Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease: Effect of acute exposure to low ethanol concentrations

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Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease : Effect of acute exposure to low ethanol concentrations. / Parlesak, Alexandr; Schäfer, Christian; Paulus, Sonja Barbara; Hammes, Susanne; Diedrich, Jens Peter; Bode, Christiane.

In: Alcoholism: Clinical and Experimental Research, Vol. 27, No. 3, 2003, p. 503-508.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Parlesak, A, Schäfer, C, Paulus, SB, Hammes, S, Diedrich, JP & Bode, C 2003, 'Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease: Effect of acute exposure to low ethanol concentrations', Alcoholism: Clinical and Experimental Research, vol. 27, no. 3, pp. 503-508. https://doi.org/10.1097/01.ALC.0000056688.27111.49

APA

Parlesak, A., Schäfer, C., Paulus, S. B., Hammes, S., Diedrich, J. P., & Bode, C. (2003). Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease: Effect of acute exposure to low ethanol concentrations. Alcoholism: Clinical and Experimental Research, 27(3), 503-508. https://doi.org/10.1097/01.ALC.0000056688.27111.49

Vancouver

Parlesak A, Schäfer C, Paulus SB, Hammes S, Diedrich JP, Bode C. Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease: Effect of acute exposure to low ethanol concentrations. Alcoholism: Clinical and Experimental Research. 2003;27(3):503-508. https://doi.org/10.1097/01.ALC.0000056688.27111.49

Author

Parlesak, Alexandr ; Schäfer, Christian ; Paulus, Sonja Barbara ; Hammes, Susanne ; Diedrich, Jens Peter ; Bode, Christiane. / Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease : Effect of acute exposure to low ethanol concentrations. In: Alcoholism: Clinical and Experimental Research. 2003 ; Vol. 27, No. 3. pp. 503-508.

Bibtex

@article{c8ca9c06dae742d2b13fe9531b43f05e,
title = "Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease: Effect of acute exposure to low ethanol concentrations",
abstract = "Background: In rodents, the development of alcoholic liver disease (ALD) after chronic alcohol feeding was shown to depend on the activity of enzymes that are necessary for production of reactive oxygen species (ROS) in phagocytes. The aim of this study was to determine the formation of ROS by resting and challenged phagocytes of patients with different stages of ALD in the presence of ethanol concentrations commonly found in the blood of alcohol abusers.Patients and Methods: The release of ROS and the phagocytosis of bacteria by neutrophils and monocytes obtained from 60 patients, who were categorized in three groups due to the severity of ALD, were compared to that of 28 healthy controls. ROS release by these phagocytes was measured after challenging with endotoxin and the addition of ethanol (22 and 44 mM). Results: Resting neutrophils but not monocytes from patients with severe stages of ALD produced significantly more ROS than those of healthy controls. Basal values of ROS production from neutrophils correlated closely to markers of the severity of ALD. ROS formation was depressed dose-dependently by ethanol in the healthy controls but not in alcohol abusers. Conclusions: Changes in the ROS metabolism of phagocytes found in this study might contribute to both the development of ALD and the impaired immune response occurring in patients with severe ALD.",
keywords = "Alcohol-Induced Liver Damage, Chemiluminescence, Ethanol, Phagocytosis, Reactive Oxygen Species",
author = "Alexandr Parlesak and Christian Sch{\"a}fer and Paulus, {Sonja Barbara} and Susanne Hammes and Diedrich, {Jens Peter} and Christiane Bode",
note = "(Ekstern)",
year = "2003",
doi = "10.1097/01.ALC.0000056688.27111.49",
language = "English",
volume = "27",
pages = "503--508",
journal = "Alcoholism: Clinical and Experimental Research",
issn = "0145-6008",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - Phagocytosis and production of reactive oxygen species by peripheral blood phagocytes in patients with different stages of alcohol-induced liver disease

T2 - Effect of acute exposure to low ethanol concentrations

AU - Parlesak, Alexandr

AU - Schäfer, Christian

AU - Paulus, Sonja Barbara

AU - Hammes, Susanne

AU - Diedrich, Jens Peter

AU - Bode, Christiane

N1 - (Ekstern)

PY - 2003

Y1 - 2003

N2 - Background: In rodents, the development of alcoholic liver disease (ALD) after chronic alcohol feeding was shown to depend on the activity of enzymes that are necessary for production of reactive oxygen species (ROS) in phagocytes. The aim of this study was to determine the formation of ROS by resting and challenged phagocytes of patients with different stages of ALD in the presence of ethanol concentrations commonly found in the blood of alcohol abusers.Patients and Methods: The release of ROS and the phagocytosis of bacteria by neutrophils and monocytes obtained from 60 patients, who were categorized in three groups due to the severity of ALD, were compared to that of 28 healthy controls. ROS release by these phagocytes was measured after challenging with endotoxin and the addition of ethanol (22 and 44 mM). Results: Resting neutrophils but not monocytes from patients with severe stages of ALD produced significantly more ROS than those of healthy controls. Basal values of ROS production from neutrophils correlated closely to markers of the severity of ALD. ROS formation was depressed dose-dependently by ethanol in the healthy controls but not in alcohol abusers. Conclusions: Changes in the ROS metabolism of phagocytes found in this study might contribute to both the development of ALD and the impaired immune response occurring in patients with severe ALD.

AB - Background: In rodents, the development of alcoholic liver disease (ALD) after chronic alcohol feeding was shown to depend on the activity of enzymes that are necessary for production of reactive oxygen species (ROS) in phagocytes. The aim of this study was to determine the formation of ROS by resting and challenged phagocytes of patients with different stages of ALD in the presence of ethanol concentrations commonly found in the blood of alcohol abusers.Patients and Methods: The release of ROS and the phagocytosis of bacteria by neutrophils and monocytes obtained from 60 patients, who were categorized in three groups due to the severity of ALD, were compared to that of 28 healthy controls. ROS release by these phagocytes was measured after challenging with endotoxin and the addition of ethanol (22 and 44 mM). Results: Resting neutrophils but not monocytes from patients with severe stages of ALD produced significantly more ROS than those of healthy controls. Basal values of ROS production from neutrophils correlated closely to markers of the severity of ALD. ROS formation was depressed dose-dependently by ethanol in the healthy controls but not in alcohol abusers. Conclusions: Changes in the ROS metabolism of phagocytes found in this study might contribute to both the development of ALD and the impaired immune response occurring in patients with severe ALD.

KW - Alcohol-Induced Liver Damage

KW - Chemiluminescence

KW - Ethanol

KW - Phagocytosis

KW - Reactive Oxygen Species

U2 - 10.1097/01.ALC.0000056688.27111.49

DO - 10.1097/01.ALC.0000056688.27111.49

M3 - Journal article

C2 - 12658117

AN - SCOPUS:0037345426

VL - 27

SP - 503

EP - 508

JO - Alcoholism: Clinical and Experimental Research

JF - Alcoholism: Clinical and Experimental Research

SN - 0145-6008

IS - 3

ER -

ID: 306589891