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Lupinine is a quinolizidine alkaloid present in the Lupinus genus (colloquially referred to as lupins) of flowering plants of the family Fabaceae.[1] The scientific literature contains many reports on the isolation and synthesis of this compound as well as a vast number of studies on its biological synthesis from its natural precursor, lysine. Studies have shown that lupinine hydrochloride is a mildly toxic acetylcholinesterase inhibitor and that lupinine has an inhibitory effect on acetylcholine receptors.[2][3] It has been historically employed as a natural insecticide.[4] The characteristically bitter taste of lupin beans, which come from the seeds of Lupinus plants, is attributable to the quinolizidine alkaloids which they contain, rendering them unsuitable for human and animal consumption unless handled properly.[5][6] However, because lupin beans have potential nutritional value due to their high protein content[7], efforts have been made to reduce their alkaloid content through the development of "sweet" varieties of Lupinus.[8][9]

Toxicity[edit]

Lupinine is a hepatotoxic toxin prevalent in the seeds of leguminous herbs of the genus Lupinus.[8] Lupinine and other quinolizidine alkaloids give a bitter taste to naturally growing lupin flowers.[3] Due to the toxicity of quinolizidine alkaloids, lupin beans are soaked overnight and rinsed to remove some of their alkaloid content.[6] However, when the cooking procedure is insufficient, 10 grams of seeds are able to liberate as much as 100 milligrams of lupinine.[10]

The neurotoxicity of lupinine has been known within veterinary medical circles for some time due to the use of lupins as a forage feed with a high protein content.[8] It is found to produce lupinosis, which is a morbid, and often fatal condition that results in acute atrophy of liver function and which affects domestic animals such as cattle and sheep.[8] When ingested by humans, quinolizidine alkaloid poisoning causes trembling, shaking, excitation, and convulsions.[11] Lupinine, in addition to being orally toxic to mammals, is also an insect antifeedant as well as a growth inhibitor for the grasshopper.[12]

Relative Toxicity[edit]

Quinolizidine Alkaloids in Lupins

Lupinine, in comparison to other quinolizidine alkaloids commonly found in Lupins, such as lupanine and sperteine, shows a lower toxicity. Lupinine, with a minimal lethal dose of 28-30 mg/kg and a toxic dose of 25-28 mg/kg, is about 85 percent as toxic as d-lupanine and about 90 percent as toxic as sparteine. The relative toxicity of lupinine with other quinolizidine alkaloids commonly found in Lupins is shown in the table below.[13]

Relative Toxicity of Quinolizidine Alkaloids
Substance Minimal Lethal Dose (mg/Kg)[13] Toxic Dose (mg/Kg)[13]
Lupinine 28-30 25-28
Lupanine 22-25 21-24
Sparteine 23-30 21-31

Mechanism of action[edit]

Structural comparison of lupinine and acetylcholine.

Studies on the hydrochloride of lupinine have shown it to be a reversible inhibitor of acetylcholinesterases.[2] Lupinine, a nitrogen-containing heterocycle, has a structure similar to the ammonium “head” of the acetylcholinesterase endogenous agonist, acetylcholine.[14] At physiological pH, the amine of lupinine is protonated which leads to ion-ion interaction with the acetylcholinesterase anionic site in the same manner as the ammonium on acetylcholine interacts.[14] Previous studies of reversible onium inhibitors similar to lupinine have shown that the ammonium groups (corresponding to the protonated amine of lupinine) enter the gorge of the active center of the acetylcholinesterase in the region of the Trp84 residue.[2] This leads to the formation of an enzyme-sorption complex with the anionic portion of the acetylcholinesterase located on the active site of lupinine, namely the amine.[14] This complex blocks the access of acetylcholine to the active center which decreases the catalytic hydrolysis and subsequent breakdown of acetylcholine by acetylcholinesterase.[14] Enzyme inactivation leads to an accumulation of acetylcholine in the body, hyperstimulation of the muscarinic and nicotinic acetylcholine receptors, and subsequent disruption of neurotransmission.[15] However, it was found that the time of incubation did not affect the inhibition, leading to the conclusion that lupinine is a reversible inhibitor.[2]

Studies have also shown that lupinine has a binding affinity for both muscarinic and nicotinic acetylcholine receptors. Lupinine was found to have an IC50 value of >500 µM for nicotinic receptors and an IC50 value of 190 µM for muscarinic receptors. However, it has yet to be determined whether this affinity is agonistic or antagonistic in nature.[16]

Synthesis[edit]

Biosynthesis of lupinine.

Biological[edit]

Lupinine is naturally biosynthesized from l-lysine in the Lupinus genes of plants along with various other quinolizidine alkaloids. In the biosynthetic process, lysine is first decarboxylated into cadaverine, which is then oxidatively deaminated to the corresponding aldehyde. The aldehyde is then spontaneously cyclized into two tautmers which couple through an aldol type mechanism in which the allylic amine attacks the iminium, forming a dissymmetric dimeric intermediate which is then hydrated. The primary amine is then oxidized and an intramolecular condensation occurs, giving the quinolizidinealdehyde. The aldehyde is then reduced to an alcohol, giving, enantioselectively, (-)- lupinine.[17][18]

Synthetic[edit]

Lupinine has a chiral carbon atom; therefore, total syntheses of lupinine need to be enantioselective for (-)-lupinine in order to provide the biologically active product. The first racemic total synthesis of lupinine occurred in 1937 by Clemo, Morgan, and Raper.[19] Six more total syntheses of lupinine followed between 1940-1956, with the first enantioselevtice synthesis of lupinine occurring in 1966 by Goldberg and Ragade.[20] Since that initial enantioselective synthesis, there have been numerous total syntheses of both enantio-pure and racemic lupinine. One synthesis, notable because it describes the preparation of all four stereoisomers of lupinine, and containing many references to earlier work in this field, was published by Ma and Ni. Another total synthesis of specific note due to the enantioselectivity and limited number of steps is by Santos et al. In 2010, Santos et al. synthesized enantioselective (-)- lupinine in 36% yield over eight steps using a double Mitsunobu Reaction.[21] First, they employed asymmetric addition of the starting materials using a Lewis acid, followed by treatment with a reducing agent and a base. This gave the (R,R)-alcohol. This configuration was inverted using a Mitsunobu reaction followed by hydrolysis, affording the (R,S) configuration of the alcohol. The alcohol was then reduced with alane, underwent another Mitsunobu reaction, was hydrolyzed to the acid and finally reduced to (-)-lupinine via alane reduction.[21]

Total retrosynthesis of Lupinine by Santos et al.

Applications[edit]

Drawing of a culicine mosquito larva.

Pest Control[edit]

Lupinine is an insect antifeedant.[12] Studies of its insecticide activity have shown it to be effective against culicine mosquito larvae which are vectors for viruses, filarial worms, and avian malaria.[4][22]

Botany[edit]

Lupins are often found growing with Castilleja (Indian paintbrush) which uses lupins as a host and confers lupinine and other alkaloids to Catilleja, which works in tandem with the increase in nitrogen fixation to increase parasitic reproduction rates and potentially reduce herbivory activity; however, studies have shown mixed results in the efficacy of alkaloid transfer in prevention of herbivory activity.[23]

Pre-clinical[edit]

It has been found that lupinine shows moderate antiglycation activity with an IC50 value of 7.12.176 ± 7.745 µM in vitro. Protein glycation is one of the main causes of late stage diabetic complications. In this process, proteins and sugars couple, leading to the formation of advanced glycation end-products which alter the structure and function of the proteins. The end-products lead to damage within most vital organs including nephropathy of the kidney and nerves, cataracts in the eyes, and atherosclerosis of the blood vessels which leads to impaired wound healing. This glycation process naturally increases with old age and is a well-known cause of pre-mature aging. The key therapeutic approach to prevention of this process is inhibition of the end-product formation which has been found to be facilitated by lupinine. It is hypothesized that the amine of lupinine may interact with the sugar, making it unavailable for binding with the protein. It was also found that lupinine lacks cytoxicity and therefore could function as a safe and effective antiglycation agent. However, it should be noted that since these findings are pre-clinical and have not been reproduced, they may not translate consistently into clinical effects on people and future studies are necessary to determine the efficacy of lupinine in preventing protein glycation in humans.[24]

Regulations[edit]

The European Chemicals Agency (ECA) labels lupinine under the hazard statement codes H302, H312, and H332, which indicate that lupinine is harmful if swallowed, harmful in contact with skin, and harmful if inhaled, respectively. It is given a GHS07 labeling which indicates its acute oral toxicity is category 4.[25]

In popular culture[edit]

Lupins, the plant genus that produces quinolizadine alkaloids, such as lupinine, are consumed in the Monty Python’s Flying Circus episode, Dennis Moore, in which they are stolen from the rich and given to the poor and then consumed in “lupin soup, roast lupin, steamed lupin, braised lupin in lupin sauce, lupin in a basket with … lupins, lupin meringue pie, lupin sorbet”.[26]

  1. ^ Wink, Michael; Meißner, Carsten; Witte, Ludger (January 1995). "Patterns of quinolizidine alkaloids in 56 species of the genus Lupinus". Phytochemistry. 38 (1): 139–153. doi:10.1016/0031-9422(95)91890-d. ISSN 0031-9422.
  2. ^ a b c d Rozengart, E. V.; Basova, N. E. (2001-11-01). "Ammonium Compounds with Localized and Delocalized Charge as Reversible Inhibitors of Cholinesterases of Different Origin". Journal of Evolutionary Biochemistry and Physiology. 37 (6): 604–610. doi:10.1023/A:1014414126143. ISSN 0022-0930.
  3. ^ a b . doi:10.17590/20170530-142504 http://www.bfr.bund.de/cm/349/risk-assessment-of-the-occurrence-of-alkaloids-in-lupin-seeds.pdf. {{cite journal}}: Cite journal requires |journal= (help); Missing or empty |title= (help)
  4. ^ a b Campbell, F. L.; Sullivan, W. N.; Smith, C. R. (1933-04-01). "The Relative Toxicity of Nicotine, Anabasine, Methyl Anabasine, and Lupinine for Culicine Mosquito Larvae". Journal of Economic Entomology. 26 (2): 500–509. doi:10.1093/jee/26.2.500. ISSN 1938-291X.
  5. ^ Bleitgen, R.; Gross, R.; Gross, U. (1979-06-01). "Die Lupine — ein Beitrag zur Nahrungsversorgung in den Anden". Zeitschrift für Ernährungswissenschaft (in German). 18 (2): 104–111. doi:10.1007/BF02023724. ISSN 0044-264X.
  6. ^ a b Róbertsdóttir,, Anna Rósa. Icelandic herbs and their medicinal uses. Berkeley, California. ISBN 9781623170226. OCLC 910979700.{{cite book}}: CS1 maint: extra punctuation (link)
  7. ^ Yáñez, Enrique; Ivanović, D.; Owen, D.F.; Ballester, D. (1983). "Chemical and Nutritional Evaluation of Sweet Lupines". Annals of Nutrition and Metabolism. 27 (6): 513–520. doi:10.1159/000176728. ISSN 1421-9697.{{cite journal}}: CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link)
  8. ^ a b c d Introduction to neurobehavioral toxicology : food and environment. Niesink, Raymundus Johannes Maria, 1953-. Boca Raton: CRC Press. 1999. ISBN 0849378028. OCLC 39764034.{{cite book}}: CS1 maint: others (link)
  9. ^ Torres Tello, F.; Nagata, A.; Dreifuss Spiegel, W. (June 1980). "[Methods of eliminating alkaloids from the seeds of Lupinus mutabilis Sweet]". Archivos Latinoamericanos De Nutricion. 30 (2): 200–209. ISSN 0004-0622. PMID 7212919.
  10. ^ Kirkensgaard, Kristine (2017-12-11). "Lupinine - the chemical stopping you from eating Lupin". natoxaq.ku.dk. Retrieved 2018-04-27.
  11. ^ Resta, Donatella; Boschin, Giovanna; D'Agostina, Alessandra; Arnoldi, Anna (2008-04). "Evaluation of total quinolizidine alkaloids content in lupin flours, lupin-based ingredients, and foods". Molecular Nutrition & Food Research. 52 (4): 490–495. doi:10.1002/mnfr.200700206. ISSN 1613-4125. {{cite journal}}: Check date values in: |date= (help)
  12. ^ a b Dictionary of plant toxins. Harborne, J. B. (Jeffrey B.), Baxter, Herbert, 1928-, Moss, Gerard P. Chichester: Wiley. 1996. ISBN 0471951072. OCLC 34281328.{{cite book}}: CS1 maint: others (link)
  13. ^ a b c Couch, James (1926). "Relative Toxicity of the Lupine Alkaloids". Journal of Agricultural Research. XXXII: 51–67.
  14. ^ a b c d Tilyabaev, Z.; Abduvakhabov, A. A. (1998-05-01). "Alkaloids ofAnabasis aphylla and their cholinergic activities". Chemistry of Natural Compounds. 34 (3): 295–297. doi:10.1007/BF02282405. ISSN 0009-3130.
  15. ^ Colovic, Mirjana B.; Krstic, Danijela Z.; Lazarevic-Pasti, Tamara D.; Bondzic, Aleksandra M.; Vasic, Vesna M. (2013-04-01). "Acetylcholinesterase Inhibitors: Pharmacology and Toxicology". Current Neuropharmacology. 11 (3): 315–335. doi:10.2174/1570159x11311030006. ISSN 1570-159X. PMC 3648782. PMID 24179466.{{cite journal}}: CS1 maint: PMC format (link)
  16. ^ Schmeller, Thorsten; Sauerwein, Martina; Sporer, Frank; Wink, Michael; Müller, Walter E. (September 1994). "Binding of Quinolizidine Alkaloids to Nicotinic and Muscarinic Acetylcholine Receptors". Journal of Natural Products. 57 (9): 1316–1319. doi:10.1021/np50111a026. ISSN 0163-3864.
  17. ^ Golebiewski, W. Marek; Spenser, Ian D. (1985-10-01). "Biosynthesis of the lupine alkaloids. I. Lupinine". Canadian Journal of Chemistry. 63 (10): 2707–2718. doi:10.1139/v85-450. ISSN 0008-4042.
  18. ^ Spenser, I. D. (1985-01-01). "Stereochemical aspects of the biosynthetic routes leading to the pyrrolizidine and the quinolizidine alkaloids". Pure and Applied Chemistry. 57 (3): 453–470. doi:10.1351/pac198557030453. ISSN 1365-3075.
  19. ^ Clemo, G. R.; Morgan, W. McG.; Raper, R. (1937). "199. The lupin alkaloids. Part XII. The synthesis of dl-lupinine and dl-isolupinine". Journal of the Chemical Society (Resumed). 0 (0): 965. doi:10.1039/jr9370000965. ISSN 0368-1769.
  20. ^ Goldberg, Stanley I.; Ragade, Indukanth (April 1967). "A total synthesis of optically active lupinine without benefit of resolution". The Journal of Organic Chemistry. 32 (4): 1046–1050. doi:10.1021/jo01279a039. ISSN 0022-3263.
  21. ^ a b Santos, Leonardo; Mirabal-Gallardo, Yaneris; Shankaraiah, Nagula; Simirgiotis, Mario (2010-12-08). "Short Total Synthesis of (-)-Lupinine and (-)-Epiquinamide by Double Mitsunobu Reaction". Synthesis. 2011 (01): 51–56. doi:10.1055/s-0030-1258356. ISSN 0039-7881.
  22. ^ Molina-Cruz, Alvaro; Lehmann, Tovi; Knöckel, Julia (2013-11). "Could culicine mosquitoes transmit human malaria?". Trends in Parasitology. 29 (11): 530–537. doi:10.1016/j.pt.2013.09.003. ISSN 1471-4922. {{cite journal}}: Check date values in: |date= (help)
  23. ^ Adler, Lynn S. (2003-08). "HOST SPECIES AFFECTS HERBIVORY, POLLINATION, AND REPRODUCTION IN EXPERIMENTS WITH PARASITIC CASTILLEJA". Ecology. 84 (8): 2083–2091. doi:10.1890/02-0542. ISSN 0012-9658. {{cite journal}}: Check date values in: |date= (help)
  24. ^ Abbas, Ghulam; Al-Harrasi, Ahmed Suliman; Hussain, Hidayat; Sattar, Samina Abdul; Choudhary, M. Iqbal (2017-02-18). "Identification of natural products and their derivatives as promising inhibitors of protein glycation with non-toxic nature against mouse fibroblast 3T3 cells". International Journal of Phytomedicine. 8 (4): 533–539. doi:10.5138/09750185.1924. ISSN 0975-0185.
  25. ^ "Classifications - CL Inventory". www.echa.europa.eu. Retrieved 2018-04-25.
  26. ^ "Dennis Moore". Monty Python's Flying Circus. 3 January 1973. BBC.
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