Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1993 Jul;39(3-4):210-7.
doi: 10.1007/BF01998975.

Is copper pro- or anti-inflammatory? A reconciling view and a novel approach for the use of copper in the control of inflammation

Affiliations
Review

Is copper pro- or anti-inflammatory? A reconciling view and a novel approach for the use of copper in the control of inflammation

G Berthon. Agents Actions. 1993 Jul.

Abstract

The anti-inflammatory role of copper is well-known although still largely unexplained. On the other hand, the capacity of copper to induce the formation of damaging .OH radicals in vivo is no longer debated. These two aspects of the physiological activity of copper have been considered to be paradoxical. Arguments developed here show that they may actually derive from a single chemical process, the type of physiological effect observed depending on the ligand bound to the copper ions involved in Fenton chemistry. Both iron and copper are Fenton catalysts. Given its intrinsic coordination properties, however, copper induces more site-specific .OH damage to the ligands bound to it. It, therefore, appears that copper complexes with specific .OH-inactivating ligands (OILs) can be used as "lures" for the Fenton reaction, .OH radicals preferentially formed on these being immediately inactivated. The hypothesis is thus put forward here that copper-OIL complexes acting as effective Fenton catalysts are potential "catalase-like" anti-inflammatory drugs.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Biochem J. 1987 May 1;243(3):709-14 - PubMed
    1. Philos Trans R Soc Lond B Biol Sci. 1985 Dec 17;311(1152):659-71 - PubMed
    1. Biochem J. 1991 Feb 1;273 ( Pt 3):601-4 - PubMed
    1. Proc Natl Acad Sci U S A. 1990 Jul;87(13):5006-10 - PubMed
    1. Int J Radiat Oncol Biol Phys. 1992;22(3):607-12 - PubMed

MeSH terms

Substances