| Literature DB >> 32824863 |
Dorota Żyżelewicz1, Kamila Kulbat-Warycha1, Joanna Oracz1, Kacper Żyżelewicz2.
Abstract
Due to the growing problem of obesity associated with type 2 diabetes and cardiovascular diseases, causes of obesity are extensively investigated. In addition to a high caloric diet and low physical activity, gut microbiota disturbance may have a potential impact on excessive weight gain. Some reports indicate differences in the composition of the intestinal microflora of obese people in comparison to lean. Bioactive compounds of natural origin with beneficial and multifaceted effects on the body are more frequently used in prevention and treatment of many metabolic diseases including obesity. Sideritis scardica is traditionally consumed as mountain tea in the Balkans to strengthen the body and improve mood. Many reports indicate a positive effect on digestive system, weight loss, and prevention of insulin resistance. Additionally, it exhibits antioxidant activity and anti-inflammatory effects. The positive effect of Sideritis scardica extracts on memory and general cognitive abilities is indicated as well. The multilevel positive effect on the body appears to originate from the abundant occurrence of phenolic compounds, especially phenolic acids in Sideritis scardica extracts. However, mechanisms underlying their action require careful discussion and further research. Therefore, the objective of this review is to summarize the available knowledge on the role and mechanism of action of biologically active compounds of Sideritis scardica and other related species from the genus Sideritis.Entities:
Keywords: Sideritis scardica; anti-inflammatory and neuroprotective properties; antioxidant; biological active compounds; gut microbiota; polyphenols
Mesh:
Substances:
Year: 2020 PMID: 32824863 PMCID: PMC7464829 DOI: 10.3390/molecules25163763
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411
Main phenolic compounds found in Sideritis species.
| Compound | Ref. |
|---|---|
|
| |
| Lavandulifolioside | [ |
| Verbascoside | [ |
| Forsythoside A | [ |
| Echinacoside | [ |
| Isoverbascoside | [ |
| Samioside | [ |
| Leucoseptoside A | [ |
| Allysonoside | [ |
| Martynoside | [ |
|
| |
| 3′- | [ |
| 4′- | [ |
| 4′- | [ |
| 4′- | [ |
| 3′- | [ |
| 4′- | [ |
| Isoscutellarein 7- | [ |
| Isoscutellarein 7- | [ |
| Isoscutellarein 7- | [ |
| Hypolaetin 7- | [ |
| Hypolaetin 7- | [ |
| Apigenin 7-(4″- | [ |
| Apigenin 7-(6″- | [ |
| Apigenin 7- | [ |
| Apigenin 7- | [ |
| Luteolin 7- | [ |
| Luteolin 7- | [ |
| Luteolin 7-O-[6‴-O-acetyl]-allosyl(1→2)glucoside | [ |
| Luteolin 7-O-[6‴- | [ |
| Hypolaetin 7- | [ |
| Apigenin 7- | [ |
| Chryseriol 7- | [ |
|
| |
| 3-Caffeoylquinic acid | [ |
| 5-Caffeoylquinic acid | [ |
| 6- | [ |
| [ | |
| Feruloylquinic acid | [ |
Figure 1Main polyphenolic compounds and essential oils of Sideritis scardica [18].
Biological activity of most common Sideritis scardica phenolic compounds.
| Polyphenols | Biological Activity | Ref. |
|---|---|---|
|
| ||
| Lavandulifolioside | antiarrhythmic effect | [ |
| Verbascoside | antioxidant activity | [ |
| Forsythoside | anti-inflammatory activity | [ |
| antioxidant activity | [ | |
|
| ||
| Apigenin | antioxidant activity | [ |
| Luteolin | antioxidant and anti-inflammatory activities | [ |
| Isoscutellarein | moderate to weak cytotoxicity to cancer cells | [ |
| Hypolaetin | anti-inflammatory activity | [ |
|
| ||
| Caffeoylquinic acid | antioxidant activity | [ |
| antioxidant activity | [ | |
| Feruloylquinic acid | antioxidant activity | [ |
Biological properties of Sideritis plant extracts.
| Biological Function | Extract | Ref. |
|---|---|---|
| Antioxidant activity | [ | |
| Anxiolytic, cognitive improving and neuroprotective properties | [ | |
| Inhibition of lipid peroxidation | herbal tea from | [ |
| Anti-inflammatory activity | [ | |
| Antimicrobial properties | [ | |
| Gastroprotective effect | [ | |
| Anti-obesity and antidiabetic properties | [ | |
| Chemopreventive activity | [ |
Summary of the main metabolites and colonic catabolites of the most common Sideritis scardica phenolic compounds.
| Polyphenol Class | Compounds | Phase I and II Possible Metabolites | Potential Microorganisms Involved | Microbial Biotransformation | Possible Gut Microbial Metabolites | Ref. |
|---|---|---|---|---|---|---|
| Flavonoids | Hypolaetin | Hypolaetin sulfate, glucuronide, diglucuronide, and glucuronide-sulfate | Human and mice fecal flora | Hydrolysis by gut microflora into their aglycones | Hypolaetin, isoscutellarein, and methylhypolaetin | [ |
| Methylhypolaetin | Methylhypolaetin sulfate, glucuronide, and glucuronide + pentose | |||||
| Isoscutellarein | Isoscutellarein sulfate, glucuronide, and glucuronide-sulfate | |||||
| Methylisoscutellarein | Isoscutellarein disulfate, glucuronide, and diglucuronide | |||||
| Apigenin | Apigenin disulfate, glucuronide, diglucuronide, and glucuronide-sulfate | Human and rats fecal flora | Hydrolysis by gut microflora to simple phenolic acids | 3-(4-Hydroxyphenyl)propionic acid, 3-(3-hydroxyphenyl)propionic acid, 3-(3,4-dihydroxyphenyl)propionic acid, phenylacetic acid, 4-hydroxycinnamic acid, phloretin | [ | |
| Luteolin | Luteolin glucuronide and sulfate, o-methyl luteolin (diosmetin or chrysoeryol) | Human and rats fecal flora | Hydrolysis by gut microflora to simple phenolic acids | 3-(3,4-dihydroxyphenyl)propionic acid, 3-(4-hydroxyphenyl)propionic acid and 4-hydroxycinnamic acid, phloretin, eriodictyol, and phloroglucinol | [ | |
| Phenylethanoid glycosides | Verbascoside (acteoside) | Methyl acteoside, dimethyl acteoside, methyl acteosideglucuronide, dimethyl acteosideglucuronide, caffeic acid sulfate and glucuronide, methyl caffeic acid sulfate, hydroxytyrosolsulfate and glucuronide, homovanillic alcohol sulfate and glucuronide, homovanillin glucuronide, homovanillic acid, homovanillic acid sulfate and glucuronide, ferulic acid, ferulic acid glucuronide, and homoprotocatechuic acid | Human and rats fecal flora | Deglycosylation, de-rhamnose, de-HT, de-caffeoyl, deacetylation, reduction, acetylation, and sulfate conjugation | Caffeic acid,3-hydroxyphenylpropionic acid and hydroxytyrosol | [ |
| Phenolic acids | Caffeoylquinic acid | Caffeoylquinic acid sulfate, disulfate, and glucuronide, caffeic acid glucuronide-sulfate, dimethylcaffeic acid glucuronide, quinic acid trisulfate, glucuronide, and glucuronide-sulfate | Human fecal flora | Deesterification, reduction of a double bond, dihydroxylation and futher | Dihydrocaffeic acid, dihydro-isoferulic acid, 3-hydroxyphenylpropionic acid and benzoic acid | [ |
| Feruloylquinic acid | Ferulic acid sulfate, glucuronide, and glucuronide-sulfate, feruloylquinic acid disulfate, glucuronide, and dimethylferuloylquinic acid glucuronide | Feruloylglycine, dihydroferulic acid, and 3-(4-hydroxyphenyl)-propionic acid, benzoic acid, 3-(4-hydroxyphenyl)propionic acid, vanillin | [ | |||
| Coumaric acid glucuronide | 3-Hydroxyphenylpropionic acid, benzoic acid, 3-(4-hydroxyphenyl)propionic acid, vanillin | [ |