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Pinnatoxin

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Pinnatoxin A (yellow) bound to the Aplysia californica acetylcholine-binding protein, illustrating the binding site at the interfaces between pentamer subunits. From PDB: 4XHE​.[1]

Pinnatoxins are paralytic chemical compounds that inhibit neuronal and muscle-type nicotinic acetylcholine receptors. Although first discovered in shellfish, they are produced by the peridinoid dinoflagellate Vulcanodinium rugosum. Eight subtypes, designated pinnatoxin A-H, have been described.

Discovery and distribution

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Pinnatoxins are neurotoxins named after the genus Pinna, a group of bivalve molluscs, in reference to their original isolation from members of the group, Pinna attenuata[2][a] and later Pinna muricata.[3] The causative organism producing the toxin was later identified as the dinoflagellate Vulcanodinium rugosum.[4] The presence of the toxin has been identified in various locations, including the Pacific Ocean,[5][6] the Persian Gulf,[7] the Mediterranean sea,[8] waters near Canada,[9] Scandinavia,[5] and South China,[10] and in water samples in Ireland.[11]

Chemistry

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Pinnatoxins are part of the cyclic imine group of marine toxins. This group currently consists of pinnatoxins, pteriatoxins, spirolides, gymnodimines, spiro-prorocentimine and portimine. Eight different types of pinnatoxins have been described, named pinnatoxin A to H.[12][13][14][15][16]

All the pinnatoxins contain several key structural elements. The structure of pinnatoxin is composed of a cyclic imine (A ring) spirolinked to a cyclohexene ring (G ring), a dispiro 6,5,6 tricyclic ketal at C12-C23 (rings B, C, D), a bridged bicyclic ketal at C25-C30 (rings E, F) and a 27-membered macrocyclic ring spanning C5-C31.[12][13][14][15][16]

Toxin Molecular formula Molecular weight (Da) 2D structure
Pinnatoxin A C41H61NO9 712.4444
Pinnatoxin B, C C42H64N2O9 741.4707
Pinnatoxin D C45H67NO10 782.4845
Pinnatoxin E C45H69NO10 784.5008
Pinnatoxin F C45H67NO9 766.4889
Pinnatoxin G C42H63NO7 694.4683
Pinnatoxin H C43H65NO7 708.4834

Table: molecular formula and molecular weight of pinnatoxins[12][13][14][15][16]

Target

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Pinnatoxin A, G, E and F display a high-affinity antagonism for the neuronal α7 and muscle α12βϒδ nicotine acetylcholine receptors (nAChRs).[17][18][19][20] The affinity of pinnatoxins for nAChR subtypes is the result of a selectivity mechanism: the bulky bridged EF-ketal ring, specific for pinnatoxins, is able to interact with the sequence-variable loop F of the nAChRs.[17]

The inhibitory potency of pinnatoxin A depends on the nAChR subtype. It has the following ranking in selectivity: α7> α12βϒδ>α4β2. Pinnatoxin A has a 300-fold greater potency toward the α7 than to the α4β2 nAChR. Furthermore, the blocking of α7 appears to be irreversible.[17]

Pinnatoxin G shows no selectivity between the two neuronal subtypes α7 en α4β2 nAChRs. In contrast, pinnatoxin G interacts with 25-fold higher affinity than pinnatoxin A on the muscle-type nAChR. So the selectivity rank ordering of pinnatoxin G is α12βϒδ> α7 > α3β2 α4β2. Pinnatoxin E and F have the same order of selectivity for these receptors, although they differ in their potency. The rank order of potency at all receptors is F>G>E.[17][18][19]

Mode of action

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Pinnatoxins are potent inhibitors of neuronal and muscle type nicotine acetylcholine receptors (nAChRs).[15][17][18][19] They block the nAChR through adherence to the receptor binding site. Different subregions of the pinnatoxin molecule have multiple anchoring points in the receptor-binding site, through which they dictate the tight binding between the opposing loops C and F at the nAChR subunit interface.[17][19]

When pinnatoxin G and F are bound to the nAChR, they can both reduce or even abolish the amplitude of miniature endplate potentials and nerve-evoked endplate potentials. They do not have an effect on the firing frequency or resting membrane potential. This is characteristic of a postsynaptic mechanism of action.[20]

Toxicity

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As of today, no pinnatoxin or cyclic imine has been linked to human poisoning.[10][16][21] The toxic effects of pinnatoxin E-H have, however, been examined on female Swiss albino mice.[10][16][21]

The symptoms exhibited by mice exposed to a lethal dose of pinnatoxin by intraperitoneal injection are very similar between pinnatoxin E, F, G and H.[10][16][21] The symptoms start off with a period of hyperactivity until 10–20 minutes after injection, when an abrupt decrease in activity occurs. In the case of pinnatoxin H injection, mice become immobile instead of hyperactive.[16] During this decrease in activity/occurrence of immobility, abdominal breathing and extension of the hind legs are observed. In some cases, mice suffer from slight exophthalmia. After this period, during which the respiration rate remains normal, the respiration rate declines rapidly within a 2 to 3-minute time interval. Death is preceded by a brief period of running movements, the occurrence of cyanosis and severe exophthalmos. The time between dosing and death varies between 14 and 50 minutes.[10][21]

Apart from the greater time to onset of inactivity and abdominal breathing at lethal doses (25–40 minutes), and the time to death (approximately 1.3 hours), the symptoms after pinnatoxin E, F or G admission by gavage do not differ much from admission by intraperitoneal injection.[10] In contrast, the time to death after admission of pinnatoxin H by intraperitoneal injection or gavage did not differ.[21]

The behavioural abnormalities observed in mice after a sublethal dose start off with a hyperactive or immobile period shortly after toxin admission, and end with a full recovery.[10][16][21] Furthermore, none of the toxins described above lead to aberrant behaviour or abnormal appearance during a subsequent 14-day observation period, nor do they result in any atypical observations at necropsy.[10][16][21] However, the symptoms after the hyperactive/immobile period until full recovery, differ between the pinnatoxins:

  • After pinnatoxin E dosing, mice become very lethargic, achieving full recovery within an hour.[21]
  • A sublethal pinnatoxin F dosing results in immobility, without full recovery until 2–3 hours after toxin admission.[21]
  • A sublethal pinnatoxin H dosing results in immobility as well, with full recovery after an unspecified time span.[16]
  • 9–13 minutes after pinnatoxin G admission, mice become very lethargic and show an abdominal breathing pattern, while the respiration rate remains normal. Full recovery occurs within 2 hours.[10][21]

References

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  1. ^ Reference cited in [1]
  1. ^ a b Bourne, Yves; Sulzenbacher, Gerlind; Radić, Zoran; Aráoz, Rómulo; Reynaud, Morgane; Benoit, Evelyne; Zakarian, Armen; Servent, Denis; Molgó, Jordi; Taylor, Palmer; Marchot, Pascale (June 2015). "Marine Macrocyclic Imines, Pinnatoxins A and G: Structural Determinants and Functional Properties to Distinguish Neuronal α7 from Muscle α12βγδ nAChRs". Structure. 23 (6): 1106–1115. doi:10.1016/j.str.2015.04.009. PMC 4461042. PMID 26004441.
  2. ^ Zheng, SZ; Huang, FL; Chem, SC; Tan, SF; Zuo, JB; Peng, J; Xie, RW (1990). "The isolation and bioactivities of pinnatoxin". Chin J Mar Drugs. 9: 33–55.
  3. ^ Uemura, Daisuke; Chou, Tong; Haino, Takeharu; Nagatsu, Akito; Fukuzawa, Seketsu; Zheng, Shu-zhen; Chen, Hai-sheng (January 1995). "Pinnatoxin A: a toxic amphoteric macrocycle from the Okinawan bivalve Pinna muricata". Journal of the American Chemical Society. 117 (3): 1155–1156. Bibcode:1995JAChS.117.1155U. doi:10.1021/ja00108a043.
  4. ^ Rhodes, Lesley; Smith, Kirsty; Selwood, Andrew; McNabb, Paul; Munday, Rex; Suda, Shoichiro; Molenaar, Sam; Hallegraeff, Gustaaf (November 2011). "Dinoflagellate Vulcanodinium rugosum identified as the causative organism of pinnatoxins in Australia, New Zealand and Japan". Phycologia. 50 (6): 624–628. Bibcode:2011Phyco..50..624R. doi:10.2216/11-19.1. S2CID 85760231.
  5. ^ a b Rundberget T, Aasen JA, Selwood AI, Miles CO. Pinnatoxins and spirolides in Norwegian blue mussels and seawater. Toxicon. 2011 Dec 1;58(8):700-11.
  6. ^ Rhodes L, Smith K, Selwood A, McNabb P, van Ginkel R, Holland P, et al. Production of pinnatoxins by a peridinoid dinoflagellate isolated from Northland, New Zealand. Harmful Algae. 2010 May;9(4):384-9.
  7. ^ Al Muftah A, Selwood AI, Foss AJ, Al-Jabri HM, Potts M, Yilmaz M. Algal toxins and producers in the marine waters of Qatar, Arabian Gulf. Toxicon. 2016 Sep 21;122:54-66.
  8. ^ Abadie E, Kaci L, Berteaux T, Hess P, Sechet V, Masseret E, et al. Effect of Nitrate, Ammonium and Urea on Growth and Pinnatoxin G Production of Vulcanodinium rugosum. Mar Drugs. 2015 Sep;13(9):5642-56.
  9. ^ McCarron P, Rourke WA, Hardstaff W, Pooley B, Quilliam MA. Identification of pinnatoxins and discovery of their fatty acid ester metabolites in mussels ( Mytilus edulis ) from eastern Canada. J Agric Food Chem. 2012 Feb 15;60(6):1437-46.
  10. ^ a b c d e f g h i Munday R, Selwood AI, Rhodes L. Acute toxicity of pinnatoxins E, F and G to mice. Toxicon. 2012 Nov;60(6):995-9.
  11. ^ McCarthy M, Bane V, Garcia-Altares M, van Pelt FN, Furey A, O'Halloran J. Assessment of emerging biotoxins (pinnatoxin G and spirolides) at Europe's first marine reserve: Lough Hyne. Toxicon. 2015 Dec 15;108:202-9.
  12. ^ a b c Uemura D, Chou T, Haino T, Nagatsu A, Fukuzawa S, Zheng SZ, et al. Pinnatoxin-a - a Toxic Amphoteric Macrocycle from the Okinawan Bivalve Pinna-Muricata. J Am Chem Soc. 1995 Jan 25;117(3):1155-6.
  13. ^ a b c Takada N, Umemura N, Suenaga K, Chou T, Nagatsu A, Haino T, et al. Pinnatoxins B and C, the most toxic components in the pinnatoxin series from the Okinawan bivalve Pinna muricata. Tetrahedron Lett. 2001 May 14;42(20):3491-4.
  14. ^ a b c Chou T, Haino T, Kuramoto M, Uemura D. Isolation and structure of pinnatoxin D, a new shellfish poison from the Okinawan bivalve Pinna muricata. Tetrahedron Lett. 1996 Jun 3;37(23):4027-30.
  15. ^ a b c d Selwood AI, Miles CO, Wilkins AL, van Ginkel R, Munday R, Rise F, et al. Isolation, Structural Determination and Acute Toxicity of Pinnatoxins E, F and G. J Agr Food Chem. 2010 May 26;58(10):6532-42.
  16. ^ a b c d e f g h i j Selwood AI, Wilkins AL, Munday R, Gu HF, Smith KF, Rhodes LL, et al. Pinnatoxin H: a new pinnatoxin analogue from a South China Sea Vulcanodinium rugosum isolate. Tetrahedron Lett. 2014 Oct 1;55(40):5508-10.
  17. ^ a b c d e f Bourne Y, Sulzenbacher G, Radic Z, Araoz R, Reynaud M, Benoit E, et al. Marine Macrocyclic Imines, Pinnatoxins A and G: Structural Determinants and Functional Properties to Distinguish Neuronal alpha7 from Muscle alpha1(2)betagammadelta nAChRs. Structure. 2015 Jun 2;23(6):1106-15.
  18. ^ a b c Araoz R, Servent D, Molgo J, Iorga BI, Fruchart-Gaillard C, Benoit E, et al. Total synthesis of pinnatoxins A and G and revision of the mode of action of pinnatoxin A. J Am Chem Soc. 2011 Jul 13;133(27):10499-511.
  19. ^ a b c d Hellyer SD, Indurthi D, Balle T, Runder-Varga V, Selwood AI, Tyndall JD, et al. Pinnatoxins E, F and G target multiple nicotinic receptor subtypes. J. Neurochem. 2015 Nov;135(3):479-91.
  20. ^ a b Hellyer SD, Selwood AI, Rhodes L, Kerr DS. Neuromuscular blocking activity of pinnatoxins E, F and G. Toxicon. 2013 Dec 15;76:214-20.
  21. ^ a b c d e f g h i j Selwood AI, Miles CO, Wilkins AL, van Ginkel R, Munday R, Rise F, et al. Isolation, structural determination and acute toxicity of pinnatoxins E, F and G. J Agric Food Chem. 2010 May 26;58(10):6532-42.
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