Natural Detox Protocols

Detox Protocols in prepared form
Detox Protocols — prepared form, typical clinical or supplement presentation.
Detox Protocols body-systems response
Illustration of the body’s organs and circulation, which carry and clear chemicals.
Detox Protocols active compounds at the cellular level
Illustration of cells at microscopic scale.

🫀 Interactive Visualization How Your Liver Actually Detoxifies Watch Phase I make a toxin more reactive and Phase II neutralise it. Launch →

Table of Contents

  1. What Detoxification Actually Means
  2. Modern Chemical Exposures
  3. Symptoms Detox Programs Attribute to “Toxicity”
  4. The Liver as the Primary Detox Organ
  5. Phase I Detoxification: Cytochrome P450
  6. Phase II Detoxification: Conjugation Pathways
  7. Phase III Detoxification: Transport and Elimination
  8. Heavy Metals: Chelation and Binders
  9. Foods and Supplements Studied for Detox Pathways
  10. The Lymphatic System
  11. Sweating and Sauna
  12. Colon Health and Elimination
  13. Hydration and Detoxification
  14. Juice Cleansing: Claims and Findings
  15. What Detox Diets Include and Exclude
  16. Detox Reactions and the Herxheimer Response
  17. Program Timelines: What Has Been Tested
  18. Cautions and Contraindications
  19. Key Research Papers
  20. Connections
  21. Featured Videos

What Detoxification Actually Means

In physiology, detoxification (biotransformation) is the continuous process by which the body chemically changes and eliminates foreign compounds and its own metabolic waste. It takes place mainly in the liver, with the kidneys, gut, lungs and skin also involved. In medicine, “detoxification” also names specific treatments for poisoning, drug overdose or alcohol withdrawal. Commercial “detox” programs and products are a third, separate use of the word: a 2015 critical review found very little clinical evidence for detox diets and, to the authors’ knowledge, no randomized controlled trials of commercial detox diets in humans (Klein & Kiat 2015).

Textbooks and reviews describe the liver’s handling of fat-soluble chemicals in phases:

Naturopathic writers present detox programs as a way of supplying the nutrients and conditions these pathways use. A 2015 review of clinical and in vivo studies of foods and food-derived compounds cautions that current research has limitations, that many nutrients have biphasic, dose-dependent effects, and that genetic differences can change outcomes; one such review concluded that a whole-foods approach may be prudent (Hodges & Minich 2015). The sections below separate what the physiology shows from what detox programs claim. The liver’s chemistry is covered in depth on the Liver Phase 1 and Phase 2 page, and the evidence on commercial cleanses on the Liver Detox page.

Modern Chemical Exposures

Detox programs start from the premise that modern chemical exposure exceeds the body’s capacity to clear it. Exposure to industrial chemicals is real and measurable; whether it overwhelms normal clearance in a given person, and whether a detox program changes that, are separate questions that the research has not answered for commercial programs.

Detox literature uses the term total body burden for the sum of these exposures. Some persistent pollutants are measurable in blood, fat and other tissues, but no study found has validated a test for a “toxic overload” that a detox program then corrects.

Symptoms Detox Programs Attribute to “Toxicity”

Naturopathic and detox-program writers list the following symptoms as possible signs that detoxification pathways are overloaded:

These symptoms are common and have many causes. No study found has validated this list as a way to identify impaired detoxification, and the 2015 Klein & Kiat review found no randomized controlled trial showing that a commercial detox diet relieves them. Several of them have treatable medical causes.

The Liver as the Primary Detox Organ

The liver is the main organ of biotransformation. It receives blood from the gut through the portal vein, so most compounds absorbed from food pass through it before reaching the rest of the body.

Alcohol, some medications (most prominently acetaminophen in overdose), viral hepatitis and fatty liver disease are the established causes of liver damage; these are covered, with sources, on the Liver Detox page.

Phase I Detoxification: Cytochrome P450

Phase I is carried out mainly by the cytochrome P450 (CYP) enzymes, located in the endoplasmic reticulum of liver cells and other tissues. Of 57 putatively functional human CYPs, about a dozen, in the CYP1, 2 and 3 families, are responsible for the biotransformation of most foreign substances, including 70–80% of drugs in clinical use; the most highly expressed in the liver are CYP3A4, 2C9, 2C8, 2E1 and 1A2 (Zanger & Schwab 2013).

Oxidation

Oxidation, which adds an oxygen atom or removes hydrogen, is the most common Phase I reaction and the main route for many drugs, environmental chemicals and steroid hormones. Enzymes involved include CYP1A2, CYP2D6, CYP2C9, CYP2C19 and CYP3A4. Genetic variants in several of these (notably CYP2D6, 2C19 and 2C9) produce poor, intermediate, extensive and ultrarapid metabolizer types (Zanger & Schwab 2013).

Reduction

Some compounds undergo reduction, in which electrons are added to the molecule; nitro and azo compounds are examples.

Hydrolysis

Hydrolysis uses water to split chemical bonds, commonly ester and amide bonds.

Reactive intermediates: Some chemicals are turned into more toxic metabolites along the way (Grant 1991). The best-known example is acetaminophen, whose reactive metabolite is normally neutralized by glutathione; acetylcysteine is the standard treatment for acetaminophen poisoning (Heard 2008). Detox writers describe an “overactive Phase I with a sluggish Phase II” as a dangerous imbalance; that framing comes from the naturopathic literature, and no test or trial found measures it in otherwise healthy people.

Nutrients named for Phase I: A 1998 review in an alternative-medicine journal lists riboflavin, niacin, vitamin B6, folic acid, vitamin B12, glutathione, branched-chain amino acids, flavonoids and phospholipids as nutrients used in Phase I, and carotenes, vitamins C and E, selenium, copper, zinc, manganese, coenzyme Q10 and other plant compounds as antioxidant protection against its reactive by-products (Liska 1998). Some are genuine enzyme cofactors (riboflavin and niacin in the NADPH system that supplies electrons to P450 enzymes). No trial found has shown that taking extra amounts improves detoxification in people who are not deficient.

Phase II Detoxification: Conjugation Pathways

Phase II attaches a water-soluble group to a compound so that it can be excreted in bile or urine. Several types of conjugation reaction are described, including glucuronidation, sulfation, and glutathione and amino acid conjugation, each requiring cofactors replenished from the diet (Liska 1998); detox literature usually lists six.

Glutathione Conjugation

Glutathione S-transferases join glutathione, a tripeptide of cysteine, glutamic acid and glycine, to reactive electrophiles, including some Phase I intermediates and carcinogens. Glutathione is the most abundant antioxidant the body makes (Richie 2015), and detox writers often call it the “master antioxidant.” Its depletion is the key step in acetaminophen liver injury (Heard 2008). Detox protocols name N-acetylcysteine (NAC), alpha-lipoic acid, selenium, vitamins C and E and sulfur-containing foods as supports for glutathione; the human evidence for those used as supplements is described under Foods and Supplements below.

Methylation

Methylation transfers a methyl group from S-adenosylmethionine (SAMe). It is used for catechol estrogens and dopamine (via COMT), histamine and inorganic arsenic. Folate, vitamin B12, vitamin B6, betaine (trimethylglycine) and choline feed the methyl-donor cycle. A common variant in the MTHFR gene lowers that enzyme’s activity and, in people who carry two copies, raises blood homocysteine (Frosst 1995).

Sulfation

Sulfation attaches a sulfate group to compounds including thyroid and steroid hormones, bile acids, neurotransmitters and many drugs. The sulfate comes largely from the breakdown of sulfur amino acids in foods such as eggs, garlic, onions and cruciferous vegetables; molybdenum is the cofactor of sulfite oxidase, which converts sulfite to sulfate. The claim, common in detox literature, that sulfation capacity is depleted by chronic toxic exposure is not supported by any study found.

Glucuronidation

Glucuronidation joins compounds to glucuronic acid. It handles bilirubin, steroid and thyroid hormones, many drugs and environmental chemicals. Beta-glucuronidase, an enzyme present in tissues and produced by gut bacteria, can split these conjugates and release the original compound. D-glucaric acid, found in grapefruit, apples, oranges and cruciferous vegetables, forms D-glucaro-1,4-lactone, a beta-glucuronidase inhibitor; calcium D-glucarate supplements are a source of it, and most of the studies of it found are in animal models of cancer (Zółtaszek 2008).

Acetylation

N-acetyltransferase enzymes attach an acetyl group from acetyl-CoA to aromatic amines, hydrazines and sulfonamide drugs. Coenzyme A is made from pantothenic acid (vitamin B5). Inherited differences in these enzymes produce slow and fast acetylators, who process some drugs, such as isoniazid, at different rates.

Amino Acid Conjugation

This pathway joins compounds to amino acids, mainly glycine, taurine and glutamine. Glycine conjugation converts benzoic acid, a food preservative, to hippuric acid, and salicylic acid to salicyluric acid. Detox writers present bone broth, collagen and glycine supplements as supports for this pathway; no trial found has tested that.

Phase III Detoxification: Transport and Elimination

“Phase III” is the name given to the membrane transporters that move compounds and their conjugates across cell membranes, into bile, the gut or urine. Without efficient transport, conjugates can accumulate within cells.

Factors detox protocols name for Phase III:

Heavy Metals: Chelation and Binders

Metals are elements and are not broken down; some, such as lead and cadmium, are retained for years in bone and kidney. Toxic-metal exposure is diagnosed by blood or urine testing, and the evidence on specific metals is covered on the Heavy Metals page. Detox protocols use two kinds of agents: chelators that act in the body, and binders that act in the gut.

Chelation

Chelating drugs, including succimer (DMSA), dimercaprol, D-penicillamine and calcium disodium EDTA, bind lead and other metals and increase their excretion; they also remove minerals such as zinc and, in some cases, calcium. A 2006 CDC report described three deaths from chelation-related hypocalcemia leading to cardiac arrest, advised clinicians unfamiliar with chelation to consult an expert, and stated that disodium EDTA (Na2EDTA) should not be given to children (CDC 2006). The U.S. National Center for Complementary and Integrative Health (NCCIH) notes that CDC recommends chelation for removing toxic metals only in some specific serious cases. Plant foods and supplements described as “natural chelators” have not been tested against these drugs in comparable trials, with the exception of the small garlic trial described below.

Binders and Other Agents Used in Detox Protocols

The “mobilize and bind” principle: Detox practitioners teach that metals mobilized from tissue need a binder in the gut, or they may be redistributed to more sensitive organs such as the brain. This principle comes from practitioner protocols; no clinical trial found has tested it. The binder evidence is set out in detail on the Binders: Charcoal, Chlorella, and Beyond page.

Foods and Supplements Studied for Detox Pathways

Detox protocols name specific foods, herbs and supplements as supports for the liver’s pathways. Some have been tested in people; many have been studied only in cells or animals.

Cruciferous Vegetables

Broccoli, cauliflower, Brussels sprouts, cabbage and kale contain glucosinolates, which form isothiocyanates such as sulforaphane, potent inducers of Phase II enzymes. Three-day-old sprouts of certain broccoli and cauliflower cultivars contain 10 to 100 times more glucoraphanin, the precursor of sulforaphane, than the mature plants (Fahey 1997). In a 12-week randomized trial in 291 participants from a rural area of China with substantial exposure to airborne pollutants, a broccoli-sprout beverage increased urinary excretion of the glutathione-derived conjugates of benzene (61%) and acrolein (23%), but not crotonaldehyde, compared with placebo (Egner 2014).

Sulfur-Rich Foods

Garlic, onions, leeks, shallots and eggs supply sulfur amino acids, which are raw materials for glutathione and sulfation. In a randomized trial in workers with chronic occupational lead poisoning, garlic (1,200 µg allicin three times daily for 4 weeks) lowered blood lead with no significant difference from the chelating drug D-penicillamine, and the authors judged garlic safer clinically (Kianoush 2012).

Supplements Named in Detox Protocols

Detox protocols often give daily doses for these supplements; the doses above are the ones the trials used, and none was a trial of a detox program.

The Lymphatic System

The lymphatic system returns fluid, proteins, fats and immune cells from the tissues to the bloodstream, passing through lymph nodes on the way. It has no central pump; it uses extrinsic pumping, from the compression of lymphatic vessels by surrounding tissue forces such as muscle movement, and intrinsic pumping, from rapid contractions of the lymphatic vessels’ own muscle (Zawieja 2009). Detox protocols describe it as a waste-removal network and offer several practices to move lymph.

Dry Brushing

Dry skin brushing, in which a natural-bristle brush is stroked over dry skin toward the heart, is described by proponents as stimulating lymph flow and exfoliating the skin. A PubMed search found no controlled study of dry brushing and lymph flow or detoxification.

Rebounding

Proponents describe bouncing on a mini trampoline (rebounding) as opening and closing lymphatic valves, and often cite a NASA study. That 1980 study, in 8 young men, compared body acceleration and oxygen uptake during treadmill running and trampoline jumping, and found that at similar heart rates and oxygen uptake the biomechanical stimulus was greater with jumping; it was aimed at preventing deconditioning in weightlessness and did not measure lymph flow (Bhattacharya 1980). The “68 percent more efficient than jogging” figure often attributed to it does not appear in the abstract.

Movement

Muscle contraction during walking, swimming, yoga and other activity is one of the extrinsic forces that move lymph (Zawieja 2009). Studies of physical activity and detoxification as an outcome were not found.

Sweating and Sauna

Sweat carries small amounts of metals and some industrial chemicals out of the body. Small descriptive studies led by Stephen Genuis (20 participants each, no comparison group) found arsenic, cadmium, lead, mercury, BPA, phthalates and some PCB congeners in induced sweat (Genuis 2011), and a 2012 systematic review by Margaret Sears and colleagues called for properly sized trials (Sears 2012). A 2019 review of sweat-gland physiology concluded that the role of sweating in eliminating waste products and toxicants “seems to be minor” compared with the kidneys and gastrointestinal tract, and that studies suggesting a larger role may reflect methodological problems such as skin-surface contamination (Baker 2019).

Sauna Types

Exercise-Induced Sweating

The BUS studies also collected sweat during exercise. The suggestion, found in detox protocols, that showering promptly prevents excreted toxins from being reabsorbed through the skin has not been tested in any study found.

Fluids and electrolytes: The 2019 review gives sweat concentrations of roughly 10–90 mmol/L for sodium and for chloride and 2–8 mmol/L for potassium; it found people with high sweat sodium at increased risk of salt imbalance during prolonged heavy sweating (Baker 2019). Among deaths in Finnish saunas in 1990–2002, half of those who died were under the influence of alcohol (Kenttämies & Karkola 2008). Session schedules, temperatures, the Hubbard niacin-sauna regimen and its trial, and the full list of hazards are covered on the Sweating and Sauna Therapy page.

Colon Health and Elimination

Compounds that the liver excretes into bile pass into the intestine, where some are reabsorbed and returned to the liver (enterohepatic recirculation). Detox protocols therefore treat bowel regularity as part of detoxification.

Hydration and Detoxification

The kidneys excrete water-soluble compounds and conjugates in urine, and dehydration reduces urine output and contributes to constipation. Detox protocols commonly set water targets, such as half the body weight (in pounds) as ounces of water a day. A 2002 review that looked for the origin of the “eight glasses a day” advice found no scientific studies supporting it for healthy adults in a temperate climate, while noting that larger intakes are called for in some diseases and with vigorous work and exercise, especially in heat (Valtin 2002). No study found has shown that drinking extra water during a detox program increases toxin removal. NCCIH notes that drinking large amounts of water and herbal tea while eating nothing for days could lead to dangerous electrolyte imbalances.

Juice Cleansing: Claims and Findings

Juice cleanses are among the most popular detox approaches. A 2017 review of popular weight-loss strategies attributes the short-term weight loss of juicing and detox diets to extremely low calorie intake and found that they tend to lead to weight gain once a normal diet resumes (Obert 2017).

Claims Made for Juice Cleanses

Concerns Raised in the Research

Naturopathic writers commonly describe limiting a juice cleanse to three to five days, favoring vegetable juices over fruit, and adding protein and a separate fiber source. These are practitioner conventions; no trial compared them.

What Detox Diets Include and Exclude

Naturopathic detox eating plans are built from whole foods and exclude processed foods. They have not been tested as detox programs in randomized trials (Klein & Kiat 2015), though many of the foods they include are part of ordinary healthy diets.

Foods Commonly Included

Foods Commonly Excluded, and the Reasons Given

Detox Reactions and the Herxheimer Response

Detox protocols describe a temporary worsening of symptoms early in a program, which they call a “healing crisis” or “Herxheimer reaction” and attribute to toxins being mobilized faster than they are eliminated, or to the die-off of microorganisms.

In medicine, the Jarisch–Herxheimer reaction is a specific event: within 24 hours of antibiotic treatment for the spirochetal infections syphilis, Lyme disease, leptospirosis and relapsing fever, patients develop shaking chills, a rise in temperature and intensified skin rashes, which usually resolve a few hours later. It is regarded as an adverse effect of antibiotics, is caused by spirochetal components and inflammatory cytokines, and is rarely fatal except in newborns and in pregnancy (Butler 2017). No study found has shown that detox programs produce a reaction of this kind, or that symptoms during a detox program are a sign of toxins leaving the body.

Symptoms Reported During Detox Programs

Several of these can also come from ordinary causes during a program, such as caffeine withdrawal, low calorie intake, laxatives or dehydration; NCCIH notes that detox programs may include laxatives, which can cause diarrhea and dehydration.

What Practitioners Describe Doing

Practitioners describe slowing the program down, drinking more water, keeping bowel movements regular, using binders, resting, and taking Epsom salt baths. The claim that magnesium sulfate baths “draw toxins through the skin” or deliver useful magnesium is not supported: a 2017 review concluded that the promotion of transdermal magnesium is scientifically unsupported (Gröber 2017). Severe or persistent symptoms during a program are a reason for medical assessment.

Program Timelines: What Has Been Tested

Naturopathic programs are commonly structured in phases. The schedule below is how such programs are described; it is a practitioner framework, and no trial found has compared one detox schedule with another or with no program.

Preparation Phase (1 to 2 Weeks)

Active Detox Phase (2 to 6 Weeks)

Transition Phase (1 to 2 Weeks)

Maintenance Phase (Ongoing)

The closest thing to a tested program is the Hubbard regimen of niacin, exercise and several hours a day of sauna for four to six weeks: its one randomized trial, a 2019 pilot in 32 veterans with Gulf War illness, did not report toxicant levels (covered on the Sweating and Sauna Therapy page). Practitioners often describe heavy-metal programs as lasting months; there are no trial data on how long such programs take or whether they lower body burden.

Cautions and Contraindications

The research raises concerns about several detox practices and about particular groups of people.

Naturopathic detoxification is framed by its practitioners as supporting the body’s own capacity to heal. Decisions about detox programs, supplements and chelation, especially alongside prescription medicines, belong with a clinician.


Back to Table of Contents

Key Research Papers

  1. Klein AV, Kiat H (2015). Detox diets for toxin elimination and weight management: a critical review of the evidence. J Hum Nutr Diet 28(6):675-86 — PubMed PMID: 25522674
  2. National Center for Complementary and Integrative Health (NIH). “Detoxes” and “Cleanses”: What You Need To Know — nccih.nih.gov
  3. Hodges RE, Minich DM (2015). Modulation of Metabolic Detoxification Pathways Using Foods and Food-Derived Components: A Scientific Review with Clinical Application. J Nutr Metab 2015:760689 — PubMed PMID: 26167297
  4. Liska DJ (1998). The detoxification enzyme systems. Altern Med Rev 3(3):187-98 — PubMed PMID: 9630736
  5. Grant DM (1991). Detoxification pathways in the liver. J Inherit Metab Dis 14(4):421-30 — PubMed PMID: 1749210
  6. Zanger UM, Schwab M (2013). Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation. Pharmacol Ther 138(1):103-41 — PubMed PMID: 23333322
  7. Wang Z, Walker GW, Muir DCG, Nagatani-Yoshida K (2020). Toward a Global Understanding of Chemical Pollution: A First Comprehensive Analysis of National and Regional Chemical Inventories. Environ Sci Technol 54(5):2575-2584 — PubMed PMID: 31968937
  8. Gore AC, Chappell VA, Fenton SE, et al. (2015). EDC-2: The Endocrine Society’s Second Scientific Statement on Endocrine-Disrupting Chemicals. Endocr Rev 36(6):E1-E150 — PubMed PMID: 26544531
  9. Bilzer M, Roggel F, Gerbes AL (2006). Role of Kupffer cells in host defense and liver disease. Liver Int 26(10):1175-86 — PubMed PMID: 17105582
  10. Heard KJ (2008). Acetylcysteine for acetaminophen poisoning. N Engl J Med 359(3):285-92 — PubMed PMID: 18635433
  11. Frosst P, Blom HJ, Milos R, et al. (1995). A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10(1):111-3 — PubMed PMID: 7647779
  12. Zółtaszek R, Hanausek M, Kiliańska ZM, Walaszek Z (2008). [The biological role of D-glucaric acid and its derivatives: potential use in medicine] (article in Polish, English abstract). Postepy Hig Med Dosw (Online) 62:451-62 — PubMed PMID: 18772850
  13. Centers for Disease Control and Prevention (2006). Deaths associated with hypocalcemia from chelation therapy — Texas, Pennsylvania, and Oregon, 2003-2005. MMWR Morb Mortal Wkly Rep 55(8):204-7 — PubMed PMID: 16511441
  14. Uchikawa T, Yasutake A, Kumamoto Y, et al. (2010). The influence of Parachlorella beyerinckii CK-5 on the absorption and excretion of methylmercury (MeHg) in mice. J Toxicol Sci 35(1):101-5 — PubMed PMID: 20118630
  15. Merino JJ, Parmigiani-Izquierdo JM, Toledano Gasca A, Cabaña-Muñoz ME (2019). The Long-Term Algae Extract (Chlorella and Fucus sp) and Aminosulphurate Supplementation Modulate SOD-1 Activity and Decrease Heavy Metals (Hg++, Sn) Levels in Patients with Long-Term Dental Titanium Implants and Amalgam Fillings Restorations. Antioxidants (Basel) 8(4):101 — PubMed PMID: 31014007
  16. Omura Y, Shimotsuura Y, Fukuoka A, Fukuoka H, Nomoto T (1996). Significant mercury deposits in internal organs following the removal of dental amalgam, & development of pre-cancer on the gingiva and the sides of the tongue and their represented organs as a result of inadvertent exposure to strong curing light & effective treatment: a clinical case report. Acupunct Electrother Res 21(2):133-60 — PubMed PMID: 8914687
  17. Aga M, Iwaki K, Ueda Y, et al. (2001). Preventive effect of Coriandrum sativum (Chinese parsley) on localized lead deposition in ICR mice. J Ethnopharmacol 77(2-3):203-8 — PubMed PMID: 11535365
  18. Chyka PA, Seger D, Krenzelok EP, Vale JA; American Academy of Clinical Toxicology; European Association of Poisons Centres and Clinical Toxicologists (2005). Position paper: Single-dose activated charcoal. Clin Toxicol (Phila) 43(2):61-87 — PubMed PMID: 15822758
  19. Neuvonen PJ, Olkkola KT (1988). Oral activated charcoal in the treatment of intoxications. Role of single and repeated doses. Med Toxicol Adverse Drug Exp 3(1):33-58 — PubMed PMID: 3285126
  20. Wang P, Afriyie-Gyawu E, Tang Y, et al. (2008). NovaSil clay intervention in Ghanaians at high risk for aflatoxicosis: II. Reduction in biomarkers of aflatoxin exposure in blood and urine. Food Addit Contam Part A 25(5):622-34 — PubMed PMID: 18478481
  21. Kraljević Pavelić S, Simović Medica J, Gumbarević D, Filošević A, Pržulj N, Pavelić K (2018). Critical Review on Zeolite Clinoptilolite Safety and Medical Applications in vivo. Front Pharmacol 9:1350 — PubMed PMID: 30538633
  22. Eliaz I, Hotchkiss AT, Fishman ML, Rode D (2006). The effect of modified citrus pectin on urinary excretion of toxic elements. Phytother Res 20(10):859-64 — PubMed PMID: 16835878
  23. Fahey JW, Zhang Y, Talalay P (1997). Broccoli sprouts: an exceptionally rich source of inducers of enzymes that protect against chemical carcinogens. Proc Natl Acad Sci U S A 94(19):10367-72 — PubMed PMID: 9294217
  24. Egner PA, Chen JG, Zarth AT, et al. (2014). Rapid and sustainable detoxication of airborne pollutants by broccoli sprout beverage: results of a randomized clinical trial in China. Cancer Prev Res (Phila) 7(8):813-823 — PubMed PMID: 24913818
  25. Kianoush S, Balali-Mood M, Mousavi SR, et al. (2012). Comparison of therapeutic effects of garlic and d-Penicillamine in patients with chronic occupational lead poisoning. Basic Clin Pharmacol Toxicol 110(5):476-81 — PubMed PMID: 22151785
  26. Rambaldi A, Jacobs BP, Gluud C (2007). Milk thistle for alcoholic and/or hepatitis B or C virus liver diseases. Cochrane Database Syst Rev (4):CD003620 — PubMed PMID: 17943794
  27. Fried MW, Navarro VJ, Afdhal N, et al. (2012). Effect of silymarin (milk thistle) on liver disease in patients with chronic hepatitis C unsuccessfully treated with interferon therapy: a randomized controlled trial. JAMA 308(3):274-82 — PubMed PMID: 22797645
  28. Richie JP Jr, Nichenametla S, Neidig W, et al. (2015). Randomized controlled trial of oral glutathione supplementation on body stores of glutathione. Eur J Nutr 54(2):251-63 — PubMed PMID: 24791752
  29. Allen J, Bradley RD (2011). Effects of oral glutathione supplementation on systemic oxidative stress biomarkers in human volunteers. J Altern Complement Med 17(9):827-33 — PubMed PMID: 21875351
  30. Packer L, Witt EH, Tritschler HJ (1995). alpha-Lipoic acid as a biological antioxidant. Free Radic Biol Med 19(2):227-50 — PubMed PMID: 7649494
  31. Dawson EB, Evans DR, Harris WA, et al. (1999). The effect of ascorbic acid supplementation on the blood lead levels of smokers. J Am Coll Nutr 18(2):166-70 — PubMed PMID: 10204833
  32. Zawieja DC (2009). Contractile physiology of lymphatics. Lymphat Res Biol 7(2):87-96 — PubMed PMID: 19534632
  33. Bhattacharya A, McCutcheon EP, Shvartz E, Greenleaf JE (1980). Body acceleration distribution and O2 uptake in humans during running and jumping. J Appl Physiol Respir Environ Exerc Physiol 49(5):881-7 — PubMed PMID: 7429911
  34. Genuis SJ, Birkholz D, Rodushkin I, Beesoon S (2011). Blood, urine, and sweat (BUS) study: monitoring and elimination of bioaccumulated toxic elements. Arch Environ Contam Toxicol 61(2):344-57 — PubMed PMID: 21057782
  35. Genuis SJ, Beesoon S, Birkholz D, Lobo RA (2012). Human excretion of bisphenol A: blood, urine, and sweat (BUS) study. J Environ Public Health 2012:185731 — PubMed PMID: 22253637
  36. Sears ME, Kerr KJ, Bray RI (2012). Arsenic, cadmium, lead, and mercury in sweat: a systematic review. J Environ Public Health 2012:184745 — PubMed PMID: 22505948
  37. Baker LB (2019). Physiology of sweat gland function: The roles of sweating and sweat composition in human health. Temperature (Austin) 6(3):211-259 — PubMed PMID: 31608304
  38. Laukkanen T, Khan H, Zaccardi F, Laukkanen JA (2015). Association between sauna bathing and fatal cardiovascular and all-cause mortality events. JAMA Intern Med 175(4):542-8 — PubMed PMID: 25705824
  39. Patrick RP, Johnson TL (2021). Sauna use as a lifestyle practice to extend healthspan. Exp Gerontol 154:111509 — PubMed PMID: 34363927
  40. Kenttämies A, Karkola K (2008). Death in sauna. J Forensic Sci 53(3):724-9 — PubMed PMID: 18471223
  41. Goldin BR, Gorbach SL (1984). The effect of milk and lactobacillus feeding on human intestinal bacterial enzyme activity. Am J Clin Nutr 39(5):756-61 — PubMed PMID: 6424430
  42. Lam LK, Sparnins VL, Wattenberg LW (1982). Isolation and identification of kahweol palmitate and cafestol palmitate as active constituents of green coffee beans that enhance glutathione S-transferase activity in the mouse. Cancer Res 42(4):1193-8 — PubMed PMID: 7059995
  43. Acosta RD, Cash BD (2009). Clinical effects of colonic cleansing for general health promotion: a systematic review. Am J Gastroenterol 104(11):2830-6 — PubMed PMID: 19724266
  44. Valtin H (2002). “Drink at least eight glasses of water a day.” Really? Is there scientific evidence for “8 x 8”? Am J Physiol Regul Integr Comp Physiol 283(5):R993-1004 — PubMed PMID: 12376390
  45. Obert J, Pearlman M, Obert L, Chapin S (2017). Popular Weight Loss Strategies: a Review of Four Weight Loss Techniques. Curr Gastroenterol Rep 19(12):61 — PubMed PMID: 29124370
  46. Getting JE, Gregoire JR, Phul A, Kasten MJ (2013). Oxalate nephropathy due to ‘juicing’: case report and review. Am J Med 126(9):768-72 — PubMed PMID: 23830537
  47. Butler T (2017). The Jarisch-Herxheimer Reaction After Antibiotic Treatment of Spirochetal Infections: A Review of Recent Cases and Our Understanding of Pathogenesis. Am J Trop Med Hyg 96(1):46-52 — PubMed PMID: 28077740
  48. Gröber U, Werner T, Vormann J, Kisters K (2017). Myth or Reality-Transdermal Magnesium? Nutrients 9(8):813 — PubMed PMID: 28788060
  49. Bailey DG, Malcolm J, Arnold O, Spence JD (1998). Grapefruit juice-drug interactions. Br J Clin Pharmacol 46(2):101-10 — PubMed PMID: 9723817
  50. Markowitz JS, Donovan JL, DeVane CL, et al. (2003). Effect of St John’s wort on drug metabolism by induction of cytochrome P450 3A4 enzyme. JAMA 290(11):1500-4 — PubMed PMID: 13129991

PubMed Topic Searches

  1. Glutathione and detoxification — PubMed search
  2. Cytochrome P450 phase I detoxification — PubMed search
  3. Heavy metal chelation therapy — PubMed search
  4. Sauna and sweat toxin excretion — PubMed search
  5. Cruciferous vegetables and liver detoxification — PubMed search
  6. Milk thistle (silymarin) and liver function — PubMed search
  7. Herxheimer reaction research — PubMed search

↑ Back to Table of Contents

Connections

↑ Back to Table of Contents

Detox Protocols — scientific infographic poster