Saponins are a class of chemical compounds found in particular abundance in various plant species. More specifically, they are amphipathic glycosides grouped phenomenologically by the soap-like foaming they produce when shaken in aqueous solutions, and structurally by having one or more hydrophilic glycoside moieties combined with a lipophilic triterpene derivative.
- 1 Structural variety and biosynthesis
- 2 Sources
- 3 Test
- 4 Role in plant ecology and impact on animal foraging
- 5 Ethnobotany
- 6 Established research bioactivities and therapeutic claims
- 7 List of saponins
- 8 See also
- 9 References
- 10 External links
Structural variety and biosynthesis
The aglycone (glycoside-free) portions of the saponins are termed sapogenins. The number of saccharide chains attached to the sapogenin/aglycone core can vary – giving rise to another dimension of nomenclature (monodesmosidic, bidesmosidic, etc.) – as can the length of each chain. A somewhat dated compilation has the range of saccharide chain lengths being 1–11, with the numbers 2-5 being the most frequent, and with both linear and branched chain saccharides being represented. Dietary monosaccharides such as D-glucose and D-galactose are among the most common components of the attached chains.
The lipophilic aglycone can be any one of a wide variety of polycyclic organic structures originating from the serial addition of 10-carbon (C10) terpene units to compose a C30 triterpene skeleton, often with subsequent alteration to produce a C27 steroidal skeleton. The subset of saponins that are steroidal have been termed saraponins; Aglycone derivatives can also incorporate nitrogen, so some saponins also present chemical and pharmacologic characteristics of alkaloid natural products. The figure at right above presents the structure of the alkaloid phytotoxin solanine, a monodesmosidic, branched-saccharide steroidal saponin. (The lipophilic steroidal structure is the series of connected six- and five-membered rings at the right of the structure, while the three oxygen-rich sugar rings are at left and below. Note the nitrogen atom inserted into the steroid skeleton at right.)
Saponins have historically been understood to be plant-derived, but they have also been isolated from marine organisms. Saponins are indeed found in many plants, and derive their name from the soapwort plant (genus Saponaria, family Caryophyllaceae), the root of which was used historically as a soap. Saponins are also found in the botanical family Sapindaceae, with its defining genus Sapindus (soapberry or soapnut), and in the closely related families Aceraceae (maples) and Hippocastanaceae (horse chestnuts; ref. needed). It is also found heavily in Gynostemma pentaphyllum (Gynostemma, Cucurbitaceae) in a form called gypenosides, and ginseng or red ginseng (Panax, Araliaceae) in a form called ginsenosides. Within these families, this class of chemical compounds is found in various parts of the plant: leaves, stems, roots, bulbs, blossom and fruit. Commercial formulations of plant-derived saponins, e.g., from the soap bark (or soapbark) tree, Quillaja saponaria, and those from other sources are available via controlled manufacturing processes, which make them of use as chemical and biomedical reagents.
- Froth Test
Uses plant Gogo (bark) Entada phaseoloides as control. The positive result shows a honeycomb froth that is higher than 2 cm that persists for 10 minutes or longer.
Blood Agar Media (BAM): Is an agar cup semi-quantitative method that shows positive result of hemolytic halos.
Role in plant ecology and impact on animal foraging
In plants, saponins may serve as anti-feedants, and to protect the plant against microbes and fungi. Some plant saponins (e.g. from oat and spinach) may enhance nutrient absorption and aid in animal digestion. However, saponins are often bitter to taste, and so can reduce plant palatability (e.g., in livestock feeds), or even imbue them with life-threatening animal toxicity. Data makes clear that some saponins are toxic to cold-blooded organisms and insects at particular concentrations. Further research is needed to define the roles of these natural products in their host organisms, which have been described as "poorly understood" to date.
Although prohibited by law, fish poison plants are still widely used by indigenous tribes in Guyana.
On the Indian Subcontinent, the Gond tribes are known for their use of plant extracts in poison fishing.
Many of California's Native American tribes traditionally used soaproot, (genus Chlorogalum) and/or the root of various yucca species, which contain saponin, as a fish poison. They would pulverize the roots, mixing in water to create a foam, and then add the suds to a stream. This would kill or incapacitate the fish, which could be gathered easily from the surface of the water. Among the tribes using this technique were the Lassik, the Luiseño, the Yuki, the Yokut, the Chilula, the Wailaki, the Miwok, the Kato, the Mattole, the Nomlaki and the Nishinam.
Established research bioactivities and therapeutic claims
One research use of the saponin class of natural products involves their complexation with cholesterol to form pores in cell membrane bilayers, e.g., in red cell (erythrocyte) membranes, where complexation leads to red cell lysis (hemolysis) on intravenous injection. In addition, the amphipathic nature of the class gives them activity as surfactants that can be used to enhance penetration of macromolecules such as proteins through cell membranes.
Saponins from the Gypsophila paniculata (baby’s breath) plant have been shown to significantly augment the cytotoxicity of immunotoxins and other targeted toxins directed against human cancer cells. The research groups of Professor Hendrik Fuchs (Charité University, Berlin, Germany) and Dr David Flavell (Southampton General Hospital, United Kingdom) are working together toward the development of Gypsophila saponins for use in combination with immunotoxins or other targeted toxins for patients with leukaemia, lymphoma and other cancers.
Saponins have also been used as adjuvants in vaccines, e.g. Quil A component QS-21, isolated from the bark of Quillaja saponaria Molina, to stimulate both the Th1 immune response and the production of cytotoxic T-lymphocytes (CTLs) against exogenous antigens make them ideal for use in subunit vaccines and vaccines directed against intracellular pathogens as well as for therapeutic cancer vaccines but with the aforementioned side-effects of hemolysis.
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Saponins (via the plant Tribulus terrestris) are being promoted commercially as dietary supplements and nutraceuticals. There is evidence of the presence of saponins in traditional medicine preparations from licorice, where oral administrations might be expected to lead to hydrolysis of glycoside from terpenoid (and obviation of any toxicity associated with the intact molecule).
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But as is often the case with wide-ranging commercial therapeutic claims for natural products:
- the claims for organismal/human benefit are often based on very preliminary biochemical or cell biological studies; and
- mention is generally omitted of the possibilities of individual chemical sensitivity, or to the general toxicity of specific agents, and high toxicity of selected cases.
While such statements require constant review (and despite the myriad web claims to the contrary), it appears that there are very limited US, EU, etc. agency-approved roles for saponins in human therapy. Therapeutic benefit is a result of careful administration of an appropriate dose. Very great care needs to be exercised in evaluating or acting on specific claims of therapeutic benefit from ingesting saponin-type and other natural products.
Use in animal feeding
Saponins are used widely for their effects on ammonia emissions in animal feeding. The mode of action seems to be an inhibition of the urease enzyme, which splits up excreted urea in feces into ammonia and carbon dioxide. Animal trials have shown that a reduced ammonia level in farming operations causes less damages to the respiratory tract of animals, and may help to make them less vulnerable to diseases.
List of saponins
- Soyasapogenol A, a triterpenoid saponin in soybean
- Soyasapogenol B, a triterpenoid saponin in soybean
- Dioscin, steroidal triterpene saponin found in wild yams
- Hostettmann, K.; A. Marston (1995). Saponins. Cambridge: Cambridge University Press. p. 3ff. ISBN 0-521-32970-1. OCLC 29670810.
- "Saponins". Cornell University. 14 August 2008. Retrieved 23 February 2009.
- "Project Summary: Functional Genomics of Triterpene Saponin Biosynthesis in Medicago Truncatula". Retrieved 23 February 2009.
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- Riguera, Ricardo (August 1997). "Isolating bioactive compounds from marine organisms". Journal of Marine Biotechnology. 5 (4): 187–193.
- Liener, Irvin E (1980). Toxic constituents of plant foodstuffs. New York City: Academic Press. p. 161. ISBN 0-12-449960-0. OCLC 5447168.[verification needed]
- "Saponin from quillaja bark". Sigma-Aldrich. Retrieved 23 February 2009.
- Antibacterial activity of leave extracts of Nymphaea lotus (Nymphaeaceae) on Methicillin resistant Staphylococcus aureus (MRSA) and Vancomycin resistant Staphylococcus aureus (VRSA) isolated from clinical samples. Akinjogunla OJ, Yah CS, Eghafona NO and Ogbemudia FO, Annals of Biological Research, 2010, 1 (2), pages 174-184
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- Jonathan G. Cannon, Robert A. Burton, Steven G. Wood, and Noel L. Owen (2004), "Naturally Occurring Fish Poisons from Plants", J. Chem. Educ., 81 (10): 1457, doi:10.1021/ed081p1457
- C. E. Bradley, "Arrow and fish poison of the American southwest", Division of Biology, California Institute of Technology
- Tinde Van Andel, The diverse uses of fish-poison plants in Northwest Guyana
- Murthy E N, Pattanaik, Chiranjibi, Reddy, C Sudhakar, Raju, V S (2010), Piscicidal plants used by Gond tribe of Kawal wildlife sanctuary, Andhra Pradesh, India, pp. 97–101
- Campbell, Paul (1999). Survival skills of native California. Gibbs Smith. p. 433. ISBN 978-0-87905-921-7.
- Francis, George; Zohar Kerem; Harinder P. S. Makkar; Klaus Becker (December 2002). "The biological action of saponins in animal systems: a review". British Journal of Nutrition. 88 (6): 587–605. doi:10.1079/BJN2002725. PMID 12493081.
- Effect of incorporation of the adjuvant Quil A on structure and immune stimulatory capacity of liposomes
- Sun, Hong-Xiang; Xie, Yong; Ye, Yi-Ping (2009). "Advances in saponin-based adjuvants". Vaccine. 27 (12): 1787–1796. doi:10.1016/j.vaccine.2009.01.091.
- Skene, Caroline D.; Philip Sutton (September 2006). "Saponin-adjuvanted particulate vaccines for clinical use". Methods. 40 (1): 53–9. doi:10.1016/j.ymeth.2006.05.019. PMID 16997713.
- "Tribulus". WebMD. Retrieved July 31, 2015.
- Asl, Marjan Nassiri; Hossein Hosseinzadeh (June 2008). "Review of pharmacological effects of Glycyrrhiza sp. and its bioactive compounds". Phytotherapy Research. 22 (6): 709–24. doi:10.1002/ptr.2362. PMID 18446848.
- Xu R; Zhao W; Xu J; Shao B; Qin G (1996). "Studies on bioactive saponins from Chinese medicinal plants". Advances in Experimental Medicine and Biology. Advances in Experimental Medicine and Biology. 404: 371–82. doi:10.1007/978-1-4899-1367-8_30. ISBN 978-1-4899-1369-2. PMID 8957308.
- "MetaCyc Pathway: saponin biosynthesis IV". Retrieved 23 February 2009.
- "Saponin". J.T. Baker. Retrieved 23 February 2009.
- Zentner, Eduard (July 2011). "Effects of phytogenic feed additives containing quillaja saponaria on ammonia in fattening pigs" (PDF). Retrieved 27 November 2012.
|Wikimedia Commons has media related to Saponines.|
- Medical Dictionary on Saponin
- Saponins in Wine, by ScienceDaily, accessed Sep 9,2003
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- Saponins: Suprising [sic] benefits of desert plants
- Other uses of Quillaja Saponins and derived products, some works of different authors.
- How to survive the world's worst diet
- Quillia Extracts JECFA Food Additives Series 48