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Biochemical and biophysical research communications2000; 273(3); 816-819; doi: 10.1006/bbrc.2000.3021

Histidin as a mercurial poisoning inhibitor.

Abstract: Histidin has been shown to effectively inhibit coagulation of horse oxyhemoglobin (HbO(2)) modified by mercury(II) ion bound to reactive thiol groups of protein. Kinetic parameters were measured and the histidin-to-mercury binding constant was kinetically estimated. Histidin, as other pharmaceutically acceptable compounds with some mercury-binding capacity, has been suggested to alleviate mercury intoxication conditions.
Publication Date: 2000-07-13 PubMed ID: 10891329DOI: 10.1006/bbrc.2000.3021Google Scholar: Lookup
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  • Journal Article

Summary

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The research article shows that Histidin, a compound, can potentially reduce mercury poisoning by inhibiting the coagulation of horse oxyhemoglobin caused by the mercury ion.

Research Methodology and Findings

  • The researchers studied the effect of Histidin on coagulation of horse oxyhemoglobin (HbO(2)) caused by the mercury ion (II) attached to the protein’s reactive thiol groups. Coagulation refers to the process by which blood or a similar substance becomes semi-solid, changing from a liquid to a gel-like or a solid state.
  • During the instruction, the researchers calculated kinetic parameters. Kinetics is a branch of science that deals with the rates of chemical reactions, and here it was used to understand the behavior of different compounds and chemicals in the introduced histidin-to-mercury environment.
  • The binding constant between histidin and mercury was also determined using the kinetic study. A binding constant is an equilibrium constant for the formation of a complex in solution. Determining a binding constant is essential to understand the affinity between two molecules.

Implications of the Study

  • The experiment indicated that Histidin has the ability to bind with mercury. Because of this property, Histidin can potentially be used to mitigate the harmful effects of mercury poisoning.
  • Mention was also made of other pharmaceutically acceptable compounds that possess some mercury-binding capacity. These compounds, like Histidin, could be developed into treatments to alleviate mercury intoxication conditions.

Conclusion

  • This research opens up new possibilities in the treatment of mercury intoxication conditions. It explains a novel use of Histidin and potentially other similar compounds.
  • However, it should be noted that this research is at its initial stages. Further studies are needed to determine the effectiveness of Histidin and its safe usage dosage in human subjects.

Cite This Article

APA
Myshkin AE, Khromova VS. (2000). Histidin as a mercurial poisoning inhibitor. Biochem Biophys Res Commun, 273(3), 816-819. https://doi.org/10.1006/bbrc.2000.3021

Publication

ISSN: 0006-291X
NlmUniqueID: 0372516
Country: United States
Language: English
Volume: 273
Issue: 3
Pages: 816-819

Researcher Affiliations

Myshkin, A E
  • Institute of Biochemical Physics of the Russian Academy of Sciences, Kosygin St. 4, Moscow V-334, 117977, Russia. myshkin@photonics.ru
Khromova, V S

    MeSH Terms

    • Animals
    • Histidine / chemistry
    • Histidine / pharmacology
    • Horses
    • Kinetics
    • Mercury Poisoning / prevention & control
    • Methemoglobin / chemistry

    Citations

    This article has been cited 1 times.
    1. Stratton A, Ericksen M, Harris TV, Symmonds N, Silverstein TP. Mercury(II) binds to both of chymotrypsin's histidines, causing inhibition followed by irreversible denaturation/aggregation. Protein Sci 2017 Feb;26(2):292-305.
      doi: 10.1002/pro.3082pubmed: 27859834google scholar: lookup