نتایج جستجو برای: myeloperoxidase deficiency

تعداد نتایج: 143382  

2017
Mandeep Atwal Emma L. Lishman Caroline A. Austin Ian G. Cowell

Myeloperoxidase is expressed exclusively in granulocytes and immature myeloid cells and transforms the topoisomerase II (TOP2) poisons etoposide and mitoxantrone to chemical forms that have altered DNA damaging properties. TOP2 poisons are valuable and widely used anticancer drugs, but they are associated with the occurrence of secondary acute myeloid leukemias. These factors have led to the hy...

Journal: :The Journal of biological chemistry 2005
Valdecir F Ximenes Sueli de O Silva Maria R Rodrigues Luiz H Catalani Ghassan J Maghzal Anthony J Kettle Ana Campa

Myeloperoxidase uses hydrogen peroxide to oxidize numerous substrates to hypohalous acids or reactive free radicals. Here we show that neutrophils oxidize melatonin to N(1)-acetyl-N(2)-formyl-5-methoxykynuramine (AFMK) in a reaction that is catalyzed by myeloperoxidase. Production of AFMK was highly dependent on superoxide but not hydrogen peroxide. It did not require hypochlorous acid, singlet...

Journal: :Free radical research communications 1991
V V Subrahmanyam P Kolachana M T Smith

Benzene, a known human myelotoxin and leukemogen is metabolized by liver cytochrome P-450 monooxygenase to phenol. Further hydroxylation of phenol by cytochrome P-450 monooxygenase results in the formation of mainly hydroquinone, which accumulates in the bone marrow. Bone marrow contains high levels of myeloperoxidase. Here we report that phenol hydroxylation to hydroquinone is also catalyzed b...

Journal: :The Journal of clinical investigation 1999
M M Anderson J R Requena J R Crowley S R Thorpe J W Heinecke

Reactive aldehydes derived from reducing sugars and peroxidation of lipids covalently modify proteins and may contribute to oxidative tissue damage. We recently described another mechanism for generating reactive aldehydes from free alpha-amino acids. The pathway begins with myeloperoxidase, a heme enzyme secreted by activated neutrophils. Conversion of alpha-amino acids to aldehydes requires h...

Journal: :Annals of the rheumatic diseases 1991
H L Nurcombe R C Bucknall S W Edwards

Synovial fluid isolated from 16 patients with rheumatoid arthritis activated luminol dependent chemiluminescence in bloodstream neutrophils, and the maximal activity stimulated varied over a 50-fold range. In contrast, these same fluids only activated a much lower range (two- to threefold) of maximal rates of lucigenin dependent chemiluminescence and cytochrome c reduction, two assays which onl...

Journal: :Archives of Iranian medicine 2011
Ashraf Mohamadkhani Ferdous Rastgar Jazii Kourosh Sayehmiri Saeideh Jafari-Nejad Laleh Montaser-Kouhsari Hossein Poustchi Ghodratollah Montazeri

BACKGROUND Hepatitis B virus initiates a complicated cascade process leading to chronic hepatitis B, cirrhosis, and hepatocellular carcinoma. In inflammatory situations, myeloperoxidase is released in plasma and binds to apolipoprotein A-1 in high-density lipoproteins. This study aims to evaluate the level of plasma myeloperoxidase as well as the pattern of plasma proteins in patients with chro...

2009
Mark A. Little Lucy Smyth Alan D. Salama Sriparna Mukherjee Jennifer Smith Dorian Haskard Sussan Nourshargh H. Terence Cook Charles D. Pusey

The morbidity burden associated with anti-neutrophil cytoplasmic autoantibody-associated vasculitis is increasing, and many novel biological therapies are now entering the drug development pipeline. There is thus an urgent need to develop a representative animal model to facilitate testing of these agents. We previously examined the effect of antineutrophil cytoplasmic autoantibody on leukocyte...

Journal: :The Journal of biological chemistry 2000
C J van Dalen C C Winterbourn R Senthilmohan A J Kettle

Myeloperoxidase is a heme enzyme of neutrophils that uses hydrogen peroxide to oxidize chloride to hypochlorous acid. Recently, it has been shown to catalyze nitration of tyrosine. In this study we have investigated the mechanism by which it oxidizes nitrite and promotes nitration of tyrosyl residues. Nitrite was found to be a poor substrate for myeloperoxidase but an excellent inhibitor of its...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2008
Dao-Quan Peng Gregory Brubaker Zhiping Wu Lemin Zheng Belinda Willard Michael Kinter Stanley L Hazen Jonathan D Smith

OBJECTIVE Apolipoprotein A-I (apoAI) acts as an ABCA1-dependent acceptor of cellular phospholipids and cholesterol during the biogenesis of HDL, but this activity is susceptible to oxidative inactivation by myeloperoxidase. We tried to determine which residues mediated this inactivation and create an oxidant-resistant apoAI variant. METHODS AND RESULTS Mass spectrometry detected the presence ...

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