Tetrodotoxin

Tetrodotoxin
Names
IUPAC name
(4R,4aR,5R,6S,7S,8S,8aR,10S,12S)-2-azaniumylidene-4,6,8,12-tetrahydroxy-6-(hydroxymethyl)-2,3,4,4a,5,6,7,8-octahydro-1H-8a,10-methano-5,7-(epoxymethanooxy)quinazolin-10-olate
Other names
anhydrotetrodotoxin, 4-epitetrodotoxin, tetrodonic acid, TTX
Identifiers
4368-28-9 YesY
ChEBI CHEBI:9506 N
ChEMBL ChEMBL507974 N
ChemSpider 9349691 N
2616
Jmol 3D model Interactive image
KEGG C11692 N
PubChem 11174599
Properties
C11H17N3O8
Molar mass 319.268
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Tetrodotoxin, frequently abbreviated as TTX, is a potent neurotoxin. Its name derives from Tetraodontiformes, an order that includes pufferfish, porcupinefish, ocean sunfish, and triggerfish; several species that carry the toxin. Although tetrodotoxin was discovered in these fish and found in several other aquatic animals (e.g., in blue-ringed octopuses, rough-skinned newts, and moon snails), it is actually produced by certain infecting or symbiotic bacteria like Pseudoalteromonas, Pseudomonas, and Vibrio as well as other species found in the animals.

Tetrodotoxin inhibits the firing of action potentials in nerves by binding to the voltage-gated sodium channels in nerve cell membranes and blocking the passage of sodium ions (responsible for the rising phase of an action potential) into the nerve cell.[1]

Its mechanism of action, selective blocking of the sodium channel, was shown definitively in 1964 by Toshio Narahashi and John W. Moore at Duke University, using the sucrose gap voltage clamp technique.[2]

Sources in nature

Apart from their bacterial species of most likely ultimate biosynthetic origin (see below), tetrodotoxin has been isolated from widely differing animal species, including:[3]

Tarichatoxin was shown to be identical to TTX in 1964 by Mosher and coworkers,[7][8] and the identity of maculotoxin and TTX was reported in Science in 1978,[9] and the synonymity of these two toxins is supported in modern reports (e.g., at Pubchem[10] and in modern toxicology textbooks[11]) though historic monographs questioning this continue in reprint.[12]

The toxin is variously used by metazoans as a defensive biotoxin to ward off predation, or as both a defensive and predatory venom (e.g., in octopi, chaetognaths, and ribbon worms). Even though the toxin acts as a defense mechanism, some predators such as the common garter snake have developed insensitivity to TTX, which allows them to prey upon toxic newts.[13]

The association of TTX with consumed, infecting, or symbiotic bacterial populations within the metazoan species from which it is isolated is, as of 2016, relatively clear;[3] presence of TTX-producing bacteria within a metazoan's microbiome is determined by culture methods, the presence of the toxin by chemical analysis, and the association of the bacteria with TTX production by toxicity assay of media in which suspected bacteria are grown.[4] As Lago et al. note, "there is good evidence that uptake of bacteria producing TTX is an important element of TTX toxicity in marine metazoans that present this toxin."[4] TTX-producing bacteria include Actinomyces, Aeromonas, Alteromonas, Bacillus, Pseudomonas, and Vibrio species;[4] in the following animals, specific bacterial species have been implicated:[3]

  • Vibrio species including Vibrio alginolyticus, from the puffer fish, Fugu vermicularis,[3][1][4][14]
  • Vibrio alginolyticus, from the starfish species Astropecten polyanthus,[1][4]
  • Aeromonas species from the puffer fish, Takifugu obscures,[1][4]
  • both Vibrio, Pseudomonas, and Aeromonas species from gastropod Niotha clathrata,[1][4][3]
  • Alteromonas, Bacillus, Pseudomonas, and Vibrio species from blue-ringed octopi, species Hapalochlaena macula,[1][4][3][15]
  • Vibrio species, including Vibrio alginolyticus again, in arrow worms, phylum Chaetognatha,[3][16] and
  • Vibrio species, again, in ribbon worms, phylum Nemertea.[3][17]

The association of bacterial species with the production of the toxin is unequivocal—Lago and coworkers state, "[e]ndocellular symbiotic bacteria have been proposed as a possible source of eukaryotic TTX by means of an exogenous pathway,"[4] and Chau and coworkers note that the "widespread occurrence of TTX in phylogenetically distinct organisms… strongly suggests that symbiotic bacteria play a role in TTX biosynthesis"[3]—although the correlation has been extended to most but not all metazoans in which the toxin has been identified.[3][4][1] To the contrary, there has been a failure in a single case, that of newts (Taricha granulosa), to detect TTX-producng bacteria in the tissues with highest toxin levels (skin, ovaries, muscle), using PCR methods, although technical concerns about the approach have been raised.[3] Critically for the general argument, Takifugu rubripes puffers captured and raised in laboratory on controlled, TTX-free diets "lose toxicity over time," while cultured, TTX-free Fugu niphobles puffers fed on TTX-containing diets saw TTX in the livers of the fishes increase to toxic levels.[3] Hence, as bacterial species that produce TTX are broadly present in aquatic sediments, a strong case is made for ingestion of TTX and/or TTX-producing bacteria, with accumulation and possible subsequent colonization and production.[3] Nevertheless, absent clear biosynthetic pathways (shown present in bacteria but absent in metazoans),[18] it remains to be fully established is whether TTX in all metazoan species arises through bacterial participation, and whether the amounts of toxin observed is a result of ingestion, ingestion and colonization, or some other mechanism.[1][4][3]

Biochemistry

Tetrodotoxin binds to what is known as site 1 of the fast voltage-gated sodium channel.[19] Site 1 is located at the extracellular pore opening of the ion channel. The binding of any molecules to this site will temporarily disable the function of the ion channel. Saxitoxin, neosaxitoxin and several of the conotoxins also bind the same site.

The use of this toxin as a biochemical probe has elucidated two distinct types of voltage-gated sodium channels present in humans: the tetrodotoxin-sensitive voltage-gated sodium channel (TTX-s Na+ channel) and the tetrodotoxin-resistant voltage-gated sodium channel (TTX-r Na+ channel). Tetrodotoxin binds to TTX-s Na+ channels with a binding affinity of 5-15 nM, while the TTX-r Na+ channels bind TTX with low micromolar affinity.[20] Nerve cells containing TTX-r Na+ channels are located primarily in cardiac tissue, while nerve cells containing TTX-s Na+ channels dominate the rest of the body.

TTX and its analogs have historically been important agents for use as chemical tool compounds, for use in channel characterization and in fundamental studies of channel function.[21][22] The prevalence of TTX-s Na+ channels in the central nervous system makes tetrodotoxin a valuable agent for the silencing of neural activity within a cell culture.

Chemical synthesis

In 1964 a team of Scientists led by Robert B. Woodward at Harvard University elucidated the structure of tetrodotoxin.[23] The structure was confirmed by X-ray crystallography in 1970.[24] Yoshito Kishi and coworkers at Nagoya University, Nagoya, Japan, (now at Harvard University) reported the first total synthesis of D,L-tetrodotoxin in 1972.[25][26] M. Isobe and coworkers at Nagoya University, Japan[27][28][29] and J. Du Bois et al. at Stanford University, U.S., reported the asymmetric total synthesis of tetrodotoxin in 2003.[30] The two 2003 syntheses used very different strategies, with Isobe's route based on a Diels-Alder approach and Du Bois's work using C-H bond activation. Since then, methods have rapidly advanced, with several new strategies for the synthesis of tetrodotoxin having been developed.[31][32]

Poisoning

Toxicity

TTX is extremely toxic. The Material Safety Data Sheet for TTX lists the oral median lethal dose (LD50) for mice as 334 μg per kg.[33] For comparison, the oral LD50 of potassium cyanide for mice is 8.5 mg per kg,[34] demonstrating that even orally, TTX is more poisonous than cyanide. TTX is even more dangerous if injected; the amount needed to reach a lethal dose by injection is only 8 μg per kg in mice.[35]

The toxin can enter the body of a victim by ingestion, injection, or inhalation, or through abraded skin.[36]

Poisoning occurring as a consequence of consumption of fish from the order Tetraodontiformes is extremely serious. The organs (e.g. liver) of the pufferfish can contain levels of tetrodotoxin sufficient to produce the described paralysis of the diaphragm and corresponding death due to respiratory failure.[37] Toxicity varies between species and at different seasons and geographic localities, and the flesh of many pufferfish may not be dangerously toxic.[1]

The mechanism of toxicity is through the blockage of fast voltage-gated sodium channels, which are required for the normal transmission of signals between the body and brain.[38] As a result, TTX causes loss of sensation, and paralysis of voluntary muscles including the diaphragm and intercostal muscles, stopping breathing.[39]

History

A Chinese Pharmacopoeia

The therapeutic use of puffer fish (tetraodon) eggs was mentioned in the first Chinese pharmacopea (Pen-T’ so Ching, The Book of Herbs, allegedly 2838-2698 BC by Shénnóng Běn Cǎo Jīng; but a later date is more likely), where they were classified as having ‘medium’ toxicity, but could have a tonic effect when used at the correct dose. The principle use was “to arrest convulsive diseases”.[40] In the Pen-T’ so Kang Mu (Index Herbacea or The Great Herbal by Li Shih-Chen, 1596) some types of the fish Ho-Tun (the current Chinese name for tetraodon) were also recognized as both toxic and (at the right dose) could be used to prepare a tonic. Increased toxicity in Ho-Tun was noted in fish caught at sea (rather than river) after the month of March. It was recognized that the most poisonous parts were the liver and eggs, but that toxicity could be reduced by soaking the eggs,[40] noting that tetrodotoxin is slightly water soluble, and soluble at 1 mg/mL in slightly acidic solutions.[41]

The German physician Engelbert Kaempfer, in his "A History of Japan" (translated and published in English in 1727), described how well known the toxic effects of the fish were, to the extent that it would be used for suicide and that the Emperor specifically decreed that soldiers were not permitted to eat it. There is also evidence from other sources that knowledge of such toxicity was widespread throughout southeast Asia and India.[40]

The first recorded cases of TTX poisoning affecting Westerners are from the logs of Captain James Cook from 7 September 1774.[37] On that date Cook recorded his crew eating some local tropic fish (pufferfish), then feeding the remains to the pigs kept on board. The crew experienced numbness and shortness of breath, while the pigs were all found dead the next morning. In hindsight, it is clear that the crew survived a mild dose of tetrodotoxin, while the pigs ate the pufferfish body parts that contain most of the toxin, thus being fatally poisoned.

The toxin was first isolated and named in 1909 by Japanese scientist Dr. Yoshizumi Tahara.[37] It was one of the agents studied by Japan's Unit 731, which evaluated biological weapons on human subjects in the 1930s.[42]

Symptoms and treatment

The diagnosis of pufferfish poisoning is based on the observed symptomatology and recent dietary history.[43]

Symptoms typically develop within 30 minutes of ingestion, but may be delayed by up to four hours; however, if the dose is fatal, symptoms are usually present within 17 minutes of ingestion.[37] Paresthesia of the lips and tongue is followed by developing paresthesia in the extremities, hypersalivation, sweating, headache, weakness, lethargy, incoordination, tremor, paralysis, cyanosis, aphonia, dysphagia, and seizures. The gastrointestinal symptoms are often severe and include nausea, vomiting, diarrhea, and abdominal pain; death is usually secondary to respiratory failure.[39][43] There is increasing respiratory distress, speech is affected, and the victim usually exhibits dyspnea, cyanosis, mydriasis, and hypotension. Paralysis increases, and convulsions, mental impairment, and cardiac arrhythmia may occur. The victim, although completely paralyzed, may be conscious and in some cases completely lucid until shortly before death, which generally occurs within 4 to 6 hours (range ~20 minutes to ~8 hours). However, some victims enter a coma.[39][44]

If the patient survives 24 hours, recovery without any residual effects will usually occur over a few days.[43]

Therapy is supportive and based on symptoms, with aggressive early airway management.[37] If ingested, treatment can consist of emptying the stomach, feeding the victim activated charcoal to bind the toxin, and taking standard life-support measures to keep the victim alive until the effect of the poison has worn off.[37] Alpha adrenergic agonists are recommended in addition to intravenous fluids to combat hypotension; anticholinesterase agents "have been proposed as a treatment option but have not been tested adequately".[44]

No antidote has been developed and approved for human use, but a primary research report (preliminary result) indicates that a monoclonal antibody specific to tetrodotoxin is in development by USAMRIID that was effective, in the one study, for reducing toxin lethality in tests on mice.[45]

Geographic frequency of toxicity

Poisonings from tetrodotoxin have been almost exclusively associated with the consumption of pufferfish from waters of the Indo-Pacific ocean regions, but pufferfishes from other regions are much less commonly eaten. Several reported cases of poisonings, including fatalities, involved pufferfish from the Atlantic Ocean, Gulf of Mexico, and Gulf of California. There have been no confirmed cases of tetrodotoxicity from the Atlantic pufferfish, Sphoeroides maculatus, but in three studies, extracts from fish of this species were highly toxic in mice. Several recent intoxications from these fishes in Florida were due to saxitoxin, which causes paralytic shellfish poisoning with very similar symptoms and signs. The trumpet shell Charonia sauliae has been implicated in food poisonings, and evidence suggests it contains a tetrodotoxin derivative. There have been several reported poisonings from mislabelled pufferfish, and at least one report of a fatal episode in Oregon when an individual swallowed a rough-skinned newt Taricha granulosa.[46]

In 2009, a major scare in the Auckland Region of New Zealand was sparked after several dogs died eating Pleurobranchaea maculata (grey side-gilled seaslug) on beaches.[47] Children and pet owners were asked to avoid beaches, and recreational fishing was also interrupted for a time. After exhaustive analysis, it was found that the sea slugs must have ingested tetrodotoxin.[48]

Statistical factors

Statistics from the Tokyo Bureau of Social Welfare and Public Health indicate 20–44 incidents of fugu poisoning per year between 1996 and 2006 in the entire country, leading to 34–64 hospitalizations and 0–6 deaths per year, for an average fatality rate of 6.8%.[49] Of the 23 incidents recorded within Tokyo between 1993 and 2006, only one took place in a restaurant, while the others all involved fishermen eating their catch.[49] From 2006 through 2009 in Japan there were 119 incidents involving 183 people but only 7 people died.[50]

Only a few cases have been reported in the United States, and outbreaks in countries outside the Indo-Pacific area are rare. In Haiti, tetrodotoxin is thought to have been used in voodoo preparations, in so-called zombie poisons, where subsequent careful analysis has repeatedly called early studies into question on technical grounds, and have failed to identify the toxin in any preparation,[51][52][53] such that discussion of the matter has all but disappeared from the primary literature since the early 1990s. Kao and Yasumoto concluded in the first of their papers in 1986 that "the widely circulated claim in the lay press to the effect that tetrodotoxin is the causal agent in the initial zombification process is without factual foundation.”[51]:748

Genetic background is not a factor in susceptibility to tetrodotoxin poisoning. This toxicosis may be avoided by not consuming animal species known to contain tetrodotoxin, principally pufferfish; other tetrodotoxic species are not usually consumed by humans.

Fugu as a food

Poisoning from tetrodotoxin is of particular public health concern in Japan, where pufferfish "fugu" is a traditional delicacy. It is prepared and sold in special restaurants where trained and licensed chefs carefully remove the viscera to reduce the danger of poisoning.[54] There is potential for misidentification and mislabelling, particularly of prepared, frozen fish products.

Food analysis

The mouse bioassay developed for paralytic shellfish poisoning (PSP) can be used to monitor tetrodotoxin in pufferfish and is the current method of choice. An HPLC method with post-column reaction with alkali and fluorescence has been developed to determine tetrodotoxin and its associated toxins. The alkali degradation products can be confirmed as their trimethylsilyl derivatives by gas chromatography/mass spectrometry.

Detection in body fluids

Tetrodotoxin may be quantified in serum, whole blood or urine to confirm a diagnosis of poisoning in hospitalized patients or to assist in the forensic investigation of a case of fatal overdosage. Most analytical techniques involve mass spectrometric detection following gas or liquid chromatographic separation.[55]

Modern therapeutic research

Tetrodotoxin has been investigated as a possible treatment for cancer-associated pain. Early clinical trials demonstrate significant pain relief in some patients.[56][57]

In addition to the cancer pain application mentioned, mutations in one particular TTX-sensitive Na+ channel are associated with some migraine headaches,[58] although it is unclear as to whether this has any therapeutic relevance for most people with migraine.[59]

Tetrodotoxin has been used clinically to relieve the headache associated with heroin withdrawal.[60]

Regulation

In the U.S., tetrodotoxin appears on the select agents list of the Department of Health and Human Services,[61] and scientists must register with HHS to use tetrodotoxin in their research. However, investigators possessing less than 100 mg are exempt from regulation.[62]

Popular culture

Tetrodotoxin serves as a plot device for characters to fake death, as in the films "Hello Again" (1987) and Captain America: The Winter Soldier (2014), and in episodes of Nikita and Chuck. In Law Abiding Citizen (2009) its paralysis is presented as a method of assisting torture. The toxin is used as a weapon in Covert Affairs.[63][64]

Based on the presumption that tetrodotoxin is not always fatal, but at near-lethal doses can leave a person extremely unwell with the person remaining conscious,[43] tetrodotoxin has been alleged to result in zombieism, and has been suggested as an ingredient in Haitian Vodou preparations.[65] This idea appeared earlier, in the 1938 non-fiction book Tell My Horse by Zora Neale Hurston—reporting multiple accounts of purported tetrodotoxin poisoning in Haiti, by a voodoo sorcerer called the Bokor[66]—and popularized by Harvard-trained ethnobotanist Wade Davis,[65] but has been dismissed by the scientific community since the 1990s based on analytical chemistry-based tests of multiple preparations and review of earlier reports (see above).[51][52][53]

See also

References

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  3. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 For a more comprehensive list of TTX-producing bacterial species associated with metazoans from which the toxin has been isolated or toxicity observed, and for a thorough discussion of the research literature regarding bacterial origins (and the remaining contrary perspectives, e.g., in newts), as well as for a thorough speculative discussion regarding biosynthesis, see Chau R, Kalaitzis JA, Neilan BA (Jul 2011). "On the origins and biosynthesis of tetrodotoxin" (print, online review). Aquatic Toxicology 104 (1-2): 61–72. doi:10.1016/j.aquatox.2011.04.001. PMID 21543051.
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  62. ↑ "Permissible Toxin Amounts". Federal Select Agent Program. United States Centers for Disease Control and Prevention. Retrieved 17 March 2013.
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Further reading

  • Bane V, Lehane M, Dikshit M, O'Riordan A, Furey A (2014). "Tetrodotoxin: chemistry, toxicity, source, distribution and detection". Toxins 6 (2): 693–755. doi:10.3390/toxins6020693. PMC 3942760. PMID 24566728. 
  • Lago J, Rodríguez LP, Blanco L, Vieites JM, Cabado AG (2015). "Tetrodotoxin, an Extremely Potent Marine Neurotoxin: Distribution, Toxicity, Origin and Therapeutical Uses". Marine Drugs 13 (10): 6384–406. doi:10.3390/md13106384. PMC 4626696. PMID 26492253. 
  • Moczydlowski EG (2013). "The molecular mystique of tetrodotoxin". Toxicon : Official Journal of the International Society on Toxinology 63: 165–83. doi:10.1016/j.toxicon.2012.11.026. PMID 23261990. 
  • Lange WR (1990). "Puffer fish poisoning". American Family Physician 42 (4): 1029–33. PMID 2220511. 
  • Nagashima Y, Matsumoto T, Kadoyama K, Ishizaki S, Taniyama S, Takatani T, Arakawa O, Terayama M (2012). "Tetrodotoxin poisoning due to smooth-backed blowfish, Lagocephalus inermis and the toxicity of L. inermis caught off the Kyushu coast, Japan". Shokuhin Eiseigaku Zasshi. Journal of the Food Hygienic Society of Japan 53 (2): 85–90. PMID 22688023. 
  • Padera RF, Tse JY, Bellas E, Kohane DS (2006). "Tetrodotoxin for prolonged local anesthesia with minimal myotoxicity". Muscle & Nerve 34 (6): 747–53. doi:10.1002/mus.20618. PMID 16897761. 
  • "Tetrodotoxin poisoning associated with eating puffer fish transported from Japan--California, 1996". MMWR. Morbidity and Mortality Weekly Report 45 (19): 389–91. 1996. PMID 8609880. 
  • Cole JB, Heegaard WG, Deeds JR, McGrath SC, Handy SM (2015). "Tetrodotoxin poisoning outbreak from imported dried puffer fish--Minneapolis, Minnesota, 2014". MMWR. Morbidity and Mortality Weekly Report 63 (51): 1222–5. PMID 25551594. 
  • Liu SH, Tseng CY, Lin CC (2015). "Is neostigmine effective in severe pufferfish-associated tetrodotoxin poisoning?". Clinical Toxicology (Philadelphia, Pa.) 53 (1): 13–21. doi:10.3109/15563650.2014.980581. PMID 25410493. 
  • Rivera VR, Poli MA, Bignami GS (1995). "Prophylaxis and treatment with a monoclonal antibody of tetrodotoxin poisoning in mice". Toxicon : Official Journal of the International Society on Toxinology 33 (9): 1231–7. PMID 8585093. 
  • Chang FC, Spriggs DL, Benton BJ, Keller SA, Capacio BR (1997). "4-Aminopyridine reverses saxitoxin (STX)- and tetrodotoxin (TTX)-induced cardiorespiratory depression in chronically instrumented guinea pigs". Fundamental and Applied Toxicology : Official Journal of the Society of Toxicology 38 (1): 75–88. PMID 9268607. 
  • Ahasan HA, Mamun AA, Karim SR, Bakar MA, Gazi EA, Bala CS (2004). "Paralytic complications of puffer fish (tetrodotoxin) poisoning". Singapore Medical Journal 45 (2): 73–4. PMID 14985845. 
  • How CK, Chern CH, Huang YC, Wang LM, Lee CH (2003). "Tetrodotoxin poisoning". The American Journal of Emergency Medicine 21 (1): 51–4. doi:10.1053/ajem.2003.50008. PMID 12563582. 

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