Asiatic acid, a pentacyclic triterpene from Centella asiatica, is neuroprotective in a mouse model of focal cerebral ischemia

  • Rajanikant G. Krishnamurthy
  • , Marie Claude Senut
  • , Daniel Zemke
  • , Jiangyong Min
  • , Mark B. Frenkel
  • , Eric J. Greenberg
  • , Seong Woon Yu
  • , Nick Ahn
  • , John Goudreau
  • , Mounzer Kassab
  • , Kiran S. Panickar
  • , Arshad Majid

Research output: Contribution to journalArticlepeer-review

144 Scopus citations

Abstract

Asiatic acid, a triterpenoid derivative from Centella asiatica, has shown biological effects such as antioxidant, antiinflammatory, and protection against glutamate- or β-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.

Original languageEnglish
Pages (from-to)2541-2550
Number of pages10
JournalJournal of Neuroscience Research
Volume87
Issue number11
DOIs
StatePublished - 15 Aug 2009

Keywords

  • Apoptosis
  • Blood-brain barrier
  • Infarct volume
  • Mitochondria
  • Oxygen-glucose deprivation

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