Time-dependent dual mode of action of COX-2 inhibition on mouse serum corticosterone levels
•Short-term COX-2 inhibition increased corticosterone levels,•Long-term COX-2 inhibition lowered corticosterone levels,•Corticosterone levels are regulated through a COX-2-dependent mechanism in mice. To elucidate the effect of cyclooxygenase-2 (COX-2) inhibition on corticosterone release, mice were...
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| Vydáno v: | Steroids Ročník 207; s. 109438 |
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| Médium: | Journal Article |
| Jazyk: | angličtina |
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Elsevier Inc
01.07.2024
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| ISSN: | 0039-128X, 1878-5867, 1878-5867 |
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| Abstract | •Short-term COX-2 inhibition increased corticosterone levels,•Long-term COX-2 inhibition lowered corticosterone levels,•Corticosterone levels are regulated through a COX-2-dependent mechanism in mice.
To elucidate the effect of cyclooxygenase-2 (COX-2) inhibition on corticosterone release, mice were divided into a group receiving NS398, a selective COX-2 inhibitor at a dose of 3 mg/kg for seven days, and a group receiving NS398 for fourteen days. After this time, the mice were sacrificed, and blood serum was collected. An ELISA protocol was used to analyze serum corticosterone levels. Short-term COX-2 inhibition increased corticosterone levels, while long-term inhibition lowered them. The exact schedule of experiments was repeated after the lipopolysaccharide (LPS) Escherichia coli challenge in mice to check the influence of stress stimuli on the tested parameters. In this case, we observed increases in corticosterone levels, significant in a seven-day pattern. These results indicate that corticosterone levels are regulated through a COX-2-dependent mechanism in mice. |
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| AbstractList | •Short-term COX-2 inhibition increased corticosterone levels,•Long-term COX-2 inhibition lowered corticosterone levels,•Corticosterone levels are regulated through a COX-2-dependent mechanism in mice.
To elucidate the effect of cyclooxygenase-2 (COX-2) inhibition on corticosterone release, mice were divided into a group receiving NS398, a selective COX-2 inhibitor at a dose of 3 mg/kg for seven days, and a group receiving NS398 for fourteen days. After this time, the mice were sacrificed, and blood serum was collected. An ELISA protocol was used to analyze serum corticosterone levels. Short-term COX-2 inhibition increased corticosterone levels, while long-term inhibition lowered them. The exact schedule of experiments was repeated after the lipopolysaccharide (LPS) Escherichia coli challenge in mice to check the influence of stress stimuli on the tested parameters. In this case, we observed increases in corticosterone levels, significant in a seven-day pattern. These results indicate that corticosterone levels are regulated through a COX-2-dependent mechanism in mice. To elucidate the effect of cyclooxygenase-2 (COX-2) inhibition on corticosterone release, mice were divided into a group receiving NS398, a selective COX-2 inhibitor at a dose of 3 mg/kg for seven days, and a group receiving NS398 for fourteen days. After this time, the mice were sacrificed, and blood serum was collected. An ELISA protocol was used to analyze serum corticosterone levels. Short-term COX-2 inhibition increased corticosterone levels, while long-term inhibition lowered them. The exact schedule of experiments was repeated after the lipopolysaccharide (LPS) Escherichia coli challenge in mice to check the influence of stress stimuli on the tested parameters. In this case, we observed increases in corticosterone levels, significant in a seven-day pattern. These results indicate that corticosterone levels are regulated through a COX-2-dependent mechanism in mice. To elucidate the effect of cyclooxygenase-2 (COX-2) inhibition on corticosterone release, mice were divided into a group receiving NS398, a selective COX-2 inhibitor at a dose of 3 mg/kg for seven days, and a group receiving NS398 for fourteen days. After this time, the mice were sacrificed, and blood serum was collected. An ELISA protocol was used to analyze serum corticosterone levels. Short-term COX-2 inhibition increased corticosterone levels, while long-term inhibition lowered them. The exact schedule of experiments was repeated after the lipopolysaccharide (LPS) Escherichia coli challenge in mice to check the influence of stress stimuli on the tested parameters. In this case, we observed increases in corticosterone levels, significant in a seven-day pattern. These results indicate that corticosterone levels are regulated through a COX-2-dependent mechanism in mice.To elucidate the effect of cyclooxygenase-2 (COX-2) inhibition on corticosterone release, mice were divided into a group receiving NS398, a selective COX-2 inhibitor at a dose of 3 mg/kg for seven days, and a group receiving NS398 for fourteen days. After this time, the mice were sacrificed, and blood serum was collected. An ELISA protocol was used to analyze serum corticosterone levels. Short-term COX-2 inhibition increased corticosterone levels, while long-term inhibition lowered them. The exact schedule of experiments was repeated after the lipopolysaccharide (LPS) Escherichia coli challenge in mice to check the influence of stress stimuli on the tested parameters. In this case, we observed increases in corticosterone levels, significant in a seven-day pattern. These results indicate that corticosterone levels are regulated through a COX-2-dependent mechanism in mice. |
| ArticleNumber | 109438 |
| Author | Tabecka-Lonczynska, Anna Sowa-Kućma, Magdalena Misztak, Paulina Stachowicz, Katarzyna Pańczyszyn-Trzewik, Patrycja |
| Author_xml | – sequence: 1 givenname: Patrycja surname: Pańczyszyn-Trzewik fullname: Pańczyszyn-Trzewik, Patrycja organization: Medical College of Rzeszów University, Institute of Medical Science, Department of Human Physiology, 35-310 Rzeszow, Kopisto Street 2a, Poland – sequence: 2 givenname: Magdalena surname: Sowa-Kućma fullname: Sowa-Kućma, Magdalena organization: Medical College of Rzeszów University, Institute of Medical Science, Department of Human Physiology, 35-310 Rzeszow, Kopisto Street 2a, Poland – sequence: 3 givenname: Paulina surname: Misztak fullname: Misztak, Paulina organization: Maj Institute of Pharmacology, Polish Academy of Sciences, Smętna 12, 31-343 Kraków, Poland – sequence: 4 givenname: Anna surname: Tabecka-Lonczynska fullname: Tabecka-Lonczynska, Anna organization: Department of Biotechnology and Cell Biology, Medical College, University of Information Technology and Management in Rzeszow, Sucharskiego 2, 35-225 Rzeszow, Poland – sequence: 5 givenname: Katarzyna surname: Stachowicz fullname: Stachowicz, Katarzyna email: stachow@if-pan.krakow.pl organization: Maj Institute of Pharmacology, Polish Academy of Sciences, Smętna 12, 31-343 Kraków, Poland |
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| Keywords | COX-2 NS398 Corticosterone LPS |
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| SubjectTerms | Animals Corticosterone Corticosterone - blood COX-2 Cyclooxygenase 2 - blood Cyclooxygenase 2 - metabolism Cyclooxygenase 2 Inhibitors - pharmacology Lipopolysaccharides - pharmacology LPS Male Mice Nitrobenzenes - pharmacology NS398 Sulfonamides - pharmacology Time Factors |
| Title | Time-dependent dual mode of action of COX-2 inhibition on mouse serum corticosterone levels |
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