Indications
Herbal products have become increasingly popular, especially among individuals with chronic diseases. Herbalists and physicians alike used the milk thistle (Silybum marianum), an annual or biennial herb from the Mediterranean region, for hundreds of years to treat a wide range of liver pathology, including fatty liver disease, hepatitis, and cirrhosis, and to protect the liver from environmental toxins.[1] Today, millions of people consume milk thistle to support healthy liver function. The ripe seeds are primarily the medicinal part of the plant.[2]
Researchers have focused their efforts on studying silymarin, a mixture of flavonolignans extracted from milk thistle, and the most active ingredient of this extract, silybin.[3] Silymarin and silybin have become some of the most prescribed natural compounds, and the 2 names are often interchangeable. However, each has a different clinical purpose, but there are no definitive results in terms of clinical efficacy. Currently, herbal products such as milk thistle in the United States are not considered drugs and do not have the same level of regulation as drugs from the US Food and Drug Administration (FDA).[4] Like most herbal products, the FDA does not approve or recommend milk thistle as a treatment for any medical condition.
Recent studies have focused on the role of milk thistle in treating nonalcoholic fatty liver disease, a common hepatic manifestation of metabolic syndrome. The prevalence of NAFLD in Western countries is approximately 20% to 30%.[5][6] Currently, there is no consensus approach when it comes to the treatment of NAFLD. Most clinicians approach the disease by emphasizing lifestyle modification, including diet, weight loss, and limiting alcohol intake. However, study results suggest milk thistle can benefit patients with NAFLD. Data indicate that silymarin treatment correlated with reduced insulin resistance and decreased fasting insulin levels significantly. Patients treated with 600 mg/d of silymarin for 12 months demonstrated lower fasting insulin levels.[7] A separate clinical trial evaluated silymarin's effectiveness compared to metformin and pioglitazone in NAFLD patients. Research showed that patients treated with silymarin had significantly lower transaminase levels than those treated with metformin or pioglitazone.[8]
In a sample of 25 patients treated for 4 months with 200 mg of silymarin 3 times a day before meals, there was a significant reduction in blood glucose levels (from 156 ± 46 mg/dL to 133 ± 39 mg/dL) compared to an increase in the placebo-treated group. In the same period, their HbA1c levels also dropped by an average of 1 point. The same group of patients also demonstrated significantly reduced total cholesterol, triglycerides, and LDL levels.[9][10] Another study aimed to evaluate the efficacy of combined treatment, which includes vitamin E, silybin, and phospholipids, and demonstrated that this complex improves liver damage, especially plasma markers of liver fibrosis and insulin resistance.[11] In Europe, intravenous preparations of purified silibinin are approved as an antidote to Amanita phalloides, a mushroom toxin that causes severe liver damage.[12]
Early lab studies suggest that silymarin and other active molecules in milk thistle may exhibit anti-cancer effects, including interfering with cancer cell division and reproduction, shortening cancer cell lifespan, and reducing the blood supply to tumors. Other research suggests milk thistle acts synergistically with chemotherapy. More research is necessary to determine whether milk thistle can exhibit this activity in vivo.[13][14][15][16]
Mechanism of Action
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Mechanism of Action
Milk thistle exhibits its hepatoprotective properties by 3 major mechanisms: an antioxidant, an anti-inflammatory, and an antifibrotic substance.[17] The anti-inflammatory properties of milk thistle are attributable to its ability to regulate cytokines responsible for inducing inflammation. Milk thistle has been shown to down-regulate and inhibit the expression of COX-2, a key mediator of inflammatory pathways.[17][18] Silymarin also inhibits the transduction cascade controlled by NF-κB. This protein complex induces the expression of pro-inflammatory genes responsible for encoding cytokines directly involved in the inflammatory process. NF-κB also regulates the survival of inflammatory T-cells. Studies done on mice showed silybin reduced liver and plasma content of pro-inflammatory cytokines while increasing IL-10, a cytokine whose function is to decrease and regulate the inflammatory response.[19][20]
Milk thistle has also shown antioxidant properties in hepatocytes and can inhibit free radicals derived from the metabolism of toxic substances such as ethanol, acetaminophen, and carbon tetrachloride. This herb stimulates protein synthesis by protecting cell membranes from free radical-induced damage and directly inhibiting radical formation. Milk thistle can also act as a free radical scavenger and increase the intracellular content of scavengers.[21] Studies have shown that silymarin increases superoxide dismutase activity and serum glutathione and glutathione peroxidase levels.[22][23] Silybin can also act as an iron chelator, further strengthening its antioxidant properties.[24]
In addition to its anti-inflammatory and antioxidant properties, silybin also shows promise as an antifibrotic agent, which is attributable to its ability to decrease platelet-derived growth factor (PDGF)-induced DNA synthesis in cells, which inhibits the transformation of stellate hepatocytes into myofibroblasts. By reducing myofibroblasts, silybin indirectly prevents the deposition of collagen fibers that lead to the progression of liver injury.[17] Finally, silybin has demonstrated an association with a significant reduction of TGF-β, a key regulator in the pathogenesis of liver fibrosis.[25]
Pharmacokinetics
Absorption: Small studies have demonstrated that flavonolignans were rapidly absorbed and eliminated after oral administration of standardized milk thistle extract.[26][27]
Distribution: Pharmacokinetic parameters appear to indicate a dose-dependent volume of distribution of some component phytochemicals in single-dose escalation assessments, with some of these compounds only detectable at the highest dose.[26]
Metabolism: Research indicates that silymarin extracts undergo extensive metabolism; most of milk thistle's phytochemicals are subject to phase II hepatic metabolic processes (eg, glucuronidation, sulfation).[26] Other research also concluded that since milk thistle flavonolignans are extensively modified following oral dosing and are recovered in the urine as sulpho- and glucuronyl conjugates, this analysis demonstrates a strong link to hepatic phase II metabolism.[27]
Elimination: The parent compounds found in milk thistle and their metabolites may enter the internal circulation and are excreted in the bile or urine. Milk thistle flavonolignans metabolites are recovered in urine.[27]
Administration
Available Dosage Forms and Adult Dosing
Like most herbal supplements, milk thistle is orally administered and is available in capsules, tablets, or as a liquid extract containing ethanol-extracted silymarin in doses of 250 to 750 mg. The daily dosage varies, but the typical dose frequency is 2 to 3 times daily. Research shows that silymarin is generally safe in humans at standard therapeutic doses and is even well tolerated at higher doses of 700 mg 3 times a day for 24 weeks.[28]
Special Patient Populations
Hepatic impairment: Despite milk thistle's use in patients with and without liver disease, it has not been implicated in altering liver function tests or causing clinically relevant acute hepatic injury.[1]
Renal impairment: There is little evidence regarding dosing milk thistle in patients with renal impairment, and in fact, some research suggests milk thistle may be renoprotective.[29]
Pregnancy considerations: Caution is recommended during pregnancy, as more studies are needed on milk thistle and pregnancy, especially in humans.[30]
Breastfeeding considerations: Limited data indicate that the silymarin components of milk thistle are not excreted into breast milk in measurable amounts.[31]
Pediatric patients: No studies exist examining whether pediatric use of milk thistle is safe.
Older patients: No data implicates milk thistle as causing problems in older patients. Clinicians should exercise caution and monitor older patients who take milk thistle.
Adverse Effects
According to pharmacological studies, silymarin is recognized as a safe herbal product since taking it at therapeutic doses is not toxic.[17] Although rare, some of the adverse effects of milk thistle include:
- Gastroenteritis
- Diarrhea
- Headache
- Bloating
- Dermatological symptoms (eg, hives, rash, pruritus)
Oral silymarin generally has few, if any, adverse effects and is well-tolerated even at higher doses. Milk thistle may prompt an allergic reaction in individuals sensitive to the Asteraceae/Compositae plant family (eg, ragweed, chrysanthemums, marigolds).
Drug-Drug Interactions
- Milk thistle does not have any documented significant drug-drug interactions. However, since it does exert some effect on the CYP450 enzyme system, it might affect certain drugs, including diazepam and warfarin. However, this effect is not potent or even moderate at recommended doses.[32] Some researchers have noted an association between milk thistle and bleeding in patients on blood thinners.[33] Caution is advised with narrow therapeutic window medications.[30]
- Since milk thistle appears to be able to lower blood sugar, it may have an additive effect with other medications for type 2 diabetes.[34]
- Milk thistle may affect the hepatic metabolism of raloxifene by inhibiting raloxifene glucuronidation.[35]
Contraindications
There are currently no documented contraindications to using milk thistle. However, there is little information about milk thistle's interactions with cancer drugs, radiation therapy, or other medications.[2]
Monitoring
As with most herbal products, there is no definitive way to monitor blood levels of milk thistle or its compounds, and little data is available on the therapeutic index of the supplement. However, silymarin has been shown to decrease the activity of cytochrome P-450 enzymes and UDP-glucuronosyltransferase (UGT) enzymes, prompting healthcare providers to caution patients against co-administration of milk thistle and specific pharmaceutical agents.
Toxicity
Asymptomatic liver toxicity in clinical trials performed on cancer patients has been reported; researchers observed an increase in ALT and bilirubin levels. However, this observation was at extremely high doses of silybin (between 10 to 20 g/d).[17]
Enhancing Healthcare Team Outcomes
Research has indicated that milk thistle has the potential to reduce biochemical changes seen in patients with NAFLD, and multiple pharmacological studies have demonstrated why many consider the plant to be a hepatoprotective substance. Based on the data available, many believe that milk thistle represents a viable alternative for patients with acute and chronic liver disease, especially those in whom standard therapy has failed. However, more evidence is needed to establish milk thistle's short-term and long-term effects. Other studies have shown potential therapeutic effects such as anticancer, anti-diabetic, anti-Alzheimer, and anti-Parkinson effects, so interest in researching this supplement remains high.[30]
Healthcare workers, including physicians, nurse practitioners, nursing staff, and pharmacists, should be aware that currently, there is no firm clinical evidence to recommend silybin or silymarin in the clinical setting.[36] Providers must function as an interprofessional team to ensure that all care team members know what drugs and supplements the patient might take. Physicians, advanced practice practitioners, nurses, and pharmacists need to inquire about non-prescription agents that the patient may be using, and milk thistle would be included in this query as an over-the-counter substance. The pharmacist must consider milk thistle and other OTC substances in their medication reconciliation and alert the rest of the team to its presence in the patient's regimen and any potential interactions. Nursing staff should be aware of the pharmacology of milk thistle and document it in the patient's medical record so all other healthcare team members can be informed. All healthcare team members need to make the patient understand that just because milk thistle is available over the counter does not mean it is a benign substance. This type of collaboration on the interprofessional team is crucial to managing patient outcomes effectively.
Using milk thistle is inconsistent with the established standard of care. There have been thousands of papers published on milk thistle to date, and the high publication volume suggests that interest among the research community remains high. Future research should continue to assess the mechanisms for preventing inflammatory sequelae and the cytoprotective effects of milk thistle, including silymarin and silybin. This research will allow for better recognition of cellular targets of milk thistle, leading to a more potent and selective compound that could prove clinically useful in treating a wide variety of liver pathology.
References
. Milk Thistle. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. 2012:(): [PubMed PMID: 31644124]
Nawaz A, Zaib S, Khan I, Ahmed A, Shahzadi K, Riaz H. Silybum marianum: An Overview of its Phytochemistry and Pharmacological Activities with Emphasis on Potential Anticancer Properties. Anti-cancer agents in medicinal chemistry. 2023:23(13):1519-1534. doi: 10.2174/1871520623666230412111152. Epub [PubMed PMID: 37055902]
Level 3 (low-level) evidenceBijak M. Silybin, a Major Bioactive Component of Milk Thistle (Silybum marianum L. Gaernt.)-Chemistry, Bioavailability, and Metabolism. Molecules (Basel, Switzerland). 2017 Nov 10:22(11):. doi: 10.3390/molecules22111942. Epub 2017 Nov 10 [PubMed PMID: 29125572]
Dwyer JT, Coates PM, Smith MJ. Dietary Supplements: Regulatory Challenges and Research Resources. Nutrients. 2018 Jan 4:10(1):. doi: 10.3390/nu10010041. Epub 2018 Jan 4 [PubMed PMID: 29300341]
Williams R. Global challenges in liver disease. Hepatology (Baltimore, Md.). 2006 Sep:44(3):521-6 [PubMed PMID: 16941687]
Bedogni G, Miglioli L, Masutti F, Tiribelli C, Marchesini G, Bellentani S. Prevalence of and risk factors for nonalcoholic fatty liver disease: the Dionysos nutrition and liver study. Hepatology (Baltimore, Md.). 2005 Jul:42(1):44-52 [PubMed PMID: 15895401]
Level 2 (mid-level) evidenceVelussi M, Cernigoi AM, De Monte A, Dapas F, Caffau C, Zilli M. Long-term (12 months) treatment with an anti-oxidant drug (silymarin) is effective on hyperinsulinemia, exogenous insulin need and malondialdehyde levels in cirrhotic diabetic patients. Journal of hepatology. 1997 Apr:26(4):871-9 [PubMed PMID: 9126802]
Level 1 (high-level) evidenceHajiaghamohammadi AA, Ziaee A, Oveisi S, Masroor H. Effects of metformin, pioglitazone, and silymarin treatment on non-alcoholic Fatty liver disease: a randomized controlled pilot study. Hepatitis monthly. 2012 Aug:12(8):e6099. doi: 10.5812/hepatmon.6099. Epub 2012 Aug 3 [PubMed PMID: 23087748]
Level 3 (low-level) evidenceKazazis CE, Evangelopoulos AA, Kollas A, Vallianou NG. The therapeutic potential of milk thistle in diabetes. The review of diabetic studies : RDS. 2014 Summer:11(2):167-74. doi: 10.1900/RDS.2014.11.167. Epub 2014 Aug 10 [PubMed PMID: 25396404]
Level 3 (low-level) evidenceHuseini HF, Larijani B, Heshmat R, Fakhrzadeh H, Radjabipour B, Toliat T, Raza M. The efficacy of Silybum marianum (L.) Gaertn. (silymarin) in the treatment of type II diabetes: a randomized, double-blind, placebo-controlled, clinical trial. Phytotherapy research : PTR. 2006 Dec:20(12):1036-9 [PubMed PMID: 17072885]
Level 1 (high-level) evidenceLoguercio C, Federico A, Trappoliere M, Tuccillo C, de Sio I, Di Leva A, Niosi M, D'Auria MV, Capasso R, Del Vecchio Blanco C, Real Sud Group. The effect of a silybin-vitamin e-phospholipid complex on nonalcoholic fatty liver disease: a pilot study. Digestive diseases and sciences. 2007 Sep:52(9):2387-95 [PubMed PMID: 17410454]
Level 3 (low-level) evidenceHruby K, Csomos G, Fuhrmann M, Thaler H. Chemotherapy of Amanita phalloides poisoning with intravenous silibinin. Human toxicology. 1983 Apr:2(2):183-95 [PubMed PMID: 6862461]
Rahnama S, Tehrankhah ZM, Mohajerani F, Mohammadi FS, Yeganeh ZY, Najafi F, Babashah S, Sadeghizadeh M. Milk thistle nano-micelle formulation promotes cell cycle arrest and apoptosis in hepatocellular carcinoma cells through modulating miR-155-3p /SOCS2 /PHLDA1 signaling axis. BMC complementary medicine and therapies. 2023 Sep 26:23(1):337. doi: 10.1186/s12906-023-04168-5. Epub 2023 Sep 26 [PubMed PMID: 37749575]
Jo AI, Kim MM. Silibinin Inhibits Cell Invasion through the Inhibition of MMPs, p-p38, and IL-1β in Human Fibrosarcoma Cells. Frontiers in bioscience (Landmark edition). 2023 Apr 6:28(4):64. doi: 10.31083/j.fbl2804064. Epub [PubMed PMID: 37114542]
Iqbal MA, Chattopadhyay S, Siddiqui FA, Ur Rehman A, Siddiqui S, Prakasam G, Khan A, Sultana S, Bamezai RN. Silibinin induces metabolic crisis in triple-negative breast cancer cells by modulating EGFR-MYC-TXNIP axis: potential therapeutic implications. The FEBS journal. 2021 Jan:288(2):471-485. doi: 10.1111/febs.15353. Epub 2020 May 28 [PubMed PMID: 32356386]
Kawaguchi-Suzuki M, Frye RF, Zhu HJ, Brinda BJ, Chavin KD, Bernstein HJ, Markowitz JS. The effects of milk thistle (Silybum marianum) on human cytochrome P450 activity. Drug metabolism and disposition: the biological fate of chemicals. 2014 Oct:42(10):1611-6. doi: 10.1124/dmd.114.057232. Epub 2014 Jul 15 [PubMed PMID: 25028567]
Loguercio C, Festi D. Silybin and the liver: from basic research to clinical practice. World journal of gastroenterology. 2011 May 14:17(18):2288-301. doi: 10.3748/wjg.v17.i18.2288. Epub [PubMed PMID: 21633595]
Abenavoli L, Bellentani S. Milk thistle to treat non-alcoholic fatty liver disease: dream or reality? Expert review of gastroenterology & hepatology. 2013 Nov:7(8):677-9. doi: 10.1586/17474124.2013.842893. Epub 2013 Oct 17 [PubMed PMID: 24134155]
Level 3 (low-level) evidenceSchümann J, Prockl J, Kiemer AK, Vollmar AM, Bang R, Tiegs G. Silibinin protects mice from T cell-dependent liver injury. Journal of hepatology. 2003 Sep:39(3):333-40 [PubMed PMID: 12927918]
Level 3 (low-level) evidenceBeyoğlu D, Idle JR. Metabolomic insights into the mode of action of natural products in the treatment of liver disease. Biochemical pharmacology. 2020 Oct:180():114171. doi: 10.1016/j.bcp.2020.114171. Epub 2020 Jul 22 [PubMed PMID: 32710968]
Trouillas P, Marsal P, Svobodová A, Vostálová J, Gazák R, Hrbác J, Sedmera P, Kren V, Lazzaroni R, Duroux JL, Walterová D. Mechanism of the antioxidant action of silybin and 2,3-dehydrosilybin flavonolignans: a joint experimental and theoretical study. The journal of physical chemistry. A. 2008 Feb 7:112(5):1054-63. doi: 10.1021/jp075814h. Epub 2008 Jan 15 [PubMed PMID: 18193843]
Wellington K, Jarvis B. Silymarin: a review of its clinical properties in the management of hepatic disorders. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy. 2001:15(7):465-89 [PubMed PMID: 11520257]
Level 3 (low-level) evidenceCacciapuoti F, Scognamiglio A, Palumbo R, Forte R, Cacciapuoti F. Silymarin in non alcoholic fatty liver disease. World journal of hepatology. 2013 Mar 27:5(3):109-13. doi: 10.4254/wjh.v5.i3.109. Epub [PubMed PMID: 23556042]
Borsari M, Gabbi C, Ghelfi F, Grandi R, Saladini M, Severi S, Borella F. Silybin, a new iron-chelating agent. Journal of inorganic biochemistry. 2001 Jun:85(2-3):123-9 [PubMed PMID: 11410232]
Fabregat I, Moreno-Càceres J, Sánchez A, Dooley S, Dewidar B, Giannelli G, Ten Dijke P, IT-LIVER Consortium. TGF-β signalling and liver disease. The FEBS journal. 2016 Jun:283(12):2219-32. doi: 10.1111/febs.13665. Epub 2016 Feb 22 [PubMed PMID: 26807763]
Zhu HJ, Brinda BJ, Chavin KD, Bernstein HJ, Patrick KS, Markowitz JS. An assessment of pharmacokinetics and antioxidant activity of free silymarin flavonolignans in healthy volunteers: a dose escalation study. Drug metabolism and disposition: the biological fate of chemicals. 2013 Sep:41(9):1679-85. doi: 10.1124/dmd.113.052423. Epub 2013 Jul 8 [PubMed PMID: 23835761]
Calani L, Brighenti F, Bruni R, Del Rio D. Absorption and metabolism of milk thistle flavanolignans in humans. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2012 Dec 15:20(1):40-6. doi: 10.1016/j.phymed.2012.09.004. Epub 2012 Oct 13 [PubMed PMID: 23072776]
Raclariu-Manolică AC, Socaciu C. Detecting and Profiling of Milk Thistle Metabolites in Food Supplements: A Safety-Oriented Approach by Advanced Analytics. Metabolites. 2023 Mar 17:13(3):. doi: 10.3390/metabo13030440. Epub 2023 Mar 17 [PubMed PMID: 36984880]
Rafieian-Kopaie M, Nasri H. Silymarin and diabetic nephropathy. Journal of renal injury prevention. 2012:1(1):3-5. doi: 10.12861/jrip.2012.02. Epub 2012 Jan 1 [PubMed PMID: 25340091]
Soleimani V, Delghandi PS, Moallem SA, Karimi G. Safety and toxicity of silymarin, the major constituent of milk thistle extract: An updated review. Phytotherapy research : PTR. 2019 Jun:33(6):1627-1638. doi: 10.1002/ptr.6361. Epub 2019 May 8 [PubMed PMID: 31069872]
. Milk Thistle. Drugs and Lactation Database (LactMed®). 2006:(): [PubMed PMID: 30000830]
Wanwimolruk S, Prachayasittikul V. Cytochrome P450 enzyme mediated herbal drug interactions (Part 1). EXCLI journal. 2014:13():347-91 [PubMed PMID: 26417265]
Hatfield J, Saad S, Housewright C. Dietary supplements and bleeding. Proceedings (Baylor University. Medical Center). 2022:35(6):802-807. doi: 10.1080/08998280.2022.2121575. Epub 2022 Sep 15 [PubMed PMID: 36304597]
Necyk C, Zubach-Cassano L. Natural Health Products and Diabetes: A Practical Review. Canadian journal of diabetes. 2017 Dec:41(6):642-647. doi: 10.1016/j.jcjd.2017.06.014. Epub 2017 Aug 18 [PubMed PMID: 28826695]
Gufford BT, Chen G, Vergara AG, Lazarus P, Oberlies NH, Paine MF. Milk Thistle Constituents Inhibit Raloxifene Intestinal Glucuronidation: A Potential Clinically Relevant Natural Product-Drug Interaction. Drug metabolism and disposition: the biological fate of chemicals. 2015 Sep:43(9):1353-9. doi: 10.1124/dmd.115.065086. Epub 2015 Jun 12 [PubMed PMID: 26070840]
Tamayo C, Diamond S. Review of clinical trials evaluating safety and efficacy of milk thistle (Silybum marianum [L.] Gaertn.). Integrative cancer therapies. 2007 Jun:6(2):146-57 [PubMed PMID: 17548793]