Alharbi Khalid Saad, Afzal Muhammad, Al-Abbasi Fahad A, Moglad Ehssan, Al-Qahtani Salwa D, Almalki Naif A R, Imam Faisal, Sayyed Nadeem, Kazmi Imran
Department of Pharmacology and Toxicology, College of Pharmacy, Qassim University, Buraydah, 51452, Al Qassim, Saudi Arabia.
Department of Pharmaceutical Sciences, Pharmacy Program, Batterjee Medical College, P.O. Box 6231, Jeddah, 21442, Saudi Arabia.
Sci Rep. 2025 Jan 24;15(1):3076. doi: 10.1038/s41598-024-83900-8.
Europinidin is a novel anthocyanidin found in the petals of Plumbago europea that exhibits several physiological effects. Research was conducted to assess europinidin's cardioprotective efficacy in a diabetic and myocardial infarction (MI) experimental model. Rat was injected through the intraperitoneal administration of 45 mg/kg of streptozotocin (STZ), while MI was induced by subcutaneously administering 85 mg/kg of isoproterenol (ISP) at 24 and 48 h prior to the sacrifice procedure. Europinidin 10 and 20 mg/day was administered orally for 4 weeks after validation of diabetes (glucose > 250 mg/dl) on the 7th day. Experimental rats were randomly allocated to control, STZ-ISP control, STZ-ISP + europinidin-10 mg, STZ-ISP + europinidin-20 mg and europinidin 20 mg perse group. Biochemicals parameters including anti-diabetic (Glucose, HbA1c, serum insulin), cardiac markers (hs-CRP, CPK-MB), dyslipidaemia (lipid analysis), anti-inflammatory (IL6, TNF-α and IL-β), oxidative stress (MDA) and antioxidant (SOD, CAT and GSH), kidney function (creatinine), liver function (AST) and pancreatic function (lipase) along with apoptosis markers (Bcl-2, caspase-3) were evaluated. In addition, histopathological indices of heart injury were investigated. In addition, molecular docking (AUTODOCK Tools 1.5.6.) and dynamics were performed. Europinidin (10 and 20 mg/day) reduced blood glucose, HbA1c, hs-CRP, and CPK-MB. It improved serum insulin, blood lipid profile and reduced inflammatory cytokines (IL-6, TNF-α, IL-β), oxidative stress and increased antioxidant enzymes (SOD, CAT and GSH). Europinidin also protected renal, hepatic functions and restored apoptosis markers (increased Bcl-2, decreased caspase-3 levels). Histopathological analysis demonstrated a reduced extent of myocardial necrosis and fibrosis. Europinidin binds in silico to proteins 1NME, 1I0E, 3I2Y and 4AQ3 with energies of -7.038, -6.682, -8.6 and - 8.761 kcal/mol, respectively. While molecular dynamics simulation studies supported the interactions of europinidin with important therapeutic target proteins. Europinidin demonstrates significant cardioprotective and anti-diabetic potential in a diabetic MI experimental model.
欧洲蓼黄素是在欧洲蓼花瓣中发现的一种新型花青素,具有多种生理作用。本研究旨在评估欧洲蓼黄素在糖尿病和心肌梗死(MI)实验模型中的心脏保护功效。通过腹腔注射45mg/kg链脲佐菌素(STZ)对大鼠进行造模,而在处死前24小时和48小时通过皮下注射85mg/kg异丙肾上腺素(ISP)诱导心肌梗死。在第7天糖尿病确诊(血糖>250mg/dl)后,口服给予欧洲蓼黄素10mg/天和20mg/天,持续4周。将实验大鼠随机分为对照组、STZ-ISP对照组、STZ-ISP + 欧洲蓼黄素10mg组、STZ-ISP + 欧洲蓼黄素20mg组和欧洲蓼黄素20mg单独给药组。评估了包括抗糖尿病指标(血糖、糖化血红蛋白、血清胰岛素)、心脏标志物(高敏C反应蛋白、肌酸磷酸激酶同工酶MB)、血脂异常(血脂分析)、抗炎指标(白细胞介素6、肿瘤坏死因子-α和白细胞介素-β)、氧化应激(丙二醛)和抗氧化指标(超氧化物歧化酶、过氧化氢酶和谷胱甘肽)、肾功能(肌酐)、肝功能(谷草转氨酶)和胰腺功能(脂肪酶)以及凋亡标志物(Bcl-2、半胱天冬酶-3)等生化参数。此外,还研究了心脏损伤的组织病理学指标。另外,进行了分子对接(AUTODOCK Tools 1.5.6.)和动力学研究。欧洲蓼黄素(10mg/天和20mg/天)可降低血糖、糖化血红蛋白、高敏C反应蛋白和肌酸磷酸激酶同工酶MB。它可改善血清胰岛素水平、血脂谱,降低炎性细胞因子(白细胞介素-6、肿瘤坏死因子-α、白细胞介素-β)、氧化应激,并增加抗氧化酶(超氧化物歧化酶、过氧化氢酶和谷胱甘肽)。欧洲蓼黄素还可保护肾脏和肝脏功能,并恢复凋亡标志物(Bcl-2水平升高,半胱天冬酶-3水平降低)的值。组织病理学分析显示心肌坏死和纤维化程度减轻。欧洲蓼黄素在计算机模拟中与蛋白质1NME、1I0E、3I2Y和4AQ3结合,能量分别为-7.038、-6.