Developmental changes in the levels and redox potentials of main hemolymph thiols/disulfides in the Jamaican field cricket Gryllus assimilis

  • Izabela A. Sadowska-Bartosz University of Rzeszów, Department of Biochemistry and Cell Biology
  • Paulina Furmaniak University of Łódź Department Environmental Chemistry
  • Edyta Bieszczad-Bedrejczuk University of Rzeszów, Department of Biochemistry and Cell Biology
  • Grzegorz Bartosz University of Łódź Department of Molecular Biophysics
  • Rafał Głowacki University of Łódź Department Environmental Chemistry

Abstract

Main thiols and disulfides were determined in the hemolymph of the Jamaican field cricket Gryllus assimilis of various developmental stages. On the basis of these data, redox potentials of the glutathione, cysteine and homocysteine redox systems were calculated. The concentrations of all thiols studied decreased during development (at a stage of 6 molts) with respect to young crickets, and increased again in adult insects. Redox potentials of the glutathione and cysteine systems increased from values of  -131.0 ± 5.6 mV and -86.9 ±17.1 mV, respectively  in young crickets to -58.0 ± 3.6 mV and -36.1 ± 4.2 mV, respectively, at the stage of 6 molts and decreased to values of -110.4 ± 24.8 mV and -66.3 ± 12.2 mV, respectively, in adult insects. Redox potentials of the glutathione and cysteine systems in the hemolymph of young and adult insects were similar to those reported for human plasma, suggesting similar redox conditions of extracellular fluids in insects and in mammals.

References

Bald E, Głowacki R (2001) 2-Chloro-1-Methylquinolinium tetrafluoroborate as effective and thiol specific UV-tagging reagent for liquid chromatography. J Liq Chromatogr Rel Techn 24: 1323-1339 doi: org/10.1081/JLC-100103450

Blanco RA, Ziegler TR, Carlson BA, Cheng PY, Park Y, Cotsonis GA, Accardi CJ, Jones DP (2007) Diurnal variation in glutathione and cysteine redox states in human plasma. Am J Clin Nutr 86: 1016-1023

Clark KD, Lu Z, Strand MR (2010) Regulation of melanization by glutathione in the moth Pseudoplusia includens. Insect Biochem Mol Biol 40: 460-467 doi: 10.1016/j.ibmb.2010.04.005

Forman HJ, Zhang H, Rinna A (2009) Glutathione: overview of its protective roles, measurement, and biosynthesis. Mol Aspects Med 30: 1-12 doi: 10.1016/j.mam.2008.08.006

Głowacki R, Bald E (2009) Fully automated method for simultaneous determination of cysteine, cysteinylglycine, glutathione and homocysteine in plasma by high performance liquid chromatography. J Chromatogr B 877: 3400-3404 doi: 10.1016/j.jchromb.2009.06.012

Głowacki R, Borowczyk K, Bald E (2012) Fast analysis of wine for total homocysteine content by high-performance liquid chromatography. Amino Acids 42: 247-251 doi: 10.1007/s00726-010-0509-3

Johnson JM, Strobel FH, Reed M, Pohl J, Jones D P (2008) A rapid LC-FTMS method for the analysis of cysteine, cystine and cysteine/cystine steady-state redox potential in human plasma. Clin Chim Acta 396: 43-48 doi: 10.1016/j.cca.2008.06.020

Jocelyn PC (1967) The standard redox potential of cysteine-cystine from the thiol-disulphide exchange reaction with glutathione and lipoic acid. Eur J Biochem 2: 327-331

Jones DP, Carlson JL, Mody VC, Cai J, Lynn MJ, Sternberg P (2000) Redox state of glutathione in human plasma. Free Radic Biol Med 28: 625-635 doi: org/10.1016/S0891-5849(99)00275-0

Kuśmierek K, Chwatko G, Głowacki R, Kubalczyk P, Bald E (2011) Ultraviolet derivatization of low-molecular-mass thiols for high performance liquid chromatography and capillary electrophoresis analysis. J Chromatogr B 879: 1290-1307 doi: 10.1016/j.jchromb.2010.10.035

Manta B, Comini M, Medeiros A, Hugo M, Trujillo, M, Radi R (2013) Trypanothione: a unique bis-glutathionyl derivative in trypanosomatids. Biochim Biophys Acta 1830: 3199-3216 doi: 10.1016/j.bbagen.2013.01.013

Meister A, Anderson ME (1983) Glutathione. Annu Rev Biochem 52: 711-760 doi: 10.1146/annurev.bi.52.070183.003431

Moriarty SE, Shah JH, Lynn M, Jiang S, Openo K, Jones DP, Sternberg P (2003) Oxidation of glutathione and cysteine in human plasma associated with smoking. Free Radic Biol Med 35: 1582-1588 doi.org/10.1016/j.freeradbiomed.2003.09.006

Newton GL, Fahey RC (2002) Mycothiol biochemistry. Arch Microbiol 178: 388-394 doi: 10.1007/s00203-002-0469-4

Paredes J, Jones DP, Wilson ME, Herndon JG (2014) Age-related alterations of plasma glutathione and oxidation of redox potentials in chimpanzee (Pan troglodytes) and rhesus monkey (Macaca mulatta). Age (Dordr) 36: 719-732 doi: 10.1007/s11357-014-9615-6

Roede JR, Uppal K, Liang Y, Promislow DE, Wachtman LM, Jones DP (2013) Characterization of plasma thiol redox potential in a common marmoset model of aging. Redox Biol 1: 387-393 doi: 10.1016/j.redox.2013.06.003

Samiec PS, Drews-Botsch C, Flagg EW, Kurtz JC, Sternberg PJr, Reed RL, Jones DP (1998) Glutathione in human plasma: decline in association with aging, age-related macular degeneration, and diabetes. Free Radic Biol Med 24: 699-704 doi: org/10.1016/S0891-5849(97)00286-4

Schafer FQ, Buettner GR (2001) Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple. Free Radic Biol Med 30: 1191-1212 doi: org/10.1016/S0891-5849(01)00480-4 doi: org/10.1016/S0891-5849(97)00286-4

Yi H, Ravilious GE, Galant A, Krishnan HB, Jez JM (2010) From sulfur to homoglutathione: thiol metabolism in soybean. Amino Acids 39: 963-978. doi: 10.1007/s00726-010-0572-9

Published
2017-07-27
Section
Articles