| Literature DB >> 30790289 |
Feiya Yang1, Lingquan Meng2,3, Panpan Han4, Dexi Chen5,6, Mingshuai Wang3, Yongguang Jiang7, Yanqiao Wu8, Yiling Wu8, Nianzeng Xing1,3.
Abstract
Chronic prostatitis is a common urological disease. The etiology of this disease and effective therapy for its treatment are yet to be elucidated. We investigated the functions of XLQ® in chronic nonbacterial prostatitis using a complete Freund's adjuvant-induced rat model. Prostates and blood samples were collected for further evaluation after oral gavage with XLQ ® or a vehicle for 4 weeks. The results showed that XLQ ® significantly decreased the prostate index, ameliorated the histopathologic changes, and reduced CD3+ and CD45+ cell infiltration in the prostate stroma. Further study showed that XLQ ® suppressed the expression of proinflammatory cytokines, such as interleukin (IL)-1β, IL-2, IL-6, IL-17A, monocyte chemoattractant protein-1, and tumor necrosis factor-α. XLQ ® showed a strong antioxidant capacity by enhancing the activities of antioxidative enzymes (e.g., total superoxide dismutase, catalase, and glutathione peroxidase) and decreasing the level of lipid peroxidation products (malondialdehyde). Moreover, XLQ ® can suppress the activation of nuclear factor-κB and P38-mitogen-activated protein kinase signaling pathways. In summary, XLQ ® has affirmative effects on chronic prostatitis, which could be attributed to its anti-inflammatory and antioxidative capacities. On the basis of these results, XLQ ® can be developed as an effective and safe therapy for chronic prostatitis.Entities:
Keywords: XLQ®; anti-inflammation; antioxidation; chronic prostatitis; signaling pathways
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Year: 2019 PMID: 30790289 DOI: 10.1002/jcp.28380
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384