Al Mousa Amal A, Abouelela Mohamed E, Mansour Ahmed, Nasr Mohamed, Ali Yasser H, Al Ghamidi Nadaa S, Abo-Dahab Youssef, Mohamed Hassan, Abo-Dahab Nageh F, Hassane Abdallah M A
Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 145111, Riyadh 4545, Saudi Arabia.
Department of Pharmacognosy, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo P.O. Box 11884, Egypt.
Curr Issues Mol Biol. 2024 Oct 19;46(10):11681-11699. doi: 10.3390/cimb46100694.
Burn injuries, which significantly affect global public health, require effective treatment strategies tailored to varying severity. Fungi are considered a sustainable, easily propagated source for lead therapeutic discovery. In this study, we explored the burn wound healing potential of through a combination of in vitro, in vivo, metabolite profiling, and in silico analysis. The in vitro scratch assays performed with human skin fibroblast cells showed promising wound healing activity. Furthermore, the burn-induced rats model showed a marked improvement in cutaneous wound healing, evidenced by an accelerated rate of wound closure and better skin regeneration after extract treatment at 14 days. The results of this study demonstrated significant enhancements in wound closure and tissue regeneration in the treated rat model, surpassing the outcomes of standard treatments. This controlled healing process, evidenced by superior collagen synthesis and angiogenesis and confirmed by histopathological studies, suggests that has potential beyond the traditionally studied fungal metabolites. The metabolite profiling of 27 bioactive compounds was further investigated by docking analysis for the potential inhibition of the NF-κB pathway, which has an important function in inflammation and wound repair. The compounds eurobenzophenone A (7), aspernolide D (16), asperphenalenone A (23), aspergilate D (15), kodaistatin A (18), and versicolactone A (14) showed the highest binding affinity to the target protein with a pose score of -16.86, -14.65, -12.65, -12.45, -12.19, and -12.08 kcal/mol, respectively. Drug-likeness properties were also conducted. The findings suggest the potential wound healing properties of as a source for lead therapeutic candidate discovery.
烧伤严重影响全球公共卫生,需要针对不同严重程度制定有效的治疗策略。真菌被认为是一种可持续、易于繁殖的先导治疗药物发现来源。在本研究中,我们通过体外、体内、代谢物谱分析和计算机模拟分析相结合的方法,探索了[具体真菌名称未给出]促进烧伤创面愈合的潜力。用人皮肤成纤维细胞进行的体外划痕试验显示出有前景的伤口愈合活性。此外,烧伤诱导的大鼠模型显示皮肤伤口愈合有显著改善,在提取物处理14天后,伤口闭合速度加快和皮肤再生更好证明了这一点。本研究结果表明,在治疗的大鼠模型中,伤口闭合和组织再生有显著增强,超过了标准治疗的效果。这种由卓越的胶原蛋白合成和血管生成所证明并经组织病理学研究证实的可控愈合过程表明,[具体真菌名称未给出]具有超越传统研究的真菌代谢物的潜力。通过对接分析进一步研究了27种生物活性化合物的代谢物谱,以探讨其对在炎症和伤口修复中起重要作用的NF-κB途径的潜在抑制作用。化合物欧苯甲酮A(7)、曲霉内酯D(16)、曲霉芬酮A(23)、曲霉酸D(15)、柯达他汀A(18)和杂色内酯A(14)对靶蛋白显示出最高的结合亲和力,其姿态分数分别为-16.86、-14.65、-12.65、-12.45、-12.19和-12.08千卡/摩尔。还进行了类药性质研究。这些发现表明[具体真菌名称未给出]作为先导治疗候选药物发现来源具有潜在的伤口愈合特性。