| Literature DB >> 32559618 |
Xiao-Hong Li1, Yan-Ru Liu1, Da-Hai Jiang1, Zhi-Shu Tang2, Da-Wei Qian3, Zhong-Xing Song1, Lin Chen1, Xin-Bo Shi1, Ning-Juan Yang1, Ya-Feng Yan1, Ai-Bing Chang1.
Abstract
Radix Paeoniae Rubra (RPR) is a traditional Chinese medicine with anti-inflammatory effects that has been used in chronic pelvic inflammation disease (CPID) therapy. However, research on the mechanism of RPR in CPID therapy is lacking. Here, we used a network pharmacology method to screen targets and found that the PTGS2 target in the arachidonic acid (AA) pathway was significantly related to CPID. Then, regarding the molecular mechanism, it was further confirmed that RPR may reduce the development of CPID by regulating the PTGS2 target. The CPID rat model was established by mixed bacterial infection. We verified the expression of PTGS2 by immunohistochemical analysis, western blotting assays to detect the expression of PTGS2 protein, and polymerase chain reaction detection of PTGS2 mRNA expression. It was observed that the PTGS2 target decreased significantly after RPR administration at different doses. It is suggested that RPR can reverse the abnormal expression of PTGS2 in CPID rats. We believe that RPR is effective in the treatment of CPID, and RPR can reduce the inflammatory symptoms of CPID by regulating the level of PTGS2 in the AA pathway.Entities:
Keywords: Anti-inflammation; Chronic pelvic inflammation disease; Mechanism; PTGS2; Radix Paeoniae Rubra
Mesh:
Substances:
Year: 2020 PMID: 32559618 DOI: 10.1016/j.biopha.2020.110052
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529