Cardiology Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russia.
Branch of M. M. Shemyakin and Yu. A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Pushchino, Moscow region, Russia.
Bull Exp Biol Med. 2024 Jan;176(3):338-341. doi: 10.1007/s10517-024-06020-3. Epub 2024 Feb 10.
A comparative analysis of the infarct-limiting activity of δ- and κ-opioid receptors (OR) agonists was carried out on a model of coronary occlusion (45 min) and reperfusion (120 min) in male Wistar rats. We used selective δ-OR agonist deltorphin II (0.12 mg/kg), δ-OR agonists BW373U86 and p-Cl-Phe DPDPE (0.1 and 1 mg/kg), selective agonists of δ-OR DPDPE (0.1 and 0.969 mg/kg), κ-OR U-50,488 (0.1 and 1 mg/kg), κ-OR GR-89696 (0.1 mg/kg), and κ-OR ICI-199,441 (0.1 mg/kg). All drugs were administered intravenously 5 min before reperfusion. Deltorphin II, BW373U86 (1 mg/kg), p-Cl-Phe DPDPE (1 mg/kg), U-50,488 (1 mg/kg), and ICI-199,441 had a cardioprotective effect. The most promising compounds for drug development are ICI-199,441 and deltorphin II.
在雄性 Wistar 大鼠的冠状动脉闭塞(45 分钟)和再灌注(120 分钟)模型上,对 δ-和 κ-阿片受体(OR)激动剂的梗死限制活性进行了比较分析。我们使用了选择性 δ-OR 激动剂 δ-内啡肽 II(0.12mg/kg)、δ-OR 激动剂 BW373U86 和 p-Cl-Phe DPDPE(0.1 和 1mg/kg)、选择性 δ-OR 激动剂 DPDPE(0.1 和 0.969mg/kg)、κ-OR U-50,488(0.1 和 1mg/kg)、κ-OR GR-89696(0.1mg/kg)和 κ-OR ICI-199,441(0.1mg/kg)。所有药物均在再灌注前 5 分钟静脉给药。δ-内啡肽 II、BW373U86(1mg/kg)、p-Cl-Phe DPDPE(1mg/kg)、U-50,488(1mg/kg)和 ICI-199,441 具有心脏保护作用。对于药物开发,最有前途的化合物是 ICI-199,441 和 δ-内啡肽 II。