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Proteomic Changes in Chick Brain Proteome Post Treatment with Lathyrus Sativus Neurotoxin, β-N-Oxalyl-L-α,β-Diaminopropionic Acid (L-ODAP): A Better Insight to Transient Neurolathyrism

  • Received : 2018.01.09
  • Accepted : 2018.06.12
  • Published : 2018.07.15

Abstract

Neurolathyrism is a neurodegenerative disorder characterized by spastic paraplegia resulting from the excessive consumption of Lathyrus sativus (Grass pea). ${\beta}$-N-Oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid (L-ODAP) is the primary neurotoxic component in this pea. The present study attempted to evaluate the proteome-wide alterations in chick brain 2 hr and 4 hr post L-ODAP treatment. Proteomic analysis of chick brain homogenates revealed several proteins involved in cytoskeletal structure, signaling, cellular metabolism, free radical scavenging, oxidative stress and neurodegenerative disorders were initially up-regulated at 2 hr and later recovered to normal levels by 4 hr. Since L-ODAP mediated neurotoxicity is mainly by excitotoxicity and oxidative stress related dysfunctions, this study further evaluated the role of L-ODAP in apoptosis in vitro using human neuroblastoma cell line, IMR-32. The in vitro studies carried out at $200{\mu}M$ L-ODAP for 4 hr indicate minimal intracellular ROS generation and alteration of mitochondrial membrane potential though not leading to apoptotic cell death. L-ODAP at low concentrations can be explored as a stimulator of various reactive oxygen species (ROS) mediated cell signaling pathways not detrimental to cells. Insights from our study may provide a platform to explore the beneficial side of L-ODAP at lower concentrations. This study is of significance especially in view of the Government of India lifting the ban on cultivation of low toxin Lathyrus varieties and consumption of this lentil.

Keywords

References

  1. Haque, A., Hossain, M., Wouters, G. and Lambein, F. (1996) Epidemiological study of lathyrism in northwestern districts of Bangladesh. Neuroepidemiology, 15, 83-91. https://doi.org/10.1159/000109893
  2. Getahun, H., Mekonnen, A., Teklehaimanot, R. and Lambein, F. (1999) Epidemic of neurolathyrism in Ethiopia. Lancet, 354, 306-307. https://doi.org/10.1016/S0140-6736(99)02532-5
  3. De falco, E. and Pardo, A. (2000) Agronomic evaluation of Italian ecotypes of Lathyrus sativus L. in a hilly area of southern Italy. Lathyrus Lathyrism Newsl., 1, 27.
  4. Kuo, Y.H., Bau, H.M., Rozan, P., Chowdhury, B. and Lambein, F. (2000) Reduction efficiency of the neurotoxin ${\beta}$-ODAP in low-toxin varieties of Lathyrus sativus seeds by solid state fermentation with Aspergillus oryzae and Rhizo- pus microsporus var chinensis. J. Sci. Food Agric., 80, 2209-2215. https://doi.org/10.1002/1097-0010(200012)80:15<2209::AID-JSFA773>3.0.CO;2-W
  5. Selye, H. (1957) Lathyrism. Rev. Can. Biol., 16, 1-2.
  6. Ludolph, A.C., Hugon, J., Dwivedi, M.P., Schaumburg, H.H. and Spencer, P.S. (1987) Studies on the etiology and pathogenesis of motor neuron disease. 1 Lathyrism: clinical findings in established cases. Brain, 110, 149-165. https://doi.org/10.1093/brain/110.1.149
  7. Spencer, P.S., Ludolph, A.C. and Kisby, G.E. (1993) Neurologic diseases associated with use of plant components with toxic potential. Environ. Res., 62, 106-113. https://doi.org/10.1006/enrs.1993.1095
  8. Getahun, H., Lambein, F. and Vanhoorne, M. (2002) Neurolathyrism in Ethiopia: assessment and comparison of knowledge and attitude of health workers and rural inhabitants. Soc. Sci. Med., 54,1513-1524. https://doi.org/10.1016/S0277-9536(01)00131-9
  9. Murti, V.V.S. and Seshadri, T.R. (1964) Toxic amino acids of plants. Curr. Sci. (India), 33, 323-329.
  10. Rao, S.L.N., Adiga, P.R. and Sarma, P.S. (1964) The isolation and characterization of ${\beta}$-N-oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid: a neurotoxin from the Seeds of Lathyrus sativus. Biochemistry, 3, 432-436. https://doi.org/10.1021/bi00891a022
  11. Ross, S.M., Roy, D.N. and Spencer, P.S. (1985) ${\beta}$-N-Oxalylamino-L-alanine: action on high-affinity transport of neurotransmitters in rat brain and spinal cord synaptosomes. J. Neurochem., 44, 886-892. https://doi.org/10.1111/j.1471-4159.1985.tb12899.x
  12. Spencer, P.S., Roy, D.N., Ludolph, A.C., Hugon, J. and Schaumburg, H.H. (1986) Lathyrism: evidence for role of the neuroexcitatory amino acid BOOA. Lancet, 2, 1066-1067.
  13. Nunn, P.B., Seelig, M., Zagoren, J.C. and Spencer, P.S. (1987) Stereospecific acute neuronotoxicity of 'uncommon' plant amino acids linked to human motor-system diseases. Brain. Res., 410, 375-379. https://doi.org/10.1016/0006-8993(87)90342-8
  14. Kuo, Y.H., Ikegami, F. and Lambein, F. (1998) Metabolic routes of ${\beta}$-(isoxazolin-5-on-2-yl)-L-alanine (BIA), the precursor of the neurotoxin ODAP (${\beta}$-n-oxalyl-l-${\alpha},{\beta}$,-diamino-propionic acid), in different legume seedlings. Phytochemistry, 49, 43-48. https://doi.org/10.1016/S0031-9422(97)01001-7
  15. Getahun, H., Lambein, F., Vanhoorne, M. and Van Der Stuyft, P. (2005) Neurolathyrism risk depends on type of grass pea preparation and on mixing with cereals and antioxidants. Trop. Med. Int. Health, 10, 169-178. https://doi.org/10.1111/j.1365-3156.2004.01370.x
  16. Van Moorhem, M., Lambien, F. and Leybaert, L. (2011) Unraveling the mechanism of ${\beta}$-N-oxalyl-${\alpha},{\beta}$-diaminopropionic acid (${\beta}$-ODAP) induced excitotoxicity and oxidative stress, relevance for neurolathyrism prevention. Food Chem. Toxicol., 49, 550-555. https://doi.org/10.1016/j.fct.2010.03.054
  17. Wu, G., Bowlus, S.B., Kim, K.S. and Haskell, B.E. (1976) L-2-Oxalylamino-3-aminopropionic acid, an isomer of Lathyrus sativus neurotoxin. Phytochemistry, 15, 1257-1259. https://doi.org/10.1016/0031-9422(76)85088-1
  18. Chase, R.A., Pearson, S., Nunn, P.B. and Lantos, P.L. (1985) Comparative toxicities of ${\alpha}$- and ${\beta}$-N-oxalyl-L-${\alpha},{\beta}$-diamino-propionic acid to rat spinal cord. Neurosci. Lett., 55, 89-94. https://doi.org/10.1016/0304-3940(85)90317-9
  19. Mehta, T., Zarghami, N.S., Parker, A.J., Cusick, P.K. and Haskell, B.E. (1979) Neurotoxicity of orally or intraperitoneally administered L-3-oxalylamino-2-aminopropionic acid in the mouse. Toxicol. Appl. Pharmacol., 48, 1-9. https://doi.org/10.1016/S0041-008X(79)80002-2
  20. Bridges, R.J., Stevens, D.R., Kahle, J.S., Nunn, P.B., Kadri, M. and Cotman, C.W. (1989) Structure-function studies on N-oxalyl-diamino-dicarboxylic acids and excitatory amino acid receptors: evidence that beta-L-ODAP is a selective non-NMDA agonist. J. Neurosci., 9, 2073-2079. https://doi.org/10.1523/JNEUROSCI.09-06-02073.1989
  21. Ross, S.M., Roy, D.N. and Spencer, P.S. (1989) Beta-N-oxalylamino-L-alanine action on glutamate receptors. J. Neurochem., 53, 710-715. https://doi.org/10.1111/j.1471-4159.1989.tb11762.x
  22. Zeevalk, G.D. and Nicklas, W. J. (1989) Acute excitotoxicity in chick retina caused by the unusual amino acids BOAA and BMAA: effects of MK-801 and kynurenate. Neurosci. Lett., 102, 284-290. https://doi.org/10.1016/0304-3940(89)90093-1
  23. Van Moorhem, M., Decrock, E., Coussee, E., Faes, L., De Vuyst, E., Vranckx, K., De Bock, M., Wang, N., D'Herde, K., Lambein, F., Callewaert, G. and Leybaert, L. (2010) L-beta-ODAP alters mitochondrial $Ca^{2+}$ handling as an early event in excitotoxicity. Cell Calcium, 47, 287-296. https://doi.org/10.1016/j.ceca.2010.01.001
  24. Sriram, K., Shankar, S.K., Boyd, M.R. and Ravindranath, V. (1998) Thiol oxidation and loss of mitochondrial complex I precede excitatory amino acid-mediated neurodegeneration. J. Neurosci., 18, 10287-10296. https://doi.org/10.1523/JNEUROSCI.18-24-10287.1998
  25. Singh, M.R., Pratap Rudra, M., Rao, S.L.N. and Singh, S. (2004) In vitro activation of protein kinase C by beta-N-oxalyl-L-alpha,beta-diaminopropionic acid, the Lathyrus sativus neurotoxin. Neurochem. Res., 29, 1343-1348. https://doi.org/10.1023/B:NERE.0000026395.25468.57
  26. Jammulamadaka, N., Burgula, S., Medisetty, R., Ilavazhagan, G., Rao, S.L.N. and Singh, S.S. (2011) ${\beta}$-N-oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid regulates mitogen-activated protein kinase signaling by down-regulation of phosphatidyleth-anolamine-binding protein 1. J. Neurochem., 118, 176-186. https://doi.org/10.1111/j.1471-4159.2011.07299.x
  27. Rao, S.L.N., Ramachandran, L.K. and Adiga, P.R. (1963) The isolation and characterization of L-homoarginine from the seeds of Lathyrus sativus. Biochemistry, 2, 298-300. https://doi.org/10.1021/bi00902a019
  28. Huang, L.F., Shi, H.L., Gao, B., Wu, H., Yang, L., Wu, X.J. and Wang, Z.T. (2014) Dencichine enhances hemostasis of activated platelets via AMPA receptors. Thromb. Res., 133, 848-854. https://doi.org/10.1016/j.thromres.2014.02.009
  29. Rao, S.L.N. (2011) A look at the brighter facets of ${\beta}$-N-oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid, homoarginine and the grass pea. Food Chem. Toxicol., 49, 620-622. https://doi.org/10.1016/j.fct.2010.06.054
  30. Khandare, A.L., Ankulu, M. and Aparna, N. (2013) Role of glutamate and nitric oxide in onset of motor neuron degeneration in neurolathyrism. Neurotoxicology, 34, 269-274. https://doi.org/10.1016/j.neuro.2012.11.004
  31. Dixit, G.P., Parihar, A.K., Bohra, A. and Singh, N.P. (2016) Achievements and prospects of grass pea (Lathyrus sativus L.) improvement for sustainable food production. Crop J., 4, 407-416. https://doi.org/10.1016/j.cj.2016.06.008
  32. Anand, U. (2016) ICMR panel clears 'unsafe' khesari dal banned in 1961. The Indian Express. New Delhi.
  33. Le Bel, C.P., Ali, S.F., McKee, M. and Bondy, S.C. (1990) Organometal-inducedincreases in oxygen reactive species: the potential of 2',7'-dichlorofluorescein diacetate as an index of neurotoxic damage. Toxicol. Appl. Pharmacol., 104, 17-24. https://doi.org/10.1016/0041-008X(90)90278-3
  34. Kim, H.B. and Yoo, B.S. (2016) Propolis inhibits UVA- induced apoptosis of human keratinocyte HaCaT cells by scavenging ROS. Toxicol. Res., 32, 345-351. https://doi.org/10.5487/TR.2016.32.4.345
  35. Roy, O.N. (1988) The neurotoxic disease lathyrism. Natl. Med. J. India, 1, 70-80.
  36. Jyothi, P., Prataprudra, M. and Rao, S.L.N. (1998) In vivo metabolism of ${\beta}$-N-oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid: the Lathyrus sativus neurotoxin in experimental animals. Nat. Toxins., 6, 189-195. https://doi.org/10.1002/(SICI)1522-7189(199809/10)6:5<189::AID-NT22>3.0.CO;2-F
  37. Rao, S.L.N., Malathi, K. and Sarma, P.S. (1969) Lathyrism. World Rev. Nutr. Diet., 10, 214-238.
  38. Von Mering, C., Jensen, L.J., Kuhn, M., Chaffron, S., Doerks, T., Krger, B., Snel, B. and Bork, P. (2007) STRING 7-recent developments in the integration and prediction of protein interactions. Nucleic. Acids. Res., 35, D358-D362. https://doi.org/10.1093/nar/gkl825
  39. Castegna, A., Aksenov, M., Thongboonkerd, V., Klein, J.B., Pierce, W.M., Booze, R., Markesbery, W.R. and Butterfield, D.A. (2002) Proteomic identification of oxidatively modified proteins in Alzheimer's disease brain. Part II. Dihydro-pyrimidinase-related protein 2, alpha-enolase and heat shock cognate 71. J. Neurochem., 82, 1524-1532. https://doi.org/10.1046/j.1471-4159.2002.01103.x
  40. Hwang, O. (2013) Role of oxidative stress in Parkinson's disease. Exp. Neurobiol., 22, 11-17. https://doi.org/10.5607/en.2013.22.1.11
  41. Lambein, F., Kuo, Y.H., Kusama-Eguchi, K. and Ikegami, F. (2007) 3-N-oxalyl-L-2,3-diaminopropanoic acid, a multifunctional plant metabolite of toxic reputation. Arkivoc, 45-52.
  42. Bridges, R.J., Hatalski, C., Shim, S.N. and Nunn, P.B. (1991) Gliotoxic properties of the Lathyrus excitotoxin ${\beta}$-N-oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid (${\beta}$-L-ODAP). Brain Res., 561, 262-268. https://doi.org/10.1016/0006-8993(91)91602-W
  43. Rao, S.L.N. (1978) Entry of beta-N-oxalyl-L-alpha,beta-diaminopropionic acid, the Lathyrus sativus neurotoxin into the central nervous sysytem of the adult rat, chick and the rhesus monkey. J. Neurochem., 30, 1467-1470. https://doi.org/10.1111/j.1471-4159.1978.tb10479.x
  44. La Bella, V. and Piccoli, F. (2000) Differential effect of ${\beta}$-N-oxalylamino-L-alanine, the Lathyrus sativus neurotoxin, and (+/−)-${\alpha}$-amino-3-hydroxy-5-methylisoxazole-4-propionate on the excitatory amino acid and taurine levels in the brain of freely moving rats. Neurochem. Int., 36, 523-530. https://doi.org/10.1016/S0197-0186(99)00152-7
  45. Roy, D.N., Nagaraja, V. and Gopalan, C. (1963) Production of neurolathyrism in chicks by injection of Lathyrus sativus concentrates. Curr. Sci., 32, 116-118.
  46. Dong, X.X., Wang, Y. and Qin, Z.H. (2009) Molecular mechanisms of excitotoxicity and their relevance to pathogenesis of neurodegenerative diseases. Acta. Pharmacol. Sin., 30, 379-387. https://doi.org/10.1038/aps.2009.24
  47. Qutub, A.A. and Popel, A.S. (2008) Reactive oxygen species regulate hypoxia-inducible factor 1 alpha differentially in cancer and ischemia. Mol. Cell. Biol., 28, 5106-5119. https://doi.org/10.1128/MCB.00060-08
  48. Eslavath, R.K., Sharma, D., Bin Omar, N.A.M., Chikati, R., Teli, M.K., Rajanikant, G.K. and Singh, S.S. (2016) ${\beta}$-N-oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid induces HRE expression by inhibiting HIF-prolyl hydroxylase-2 in normoxic conditions. Eur. J. Pharmacol., 791, 405-411. https://doi.org/10.1016/j.ejphar.2016.07.007
  49. Park, H. (2008) Novel dioxygenases, HIF-${\alpha}$ specific prolyl-hydroxylase and asparanginyl-hydroxylase: $O_2$ switch for cell survival. Toxicol. Res., 24, 101-107. https://doi.org/10.5487/TR.2008.24.2.101

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