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Neuroprotective effects of aromatic turmerone on activity deprivation-induced apoptosis in cerebellar granule neurons.

Abstract
Ar-turmerone, which is a major bioactive component found in the essential oil derived from Curcuma longa, has been reported to inhibit proliferation and induce apoptosis in cancer cell lines. Recently, ar-turmerone has been reported to increase the proliferation of neuronal stem cells, in contrast to its actions in cancer cells. These observations raise the possibility that ar-turmerone serves specific functions in neuronal cell lineages. However, the effects of ar-turmerone on postmitotic neurons remain elusive. In the present study, we investigated the neuroprotective functions of ar-turmerone in primary cerebellar granule neuronal cultures. We found that ar-turmerone increased the survival of neurons following activity deprivation. Consistently, the induction of cleaved caspase-3, a hallmark of apoptosis, was prevented by ar-turmerone, although neither the level of reactive oxygen species nor the mitochondrial membrane potential was affected. This study reports a neuroprotective function for ar-turmerone, providing new insights into the potential therapeutic applications of ar-turmerone for neurological disorders.
AuthorsYuya Saga, Yudai Hatakenaka, Miho Matsumoto, Yuri Yoshioka, Shinichi Matsumura, Nobuhiro Zaima, Yoshiyuki Konishi
JournalNeuroreport (Neuroreport) Vol. 31 Issue 18 Pg. 1302-1307 (12 16 2020) ISSN: 1473-558X [Electronic] England
PMID33165195 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Ketones
  • Neuroprotective Agents
  • Reactive Oxygen Species
  • Sesquiterpenes
  • ar-turmerone
  • Casp3 protein, mouse
  • Caspase 3
Topics
  • Animals
  • Apoptosis (drug effects)
  • Caspase 3 (drug effects, metabolism)
  • Cell Survival (drug effects)
  • Cerebellar Cortex (cytology)
  • Ketones (pharmacology)
  • Membrane Potential, Mitochondrial (drug effects)
  • Mice
  • Neurons (drug effects, metabolism)
  • Neuroprotective Agents (pharmacology)
  • Primary Cell Culture
  • Reactive Oxygen Species (metabolism)
  • Sesquiterpenes (pharmacology)

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