3D model (JSmol)
|Molar mass||398.45 g·mol−1|
|Melting point||85 to 89 °C (185 to 192 °F; 358 to 362 K)|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Ptaquiloside is a norsesquiterpene glucoside produced by bracken ferns (majorly Pteridium aquilinum) during metabolism. It is identified to be the main carcinogen of the ferns and to be responsible for their biological effects, such as haemorrhagic disease and bright blindness in livestock and oesophageal, gastric cancer in humans. Ptaquiloside has unstable chemical structure and acts as a DNA alkylating agent under physiological conditions. It was first isolated and characterized by Yamada and co-workers in 1983. The pure form ptaquiloside is a colorless amorphous compound. It is readily soluble in water and fairly soluble in ethyl acetate. Except in the plants, ptaquiloside has been detected in the milk and meat of affected livestock, as well as in the underground water and dry soil around bracken fern vegetation. The prevalence of ptaquiloside in daily sources along with its carcinogenic effects make it an increasing biological hazard in modern days.
In plants and food chains
The presence of ptaquiloside has been detected in a variety of ferns, including the species in the genera Pteridium (bracken), Pteris, Microlepia, and Hypolepis. Pteridium aquilinum (commonly known as bracken fern) is the most common ptaquiloside-containing fern with a wide geographical and ecological distribution. It is present in all continents from subtropic to subarctic areas. Bracken fern is a very adaptable plant and is capable of forming dense, rapidly expanding populations in course of the first phases of the ecological succession in forest cleanings and other disturbed rural areas. Its aggressive growth, characterized by an extensive rhizome system and rapidly growing fronds, sometimes enables it to be a dominant species in certain plant communities. The ptaquiloside content of bracken varies widely across species and changes with the part of the plant, the plant growing site and the collecting season. According to previous studies, the concentrations of ptaquiloside in bracken varied between 0 to 1% of the dry weight of the plant. Generally, ptaquiloside is found to occur in the highest concentrations in the young developing parts of bracken, such as the croziers and unfolding parts during the spring and early summer, while the concentrations of ptaquiloside in the rhizomes are rather low. However, studies on the concentrations of ptaquiloside in Danish bracken by Rasmussen et al. showed that the concentrations of ptaquiloside in the rhizomes were significantly higher than the previously reported values.
Ptaquiloside can pass into the milk produced by bracken-fed cows and sheep. In 1996, Alonso-Amelot, Smith and co-workers found that ptaquiloside was excreted in milk at a concentration of 8.6 ± 1.2% of the amount ingested by a cow from bracken, and was linearly dose-dependent. On the basis of their experiments and the assumption that a person drinks 0.5 litres of milk daily, they estimated that this person might ingest about 10 mg of ptaquiloside per day, although only some of that amount will be absorbed. Ptaquiloside can also leach from the bracken leaves into water and soil. Numerous studies have reported the presence of ptaquiloside in the underground/surface water, and soil near bracken vegetation. The degradation speed of ptaquiloside in the soil is affected by the acidity, clay content, carbon content, temperature and presumably microbioactivity. Acidic condition (pH<4) and high temperature (at least 25℃) facilitate ptaquiloside degradation, while the half-life of ptaquiloside in less acidic sandy soil is reported to be between 150 and 180 hours.
Ways of ptaquiloside exposure
Main routes that can lead to human exposure to the toxic effects of bracken fern include ingestion of the plant (particularly the croziers and young fronds), inhalation of the airborne spores, consumption of the milk and meat of affected animals, and drinking ptaquiloside contaminated water.
Mechanism of action
Ptaquiloside has unstable chemical structure and readily undergoes glucose liberation. The resulting ptaquilodienone is the active form of ptaquiloside and accounts for the observed biological effects. The cyclopropyl group in the dienone is highly reactive as an electrophile, not only because it is conjugated with the keto group, but because it also constitutes a cyclopropyl carbinol system, from which the facile formation of the stable non-classical cation is well-known.
In acidic conditions, ptaquiloside gradually undergoes aromatization with the elimination of D-glucose to afford ptaquilosin, and finally pterosin B. Under weakly alkaline conditions, ptaquiloside and its aglycone ptaquilosin are converted into an unstable conjugated dienone intermediate. This ptaquilodienone is the activated form of ptaquiloside and is regarded as the ultimate carcinogen of bracken ferns. Due to the constitution of a cyclopropyl carbinol system, ptaquilodienone is a strong electrophile and acts as a powerful alkylating agent that reacts directly with biological nucleophiles including amino acids, nucleosides, and nucleotides under weakly acidic conditions at room temperature (as shown in the scheme below).
Under physiological conditions
Under physiological conditions, ptaquiloside readily liberates glucose to produce the ptaquilodienone. The alkylation of amino acids with the dienone mostly takes place at the thiol group in cysteine, glutathione and methionine. The alkylation at the carboxylate group of each amino acid, forming the corresponding ester, is also observed to a small extent based on the previously reported literature. The dienone reacts with both adenine (majorly at N-3) and guanine (majorly at N-7) residues of DNA to form the DNA adducts. The alkylation induces spontaneous depurination and cleavage of DNA at adenine base site. In a model reaction with a deoxytetranucleotide (as shown on the right), a covalent adduct is found at a guanine residue and the N-glycosidic bond breaks to release the adduct. In 1998, Prakash, Smith and co-workers showed that the alkylation of adenine by ptaquiloside in codon 61 followed by depurination and error in the DNA synthesis resulted in the activation of H-ras proto-oncogene in the ileum of calves fed bracken.
Bracken is known to have various biological effects, such as carcinogenicity and its well-defined syndromes in livestock and laboratory animals. Ptaquiloside is proved to be responsible for several of these biological effects, some of which are species specific.
Cattle that consume bracken ferns develop acute bracken poisoning and chronic bovine enzootic haematuria (BEH). The main feature of acute bracken poisoning in cattle is the depression of bone marrow activity, which gives rise to severe leucopenia (particularly of the granulocytes), thrombocytopenia, and acute haemorrhagic crisis. However, most of the researchers believe ptaquiloside is not the direct causing agent of the acute bracken fern poisoning. The main feature of haematuria is urinary bladder tumors and haematuria in cattle after prolonged exposure to bracken. Based on the extensive studies, a positive correlation is shown between the ptquiloside concentration and the incidence of BEH.
Sheep fed by a diet containing bracken develop acute haemorrhagic disease and bright blindness. The main features of the blindness include progressive retinal atrophy and stenosis of the blood vessels. In 1993, Yamada group proved ptaquiloside was the compound causing retinal degeneration.
Rats that were given a diet containing ptaquiloside for a prolonged period developed tumors in both the ileum and urinary bladder. Prakash, Smith and co-workers showed that ptaquiloside-induced carcinogenesis was initiated by the activation of the H-ras oncogene. Other non-ruminants such as pig, rabbit, and guinea pig, also develop syndromes after ingestion of ptaquiloside, which include haematuria, tumors and organ abnormities (see the diagram).
Bracken fern increases the oncogenic risk in humans. Epidemiological survey revealed that bracken fern consumption was positively correlated with esophageal cancer and with gastric cancer in many geographical areas of the world. In 1989, Natori and co-workers showed that ptaquiloside had clastogenic effect and caused chromosomal aberration in mammalian cells. In 2003, Santos group reported significantly increased levels of chromosomal abnormalities, such as chromatid breaks in cultured peripheral lymphocytes.
Control and detection
The use of bracken fern as human food is mainly a historical question. The rhizomes of these plants served as human food in Scotland during the First World War. In America (USA, Canada), Russia, China and Japan, fern is grown commercially for human use. The usual procedure that is performed before eating the plant is to pre-treat the fern with boiling water in the presence of different chemicals, such as sodium bicarbonate and wood ash, to degrade or inactivate ptaquiloside and other toxic agents. Nevertheless, some carcinogenic activity persists even after the treatment. As shown by Kamon and Hirayama, the risk of oesophageal cancer was increased approximately by 2.1 in men and 3.7 in women who regularly consume bracken in Japan. Recent researches have suggested that sulfur-containing amino acids can potentially be used under appropriate conditions as detoxifying agents for ptaquiloside  and selenium supplementation can prevent as well as reverse the immunotoxic effects induced by ptaquiloside.
Ptaquiloside in the aqueous extract of bracken can be detected using different instrumental methods: thin-layer chromatography–densitometry (TLC-densitometry), high-performance liquid chromatography (HPLC), gas chromatography–mass spectrometry (GCMS), and liquid chromatography–mass spectrometry (LC-MS). The diagnostic tests of ptaquiloside inside cells include gene mutation detection, immunohistochemical detection of tumor biomarkers, chromosomal aberrations, oxidative stress for EBH, PCR, real-time PCR and DNase-SISPA (sequence-independent single primer amplification).
In 1989 and 1993, Yamada and co-workers reported the first enantioselective total synthesis of both the enantiomers of ptaquilosin, the aglycone of ptaquiloside. In the first step, the menthyl ester of cyclopentane-1,2-dicarboxylic acid 1 was partially hydrolyzed to afford the monomenthyl ester, which was later alkylated with methallyl bromide in the presence of HMPA to selectively produce 2. The product 2 was then converted to the acid chloride and treated with stannic chloride to effect Friedel-Crafts acylation to give enone 3. Hydride reduction, selective oxidation of the allylic alcohol, and silylation were then performed to provide compound 4. On treatment with base and a chloroethyl sulfonium salt, a mixture of spirocyclopropanes was obtained. The minor product 5a can be isomerized with p-toluenesulfonic acid to 5b with 81% yield. Desaturation by selenylation/dehydroselenation and basic peroxide oxidation afforded epoxide 6. Mild reduction, methyl Grignard addition, and oxidation gave compound 7. Methylation of the cyclopentanone under Noyori’s condition using the TASF enolate produced a mixture of isomers. The undesired isomer 8a can be equilibriumed with potassium tert-butoxide in 81% yield to exclusively generate 8b.[clarification needed] Reduction, deprotection, and oxidation afforded 9. On treatment with oxygen in warm ethyl acetate, the aldehyde on 9 was oxidized to the acyl radical for decarbonylation. Stereoselective trapping of the tertiary radical by oxygen gave the hydroperoxide 10. Under mild reduction, the naturally occurred (-)-ptaquilosin 11 was obtained. The Yamada’s synthesis proceeded in 20 steps with an overall yield of 2.9%. Similarly, the unnatural (+)-enantiomer of ptaquilosin was synthesized from the diastereomer of 2.
Multiple synthetic studies directed towards ptaquilosin 11 have been reported since 1989. In 1994, Padwa and co-workers described the synthesis of the core skeleton of ptaquilosin by a highly convergent approach. In 1995, Cossy and co-workers reported novel routes to the racemic and optically active ptaquilosin skeleton. Their properly functionalized tricyclic compound would be of great utility for the synthesis of 11.
- Kimiaki Saitoa, T.N.; Nagao, T.; Takatsuki, S.; Koyama, K.; Natori, S. (1990). "The sesquiterpenoid carcinogen of bracken fern, and some analogues, from the pteridaceae". Phytochemistry. 29 (5): 1475–1479. doi:10.1016/0031-9422(90)80104-O.
- Niwa, Haruki; Ojika, Makoto; Wakamatsu, Kazumasa; Yamada, Kiyoyuki; Ohba, Shigeru; Saito, Yoshihiko; Hirono, Iwao; Matsushita, Kazuhiro (1983). "Stereochemistry of ptaquiloside, a novel norsesquiterpene glucoside from bracken, Pteridium aquilinum var. latiusculum". Tetrahedron Letters. 24 (48): 5371–5372. doi:10.1016/S0040-4039(00)87871-5.
- Niwa, Haruki; Ojika, Makoto; Wakamatsu, Kazumasa; Yamada, Kiyoyuki; Hirono, Iwao; Matsushita, Kazuhiro (1983). "Ptaquiloside, a novel norsesquiterpene glucoside from bracken, Pteridium aquilinum var. latiusculum". Tetrahedron Letters. 24 (38): 4117–4120. doi:10.1016/S0040-4039(00)88276-3.
- Alonso-Amelot, Miguel E.; Castillo, Uvidelio; Smith, Barry L.; Lauren, Denis R. (15 August 1996). "Bracken ptaquiloside in milk". Nature. 382 (6592): 587–587. doi:10.1038/382587a0.
- Jensen, Pia H.; Jacobsen, Ole S.; Hansen, Hans Christian B.; Juhler, René K. (12 November 2008). "Quantification of Ptaquiloside and Pterosin B in Soil and Groundwater Using Liquid Chromatography−Tandem Mass Spectrometry (LC−MS/MS)". Journal of Agricultural and Food Chemistry. 56 (21): 9848–9854. doi:10.1021/jf801986u. PMID 18937485.
- Rasmussen, Lars H; Kroghsbo, Stine; Frisvad, Jens C; Hansen, Hans Christian B (April 2003). "Occurrence of the carcinogenic Bracken constituent ptaquiloside in fronds, topsoils and organic soil layers in Denmark". Chemosphere. 51 (2): 117–127. doi:10.1016/S0045-6535(02)00694-X.
- Kristanc, Luka; Kreft, Samo (June 2016). "European medicinal and edible plants associated with subacute and chronic toxicity part I: Plants with carcinogenic, teratogenic and endocrine-disrupting effects". Food and Chemical Toxicology. 92: 150–164. doi:10.1016/j.fct.2016.04.007.
- Smith, Barry L.; Seawright, Alan A.; Ng, Jack C.; Hertle, Andrew T.; Tomson, John A.; Bostock, Peter D. (1994). "Concentration of ptaquiloside, a major carcinogen in bracken fern (Pteridium spp.), from Eastern Australia and from a cultivated worldwide collection held in Sydney, Australia". Nat. Toxins. 2 (6): 347–353.
- Smith, B. L.; Seawright, A. A.; Ng, J. C.; Hertle, A. T.; Thomson, J. A.; Bostock, P. D. (1994). In Plant-Associated Toxins: Agricultural, Phytochemical and Ecological Aspects. Wallingford: S. M. Colgate and P. R. Dorling. pp. 45–50.
- Vetter, János (March 2009). "A biological hazard of our age: Bracken fern [(L.) Kuhn] — A Review". Acta Veterinaria Hungarica. 57 (1): 183–196. doi:10.1556/AVet.57.2009.1.18.
- Rasmussen, Lars Holm; Jensen, Lasse Sander; Hansen, Hans Christian Bruun (2003). "Distribution of the Carcinogenic Terpene Ptaquiloside in Bracken Fronds, Rhizomes (Pteridium aquilinum), and Litter in Denmark". Journal of Chemical Ecology. 29 (3): 771–778. doi:10.1023/A:1022885006742.
- Rasmussen, Lars Holm; Bruun Hansen, Hans Christian; Lauren, Denis (February 2005). "Sorption, degradation and mobility of ptaquiloside, a carcinogenic Bracken (Pteridium sp.) constituent, in the soil environment". Chemosphere. 58 (6): 823–835. doi:10.1016/j.chemosphere.2004.08.088.
- Virgilio, Antonella; Sinisi, Annamaria; Russo, Valeria; Gerardo, Salvatore; Santoro, Adriano; Galeone, Aldo; Taglialatela-Scafati, Orazio; Roperto, Franco (20 May 2015). "Ptaquiloside, the Major Carcinogen of Bracken Fern, in the Pooled Raw Milk of Healthy Sheep and Goats: An Underestimated, Global Concern of Food Safety". Journal of Agricultural and Food Chemistry. 63 (19): 4886–4892. doi:10.1021/acs.jafc.5b01937.
- Potter, D. M.; Baird, M. S. (1 October 2000). "Carcinogenic effects of ptaquiloside in bracken fern and related compounds". British Journal of Cancer. 83 (7): 914–920. doi:10.1054/bjoc.2000.1368. ISSN 0007-0920. PMC . PMID 10970694.
- Ojika, Makoto; Wakamatsu, Kazumasa; Niwa, Haruki; Yamada, Kiyoyuki (January 1987). "Ptaquiloside, a potent carcinogen isolated from bracken fern var. : structure elucidation based on chemical and spectral evidence, and reactions with amino acids, nucleosides, and nucleotides". Tetrahedron. 43 (22): 5261–5274. doi:10.1016/S0040-4020(01)87702-4.
- Shahin, Mahmood; Moore, Michael R.; Worrall, Simon; Smith, Barry L.; Seawright, Alan A.; Prakash, Arungundrum S. (September 1998). "H-rasActivation Is an Early Event in the Ptaquiloside-Induced Carcinogenesis: Comparison of Acute and Chronic Toxicity in Rats". Biochemical and Biophysical Research Communications. 250 (2): 491–497. doi:10.1006/bbrc.1998.9341. PMID 9753659.
- Yamada, Kiyoyuki; Ojika, Makoto; Kigoshi, Hideo (2007). "Ptaquiloside, the major toxin of bracken, and related terpene glycosides: chemistry, biology and ecology". Natural Product Reports. 24 (4): 798. doi:10.1039/B614160A. PMID 17653360.
- Smith, B.L.; Embling, P.P.; Agnew, M.P.; Lauren, D.R.; Holland, P.T. (June 1988). "Carcinogenicity of bracken fern in New Zealand". New Zealand Veterinary Journal. 36 (2): 56–58. doi:10.1080/00480169.1988.35481.
- Pinto, C.; Januário, T.; Geraldes, M.; Machado, J.; Lauren, D. R.; Smith, B. L.; Robinson, R. C. (2004). In Poisonous Plants and Related Toxins. Wallingford: CABI Publishing. pp. 564–574.
- Watson, W.; Barlow, R.; Barnett, K. (11 September 1965). "Bright blindness--a condition prevalent in Yorkshire hill sheep". Veterinary Record. 77 (37): 1060–1069. doi:10.1136/vr.77.37.1060.
- Watson, W.; Barnett, K.; Terlecki, S. (30 December 1972). "Progressive retinal degeneration (Bright Blindness) in sheep: a review". Veterinary Record. 91 (27): 665–670. doi:10.1136/vr.91.27.665.
- HIRONO, Iwao; ITO, Mitsuya; YAGYU, Shigeru; HAGA, Masanobu; WAKAMATSU, Kazumasa; KISHIKAWA, Teruaki; NISHIKAWA, Osamu; YAMADA, Kiyoyuki; OJIKA, Makoto; KIGOSHI, Hideo (1993). "Reproduction of Progressive Retinal Degeneration(Bright Blindness) in Sheep by Administration of Ptaquiloside Contained in Bracken". The Journal of Veterinary Medical Science. 55 (6): 979–983. doi:10.1292/jvms.55.979.
- Marliére, C. A.; Wathern, P.; Castro, M. C. F. M.; O'Connor, P.; Galvao, M. A. (1 January 2002). "Bracken fern (Pteridium aquilinum) ingestion and oesophageal and stomach cancer". IARC scientific publications. 156: 379–380. ISSN 0300-5038. PMID 12484211.
- Matsuoka, Atsuko; Hirosawa, Akiko; Natori, Shinasku; Iwasaki, Shigeo; Toshio, Sofuni; Motoi, Ishidate, Jr. (December 1989). "Mutagenicity of ptaquiloside, the carcinogen in bracken, and its related illudane-type sesquiterpenes". Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 215 (2): 179–185. doi:10.1016/0027-5107(89)90182-6.
- Recouso, R. C.; Santos, R. C. Stocco dos; Freitas, R.; Santos, R. C.; Freitas, A. C. de; Brunner, O.; Beçak, W.; Lindsey, C. J. (1 March 2003). "Clastogenic effect of bracken fern (Pteridium aquilinum v. arachnoideum) diet in peripheral lymphocytes of human consumers: preliminary data". Veterinary and Comparative Oncology. 1 (1): 22–29. doi:10.1046/j.1476-5829.2003.00006.x. ISSN 1476-5829.
- Sharma, Rinku; Bhat, Tej K.; Sharma, Om P. (2013). "The Environmental and Human Effects of Ptaquiloside-Induced Enzootic Bovine Hematuria: A Tumorous Disease of Cattle". Reviews of Environmental Contamination and Toxicology Volume 224. New York: Springer New York. pp. 53–95. ISBN 9781461458814.
- Kamon, S.; Hirayama, T. (1975). "Epidemiology of cancer of the oesophagus in Mye, Nara and Wakayama prefecture with special reference to the role of bracken fern。". Proc. Jpn. Cancer Assoc., 34th Annual Meeting: 211.
- Latorre AO, Caniceiro BD, Wysocki HL, Haraguchi M, Gardner DR, Górniak SL (2011). "Selenium reverses Pteridium aquilinum-induced immunotoxic effects". Food Chem. Toxicol. 49 (2): 464–70. doi:10.1016/j.fct.2010.11.026. PMID 21112370.
- Kigoshi, Hideo; Imamura, Yoshifumi; Mizuta, Kazuhiro; Niwa, Haruki; Yamada, Kiyoyuki (April 1993). "Total synthesis of natural (-)-ptaquilosin, the aglycon of a potent bracken carcinogen ptaquiloside and the (+)-enantiomer, and their DNA cleaving activities". Journal of the American Chemical Society. 115 (8): 3056–3065. doi:10.1021/ja00061a003.
- Kigoshi, Hideo; Imamura, Yoshifumi; Niwa, Haruki; Yamada, Kiyoyuki (March 1989). "Total synthesis of ptaquilosin: the aglycon of ptaquiloside, a potent bracken carcinogen". Journal of the American Chemical Society. 111 (6): 2302–2303. doi:10.1021/ja00188a054.
- Padwa, Albert; Sandanayaka, Vincent P.; Curtis, Erin A. (March 1994). "Synthetic studies toward Illudins and Ptaquilosin. A highly convergent approach via the dipolar cycloaddition of carbonyl ylides". Journal of the American Chemical Society. 116 (6): 2667–2668. doi:10.1021/ja00085a076.
- Cossy, Janine; Ibhi, Saïd; Kahn, Philippe H.; Tacchini, Laura (October 1995). "A formal synthesis of ptaquilosin the aglycon of a potent bracken carcinogen ptaquiloside". Tetrahedron Letters. 36 (43): 7877–7880. doi:10.1016/0040-4039(95)01552-S.