3-Hydroxypropylmercapturic acid (3-HPMA) is a urinary metabolite formed from acrolein, a harmful aldehyde found in cigarette smoke, automobile exhaust, industrial emissions, and some processed foods.
Acrolein, once in the body, binds with the antioxidant glutathione and undergoes further metabolic processing to become 3-HPMA. The presence of 3-HPMA in urine is a key biomarker used to assess exposure to acrolein from various sources.
Elevated levels of 3-HPMA in urine can indicate significant exposure to this toxicant, making it a valuable tool in both clinical and environmental health studies.
3-Hydroxypropylmercapturic acid (3-HPMA) is a metabolite formed as a result of exposure to acrolein, a reactive aldehyde present in various environmental sources. Acrolein is found in some processed foods, cigarette smoke, automobile exhaust, and certain industrial processes, as well as being used as an herbicide. [7.]
When acrolein enters the body, it undergoes a series of metabolic reactions. First, it conjugates with glutathione, a cellular antioxidant. This conjugate then undergoes further metabolic processing, including reduction and conversion to a mercapturic acid derivative, resulting in the formation of 3-HPMA.
The presence of 3-HPMA in urine serves as a biomarker to assess exposure to acrolein from different sources. [5.]
It has been detected in the urine of cigarette smokers, indicating exposure to acrolein from tobacco smoke. Additionally, studies have investigated the relationship between urinary 3-HPMA levels and the formation of acrolein-DNA adducts in the lungs, which are associated with potential carcinogenic effects. [1.]
Furthermore, 3-HPMA has been used as a biomarker to evaluate environmental exposure to acrolein, as it is present in various pollutants and can be ingested through contaminated food, water, or air.
Laboratory testing for 3-HPMA is primarily done in urine. The sample may be collected in a clinical setting, or from the comfort of home.
It is essential to consult with the ordering provider prior to sample collection, as specific preparation measures may be required.
Because 3-HPMA is the metabolite of a toxic compound, optimal levels are undetectable, or very low. It is essential to consult with the laboratory company used to determine their recommended reference range.
Elevated levels of 3-HPMA signify exposure to acrolein. Because it is detoxified via glutathione, supporting glutathione levels, for example with NAC supplementation, in the setting of acrolein toxicity is increasingly recommended. [4., 8.]
Low or undetectable levels of 3-HPMA is considered optimal.
Many diet and lifestyle practices have shown benefit in supporting healthy glutathione and antioxidant levels in the body:
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[2.] Glutathione depletion in chronic alcohol abuse makes lungs vulnerable to life-threatening diseases. EurekAlert! https://www.eurekalert.org/news-releases/523585
[3.] Glutathione Disulfide - an overview | ScienceDirect Topics. www.sciencedirect.com. Accessed May 30, 2024. https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/glutathione-disulfide
[4.] Gupta S, Kamil S, Sinha PR, Rodier JT, Chaurasia SS, Mohan RR. Glutathione is a potential therapeutic target for acrolein toxicity in the cornea. Toxicol Lett. 2021 Apr 1;340:33-42. doi: 10.1016/j.toxlet.2021.01.005. Epub 2021 Jan 6. PMID: 33421550; PMCID: PMC9206442.
[5.] Minet, E., Errington, G., Scherer, G. et al. An inter-laboratory comparison of urinary 3-hydroxypropylmercapturic acid measurement demonstrates good reproducibility between laboratories. BMC Res Notes 4, 391 (2011). https://doi.org/10.1186/1756-0500-4-391
[6.] Minich DM, Brown BI. A Review of Dietary (Phyto)Nutrients for Glutathione Support. Nutrients. 2019 Sep 3;11(9):2073. doi: 10.3390/nu11092073. PMID: 31484368; PMCID: PMC6770193.
[7.] Stevens JF, Maier CS. Acrolein: sources, metabolism, and biomolecular interactions relevant to human health and disease. Mol Nutr Food Res. 2008 Jan;52(1):7-25. doi: 10.1002/mnfr.200700412. PMID: 18203133; PMCID: PMC2423340.
[8.] Tomitori H, Nakamura M, Sakamoto A, Terui Y, Yoshida M, Igarashi K, Kashiwagi K. Augmented glutathione synthesis decreases acrolein toxicity. Biochem Biophys Res Commun. 2012 Feb 3;418(1):110-5. doi: 10.1016/j.bbrc.2011.12.143. Epub 2012 Jan 5. PMID: 22244891.