., for forty years, it has been generally accepted that the pathway to the production of human isoprene, and hence the origin of isoprene in exhaled breath, is through cholesterol biosynthesis via the mevalonate (MVA) pathway within the liver. However, various studies between 2001 and 2012 provide compelling evidence that human isoprene is produced in skeletal muscle tissue. A recent multi-omic investigation of genes and metabolites has revealed that this proposal is correct by showing that human isoprene predominantly results from muscular lipolytic cholesterol metabolism. Despite the overwhelming proof for a muscular pathway to isoprene production in the human body, breath research papers still reference the hepatic MVA pathway. The major aim of this perspective is review the evidence that leads to a correct interpretation for the origins of human isoprene, so that the major pathway to human isoprene production is understood and appropriately disseminated. This is important, because an accurate attribution to the endogenous origins of isoprene is needed if exhaled isoprene levels are to be correctly interpreted and for assessing isoprene as a clinical biomarker.
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揭开异戊二烯在人体内的起源--四十年的奥德赛。
呼吸研究界在寻找可作为各种疾病非侵入性生物标志物的挥发性有机化合物的过程中,发现了数百种内源性挥发物。虽然这些系统化学物质产生于正常或异常的新陈代谢活动或病理紊乱,但迄今为止,只有极少数可用于开发可用于疾病诊断或监测治疗的临床呼气测试。缺乏应用的原因是多方面的,也是复杂的,这些复杂因素限制或最终抑制了内源性挥发物在医学科学中的分析应用。其中一个复杂因素就是对内源性挥发物的生物来源缺乏了解。异戊二烯是一个主要的例外。自 1984 年以来,即四十年来,人们普遍认为人类产生异戊二烯的途径,也就是呼出气体中异戊二烯的来源,是通过肝脏中的甲羟戊酸(MVA)途径进行胆固醇生物合成。然而,2001 年至 2012 年间的多项研究提供了令人信服的证据,证明人体异戊二烯是在骨骼肌组织中产生的。最近对基因和代谢物进行的多组学调查显示,人体异戊二烯主要是通过肌肉脂肪分解胆固醇代谢产生的,从而证明了这一观点的正确性。尽管有大量证据证明异戊二烯在人体内是通过肌肉途径产生的,但仍有研究论文提到肝脏 MVA 途径。本视角的主要目的是回顾能正确解释人体异戊二烯来源的证据,从而了解人体异戊二烯产生的主要途径,并进行适当的传播。这一点非常重要,因为如果要正确解释呼出的异戊二烯水平,并将异戊二烯作为临床生物标志物进行评估,就必须准确归因于异戊二烯的内源性来源。
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来源期刊
Journal of breath research
Journal of breath research BIOCHEMICAL RESEARCH METHODS-RESPIRATORY SYSTEM
CiteScore
7.60
自引率
21.10%
发文量
49
审稿时长
>12 weeks
期刊介绍: Journal of Breath Research is dedicated to all aspects of scientific breath research. The traditional focus is on analysis of volatile compounds and aerosols in exhaled breath for the investigation of exogenous exposures, metabolism, toxicology, health status and the diagnosis of disease and breath odours. The journal also welcomes other breath-related topics. Typical areas of interest include: Big laboratory instrumentation: describing new state-of-the-art analytical instrumentation capable of performing high-resolution discovery and targeted breath research; exploiting complex technologies drawn from other areas of biochemistry and genetics for breath research. Engineering solutions: developing new breath sampling technologies for condensate and aerosols, for chemical and optical sensors, for extraction and sample preparation methods, for automation and standardization, and for multiplex analyses to preserve the breath matrix and facilitating analytical throughput. Measure exhaled constituents (e.g. CO2, acetone, isoprene) as markers of human presence or mitigate such contaminants in enclosed environments. Human and animal in vivo studies: decoding the ''breath exposome'', implementing exposure and intervention studies, performing cross-sectional and case-control research, assaying immune and inflammatory response, and testing mammalian host response to infections and exogenous exposures to develop information directly applicable to systems biology. Studying inhalation toxicology; inhaled breath as a source of internal dose; resultant blood, breath and urinary biomarkers linked to inhalation pathway. Cellular and molecular level in vitro studies. Clinical, pharmacological and forensic applications. Mathematical, statistical and graphical data interpretation.
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