Saad Muhammed A, Abdel Salam Rania M, Kenawy Sanaa A, Attia Amina S
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Pharmacol Rep. 2015 Feb;67(1):115-22. doi: 10.1016/j.pharep.2014.08.014. Epub 2014 Aug 27.
Pinocembrin is a major flavonoid molecule isolated from honey and propolis. It has versatile pharmacological and biological activities including antimicrobial, anti-inflammatory, antioxidant, and anticancer activities as well as neuroprotective effects against cerebral ischemic injury. The purpose of the current study was to determine the possible mechanisms of neuroprotection elicited by pinocembrin with specific emphasis on chronic prophylactic use before the induction of global cerebral ischemia reperfusion.
Global cerebral ischemia-reperfusion (I/R) was induced by bilateral carotid artery occlusion for 15min followed by 60min reperfusion period. Animals were randomly allocated into 3 groups (n=28): Sham operated, I/R control and rats treated with pinocembrin (10mg/kg, po) daily for 7 days then I/R was induced 1h after the last dose of pinocembrin. After reperfusion rats were killed by decapitation, brains were removed and both hippocampi separated and the following biochemical parameters were estimated; lactate dehydrogenase activity, oxidative stress markers (lipid peroxides, nitric oxide and reduced glutathione), inflammatory markers (myeloperoxidase, tumor necrosis factor-alpha, nuclear factor kappa-B, interleukin-6 and interleukin-10), apoptotic biomarkers (caspase 3 and cytochrome C), neurotransmitters (glutamate, gamma aminobutyric acid) and infarct size were assessed.
Pinocembrin ameliorated damage induced by I/R through suppressing oxidative stress, inflammatory and apoptotic markers as well as mitigating glutamate and lactate dehydrogenase activity. One of the more significant findings to emerge from this study is that pinocembrin normalized the infarct size elevated by I/R.
Pinocembrin showed a neuroprotective effects through antioxidant, anti-inflammatory and antiapoptotic mechanisms.
松属素是从蜂蜜和蜂胶中分离出的一种主要黄酮类分子。它具有多种药理和生物学活性,包括抗菌、抗炎、抗氧化和抗癌活性,以及对脑缺血损伤的神经保护作用。本研究的目的是确定松属素引发神经保护作用的可能机制,特别强调在全脑缺血再灌注诱导前进行长期预防性使用。
通过双侧颈动脉闭塞15分钟,随后再灌注60分钟来诱导全脑缺血再灌注(I/R)。将动物随机分为3组(n = 28):假手术组、I/R对照组和每天口服松属素(10mg/kg)共7天的大鼠组,在最后一剂松属素给药1小时后诱导I/R。再灌注后,通过断头处死大鼠,取出大脑,分离双侧海马,并评估以下生化参数;乳酸脱氢酶活性、氧化应激标志物(脂质过氧化物、一氧化氮和还原型谷胱甘肽)、炎症标志物(髓过氧化物酶、肿瘤坏死因子-α、核因子κB、白细胞介素-6和白细胞介素-10)、凋亡生物标志物(半胱天冬酶3和细胞色素C)、神经递质(谷氨酸、γ-氨基丁酸)并评估梗死面积。
松属素通过抑制氧化应激、炎症和凋亡标志物以及减轻谷氨酸和乳酸脱氢酶活性,改善了I/R诱导的损伤。本研究中出现的一个更显著的发现是,松属素使I/R升高的梗死面积恢复正常。
松属素通过抗氧化、抗炎和抗凋亡机制表现出神经保护作用。