Design, Synthesis and Biological Evaluation of Diosgenin-Amino Acid Derivatives with Dual Functions of Neuroprotection and Angiogenesis.
Desheng CaiJinchai QiYuqin YangWenxi ZhangFei ZhouXiaohui JiaWenbo GuoXuemei HuangFeng GaoHongshan ChenTong LiGuoping LiPenglong WangYuzhong ZhangHai-Min LeiPublished in: Molecules (Basel, Switzerland) (2019)
Diosgenin, a natural product with steroidal structure, has a wide range of clinical applications in China. It also shows great potential in the treatment of blood clots and nerve damage. To enhance the bioavailability as well as efficacy of diosgenin, eighteen diosgenin-amino acid derivatives were designed and synthesized. The neuroprotective effects of these compounds were evaluated by SH-SY5Y cell line and the biosafety was evaluated by H9c2 cell line. The results displayed that part of the derivatives' activities (EC50 < 20 μM) were higher than positive control edaravone (EC50 = 21.60 ± 3.04 μM), among which, DG-15 (EC50 = 6.86 ± 0.69 μM) exhibited the best neuroprotection. Meanwhile, biosafety evaluation showed that DG-15 had no cytotoxicity on H9c2 cell lines. Interestingly, combined neuroprotective and cytotoxic results, part of the derivatives without their protecting group were superior to compounds with protecting group. Subsequently, Giemsa staining and DAPI (4',6-diamidino-2-phenylindole) staining indicated that DG-15 had a protective effect on damaged SH-SY5Y cells by reducing apoptosis. Moreover, DG-15 showed a higher role in promoting angiogenesis at high concentrations (4 mg/mL) on the chorioallantoic membrane model. This finding displayed that DG-15 had dual functions of neuroprotection and angiogenesis, which provided further insight into designing agent for the application in treatment of ischemic stroke.
Keyphrases
- cerebral ischemia
- amino acid
- endothelial cells
- cell cycle arrest
- brain injury
- vascular endothelial growth factor
- oxidative stress
- induced apoptosis
- structure activity relationship
- subarachnoid hemorrhage
- endoplasmic reticulum stress
- blood brain barrier
- atrial fibrillation
- risk assessment
- combination therapy
- cell proliferation
- signaling pathway
- replacement therapy