Chemistry:Silibinin

From HandWiki
Short description: Chemical compound
Silibinin
Silibinin A.svg
Silibinin B.svg
Silibinin A and silibinin B structures
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration		Oral and Intravenous
ATC code
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC25H22O10
Molar mass482.441 g·mol−1
3D model (JSmol)
 ☒N☑Y (what is this?)  (verify)

Silibinin (INN), also known as silybin (both from Silybum, the generic name of the plant from which it is extracted), is the major active constituent of silymarin, a standardized extract of the milk thistle, containing a mixture of flavonolignans consisting of silibinin, isosilibinin, silychristin, silidianin, and others. Silibinin itself is a mixture of two diastereomers, silybin A and silybin B, in approximately equimolar ratio.[1] Silibinin is used in pure forms as a medication, and more frequently as an active ingredient in milk thistle–derived herbal supplements.

Medical uses

For approved drug preparations and parenteral applications in the treatment of Amanita mushroom poisoning, the water-soluble silibinin-C-2',3-dihyrogensuccinate disodium salt is used. In 2011, the same compound also received Orphan Medicinal Product Designation for the prevention of recurrent hepatitis C in liver transplant recipients by the European Commission.[2]

Silibinin is available as drug (Legalon SIL (Madaus) (D, CH, A) and Silimarit (Bionorica), a Silymarin product) in many EU countries and used in the treatment of toxic liver damage (e.g. IV treatment in case of death cap poisoning); as adjunctive therapy in chronic hepatitis and cirrhosis.[citation needed][3][4]

There is limited evidence to support use of silibinin-containing products as a supplement in people with chronic liver disease (CLD). A systematic review and meta-analysis concluded that silymarin does not affect all-cause mortality in persons with cirrhosis, but it may help prevent liver-related mortality in those patients.[5] There is mixed evidence for silibinin as an antiinflammatory agent in alcohol-related liver disease or non-alcoholic fatty liver disease and trials continue.[6] There is little evidence to support a meaningful antiviral effect of milk thistle in chronic hepatitis C.[7][8]

Potential medical uses

Silibinin is under investigation to see whether it may have a role in cancer treatment (e.g. due to its inhibition of STAT3 signalling).[9]

Silibinin also has a number of potential mechanisms that could benefit the skin. These include chemoprotective effects from environmental toxins, anti-inflammatory effects, protection from UV induced photocarcinogenesis, protection from sunburn, protection from UVB-induced epidermal hyperplasia, and DNA repair for UV induced DNA damage (double strand breaks).[10] Studies on mice demonstrate a significant protection on chronic unpredictable mild stress (CUMS) induced depressive-like behavior on mice[11] and increased cognition in aged rats as a result of consuming silymarin.[12]

Due to its immunomodulatory,[13] iron chelating and antioxidant properties, this herb has the potential to be used in beta-thalassemia patients who receive regular blood transfusions and suffer from iron overload.[14]

Pharmacology

Poor water solubility and bioavailability of silymarin led to the development of enhanced formulations. Silipide (trade name Siliphos, not to be confused with the water treatment compound of the same name, a glass-like polyphosphate containing sodium, calcium magnesium and silicate, formulated for the treatment of water problems), a complex of silymarin and phosphatidylcholine (a phospholipid in lecithin), is about 10 times more bioavailable than silymarin.[15] An earlier study had concluded Siliphos to have 4.6 fold higher bioavailability.[16][non-primary source needed] It has been also reported that silymarin inclusion complex with β-cyclodextrin is much more soluble than silymarin itself.[17] There have also been prepared glycosides of silybin, which show better water solubility and even stronger hepatoprotective effect.[18]

Silymarin, like other flavonoids, has been shown to inhibit P-glycoprotein-mediated cellular efflux.[19] The modulation of P-glycoprotein activity may result in altered absorption and bioavailability of drugs that are P-glycoprotein substrates. It has been reported that silymarin inhibits cytochrome P450 enzymes and an interaction with drugs primarily cleared by P450s cannot be excluded.[20]

Toxicity

Silibinin and all the other compounds found in silymarin, especially silychristin, blocked the MCT8 transporter according to one in vitro study.[21] There is no published clinical information showing silymarin or silibinin cause any thyroid problems. In fact, one clinical trial found that silymarin actually helped prevent thyroid suppression that is often caused by the drug lithium.[22]

There is limited research on milk thistle and silymarin in pregnant humans. However, the one known clinical trial found only benefits, including but not limited to effectively treating intrahepatic cholestasis of pregnancy.[23][24] Silymarin is also devoid of embryotoxic potential in animal models.[25][26]

A phase I clinical trial in humans with prostate cancer designed to study the effects of high dose silibinin found 13 grams daily to be well tolerated in patients with advanced prostate cancer with asymptomatic liver toxicity (hyperbilirubinemia and elevation of alanine aminotransferase) being the most commonly seen adverse event.[27]

Biotechnology

Silymarin can be produced in callus and cell suspensions of Silybum marianum and substituted pyrazinecarboxamides can be used as abiotic elicitors of flavolignan production.[28]

Biosynthesis

The biosynthesis of silibinin A and silibinin B is composed of two major parts, taxifolin and coniferyl alcohol.[29][30] Coniferyl alcohol is synthesized in milk thistle seed coat. Starting with the transformation of phenylalanine into cinnamic acid mediated by phenylalanine ammonia-lyase.[31] Cinnamic acid will then go through two rounds of oxidation by trans-cinnamate 4-monooxygenase and 4-coumarate 3-hydroxylase to give caffeic acid. The meta position alcohol is methylated by caffeic acid 3-O-methyltransferase to produce ferulic acid. From ferulic acid, the production of coniferyl alcohol is carried out by 4-hydroxycinnamate CoA ligase, cinnamoyl CoA reductase, and cinnamyl alcohol dehydrogenase. For taxifolin, its genes for the biosynthesis can be overexpressed in flowers as the transcription is light dependent. The production of taxifolin utilizes a similar pathway as for synthesizing p-coumaric acid followed by three times of carbon chain elongation with malonyl-CoA and cyclization by chalcone synthase and chalcone isomerase to yield naringenin. Through flavanone 3-hydroxylase and flavonoid 3'-monooxygenase, taxifolin is furnished. To merge taxifolin and coniferyl alcohol, taxifolin can be translocated from the flower to the seed coat through symplast pathway. Both taxifolin and coniferyl alcohol will be oxidized by ascorbate peroxidase 1 to enable the single electron reaction to couple two fragments generating silybin (silibinin A + silibinin B).

Biosynthesis of silybin (silibinin A and silibinin B)

References

  1. ↑ "Milk Thistle and Prostate Cancer: Differential Effects of Pure Flavonolignans from Silybum marianum on Antiproliferative End Points in Human Prostate Carcinoma Cells". Cancer Research 65 (10): 4448–57. 2005. doi:10.1158/0008-5472.CAN-04-4662. PMID 15899838. http://cancerres.aacrjournals.org/content/canres/65/10/4448.full.pdf. 
  2. ↑ Rottapharm|Madaus. Media Communications Legalon®. Retrieved March 6, 2017.
  3. ↑ "Silymarin/Silybin and Chronic Liver Disease: A Marriage of Many Years.". Molecules 22 (2): 191. Jan 2017. doi:10.3390/molecules22020191. PMID 28125040. 
  4. ↑ Yarnell, Eric (2010). Natural Approach to Gastroenterology 2nd ed. Wenatchee: Wild Brilliance Press. p. 1701. ISBN 978-1933350066. https://wildbrilliancepress.com/production/natural_approach_to_gastroenterology. 
  5. ↑ "An updated systematic review with meta-analysis for the clinical evidence of silymarin". Forschende Komplementärmedizin 15 (1): 9–20. 2008. doi:10.1159/000113648. PMID 18334810. https://www.zora.uzh.ch/id/eprint/12530/. 
  6. ↑ "Efficacy of silymarin in patients with non-alcoholic fatty liver disease — the Siliver trial: a study protocol for a randomized controlled clinical trial". Trials 24 (1): 177. 2023. doi:10.1186/s13063-023-07210-6. Art. No. 177. PMID 36899430. 
  7. ↑ Nelson, Angela (31 August 2022). "Does Milk Thistle Help Your Liver?". in Khatri, Minesh. https://www.webmd.com/hepatitis/milk-thistle-liver. 
  8. ↑ "Effects and tolerance of silymarin (milk thistle) in chronic hepatitis C virus infection patients: a meta-analysis of randomized controlled trials". BioMed Research International 2014: 1–9. 2014. doi:10.1155/2014/941085. Art. ID 941085. PMID 25247194. 
  9. ↑ "Response of brain metastasis from lung cancer patients to an oral nutraceutical product containing silibinin". Oncotarget 7 (22): 32006–32014. May 2016. doi:10.18632/oncotarget.7900. PMID 26959886. 
  10. ↑ "Cosmeceuticals and silibinin". Clinics in Dermatology 27 (5): 479–484. September 2009. doi:10.1016/j.clindermatol.2009.05.012. PMID 19695480. 
  11. ↑ "Therapeutic potential of silymarin in chronic unpredictable mild stress induced depressive-like behavior in mice". Journal of Psychopharmacology 32 (2): 223–235. February 2018. doi:10.1177/0269881117742666. PMID 29215318. 
  12. ↑ "Chronic Silymarin, Quercetin and Naringenin Treatments Increase Monoamines Synthesis and Hippocampal Sirt1 Levels Improving Cognition in Aged Rats". Journal of Neuroimmune Pharmacology 13 (1): 24–38. March 2018. doi:10.1007/s11481-017-9759-0. PMID 28808887. 
  13. ↑ "Serum levels of TGFβ, IL-10, IL-17, and IL-23 cytokines in β-thalassemia major patients: the impact of silymarin therapy". Immunopharmacology and Immunotoxicology 36 (4): 271–274. August 2014. doi:10.3109/08923973.2014.926916. PMID 24945737. 
  14. ↑ "Evaluating the safety and efficacy of silymarin in β-thalassemia patients: a review". Hemoglobin 39 (2): 75–80. 2015-03-04. doi:10.3109/03630269.2014.1003224. PMID 25643967. 
  15. ↑ "A review of the bioavailability and clinical efficacy of milk thistle phytosome: a silybin-phosphatidylcholine complex (Siliphos)". Alternative Medicine Review 10 (3): 193–203. 2005. PMID 16164374. http://www.thorne.com/altmedrev/.fulltext/10/3/193.pdf. Retrieved 2010-12-14. 
  16. ↑ "Pharmacokinetic studies on IdB 1016, a silybin- phosphatidylcholine complex, in healthy human subjects". Eur J Drug Metab Pharmacokinet 15 (4): 333–8. 1990. doi:10.1007/bf03190223. PMID 2088770. 
  17. ↑ "Solid state mechanochemical activation of Silybum marianum dry extract with betacyclodextrins: Characterization and bioavailability of the coground systems". Journal of Pharmaceutical Sciences 98 (11): 4119–29. 2009. doi:10.1002/jps.21704. PMID 19226635. 
  18. ↑ "Antioxidant properties of silybin glycosides". Phytotherapy Research 16 (Suppl 1): S33–S39. 2002. doi:10.1002/ptr.796. PMID 11933137. 
  19. ↑ "Herbal modulation of P-glycoprotein". Drug Metabolism Reviews 36 (1): 57–104. 2004. doi:10.1081/DMR-120028427. PMID 15072439. 
  20. ↑ "Drug-drug interactions of silymarin on the perspective of pharmacokinetics". Journal of Ethnopharmacology 121 (2): 185–93. 2009. doi:10.1016/j.jep.2008.10.036. PMID 19041708. 
  21. ↑ "Silychristin, a Flavonolignan Derived From the Milk Thistle, Is a Potent Inhibitor of the Thyroid Hormone Transporter MCT8". Endocrinology 157 (4): 1694–2301. 2016. doi:10.1210/en.2015-1933. PMID 26910310. 
  22. ↑ "Silymarin Improves Thyroid Function in Lithium-treated Bipolar Patients: A Randomized, Double-blind, Placebo-controlled Pilot Study". Current Drug Therapy 18. July 2023. doi:10.2174/1574885518666230710122712. 
  23. ↑ "Safety and toxicity of silymarin, the major constituent of milk thistle extract: An updated review". Phytotherapy Resesearch 33 (6): 1627–1638. June 2019. doi:10.1002/ptr.6361. PMID 31069872. 
  24. ↑ "Effect of silymarin in intrahepatic cholestasis of pregnancy (preliminary communication)". Revista chilena de obstetricia y ginecología. 47 (1): 22–29. 1982. PMID 6927150. 
  25. ↑ "Pharmacology of Silymarin". Clinical Drug Investigation 22 (1): 51–65. 2002. doi:10.2165/00044011-200222010-00007. http://adisonline.com/druginvestigation/Abstract/2002/22010/Pharmacology_of_Silymarin.7.aspx. 
  26. ↑ "On the pharmacology and toxicology of silymarin, an antihepatotoxic active principle from Silybum marianum (L.) gaertn". Arzneimittelforschung 18 (6): 698–704. 1968. PMID 5755807. 
  27. ↑ "A phase I and pharmacokinetic study of silybin-phytosome in prostate cancer patients". Investigational New Drugs 25 (2): 139–146. April 2007. doi:10.1007/s10637-006-9019-2. PMID 17077998. 
  28. ↑ "Substituted Pyrazinecarboxamides as Abiotic Elicitors of Flavolignan Production in Silybum marianum (L.) Gaertn Cultures in Vitro". Molecules 15 (1): 331–340. 2010. doi:10.3390/molecules15010331. PMID 20110894. 
  29. ↑ "Spatial organization of silybin biosynthesis in milk thistle [Silybum marianum (L.) Gaertn]". The Plant Journal 92 (6): 995–1004. December 2017. doi:10.1111/tpj.13736. PMID 28990236. 
  30. ↑ "Silibinin and non-melanoma skin cancers". Journal of Traditional and Complementary Medicine 10 (3): 236–244. May 2020. doi:10.1016/j.jtcme.2020.02.003. PMID 32670818. 
  31. ↑ "4-Coumarate 3-hydroxylase in the lignin biosynthesis pathway is a cytosolic ascorbate peroxidase". Nature Communications 10 (1): 1994. April 2019. doi:10.1038/s41467-019-10082-7. PMID 31040279. Bibcode: 2019NatCo..10.1994B. 

Further reading

External links



Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Silibinin&oldid=3334550"