Inthanon Kewalin, Wong-A-Nan Natthawut, Dheeranupattana Srisulak, Guerra Andres Garcia, Davies Neal M, Kesornpun Chatchai, Sangher Sasithorn, Kittakoop Prasat
Department of Biotechnology, Faculty Science and Technology, Thammasat University Lampang Campus, Lampang, 52190, Thailand.
Department of Clinical Pathology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.
Sci Rep. 2025 Feb 3;15(1):4051. doi: 10.1038/s41598-025-87945-1.
Obesity poses a significant global health challenge, necessitating the search for novel therapeutic agents to address this epidemic. Chromenes, known for their diverse bioactivities, hold promise as potential anti-obesity compounds, yet research in this area remains limited. This pioneering study represents the first exploration of synthetic chromenes as potential anti-obesity agents, unveiling the underlying molecular pathways governing adipogenesis and lipolysis. Twenty-nine chromenes were synthesized using green chemistry approaches, resulting in five novel compounds: 1, 2, 3, 4, and 5. Among them, 14 chromenes demonstrated a lack of toxicity to pre-adipocytes (PAs) and mature adipocytes (MAs) of 3T3-L1 cells. The anti-adipogenesis and lipolysis enhancement potential of these non-toxic 14 chromenes were comprehensively evaluated using Oil Red O staining technique, LDH activity measurement, and glycerol release assays. Notably, 4, 5, 21 and 25 exhibited remarkable efficacy in reducing intracellular lipid accumulation without inducing cellular stress or cell death. Molecular analysis revealed significant alterations in the expression of key transcription factors involved in adipogenesis and lipid metabolism, including PPARγ, C/EBPα, ADD-1, Pref-1, IRS-1, GLUT-4, adiponectin, FAS, aP2, ATGL, and HSL. This suggests their potential role in anti-adipogenesis. Additionally, the treatments with 4 and 25 showed potential for enhancing lipolysis, providing further evidence of their anti-obesity properties. This study presents several promising prospects for the development of synthetic chromenes as potential anti-obesity agents, opening new avenues for drug discovery and benefitting individuals worldwide in addressing obesity-related challenges to human health. In addition, predictive in silico modeling was performed on the identified candidate chromenes. This modeling provides prospective anti-HIV activity, pharmacokinetic, metabolism, and permeability data, setting the groundwork for further investigation into these potential new chemical entities.
肥胖是一项重大的全球健康挑战,因此需要寻找新的治疗药物来应对这一流行病。色烯因其多样的生物活性而有望成为潜在的抗肥胖化合物,但该领域的研究仍然有限。这项开创性研究首次探索了合成色烯作为潜在抗肥胖药物,揭示了控制脂肪生成和脂肪分解的潜在分子途径。采用绿色化学方法合成了29种色烯,得到了5种新化合物:1、2、3、4和5。其中,14种色烯对3T3-L1细胞的前脂肪细胞(PA)和成熟脂肪细胞(MA)无毒性。使用油红O染色技术、乳酸脱氢酶(LDH)活性测定和甘油释放试验,全面评估了这14种无毒色烯的抗脂肪生成和增强脂肪分解的潜力。值得注意的是,4、5、21和25在减少细胞内脂质积累方面表现出显著效果,且不会诱导细胞应激或细胞死亡。分子分析显示,参与脂肪生成和脂质代谢的关键转录因子的表达发生了显著变化,包括过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT/增强子结合蛋白α(C/EBPα)、脂肪分化相关蛋白1(ADD-1)、前脂肪细胞因子1(Pref-1)、胰岛素受体底物1(IRS-1)、葡萄糖转运蛋白4(GLUT-4)、脂联素、脂肪酸合酶(FAS)、脂肪细胞脂肪酸结合蛋白(aP2)、脂肪甘油三酯脂酶(ATGL)和激素敏感脂肪酶(HSL)。这表明它们在抗脂肪生成中具有潜在作用。此外,用4和25进行的处理显示出增强脂肪分解的潜力,进一步证明了它们的抗肥胖特性。这项研究为合成色烯作为潜在抗肥胖药物的开发提供了几个有前景的方向,为药物发现开辟了新途径,并使全球各地的人们在应对肥胖相关的健康挑战方面受益。此外,对鉴定出的候选色烯进行了计算机预测建模。该建模提供了前瞻性的抗HIV活性、药代动力学、代谢和渗透性数据,为进一步研究这些潜在的新化学实体奠定了基础。