Tang Ping, Ding Qi, Lin Juan, Yang Xinrong, Wang Yiting, Liu Fangle, Zheng Yuying, Lin Liuqing, Wang Deqin, Lin Baoqin
Experimental Center, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510405, China.
Hutchison Whampoa Guangzhou Baiyunshan Chinese Medicine Co., Ltd., Guangzhou, 510515, China.
Int J Med Sci. 2023 Sep 4;20(11):1386-1398. doi: 10.7150/ijms.87433. eCollection 2023.
Pen Yan Jing tablets (PYJ), a Chinese patent medicine, has being used for pelvic inflammatory disease (PID) effectively. This study was designed to explore the underlying mechanisms of PYJ for treating PID. A rat model of PID was established by mixed bacteria liquid plus mechanical damage. After PYJ treatment, the morphology of uteri and extent of pelvic adhesion were observed. The pathological changes were evaluated by hematoxylin-eosin (HE) staining. The protein expressions of CD68, intercellular cell adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), monocyte chemotactic protein-1 (MCP-1) and cyclooxygenase-2 (COX-2) were quantitated by immunohistochemistry. A cell model of lipopolysaccharide (LPS)-activated RAW 264.7 macrophages was performed. The cell proliferation and NO level were measured by CCK-8 and Griess method, respectively. The tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) levels were detected by ELISA. The protein kinase B (Akt)/nuclear factor kappa-B (NF-κB) pathway-related protein expressions were assayed by western blot or immunofluorescence. PYJ alleviated pelvic adhesion and inflammatory lesions of uteri in PID rats. PYJ down-regulated protein expressions of ICAM-1, VCAM-1, MCP-1, COX-2, p-Akt, p-IκB kinaseα/β (p-IKKα/β), p-IκBα, p65, and p-p65 in uteri of PID rats. Moreover, PYJ medicated serum inhibited abnormal cell proliferation, NO release, levels of TNF-α and IL-6, nuclear translocation of p65, and protein expressions of p-Akt, p-p65 and p-IκBα in LPS-activated RAW 264.7 macrophages. : Taken together, PYJ may alleviates PID through inhibiting Akt/NF-κB pathway.
盆炎净片(PYJ)是一种中成药,已被有效用于治疗盆腔炎(PID)。本研究旨在探讨PYJ治疗PID的潜在机制。通过混合菌液加机械损伤建立大鼠PID模型。给予PYJ治疗后,观察子宫形态和盆腔粘连程度。采用苏木精-伊红(HE)染色评估病理变化。通过免疫组化定量检测CD68、细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)、单核细胞趋化蛋白-1(MCP-1)和环氧化酶-2(COX-2)的蛋白表达。构建脂多糖(LPS)激活的RAW 264.7巨噬细胞细胞模型。分别采用CCK-8法和Griess法检测细胞增殖和NO水平。通过ELISA检测肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)水平。采用蛋白质印迹法或免疫荧光法检测蛋白激酶B(Akt)/核因子κB(NF-κB)通路相关蛋白表达。PYJ减轻了PID大鼠的盆腔粘连和子宫炎症病变。PYJ下调了PID大鼠子宫中ICAM-1、VCAM-1、MCP-1、COX-2、p-Akt、p-IκB激酶α/β(p-IKKα/β)、p-IκBα、p65和p-p65的蛋白表达。此外,PYJ含药血清抑制了LPS激活的RAW 264.7巨噬细胞的异常细胞增殖、NO释放、TNF-α和IL-6水平、p65核转位以及p-Akt、p-p65和p-IκBα的蛋白表达。综上所述,PYJ可能通过抑制Akt/NF-κB通路减轻PID。