Time-dependent dual mode of action of COX-2 inhibition on mouse serum corticosterone levels

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Steroids Pub Date : 2024-05-07 DOI:10.1016/j.steroids.2024.109438
Patrycja Pańczyszyn-Trzewik , Magdalena Sowa-Kućma , Paulina Misztak , Anna Tabecka-Lonczynska , Katarzyna Stachowicz
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Abstract

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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COX-2 抑制剂对小鼠血清皮质酮水平的时间依赖性双重作用模式
为了阐明环氧化酶-2(COX-2)抑制剂对皮质酮释放的影响,研究人员将小鼠分为两组,一组接受3毫克/千克剂量的选择性COX-2抑制剂NS398治疗七天,另一组接受NS398治疗十四天。之后,小鼠被处死,并收集血清。采用 ELISA 方法分析血清中的皮质酮水平。短期 COX-2 抑制会增加皮质酮水平,而长期抑制则会降低皮质酮水平。在小鼠受到脂多糖(LPS)大肠杆菌挑战后,我们重复了实验的具体安排,以检查应激刺激对测试参数的影响。在这种情况下,我们观察到皮质酮水平的升高,并以七天的模式显著增加。这些结果表明,小鼠体内的皮质酮水平是通过 COX-2 依赖性机制调节的。
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来源期刊
Steroids
Steroids 医学-内分泌学与代谢
CiteScore
5.10
自引率
3.70%
发文量
120
审稿时长
73 days
期刊介绍: STEROIDS is an international research journal devoted to studies on all chemical and biological aspects of steroidal moieties. The journal focuses on both experimental and theoretical studies on the biology, chemistry, biosynthesis, metabolism, molecular biology, physiology and pharmacology of steroids and other molecules that target or regulate steroid receptors. Manuscripts presenting clinical research related to steroids, steroid drug development, comparative endocrinology of steroid hormones, investigations on the mechanism of steroid action and steroid chemistry are all appropriate for submission for peer review. STEROIDS publishes both original research and timely reviews. For details concerning the preparation of manuscripts see Instructions to Authors, which is published in each issue of the journal.
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