Wang Zimin, Zhao Meirong, Yu Yunxia, Kong Fandong, Lin Nanxin, Wang Qi
Department of Pediatric intensive Care Medicine, Hainan Women and Children's Medical Center, Haikou 570100, China.
Key Laboratory of Chemistry and Engineering of Forest Products, State Ethnic Affairs Commission, Guangxi Key Laboratory of Polysaccharide Materials and Modification, School of of Marine Science and Biotechnology, Guangxi Minzu University, Nanning 530006, China.
Mar Drugs. 2025 Mar 26;23(4):142. doi: 10.3390/md23040142.
Diabetes mellitus has emerged as a global public health crisis, with Type 2 diabetes (T2D) constituting over 90% of cases. Current treatments are palliative, primarily focusing on blood glucose modulation. This review systematically evaluates 181 bioactive compounds isolated from 66 marine fungal strains for their inhibitory activities against key diabetes-related enzymes, including α-glucosidase, protein tyrosine phosphatase 1B (PTP1B), dipeptidyl peptidase-4 (DPP-4), glycogen synthase kinase-3β (GSK-3β), and fatty acid-binding protein 4 (FABP4). These compounds, categorized into polyketides, alkaloids, terpenoids, and lignans, exhibit multitarget engagement and nanomolar-to-micromolar potency. The review highlights the potential of marine fungal metabolites as novel antidiabetic agents, emphasizing their structural novelty and diverse mechanisms of action. Future research should focus on overcoming challenges related to yield and extraction, leveraging advanced technologies such as genetic engineering and synthetic biology to enhance drug development.
糖尿病已成为全球公共卫生危机,其中2型糖尿病(T2D)占病例的90%以上。目前的治疗方法是姑息性的,主要侧重于血糖调节。本综述系统评价了从66株海洋真菌菌株中分离出的181种生物活性化合物对关键糖尿病相关酶的抑制活性,这些酶包括α-葡萄糖苷酶、蛋白酪氨酸磷酸酶1B(PTP1B)、二肽基肽酶-4(DPP-4)、糖原合酶激酶-3β(GSK-3β)和脂肪酸结合蛋白4(FABP4)。这些化合物分为聚酮类、生物碱类、萜类和木脂素类,具有多靶点作用和纳摩尔至微摩尔级别的效力。该综述强调了海洋真菌代谢产物作为新型抗糖尿病药物的潜力,强调了它们的结构新颖性和多样的作用机制。未来的研究应集中在克服与产量和提取相关的挑战上,利用基因工程和合成生物学等先进技术来加强药物开发。