化学
突触后电位
药代动力学
肽
突触后密度
药理学
体内
体外
代谢稳定性
脂肪酸
药品
生物化学
受体
医学
生物技术
生物
作者
Klaus B. Nissen,Julie J. Andersen,Linda M. Haugaard‐Kedström,Anders Bach,Kristian Strømgaard
摘要
Dimeric peptide-based inhibitors of postsynaptic density-95 (PSD-95) can reduce ischemic brain damage and inflammatory pain in rodents. To modify the pharmacokinetic profile, we designed a series of fatty acid linked dimeric ligands, which potently inhibits PSD-95 and shows improved in vitro blood plasma stability. Subcutaneous administration in rats showed extended stability and sustained release of these ligands. This can facilitate new pharmacological uses of PSD-95 inhibitors and further exploration of PSD-95 as a drug target.
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