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Inhibition of neutrophil derived lysosomal enzymes and reactive oxygen species by a novel tetrapeptide.

作者信息

Meera R, Anand S, Ramesh C V, Puvanakrishnan R

机构信息

Department of Biotechnology, Central Leather Research Institute, Adyar, India.

出版信息

Inflamm Res. 1999 Sep;48(9):479-84. doi: 10.1007/s000110050490.

Abstract

OBJECTIVE AND DESIGN

The role of a tetrapeptide derivative PEP 1261 {Boc-Lys(Boc)-Arg-Asp-Ser(tBu)-OtBu}, corresponding to residues 39-42 of human lactoferrin, has been tested in vitro in the modulation of neutrophil function.

MATERIAL AND SUBJECTS

The level of non-enzymatic mediators of inflammation such as reactive oxygen species (ROS), enzymatic mediators such as myeloperoxidase (MPO) and lysosomal enzymes have been assessed in the presence or absence of PEP 1261 in phorbol 12-myristate 13 acetate (PMA) stimulated human neutrophils (n = 6) and also in neutrophils isolated from adjuvant induced arthritic rats (AIA) (n = 4).

TREATMENT

PEP 1261, at a concentration of 0.14 mM, was added to the neutrophil cultures.

STATISTICAL METHOD

The results were analysed by nonparametric statistics using Mann Whitney U test.

RESULTS

Addition of PEP 1261 effectively blocked the H2O2 and O2*- release, decreased the levels of MPO levels (p< 0.01) and lysosomal enzymes (p < 0.05) as compared to PMA stimulated human neutrophils. PEP 1261 was also observed to inhibit the levels of H2O2, O2*-, MPO and lysosomal enzymes (p < 0.05) as compared to PMA stimulated control rat neutrophils and neutrophils from arthritic rats.

CONCLUSIONS

The results of this study indicate that PEP 1261 could serve as an excellent antiinflammatory agent.

摘要

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