Design, Synthesis, and Biological Evaluation of Novel Multifunctional Rolipram-Tranilast Hybrids As Potential Treatment for Traumatic Brain Injury.
Junfeng LuChen ChenXiaobing DengMarvin Sh MakZeyu ZhuXixin HeJinhao LiangSwetha K MaddiliKarl Wah-Keung TsimYifan HanRongbiao PiPublished in: ACS chemical neuroscience (2020)
Traumatic brain injury (TBI) is a prevalent public healthcare concern frequently instigated by mechanical shock, traffic, or violence incidents, leading to permanent nerve damage, and there is no ideal treatment for it yet. In this study, a series of Rolipram-Tranilast hybrids were designed and synthesized. The neuroprotective activities of the Rolipram-Tranilast hybrids were evaluated both in vitro and in vivo. Compound 5 has been identified as the strongest neuroprotective molecule among the series with robust anti-oxidant and anti-inflammatory potentials. Compound 5 significantly increased the heme oxygenase-1 (HO-1) levels and the phosphorylated cAMP response elements binding protein (p-CREB) while it down-regulated phosphodiesterase-4 B (PDE4B) expression in vitro. Furthermore, compound 5 remarkably attenuated TBI and had a good safety profile in mice. Taken together, our findings suggested that compound 5 could serve as a novel promising lead compound in the treatment of TBI and other central nervous system (CNS) diseases associated with PDE4B and oxidative stress.
Keyphrases
- traumatic brain injury
- healthcare
- oxidative stress
- binding protein
- anti inflammatory
- mental health
- severe traumatic brain injury
- type diabetes
- air pollution
- poor prognosis
- combination therapy
- blood brain barrier
- risk assessment
- patient safety
- cell proliferation
- cancer therapy
- endoplasmic reticulum stress
- ischemia reperfusion injury
- heat shock
- induced apoptosis
- smoking cessation