Krishnamurthy Rajanikant G, Senut Marie-Claude, Zemke Daniel, Min Jiangyong, Frenkel Mark B, Greenberg Eric J, Yu Seong-Woon, Ahn Nick, Goudreau John, Kassab Mounzer, Panickar Kiran S, Majid Arshad
Division of Cerebrovascular Diseases and Department of Neurology and Ophthalmology, Michigan State University, East Lansing, Michigan 48824, USA.
J Neurosci Res. 2009 Aug 15;87(11):2541-50. doi: 10.1002/jnr.22071.
Asiatic acid, a triterpenoid derivative from Centella asiatica, has shown biological effects such as antioxidant, antiinflammatory, and protection against glutamate- or beta-amyloid-induced neurotoxicity. We investigated the neuroprotective effect of asiatic acid in a mouse model of permanent cerebral ischemia. Various doses of asiatic acid (30, 75, or 165 mg/kg) were administered orally at 1 hr pre- and 3, 10, and 20 hr postischemia, and infarct volume and behavioral deficits were evaluated at day 1 or 7 postischemia. IgG (blood-brain barrier integrity) and cytochrome c (apoptosis) immunostaining was carried out at 24 hr postischemia. The effect of asiatic acid on stress-induced cytochrome c release was examined in isolated mitochondrial fractions. Furthermore, its effects on cell viability and mitochondrial membrane potential were studied in HT-22 cells exposed to oxygen-glucose deprivation. Asiatic acid significantly reduced the infarct volume by 60% at day 1 and by 26% at day 7 postischemia and improved neurological outcome at 24 hr postischemia. Our studies also showed that the neuroprotective properties of asiatic acid might be mediated in part through decreased blood-brain barrier permeability and reduction in mitochondrial injury. The present study suggests that asiatic acid may be useful in the treatment of cerebral ischemia.
积雪草中的三萜类衍生物积雪草苷,已显示出多种生物学效应,如抗氧化、抗炎,以及对谷氨酸或β-淀粉样蛋白诱导的神经毒性具有保护作用。我们研究了积雪草苷在永久性脑缺血小鼠模型中的神经保护作用。在缺血前1小时以及缺血后3、10和20小时,口服给予不同剂量的积雪草苷(30、75或165mg/kg),并在缺血后第1天或第7天评估梗死体积和行为缺陷。在缺血后24小时进行IgG(血脑屏障完整性)和细胞色素c(凋亡)免疫染色。在分离的线粒体组分中检测积雪草苷对应激诱导的细胞色素c释放的影响。此外,在暴露于氧糖剥夺的HT-22细胞中研究其对细胞活力和线粒体膜电位的影响。积雪草苷在缺血后第1天显著减少梗死体积60%,在缺血后第7天减少26%,并在缺血后24小时改善神经功能结局。我们的研究还表明,积雪草苷的神经保护特性可能部分通过降低血脑屏障通透性和减少线粒体损伤来介导。本研究表明,积雪草苷可能对治疗脑缺血有用。