Organophosphorus insecticides affect normal polyamine metabolism in amphibian embryogenesis

Pesticide Biochemistry and Physiology

Volumn 101, Issue 3, 2011, Pages 240-247

  Lascano, Cecilia I ^a,b   Ferrari, Ana ^a,b   Gauna, Lidia E ^b   Cocca, Claudia ^c   Cochón, Adriana C ^c   Verrengia, Noemí ^c   Venturino, Andrés ^a,b  

^a UNIVERSIDAD NACIONAL DEL COMAHUE   (Argentina)

^b LABORATORIO ECOTONO   (Argentina)

^c UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

Malformations; Organophosphorus pesticides; Ornithine decarboxylase; Putrescine; Spermidine; Spermine

Indexed keywords

AMPHIBIA; ANURA;

EID: 81555219346     PISSN: 00483575     EISSN: 10959939     Source Type: Journal    
DOI: 10.1016/j.pestbp.2011.10.001     Document Type: Article

References (53)

1. Moinard C., Cynober L., de Bandt J.-P. Polyamines: metabolism and implications in human diseases. Clin. Nutr. 2005, 24:184-197.
2. Osborne H.B., Cormier P., Lorillon O., Maniey D., Bellé R. An appraisal of the developmental importance of polyamine changes in early Xenopus embryos. Int. J. Dev. Biol. 1993, 37:615-618.
3. Hetrick B., Khade P.K., Lee K., Stephen J., Thomas A., Joseph S. Polyamines accelerate codon recognition by transfer RNAs on the ribosome. Biochemistry 2010, 49:7179-7189.
4. Kamboj S.K., Swansonand G.T., Cull-Candy S.G. Intracellular spermine confers rectification on rat calcium-permeable AMPA and kainate receptors. J. Physiol. 1995, 486:297-303.
5. Lopatin A.N., Makhina E.N., Nichols C.G. Potassium channel block by cytoplasmic polyamines as the mechanism of intrinsic rectification. Nature 1994, 372:366-369.
6. Bueb J.L., Da Silva A., Mousli M., Landry Y. Natural polyamines stimulate G-proteins. Biochem. J. 1992, 282:545-550.
7. Tabib A., Bachrach U. Role of polyamines in mediating malignant transformation and oncogene expression. Int. J. Biochem. Cell Biol. 1999, 31:1289-1295.
8. Sava I.G., Battaglia V., Rossi C.A., Salvi M., Toninello A. Free radical scavenging action of the natural polyamine spermine in rat liver mitochondria. Free Radic. Biol. Med. 2006, 41:1272-1281.
9. Schipper R.G., Penning L.C., Verhofstad A.A. Involvement of polyamines in apoptosis. Facts and controversies: effectors or protectors?. Semin. Cancer Biol. 2000, 10:55-68.
10. López-García C., López-Contreras A.J., Cremades A., Castells M.T., Marín F., Schreiber F., Peñafiel R. Molecular and morphological changes in placenta and embryo development associated with the inhibition of polyamine synthesis during midpregnancy in mice. Endocrinology 2008, 149(10):5012-5023.
11. Pendeville H., Carpino N., Marine J.C., Takahashi Y., Muller M., Martial J.A., Cleveland J.L. The ornithine decarboxylase gene is essential for cell survival during early murine development. Mol. Cell. Biol. 2001, 21(19):6549-6558.
12. Olivier H.M., Moon B.R. The effects of atrazine on spotted salamander embryos and their symbiotic alga. Ecotoxicology 2010, 19(4):654-661.
13. Sişman T. Dichlorvos-induced developmental toxicity in zebrafish. Toxicol. Ind. Health 2010, 26(9):567-573.
14. Wang H., Huang H.H., Ding J., Wang Y.H. Embryotoxicity and teratogenicity of pesticide indoxacarb to sea urchin (Strongylocentrotus intermedius). Water Sci. Technol. 2010, 61(11):2733-2739.
15. Hart J.J., Di Tomaso J.M., Kochian L.V. Characterization of paraquat transport in protoplasts from maize (Zea mays L.) suspension cells. Plant Physiol. 1993, 103(3):963-969.
16. Mornet C., Mondory C., Gaillard C., Martinoia E. Transport of paraquat and polyamines across the vacuolar membrane of barley mesophyll cells. Plant Physiol. Biochem. 1997, 35:181-191.
17. Watanabe S., Sato S., Nagase S., Tomita M., Saito T. Change of polyamine level in various tissues of male rats intoxicated with paraquat. Toxicol. Lett. 1993, 69(2):163-170.
18. Cochón A.C., Della Penna A.B., Kristoff G., Piol M.N., San Martín de Viale L.C., Verrengia Guerrero N.R. Differential effects of paraquat on oxidative stress parameters and polyamine levels in two freshwater invertebrates. Ecotoxicol. Environ. Saf. 2007, 68(2):286-292.
19. Anguiano O.L., Caballero de Castro A., Pechen A.M., Pechen de D'Angelo A.M. The role of glutathione conjugation in the regulation of early toad embryos' tolerance to pesticides. Comp. Biochem. Physiol. C 2001, 128:35-43.
20. Bacchetta R., Mantecca P., Andrioletti M., Vismara C., Vailati G. Axial-skeletal defects caused by Carbaryl in Xenopus laevis embryos. Sci. Total Environ. 2008, 392:110-118.
21. Bonfanti P., Colombo A., Orsi F., Nizzetto I., Andrioletti M., Bacchetta R., Mantecca P., Fascio U., Vailati G., Vismara C. Comparative teratogenicity of Chlorpyrifos and Malathion on Xenopus laevis development. Aquat. Toxicol. 2004, 70:189-200.
22. Colombo A., Orsi F., Bonfanti P. Exposure to the organophosphorus pesticide chlorpyrifos inhibits acetylcholinesterase activity and affects muscular integrity in Xenopus laevis larvae. Chemosphere 2005, 61:1665-1671.
23. Venturino A., Gauna L., Bergoc R.M., Pechen de D'Angelo A.M. Effect of exogenously applied polyamines on malathion toxicity in the toad Bufo arenarum Hensel. Arch. Environ. Contam. Toxicol. 1992, 22:135-139.
24. Venturino A., Anguiano O.L., Gauna L., Cocca C., Bergoc R.M., Pechen de D'Angelo A.M. Thiols and polyamines in the potentiation of malathion toxicity in larval stages of the toad Bufo arenarum. Comp. Biochem. Physiol. C 2001, 130:191-198.
25. Fonovich de Schroeder T., Pechen de D'Angelo A.M. Dieldrin effects on phospholipid and phosphoinositide metabolism in Bufo arenarum oocytes. Comp. Biochem. Physiol. C 1991, 98:287-292.
26. Del Conte E., Sirlin J.L. Pattern series of the first embryonary stages in Bufo arenarum. Anat. Rec. 1952, 112:125-130.
27. Ferrari A., Lascano C.I., Anguiano O.L., Pechen de D'Angelo A.M., Venturino A. Antioxidant responses to azinphos methyl and carbaryl during the embryonic development of the toad Rhinella (Bufo) arenarum Hensel. Aquat. Toxicol. 2009, 93:37-44.
28. Sánchez C.P., González N.S., Algranati I.D. Stable ornithine decarboxylase in promastigotes of Leishmaina mexicana Mexicana. Biochem. Biophys. Res. Commun. 1989, 161:754-761.
29. Marcé M., Brown D.S., Capell T., Figueras X., Tiburcio A.F. Rapid high-performance liquid chromatographic method for the quantitation of polyamines as their dansyl derivatives: application to plant and animal tissues. J. Chromatogr. B 1995, 666:329-335.
30. Cochón A.C., González N., San Martín de Viale L.C. Effects of the porphyrinogenic compounds hexachlorobenzene and 3,5-diethoxycarbonyl-1,4-dihydrocollidine on polyamine metabolism. Toxicology 2002, 176:209-219.
31. Bantle J.A., Dumont J.N., Finch R.A., Linder G. Atlas of Abnormalities: A Guide for the Performance of FETAX 1991, Oklahoma State Publications, Stillwater, OK.
32. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with the Folin phenol reagent. J. Biol. Chem. 1951, 193:265-275.
33. Kusunoki S., Yasumasu Y. Inhibitory effect of alpha-hydrazinoornithine on egg cleavage in sea urchin eggs. Dev. Biol. 1978, 67:336-345.
34. Srivastava R.K. Changes in polyamines during embryonic development of atlantic salmon Salmo salar. Comp. Biochem. Physiol. B 1992, 102:97-101.
35. Russell D.H. Putrescine and spermidine biosynthesis in the development of normal and anucleolate mutants of Xenopus laevis. Proc. Natl. Acad. Sci. USA 1971, 68(3):523-547.
36. Zhao Y.C., Chi Y.J., Yu Y.S., Liu J.L., Su R.W., Ma X.H., Shan C.H., Yang Z.M. Polyamines are essential in embryo implantation: expression and function of polyamine-related genes in mouse uterus during peri-implantation period. Endocrinology 2008, 149(5):2325-2332.
37. Bettuzzi S., Davalli P., Astancolle S., Pinna C., Roncaglia R., Boraldi F., Tiozzo R., Sharrard M., Corti A. Coordinate changes of polyamine metabolism regulatory proteins during the cell cycle of normal human dermal fibroblasts. FEBS Lett. 1999, 446(1):18-22.
38. 1-acetyltransferase overexpression in kidney epithelial cells disrupts polyamine homeostasis, leads to DNA damage and causes G2 arrest. Am. J. Physiol. Cell Physiol. 2007, 292(3):1204-1215.
39. Osborne B., Duval C., Ghoda L., Omilli F., Bassez T., Coffino P. Expression and post-transcriptional regulation of ornithine decarboxylase during early Xenopus development. Eur. J. Biochem. 1991, 202:575-581.
40. Pegg A.E. Mammalian polyamine metabolism and function. IUBMB Life 2009, 61(9):880-894.
41. Pegg A.E. Regulation of ornithine decarboxylase. J. Biol. Chem. 2006, 281(21):14529-14532.
42. Kwak M.-K., Kensler T.W., Casero R.A. Induction of phase 2 enzymes by serum oxidized polyamines through activation of Nrf2: effect of the polyamine metabolite acrolein. Biochem. Biophys. Res. Commun. 2003, 305:662-670.
43. Igarashi K., Kashiwagi K. Modulation of cellular function by polyamines. Int. J. Biochem. Cell Biol. 2010, 42:39-51.
44. Shinga J., Kashiwagi K., Tashiro K., Igarashi K., Shiokawa K. Maternal and zygotic expression of mRNA for S-adenosylmethionine decarboxylase and its relevance to the unique polyamine composition in Xenopus oocytes and embryo. Biochim. Biophys. Acta 1996, 1308(1):31-40.
45. Ogasawara T., Ito K., Igarashi K. Effect of polyamines on globin synthesis in a rabbit reticulocyte polyamine-free protein synthetic system. J. Biochem. 1989, 105(2):164-167.
46. Coffino P. Polyamines in spermiogenesis: not now, darling. Proc. Natl. Acad. Sci. USA 2000, 97(9):4421-4423.
47. Thomas T., Thomas T.J. Polyamines in cell growth and cell death: molecular mechanisms and therapeutic applications. Cell. Mol. Life Sci. 2001, 58(2):244-258.
48. Scorcioni F., Corti A., Davalli P., Astancolle S., Bettuzzi S. Manipulation of the expression of regulatory genes of polyamine metabolism results in specific alterations of the cell-cycle progression. Biochem. J. 2001, 354(Pt. 1):217-223.
49. Bell M.R., Belarde J.A., Johnson H.F., Aizenman C.D. A neuroprotective role for polyamines in a Xenopus tadpole model of epilepsy. Nat. Neurosci. 2011, 14(4):505-512.
50. Halonen T., Sivenius J., Miettinen R., Halmekyto M., Kauppinen R., Sinervirta R., Alakuijala L., Alhonen L., MacDonald E., Janne J., Reikkinen P.J. Elevated seizure threshold and impaired spatial learning in transgenic mice with putrescine overproduction in the brain. Eur. J. Neurosci. 1993, 5:1233-1239.
51. Randi A.S., Hernández S., álvarez L., Sánchez M., Schwarcz M., Kleiman de Pisarev D.L. Hexachlorobenzene-induced early changes in ornithine decarboxylase and protein tyrosine kinase activities, polyamines and c-Myc, c-Fos and c-Jun proto-oncogenes in rat liver. Toxicol. Sci. 2003, 76(2):291-298.
52. Rodríguez-Caso C., Montañez R., Cascante M., Sánchez-Jiménez F., Medina M.A. Mathematical modeling of polyamine metabolism in mammals. J. Biol. Chem. 2006, 281(31):21799-21812.
53. Coffino P., Poznanski A. Killer polyamines?. J. Cell. Biochem. 1991, 45(1):54-58.