Sayed Ahmed M, Abdelkader Karim, Abdelnaser Mahmoud, Yahia Ramadan, Saber Entesar Ali, Bedaiwi Ruqaiah I, Hendawy Omnia Magdy, Elrehany Mahmoud A, Abdelmohsen Usama Ramadan
Department of Pharmacognosy, Faculty of Pharmacy, Nahda University, Beni-Suef, 62513, Egypt.
Department of Pharmacognosy, College of Pharmacy, Almaaqal University, Basrah, 61014, Iraq.
Sci Rep. 2025 Sep 24;15(1):32706. doi: 10.1038/s41598-025-90710-z.
The unprecedented dissemination of antibiotic resistance announces a close post antibiotic era, thus exploring effective alternatives is urgent. Natural products are untapped alternatives that could offer effective alternatives with low costs. Sparastolonin B (SsnB) is a natural anthracene-derivative with a reported anti-inflammatory activity; however, its potential antibacterial activity is still under-explored. Here, we investigated both antibacterial and anti-inflammatory activity of SsnB in vitro, in vivo and in silico. In vitro, SsnB showed a specific antibacterial activity against Gram-positive bacteria with MIC range of 1-4 µg/ml against S. aureus and E. faecalis. Furthermore, it displayed a profound antibacterial activity against the clinical MRSA strain K15 in both wound infection, and peritonitis infection models with overall bacterial count reductions up to 1.21 and 1.23 log-units respectively. In addition, it has significantly improved wound healing and tissue repair rates compared to the un-treated group in wound infection model. SsnB has also significantly down-regulated the expression of inflammatory mediators, TLR-2, MCP-1, CXCL-1, CXCL-2, IL-6 and IL-1β, in the treated rabbits highlighting its potential anti-inflammatory activity. Finally, in silico analysis has predicted Gyr-B as a potential target for the observed SsnB antibacterial activity. To conclude, SsnB is a promising natural compound with a dual antibacterial and anti-inflammatory activities, suggesting it as a good candidate for subsequent clinical investigation.
抗生素耐药性的空前传播预示着抗生素时代即将结束,因此探索有效的替代方案迫在眉睫。天然产物是尚未开发的替代方案,它们可以提供低成本的有效替代品。斯巴司他宁B(SsnB)是一种天然蒽衍生物,据报道具有抗炎活性;然而,其潜在的抗菌活性仍有待深入研究。在这里,我们在体外、体内和计算机模拟中研究了SsnB的抗菌和抗炎活性。在体外,SsnB对革兰氏阳性菌表现出特异性抗菌活性,对金黄色葡萄球菌和粪肠球菌的最低抑菌浓度范围为1-4μg/ml。此外,在伤口感染和腹膜炎感染模型中,它对临床耐甲氧西林金黄色葡萄球菌菌株K15均表现出显著的抗菌活性,细菌总数分别降低了1.21和1.23个对数单位。此外,在伤口感染模型中,与未治疗组相比,它显著提高了伤口愈合和组织修复率。在治疗的兔子中,SsnB还显著下调了炎症介质TLR-2、MCP-1、CXCL-1、CXCL-2、IL-6和IL-1β的表达,突出了其潜在的抗炎活性。最后,计算机模拟分析预测Gyr-B是观察到的SsnB抗菌活性的潜在靶点。总之,SsnB是一种有前途的天然化合物,具有双重抗菌和抗炎活性,表明它是后续临床研究的良好候选物。