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3-Indoleacetic Acid
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3-Indoleacetic Acid

3-Indoleacetic Acid (3-IAA) is an organic compound derived from the amino acid tryptophan through bacterial fermentation in the gut microbiome.  

This compound, characterized by an indole ring with an acetic acid side chain, is well-known as a phytohormone that regulates plant growth.  However, its role in mammalian biology has sparked significant interest.

Studies have shown that 3-IAA can activate the aryl hydrocarbon receptor (AhR) pathway, which is involved in immune function and cancer regulation. 

This has led to research exploring 3-IAA's potential in treating cancer and autoimmune diseases by modulating the AhR pathway.  Additionally, elevated levels of 3-IAA have been linked to improved responses to chemotherapy in pancreatic cancer.

However, excessive 3-IAA can indicate digestive disorders and toxicity, as well as highlighting the presence of other chronic conditions. 

Elevated 3-IAA levels have been associated with conditions such as chronic kidney disease, anxiety, depression, cardiovascular morbidity, and autism spectrum disorder (ASD).  These findings highlight the significant impact of 3-IAA on health and disease.

What is 3-Indoleacetic Acid?

3-Indoleacetic Acid, also known as 3-indoleacetic acid (3-IAA), is an organic compound derived from the amino acid tryptophan through bacterial fermentation in the gut microbiome.  Its structure consists of an indole ring with an acetic acid side chain. 

While 3-IAA is well-recognized as a phytohormone that regulates plant growth and development, it has also garnered significant interest in mammalian biology.

Several scientific studies have explored the potential role of 3-IAA in activating the aryl hydrocarbon receptor (AhR) pathway, which is involved in immune function and cancer regulation.  [16.]

This has led to investigations into the therapeutic potential of 3-IAA in treating cancer and autoimmune diseases by modulating the AhR pathway.  [15., 16.] 

In the setting of pancreatic cancer, increasing levels of 3-IAA can promote a response to chemotherapy.  [14.] 

However, excessive amounts of 3-IAA may be a marker of digestive disorders and toxicity: there is a growing body of evidence linking indole derivatives, including 3-IAA, to gastrointestinal disorders and potential toxicity.   [16.] 

This association with the gut microbiome and its metabolites has sparked interest in exploring 3-IAA and related compounds as potential biomarkers for various diseases.

3-Indoleacetic Acid in Tryptophan Metabolism  [4., 7.] 

The gut microbiota plays a crucial role in metabolizing tryptophan through various pathways, producing a diverse array of metabolites that can influence the gut-brain axis.  The production of 3-IAA is just one pathway.  

Key tryptophan metabolic pathways mediated by gut microbes include the serotonin synthesis pathway, the kynurenine pathway, indole and indole derivative production,  decarboxylation to tryptamine, and transamination to indole-3-pyruvic acid.

The gut microbiota's ability to metabolize tryptophan through these diverse pathways highlights its significant influence on tryptophan availability and the production of bioactive metabolites that can modulate various physiological processes, including those related to the gut-brain axis.

Elevated Levels of 3-Indoleacetic Acid  

Elevated levels of 3-Indoleacetic Acid have been associated with a variety of conditions including elevated inflammation, chronic kidney disease, anxiety and depression, cardiovascular morbidity and mortality, as well as in ASD.  [5., 8., 12.]

It may also be elevated in certain cancers, including gastric, hepatobiliary, and esophageal cancers.  [9.] 

What Are Organic Acids?  [2., 3.]

Organic acids are organic compounds with acidic properties.  They include a variety of functional groups like carboxyl, phenol, enol, and thiol, with carboxylic acids having the strongest acidity.

Organic acids are considered weak acids, with those containing phenol, enol, alcohol, or thiol groups being even weaker.  

Their structures vary in terms of carbon chain types—aromatic, aliphatic, alicyclic, heterocyclic—saturation, substitutions, and the number of functional groups. 

These acids play critical roles in metabolic and catabolic pathways, notably in the tricarboxylic acid cycle inside mitochondria, which is central to energy production in eukaryotes.  They are also pivotal in determining the sensory properties of fruits and vegetables.

Organic Acids and the Microbiome  [10.]

Increasingly, research highlights new relationships between the microbiome and human health.  Many organisms that comprise the microbiome produce organic acids that can then be tested for additional diagnostic capability.  

Certain organic acids in urine like hippuric acid, benzoic acid, and indoleacetic acid are metabolites produced by gut bacteria from the breakdown of amino acids, dietary polyphenols, and other substances. 

These acids provide insights into gut health and metabolic functions.  For example, elevated levels of certain acids may indicate gut dysbiosis or specific metabolic imbalances, such as phenylketonuria. 

Some organic acids known to be produced by the microbiome include: 

Benzoic Acid (BA): 

Produced from phenylalanine and polyphenol metabolism by intestinal bacteria. High levels in urine can indicate glycine deficiency or liver dysfunction.

Hippuric Acid (HA):

Formed in the liver by conjugation of benzoic acid with glycine. Elevated levels may indicate exposure to environmental toxins like toluene.

Phenylacetic Acid (PAA) and Phenylpropionic Acid (PPA): 

These acids result from phenylalanine metabolism by gut bacteria. High urinary levels can suggest dysbiosis or disorders like phenylketonuria. PAA is also associated with depression markers.

4-Hydroxybenzoic Acid (4-HBA) and 4-Hydroxyphenylacetic Acid (4-HPAA): 

Derivatives of tyrosine metabolism. 4-HBA is linked to catechin (green tea) metabolism, and 4-HPAA is useful in diagnosing small bowel diseases related to bacterial overgrowth.

3-Hydroxyphenylpropionic Acid (3-HPPA): 

A metabolite from dietary polyphenols like proanthocyanidins, indicative of robust bacterial metabolism in the intestines.

3,4-Dihydroxyphenyl Propionic Acid (3,4-DHPPA): 

Produced from dietary quinolones by clostridial species, with high levels suggesting an overgrowth.

3-Indoleacetic Acid (IAA): A breakdown product of tryptophan by gut bacteria such as Bifidobacterium and Bacteroides. Elevated levels are seen in conditions like phenylketonuria or dietary changes.

These organic acids are important markers in clinical diagnostics, helping to monitor metabolic disturbances, gut microbiota balance, and exposure to environmental toxins.

Their presence and concentration are influenced by diet, gut microbiota composition, and overall metabolic health, making them valuable indicators in clinical settings for assessing both metabolic and gastrointestinal conditions.

Organic Acid Testing in Functional Medicine

Organic Acid Testing in Functional Medicine

In functional medicine, organic acid testing is utilized to evaluate a patient's metabolic function through a simple urine test. This testing can identify metabolic imbalances that may affect a patient’s mood, energy, and overall health. 

Testing provides insights into nutrient deficiencies, dietary habits, toxic exposures, and gut microbiome activity. 

The results assist practitioners in customizing treatment plans to address specific metabolic dysfunctions and improve health outcomes. 

Additionally, it helps in assessing the impact of microbial metabolism and the efficiency of the Krebs Cycle, aiding in personalized healthcare.

Laboratory Testing for 3-Indoleacetic Acid

Test Information, Sampling Methods and Preparation

Laboratory testing for organic acids including 3-Indoleacetic Acid is typically done in urine, although it can also be tested in blood.  Testing may be ordered to diagnose an inborn metabolic disorder, or to assess metabolic function and gastrointestinal health in a functional medicine setting.  

Urine samples may be collected in a clinical setting; they can also be collected at home.  Some labs recommend or require a first morning void sample, to provide a concentrated sample.  

Interpreting 3-Indoleacetic Acid Results

Optimal Range for 3-Indoleacetic Acid Testing

Generally, falling within reference ranges for organic acids is recommended, although for many of these organic acids, a level towards the lower end of the reference range is considered optimal.  

It is essential to consult with the laboratory company used for their recommended reference range for 3-Indoleacetic Acid.  

One company reports the following reference range for 3-Indoleacetic Acid:  0.46-9.21 mcg/mg creatinine  [11.]

Clinical Significance of Elevated Levels of 3-Indoleacetic Acid

Elevated 3-Indoleacetic Acid levels may indicate conditions such as kidney or cardiovascular disease or certain cancers.  3-IAA has also been elevated in anxiety, depression, and in ASD.  [5., 8., 9., 12.]

Elevated levels may also indicate dysbiosis or overgrowth of certain bacteria that produce 3-IAA from tryptophan, including Lactobacillus, Clostridium, and Bacteroides.  [4.] 

Clinical Significance of Low Levels of 3-Indoleacetic Acid

Low levels of 3-Indoleacetic Acid are not considered clinically relevant.  

3-Indoleacetic Acid Related Biomarkers and Comparative Analysis

3-Indoleacetic Acid is typically tested along with other organic acids to gain deeper insights into metabolic pathways and physiological processes.

Organic acids that may be tested as part of a panel include: 

2-Hydroxybutyric Acid: this acid is a marker for insulin resistance and increased oxidative stress.

2-Hydroxyphenylacetic Acid: derived from phenylalanine metabolism, this acid is used as a biomarker in various metabolic assessments.

3-Hydroxybutyric Acid: a ketone body produced during fat metabolism, indicative of carbohydrate deprivation or ketogenic conditions.

3-Hydroxyisovaleric Acid: an organic acid that accumulates in leucine catabolism disorders, often elevated in maple syrup urine disease.

4-Hydroxybenzoic Acid: a derivative of tyrosine metabolism, it is linked to catechin (green tea) metabolism and may be produced by some intestinal bacteria.

4-Hydroxyphenylacetic Acid: a breakdown product of tyrosine, used in diagnosing disorders involving the degradation of aromatic amino acids.

5-Hydroxyindoleacetic Acid: the main metabolite of serotonin, used as a marker in the diagnosis of carcinoid syndrome.

Adipic Acid: a dicarboxylic acid that can also be formed metabolically in humans through the oxidation of certain fatty acids.

a-Keto-b-Methylvaleric Acid: an intermediate in isoleucine metabolism, which can accumulate in certain metabolic disorders.

a-Ketoisocaproic Acid: an intermediate in the metabolism of leucine, elevated in maple syrup urine disease.

a-Ketoisovaleric Acid: a breakdown product of valine metabolism, also linked to maple syrup urine disease.

a-Ketoglutaric Acid: a key intermediate in the citric acid cycle, essential for energy production and nitrogen transport.

Benzoic Acid: produced from phenylalanine and polyphenol metabolism by intestinal bacteria. High levels in urine can indicate glycine deficiency or liver dysfunction.

Cis-Aconitic Acid: an intermediate in the tricarboxylic acid cycle, formed by the dehydration of citric acid.

Citric Acid: a central compound in the citric acid cycle, crucial for energy production in cells.

Ethylmalonic Acid: this acid accumulates in ethylmalonic encephalopathy and is involved in fatty acid metabolism.

Fumaric Acid: an intermediate in the tricarboxylic acid (TCA) cycle, participating in energy production through its conversion to malate and subsequent participation in the generation of ATP.

Homovanillic Acid: a major metabolite of dopamine, used as a marker to monitor dopamine levels.

Hippuric Acid: formed from the conjugation of benzoic acid and glycine; elevated levels can indicate exposure to certain environmental toxins.

Hydroxymethylglutarate: an intermediate in leucine metabolism, also associated with disorders of ketogenesis and ketolysis.

Isocitric Acid: an isomer of citric acid and an important part of the citric acid cycle, pivotal in cellular energy production.

Kynurenic Acid: a product of tryptophan metabolism, known for its role as a neuroprotective agent.

Lactic Acid: produced from pyruvate via anaerobic metabolism, an indicator of hypoxia and strenuous exercise.

Malic Acid: a dicarboxylic acid found in fruits, and involved  in the citric acid cycle.

Methylmalonic Acid: an indicator of Vitamin B12 deficiency, it accumulates when the vitamin is deficient.

Methylsuccinic Acid: a dicarboxylic acid often involved in alternative pathways of fatty acid metabolism.

Orotic Acid: involved in the metabolism of pyrimidines, abnormalities in its levels can indicate metabolic disorders.

Pyroglutamic Acid: an uncommon amino acid derivative that can accumulate in glutathione synthesis disorders.

Pyruvic Acid: a key intersection in several metabolic pathways; its levels are crucial for assessing cellular respiration and metabolic function.

Quinolinic Acid: a neuroactive metabolite of the kynurenine pathway, elevated levels are associated with neurodegenerative diseases.

Suberic Acid: a dicarboxylic acid that is a biomarker in adipic aciduria, often studied in relation to fatty acid oxidation disorders.

Succinic Acid: a four-carbon dicarboxylic acid that plays a central role in the Krebs cycle, crucial for energy production.

Tricarballylic Acid: an organic acid that can inhibit aconitase in the citric acid cycle and is sometimes associated with glyphosate exposure.

Vanillylmandelic Acid: a metabolite of epinephrine and norepinephrine, used as a marker for neuroblastoma and other catecholamine-secreting tumors.

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See References

[1.] Beley GJ, Anne M, Dadia DM. Nutrigenomics in the management and prevention of metabolic disorders. Elsevier eBooks. Published online January 1, 2023:209-274. doi:https://doi.org/10.1016/b978-0-12-824412-8.00006-0 

[2.] Chahardoli A, Jalilian F, Memariani Z, Farzaei MH, Shokoohinia Y. Analysis of organic acids. Recent Advances in Natural Products Analysis. Published online 2020:767-823. doi:https://doi.org/10.1016/b978-0-12-816455-6.00026-3 

[3.] French D. Advances in Clinical Mass Spectrometry. Advances in Clinical Chemistry. 2017;79:153-198. doi:https://doi.org/10.1016/bs.acc.2016.09.003 

[4.] Gao K, Mu C, Farzi A, Zhu W. Tryptophan Metabolism: A Link Between the Gut Microbiota and Brain. Advances in Nutrition. 2019;11(3). doi:https://doi.org/10.1093/advances/nmz127

[5.] Gevi F, Zolla L, Gabriele S, Persico AM. Urinary metabolomics of young Italian autistic children supports abnormal tryptophan and purine metabolism. Mol Autism. 2016 Nov 24;7:47. doi: 10.1186/s13229-016-0109-5. PMID: 27904735; PMCID: PMC5121959.

[6.] Hou Y, Li J, Ying S. Tryptophan Metabolism and Gut Microbiota: A Novel Regulatory Axis Integrating the Microbiome, Immunity, and Cancer. Metabolites. 2023;13(11):1166. doi:https://doi.org/10.3390/metabo13111166

[7.] Hyland NP, Cavanaugh CR, Hornby PJ. Emerging effects of tryptophan pathway metabolites and intestinal microbiota on metabolism and intestinal function. Amino Acids. 2022;54(1):57-70. doi:https://doi.org/10.1007/s00726-022-03123-x

[8.] Karu N, McKercher C, Nichols DS, Davies N, Shellie RA, Hilder EF, Jose MD. Tryptophan metabolism, its relation to inflammation and stress markers and association with psychological and cognitive functioning: Tasmanian Chronic Kidney Disease pilot study. BMC Nephrol. 2016 Nov 10;17(1):171. doi: 10.1186/s12882-016-0387-3. PMID: 27832762; PMCID: PMC5103367.

[9.] Kobori K, Sakakibara H, Maruyama K, Kobayashi T, Yamaki T. [A rapid method for determining urinary indoleacetic acid concentration and its clinical significance as the tumor-marker in the diagnosis of malignant diseases]. J UOEH. 1983 Jun 1;5(2):213-20. Japanese. doi: 10.7888/juoeh.5.213. PMID: 6207579.

[10.] Lee YT, Huang SQ, Lin CH, Pao LH, Chiu CH. Quantification of Gut Microbiota Dysbiosis-Related Organic Acids in Human Urine Using LC-MS/MS. Molecules. 2022 Aug 23;27(17):5363. doi: 10.3390/molecules27175363. PMID: 36080134; PMCID: PMC9457824. 

[11.] Rupa Health.  Organic Acids Sample Report.pdf. Google Docs. https://drive.google.com/file/d/1UJk_PcOslDhV5WjuyYqGQ1CwHLU43skK/view

[12.] Sallée M, Dou L, Cerini C, Poitevin S, Brunet P, Burtey S. The aryl hydrocarbon receptor-activating effect of uremic toxins from tryptophan metabolism: a new concept to understand cardiovascular complications of chronic kidney disease. Toxins (Basel). 2014 Mar 4;6(3):934-49. doi: 10.3390/toxins6030934. PMID: 24599232; PMCID: PMC3968369.

[13.] Seashore M. The Organic Acidemias: An Overview.; 2001. Accessed May 2, 2024. https://corpora.tika.apache.org/base/docs/govdocs1/141/141031.pdf 

[14.] Seo YD, Wargo JA. From bugs to drugs: Bacterial 3-IAA enhances efficacy of chemotherapy in pancreatic cancer. Cell Reports Medicine. 2023;4(5):101039. doi:https://doi.org/10.1016/j.xcrm.2023.101039

[15.] Shen J, Yang L, You K, et al. Indole-3-Acetic Acid Alters Intestinal Microbiota and Alleviates Ankylosing Spondylitis in Mice. Frontiers in Immunology. 2022;13. doi:https://doi.org/10.3389/fimmu.2022.762580

[16.] Zhang X, Gan M, Li J, et al. Endogenous Indole Pyruvate Pathway for Tryptophan Metabolism Mediated by IL4I1. Journal of Agricultural and Food Chemistry. 2020;68(39):10678-10684. doi:https://doi.org/10.1021/acs.jafc.0c03735

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