Peripheral benzodiazepines enhance the respiratory burst of macrophage-like P388D 1 cells stimulated by arachidonic acid
International Journal of Immunopharmacology, ISSN: 0192-0561, Vol: 9, Issue: 3, Page: 269-274
1987
- 53Citations
- 4Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations53
- Citation Indexes53
- 53
- CrossRef46
- Captures4
- Readers4
Article Description
P388D 1, a murine cell with macrophage properties, responds to exogenous arachidonic acid with superoxide anion production. This oxidative burst is enhanced by peripheral and mixed type benzodiazepines and this stimulation is specifically reversed by the peripheral antagonist PK 11195. In contrast, PK 11195 is unable to antagonize a stimulation caused by a non-benzodiazepine ligand such as the chemotactic peptide fMet-Leu-Phe. The optimal concentrations were close to 10 nM and corresponded to the affinities of the compounds for the peripheral benzodiazepine receptor detected on these cells. Compared to other tissues where peripheral benzodiazepines acted only at micromolar concentrations, the macrophage with its functional receptor appears as a privileged site of action for these molecules.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0192056187900506; http://dx.doi.org/10.1016/0192-0561(87)90050-6; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0023272262&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/3038760; https://linkinghub.elsevier.com/retrieve/pii/0192056187900506; http://dx.doi.org/10.1016/0192-0561%2887%2990050-6; https://dx.doi.org/10.1016/0192-0561%2887%2990050-6
Elsevier BV
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