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In vivo imaging of reactive oxygen and nitrogen species in inflammation using the luminescent probe L-012

Kielland, Anders (author)
Department of Nutrition, Institute of Basic Medical Sciences, The Medical Faculty, Oslo, Blindern, Norway
Blom, Thomas (author)
Lund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups
Nandakumar, Kutty Selva, 1965- (author)
Lund University,Lunds universitet,Karolinska Institutet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups
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Holmdahl, Rikard (author)
Lund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups
Blomhoff, Rune (author)
Department of Nutrition, Institute of Basic Medical Sciences, The Medical Faculty, Oslo, Blindern, Norway
Carlsen, Harald (author)
Department of Nutrition, Institute of Basic Medical Sciences, The Medical Faculty, Oslo, Blindern, Norway
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 (creator_code:org_t)
Philadelphia, PA : Elsevier, 2009
2009
English.
In: Free Radical Biology & Medicine. - Philadelphia, PA : Elsevier. - 0891-5849 .- 1873-4596. ; 47:6, s. 760-766
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Production of reactive oxygen and nitrogen species (ROS/RNS) is an important part of the inflammatory response, but prolonged elevated levels of ROS/RNS as under chronic inflammation can contribute to the development of disease. Monitoring ROS/RNS in living animals is challenging due to the rapid turnover of ROS/RNS and the limited sensitivity and specificity of ROS/RNS probes. We have explored the use of the chemiluminescent probe L-012 for noninvasive imaging of ROS/RNS production during inflammation in living mice. Various inflammatory conditions were induced, and L-012-dependent luminescence was recorded with an ultrasensitive CCD camera. Strong luminescent signals were observed from different regions of the body corresponding to inflammation. The signal was reduced by administration of the SOD mimetic tempol, the NADPH oxidase inhibitor apocynin, and the inhibitor of nitric oxide synthesis L-NAME, signifying the requirement for the presence of ROS/RNS. Additionally, the L-012 signal was abolished in mice with a mutation in the Ncf1 gene, encoding a protein in the NADPH oxidase complex 2, which generates ROS/RNS during inflammation. In conclusion, L-012 is well distributed in the mouse body and mediates a strong ROS/RNS-dependent luminescent signal in vivo and is useful for monitoring the development and regulation of inflammation in living organisms. © 2009 Elsevier Inc. All rights reserved.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Chemiluminescence
Free radical
In vivo
Inflammation
L-012
Luminescence
Molecular imaging
Mouse
Optical imaging
RNS
ROS
RNS
Inflammation
L-012
In vivo
Molecular imaging
Optical imaging
Free radical
Mouse
Chemiluminescence
ROS
Luminescence

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art (subject category)

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