Respiratory burst activity in rat alveolar macrophages: particle-stimulated oxygen consumption independent of superoxide anion release.
Public Domain
-
1987/07/01
Details
-
Personal Author:
-
Description:Respiratory burst activity during stimulation of alveolar macrophages was studied in-vitro. The purpose of the study was to test the assumption that oxygen consumption stimulated by exposing alveolar macrophages to xenobiotics was used in releasing superoxide- anion (O2-). Suspensions of alveolar macrophages obtained from male Sprague-Dawley-rats were stimulated with 0 to 3000 micrograms per milliliter (microg/ml) concanavalin-A (11028710) (conA) or 0 to 6.0mg/ml zymosan (9010724) particles. Oxygen consumption and release of hydrogen-peroxide and O2- by the suspensions was monitored. The time course and dose response curves for zymosan and conA stimulated oxygen consumption did not match those for hydrogen- peroxide and O2- production. The maximum rate of oxygen consumption induced by zymosan occurred at a lower concentration than was required to release O2- or hydrogen-peroxide. ConA at concentrations above 600microg/ml decreased oxygen consumption and hydrogen-peroxide release. O2- release increased over the entire range of conA concentrations. Additionally rat alveolar macrophages were preincubated with 0 or 0.12 millimolar cytochrome-c (9007436), followed by 0.1 to 2.0mg/ml zymosan. The effects on oxygen consumption were monitored. Rat alveolar macrophages were treated with 0 or 0.1mg/ml zymosan and 0 or 5microg/ml cytochalasin-B (14930962). The effects on oxygen consumption and O2- and hydrogen- peroxide formation were monitored. Cytochrome-c inhibited zymosan induced oxygen consumption by 40 percent. Cytochalasin-B stimulated zymosan induced oxygen consumption and hydrogen-peroxide release by 98.5 and 44 percent, respectively, but had no effect on O2- production. The authors conclude that all of the stimulated increase in oxygen consumption in alveolar macrophages is not used in generating O2-. Some of the increase may be consumed by mechanical processes involving microfilament activation. [Description provided by NIOSH]
-
Subjects:
-
Keywords:
-
ISBN:9780849343322
-
Publisher:
-
Document Type:
-
Genre:
-
Place as Subject:
-
CIO:
-
Division:
-
Topic:
-
Location:
-
Pages in Document:21-37
-
NIOSHTIC Number:nn:00184745
-
Citation:Cellular chemiluminescence. Van Dyke K, Castranova V, eds. Boca Raton, FL: CRC Press, 1987 Jul; :21-37
-
CAS Registry Number:
-
Editor(s):
-
Federal Fiscal Year:1987
-
Peer Reviewed:False
-
Source Full Name:Cellular chemiluminescence
-
Collection(s):
-
Main Document Checksum:urn:sha-512:7dc847c09aedf140bc731323e8446b4703641ae07d6ad9e7b7238120dab30b8f7dcaa9b938d34d035f87873a0fe7fec262d5d13dcaf290925445e82b6de3b57d
-
Download URL:
-
File Type:
ON THIS PAGE
CDC STACKS serves as an archival repository of CDC-published products including
scientific findings,
journal articles, guidelines, recommendations, or other public health information authored or
co-authored by CDC or funded partners.
As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.
As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.
You May Also Like