Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal Damage
We examined whether Brazilian green propolis, a widely used folk medicine, has a neuroprotective function in vitro and/or in vivo. In vitro, propolis significantly inhibited neurotoxicity induced in neuronally differentiated PC12 cell cultures by either 24 h hydrogen peroxide (H2O2) exposure or 48...
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doaj-89a8e69879d34b81a40f5403dd55bbb42020-11-24T23:03:46ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882005-01-012220120710.1093/ecam/neh078Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal DamageMasamitsu Shimazawa0Satomi Chikamatsu1Nobutaka Morimoto2Satoshi Mishima3Hiroichi Nagai4Hideaki Hara5Department of Biofunctional Molecules, Gifu Pharmaceutical University, Gifu, JapanDepartment of Biofunctional Molecules, Gifu Pharmaceutical University, Gifu, JapanDepartment of Biofunctional Molecules, Gifu Pharmaceutical University, Gifu, JapanResearch Center, API Co. Ltd, Gifu, JapanDepartment of Pharmacology, Gifu Pharmaceutical University, Gifu, JapanDepartment of Biofunctional Molecules, Gifu Pharmaceutical University, Gifu, JapanWe examined whether Brazilian green propolis, a widely used folk medicine, has a neuroprotective function in vitro and/or in vivo. In vitro, propolis significantly inhibited neurotoxicity induced in neuronally differentiated PC12 cell cultures by either 24 h hydrogen peroxide (H2O2) exposure or 48 h serum deprivation. Regarding the possible underlying mechanism, propolis protected against oxidative stress (lipid peroxidation) in mouse forebrain homogenates and scavenged free radicals [induced by diphenyl-p-picrylhydrazyl (DPPH). In mice in vivo, propolis [30 or 100 mg/kg; intraperitoneally administered four times (at 2 days, 1 day and 60 min before, and at 4 h after induction of focal cerebral ischemia by permanent middle cerebral artery occlusion)] reduced brain infarction at 24 h after the occlusion. Thus, a propolis-induced inhibition of oxidative stress may be partly responsible for its neuroprotective function against in vitro cell death and in vivo focal cerebral ischemia.http://dx.doi.org/10.1093/ecam/neh078 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Masamitsu Shimazawa Satomi Chikamatsu Nobutaka Morimoto Satoshi Mishima Hiroichi Nagai Hideaki Hara |
spellingShingle |
Masamitsu Shimazawa Satomi Chikamatsu Nobutaka Morimoto Satoshi Mishima Hiroichi Nagai Hideaki Hara Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal Damage Evidence-Based Complementary and Alternative Medicine |
author_facet |
Masamitsu Shimazawa Satomi Chikamatsu Nobutaka Morimoto Satoshi Mishima Hiroichi Nagai Hideaki Hara |
author_sort |
Masamitsu Shimazawa |
title |
Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal Damage |
title_short |
Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal Damage |
title_full |
Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal Damage |
title_fullStr |
Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal Damage |
title_full_unstemmed |
Neuroprotection by Brazilian Green Propolis against In vitro and In vivo Ischemic Neuronal Damage |
title_sort |
neuroprotection by brazilian green propolis against in vitro and in vivo ischemic neuronal damage |
publisher |
Hindawi Limited |
series |
Evidence-Based Complementary and Alternative Medicine |
issn |
1741-427X 1741-4288 |
publishDate |
2005-01-01 |
description |
We examined whether Brazilian green propolis, a widely used folk medicine, has a neuroprotective function in vitro and/or in vivo. In vitro, propolis significantly inhibited neurotoxicity induced in neuronally differentiated PC12 cell cultures by either 24 h hydrogen peroxide (H2O2) exposure or 48 h serum deprivation. Regarding the possible underlying mechanism, propolis protected against oxidative stress (lipid peroxidation) in mouse forebrain homogenates and scavenged free radicals [induced by diphenyl-p-picrylhydrazyl (DPPH). In mice in vivo, propolis [30 or 100 mg/kg; intraperitoneally administered four times (at 2 days, 1 day and 60 min before, and at 4 h after induction of focal cerebral ischemia by permanent middle cerebral artery occlusion)] reduced brain infarction at 24 h after the occlusion. Thus, a propolis-induced inhibition of oxidative stress may be partly responsible for its neuroprotective function against in vitro cell death and in vivo focal cerebral ischemia. |
url |
http://dx.doi.org/10.1093/ecam/neh078 |
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