Effect of Carbon Monoxide on Bacteria‐Stimulated Cytokine Production by Placental Explants. (13th September 2012)
- Record Type:
- Journal Article
- Title:
- Effect of Carbon Monoxide on Bacteria‐Stimulated Cytokine Production by Placental Explants. (13th September 2012)
- Main Title:
- Effect of Carbon Monoxide on Bacteria‐Stimulated Cytokine Production by Placental Explants
- Authors:
- Peltier, Morgan R.
Arita, Yuko
Gurzenda, Ellen M.
Klimova, Natalia
Koo, Hschi‐Chi
Murthy, Amitasrigowri
Hanna, Nazeeh - Abstract:
- <abstract abstract-type="main" id="aji12017-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="aji12017-sec-0001" sec-type="section"> <title>Problem</title> <p>Preterm birth is frequently caused by an inflammatory response to ascending infections of the reproductive tract. Carbon monoxide (CO) has potent anti‐inflammatory properties at subtoxic concentrations. Whether or not CO can modulate inflammatory responses by placental tissues is unclear.</p> </sec> <sec id="aji12017-sec-0002" sec-type="section"> <title>Methods</title> <p>Placental explant cultures were incubated with heat‐killed <italic>Escherichia coli</italic> or <italic>Ureaplasma parvum</italic> in the presence or absence of 250 ppm CO for 24 hr. Concentrations of cytokines relative viability of the cultures were quantified.</p> </sec> <sec id="aji12017-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>Escherichia coli‐</italic> and <italic>U. parvum</italic>‐stimulated IL‐1β production was significantly inhibited by CO supplementation. <italic>Escherichia coli‐stimulated</italic>, but not <italic>U. parvum</italic>‐stimulated, IFN‐γ production was inhibited by CO. While CO inhibited PGE<sub>2</sub> production by unstimulated cells, no effects on bacteria‐stimulated prostaglandin production were detected. CO had no effect on basal or <italic>E. coli</italic>‐stimulated TNF‐α production but enhanced TNF‐α production by cultures stimulated with <italic>U. parvum</italic>. In<abstract abstract-type="main" id="aji12017-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="aji12017-sec-0001" sec-type="section"> <title>Problem</title> <p>Preterm birth is frequently caused by an inflammatory response to ascending infections of the reproductive tract. Carbon monoxide (CO) has potent anti‐inflammatory properties at subtoxic concentrations. Whether or not CO can modulate inflammatory responses by placental tissues is unclear.</p> </sec> <sec id="aji12017-sec-0002" sec-type="section"> <title>Methods</title> <p>Placental explant cultures were incubated with heat‐killed <italic>Escherichia coli</italic> or <italic>Ureaplasma parvum</italic> in the presence or absence of 250 ppm CO for 24 hr. Concentrations of cytokines relative viability of the cultures were quantified.</p> </sec> <sec id="aji12017-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>Escherichia coli‐</italic> and <italic>U. parvum</italic>‐stimulated IL‐1β production was significantly inhibited by CO supplementation. <italic>Escherichia coli‐stimulated</italic>, but not <italic>U. parvum</italic>‐stimulated, IFN‐γ production was inhibited by CO. While CO inhibited PGE<sub>2</sub> production by unstimulated cells, no effects on bacteria‐stimulated prostaglandin production were detected. CO had no effect on basal or <italic>E. coli</italic>‐stimulated TNF‐α production but enhanced TNF‐α production by cultures stimulated with <italic>U. parvum</italic>. In addition, CO tended to improve the viability of the placental cultures.</p> </sec> <sec id="aji12017-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Low concentrations of CO tended to reduce proinflammatory cytokines and to promote the production of anti‐inflammatory cytokines in a pathogen‐specific manner. These properties suggest that CO may be useful for promoting a pro‐pregnancy cytokine milieu by placental explants and may reduce the consequences of intrauterine infections.</p> </sec> </abstract> … (more)
- Is Part Of:
- American journal of reproductive immunology. Volume 69:Number 2(2013:Feb.)
- Journal:
- American journal of reproductive immunology
- Issue:
- Volume 69:Number 2(2013:Feb.)
- Issue Display:
- Volume 69, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 69
- Issue:
- 2
- Issue Sort Value:
- 2013-0069-0002-0000
- Page Start:
- 142
- Page End:
- 149
- Publication Date:
- 2012-09-13
- Subjects:
- Human reproduction -- Immunological aspects -- Periodicals
616.69206 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-0897 ↗
http://estar.bl.uk/cgi-bin/sciserv.pl?collection=journals&journal=10467408 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/aji.12017 ↗
- Languages:
- English
- ISSNs:
- 1046-7408
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0836.500000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3114.xml