Wang Peng, Jiang Huiyi, Yao Jinzhong, He Guangting, Tao Tao, Qin Zaisheng
Department of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
The Key Laboratory of Precision Anesthesia and Perioperative Organ Protection, Guangzhou, Guangdong, China.
Front Med (Lausanne). 2025 Feb 19;12:1510271. doi: 10.3389/fmed.2025.1510271. eCollection 2025.
Inflammation is a frequent precursor to the development of chronic pain. Ponicidin, a compound derived from traditional Chinese medicine, possesses immunomodulatory and anti-inflammatory properties. However, whether ponicidin mitigates inflammatory pain through its anti-inflammatory effects and potential target molecules remains to be further explored. In this study, we investigated the analgesic effects of ponicidin in a mouse model of Complete Freund's Adjuvant (CFA)-induced inflammatory pain and employed network pharmacology to predict the potential therapeutic targets of ponicidin for pain treatment.
Initially, we established a mouse model of inflammatory pain induced by Complete Freund's Adjuvant (CFA). Following the establishment of the model, the analgesic effects of ponicidin were assessed using behavioral tests, and further validation was conducted through hematoxylin and eosin (H&E) staining, enzyme-linked immunosorbent assay (ELISA), and immunofluorescence methods. Subsequently, we analyzed the potential analgesic targets of ponicidin using network pharmacology approaches and molecular docking.
In this study, we observed that ponicidin has a significant alleviating effect on CFA-induced inflammatory pain. Our results suggest that ponicidin may alleviate inflammatory pain by reducing inflammatory responses in the spinal cord and hind paw of CFA model mice. Furthermore, we found that ponicidin can mitigate the activation of macrophages in the subcutaneous tissue of the hind paw and microglia in the dorsal horn of the spinal cord. Network pharmacology analysis suggests that ponicidin may exert its analgesic effects through a multi-target, multi-pathway mechanism. Key transcription factors such as κ (), (), and () may be involved in the underlying mechanisms of ponicidin's analgesic action. Through molecular docking and experimental validation, we have identified () and () as key targets of ponicidin's analgesic effects.
Ponicidin alleviates inflammatory pain by reducing inflammatory responses in the spinal cord and hind paw of the CFA model mice. and may as key targets for the analgesic effects of ponicidin.
炎症是慢性疼痛发展的常见先兆。ponicidin是一种源自中药的化合物,具有免疫调节和抗炎特性。然而,ponicidin是否通过其抗炎作用和潜在靶分子减轻炎性疼痛仍有待进一步探索。在本研究中,我们研究了ponicidin在完全弗氏佐剂(CFA)诱导的炎性疼痛小鼠模型中的镇痛作用,并采用网络药理学预测ponicidin治疗疼痛的潜在治疗靶点。
首先,我们建立了完全弗氏佐剂(CFA)诱导的炎性疼痛小鼠模型。模型建立后,通过行为测试评估ponicidin的镇痛作用,并通过苏木精和伊红(H&E)染色、酶联免疫吸附测定(ELISA)和免疫荧光方法进行进一步验证。随后,我们使用网络药理学方法和分子对接分析ponicidin的潜在镇痛靶点。
在本研究中,我们观察到ponicidin对CFA诱导的炎性疼痛有显著缓解作用。我们的结果表明,ponicidin可能通过减少CFA模型小鼠脊髓和后爪的炎症反应来减轻炎性疼痛。此外,我们发现ponicidin可以减轻后爪皮下组织中巨噬细胞和脊髓背角中小胶质细胞的活化。网络药理学分析表明,ponicidin可能通过多靶点、多途径机制发挥其镇痛作用。关键转录因子如κ()、()和()可能参与ponicidin镇痛作用的潜在机制。通过分子对接和实验验证,我们确定()和()是ponicidin镇痛作用的关键靶点。
ponicidin通过减少CFA模型小鼠脊髓和后爪的炎症反应来减轻炎性疼痛。和可能是ponicidin镇痛作用的关键靶点。