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Chemical Compound Review

Dithioerythritol     (2S,3R)-1,4-bis- sulfanylbutane-2,3-diol

Synonyms: AmbotzRL-1019, CHEBI:17456, D8161_SIGMA, D8255_SIAL, D9680_SIAL, ...
 
 
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High impact information on Dithioerythritol

  • RESULTS: Endogenous eotaxin was undetectable in DTE-processed samples, with a mean of only 30% (SD, 13%) spike recovery [1].
  • METHODS: Induced sputum from normal and asthmatic subjects was processed with dithioerythritol (DTE) or PBS; recovery of eotaxin was assessed by means of ELISA before and after spiking with recombinant eotaxin [1].
  • While graft survivals were improved when positive crossmatch serum reactivity was due to IgM, these survivals were still significantly poorer than when the crossmatches were completely negative (86% vs. 60%, P < 0.05 for NIH-negative vs. NIH-positive, but DTE-negative, and 88% vs. 77%, P < 0.05 for AHG-negative vs. AHG-positive, but DTE-negative) [2].
  • NIH and AHG crossmatch-positive sera were treated with dithioerythritol (DTE) to establish whether reactivity was due to IgM or IgG immunoglobulin [2].
  • Without antioxidant (DTE or ascorbic acid) almost no BH(4) was detected [3].
 

Biological context of Dithioerythritol

  • Re-Tx recipients with an AHG-POS XM who are either DTE/AHG-POS or -NEG display reduced graft survivals compared with AHG-NEG Re-Tx recipients [4].
  • The reduction of SS groups by DTE (10 mM, 1 h at 23 degrees C) in the intact membrane preparation produced an increase in total number of binding sites of the high-affinity component of [3H]IMI binding by 50% [5].
  • Reversal of the cross-linking with the reducing agent dithioerythritol (DTE) restored osmotic fragility and response to lysolecithin as well as deformability [6].
 

Anatomical context of Dithioerythritol

 

Associations of Dithioerythritol with other chemical compounds

  • Compared with ascorbic acid as an antioxidant, DTE was more protective against oxidation of BH(4), particularly in samples stored over a period of 8 months [3].
  • The effects of cross-linking with 5 mM DTBP for 1 h were completely reversible after treatment with 10 mM DTE for 20 min [6].
  • NAC, NAM, DTT, and DTE were administered by subcutaneous injection or by mouth or by both routes, the other vitamins and DMSA by mouth alone [9].
  • 8. Three other activities, a protease, a corticolytic enzyme, and purine nucleoside phosphorylase, were solubilized by both DTE alone and DTE plus urea at pH 9 [10].
 

Gene context of Dithioerythritol

  • However, treatment of Re-Tx, AHG-POS sera with DTE resulted in comparably poor graft survival rates of 31% and 50% for DTE/AHG-NEG and POS crossmatches, respectively [4].
  • The minimum concentration of the thiol compound required for optimal activation of cathepsin B was found to be lowest (0.2 mM) for DTE [11].
 

Analytical, diagnostic and therapeutic context of Dithioerythritol

References

  1. Measurement of eotaxin (CCL11) in induced sputum supernatants: validation and detection in asthma. Hadjicharalambous, C., Dent, G., May, R.D., Handy, R.L., Anderson, I.K., Davies, D.E., Djukanovic, R. J. Allergy Clin. Immunol. (2004) [Pubmed]
  2. Positive pretransplant crossmatches predict early graft loss in liver allograft recipients. Katz, S.M., Kimball, P.M., Ozaki, C., Monsour, H., Clark, J., Cavazos, D., Kahan, B.D., Wood, R.P., Kerman, R.H. Transplantation (1994) [Pubmed]
  3. Plasma tetrahydrobiopterin and its pharmacokinetic following oral administration. Fiege, B., Ballhausen, D., Kierat, L., Leimbacher, W., Goriounov, D., Schircks, B., Thöny, B., Blau, N. Mol. Genet. Metab. (2004) [Pubmed]
  4. AHG and DTE/AHG procedure identification of crossmatch-appropriate donor-recipient pairings that result in improved graft survival. Kerman, R.H., Kimball, P.M., Van Buren, C.T., Lewis, R.M., DeVera, V., Baghdahsarian, V., Heydari, A., Kahan, B.D. Transplantation (1991) [Pubmed]
  5. High- and low-affinity [3H]imipramine binding sites on human platelets: separate determination and involvement of sulphur-containing bonds. Demushkin, V.P., Fomenko, A.M., Plyashkevich, Y.G., Shchurin, M.R., Brusov, O.S. Eur. J. Pharmacol. (1987) [Pubmed]
  6. Reversible cross-linking and CO treatment as an approach in red cell stabilization. Bakaltcheva, I., Leslie, S., MacDonald, V., Spargo, B., Rudolph, A. Cryobiology (2000) [Pubmed]
  7. The effect of processing on inflammatory markers in induced sputum. Louis, R., Shute, J., Goldring, K., Perks, B., Lau, L.C., Radermecker, M., Djukanovic, R. Eur. Respir. J. (1999) [Pubmed]
  8. Effect of thiols on macroconidia of Fusarium sulphureum. Barran, L.R., Schneider, E.F. Can. J. Microbiol. (1979) [Pubmed]
  9. Survival in patients with amyotrophic lateral sclerosis, treated with an array of antioxidants. Vyth, A., Timmer, J.G., Bossuyt, P.M., Louwerse, E.S., de Jong, J.M. J. Neurol. Sci. (1996) [Pubmed]
  10. Alteration by heat activation of enzymes localized in spore coats of Bacillus cereus. Srivastava, O.P., Fitz-James, P.C. Can. J. Microbiol. (1981) [Pubmed]
  11. Studies on activation and inhibition of cathepsin B from buffalo liver. Salahuddin, A., Kaur, H. J. Protein Chem. (1996) [Pubmed]
 
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