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Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats

OBJECTIVE: Alzheimer’s disease is the most common type of neurodegenerative disorder. It has been suggested that oxidative stress can be one of the pathological mechanisms of this disease. Carnosic acid (CA) is an effective antioxidant substance and recent studies have shown that its electrophilic c...

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Autores principales: Azad, Nahid, Rasoolijazi, Homa, Joghataie, Mohammad Taghi, Soleimani, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652539/
https://www.ncbi.nlm.nih.gov/pubmed/23671826
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author Azad, Nahid
Rasoolijazi, Homa
Joghataie, Mohammad Taghi
Soleimani, Sara
author_facet Azad, Nahid
Rasoolijazi, Homa
Joghataie, Mohammad Taghi
Soleimani, Sara
author_sort Azad, Nahid
collection PubMed
description OBJECTIVE: Alzheimer’s disease is the most common type of neurodegenerative disorder. It has been suggested that oxidative stress can be one of the pathological mechanisms of this disease. Carnosic acid (CA) is an effective antioxidant substance and recent studies have shown that its electrophilic compounds play a role in reversing oxidative stress. Thus we tried to find out whether CA administration protects hippocampal neurons, preventing neurodegeneration in rats. MATERIALS AND METHODS: Animals were divided into four groups: Sham-operated (sham), CA-pretreated sham-operated (sham+CA), untreated lesion (lesion) and CA-pretreated lesion (lesion+CA). Animals in all groups received vehicle or vehicle plus CA (CA: 10mg/ kg) intra-peritoneally one hour before surgery, again the same solution injected 3-4 hours after surgery (CA: 3 mg/kg) and repeated each afternoon for 12 days. A lesion was made by bilateral intra-hippocampal injection of 4 µl of beta amyloid protein (1.5 nmol/µl) or vehicle in each side. 14 days after surgery, the brains were extracted for histochemical studies. Data was expressed as mean ± SEM and analyzed using SPSS statistical software. RESULTS: Results showed that pretreatment with carnosic acid can reduce cellular death in the cornu ammonis 1 (CA1) region of the hippocampus in the lesion+CA group, as compared with the lesion group. CONCLUSION: Carnosic acid may be useful in protecting against beta amyloid-induced neurodegeneration in the hippocampus.
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spelling pubmed-36525392013-05-13 Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats Azad, Nahid Rasoolijazi, Homa Joghataie, Mohammad Taghi Soleimani, Sara Cell J Research Article OBJECTIVE: Alzheimer’s disease is the most common type of neurodegenerative disorder. It has been suggested that oxidative stress can be one of the pathological mechanisms of this disease. Carnosic acid (CA) is an effective antioxidant substance and recent studies have shown that its electrophilic compounds play a role in reversing oxidative stress. Thus we tried to find out whether CA administration protects hippocampal neurons, preventing neurodegeneration in rats. MATERIALS AND METHODS: Animals were divided into four groups: Sham-operated (sham), CA-pretreated sham-operated (sham+CA), untreated lesion (lesion) and CA-pretreated lesion (lesion+CA). Animals in all groups received vehicle or vehicle plus CA (CA: 10mg/ kg) intra-peritoneally one hour before surgery, again the same solution injected 3-4 hours after surgery (CA: 3 mg/kg) and repeated each afternoon for 12 days. A lesion was made by bilateral intra-hippocampal injection of 4 µl of beta amyloid protein (1.5 nmol/µl) or vehicle in each side. 14 days after surgery, the brains were extracted for histochemical studies. Data was expressed as mean ± SEM and analyzed using SPSS statistical software. RESULTS: Results showed that pretreatment with carnosic acid can reduce cellular death in the cornu ammonis 1 (CA1) region of the hippocampus in the lesion+CA group, as compared with the lesion group. CONCLUSION: Carnosic acid may be useful in protecting against beta amyloid-induced neurodegeneration in the hippocampus. Royan Institute 2011 2011-04-21 /pmc/articles/PMC3652539/ /pubmed/23671826 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Azad, Nahid
Rasoolijazi, Homa
Joghataie, Mohammad Taghi
Soleimani, Sara
Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats
title Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats
title_full Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats
title_fullStr Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats
title_full_unstemmed Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats
title_short Neuroprotective Effects of Carnosic Acid in an Experimental Model of Alzheimer’s Disease in Rats
title_sort neuroprotective effects of carnosic acid in an experimental model of alzheimer’s disease in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652539/
https://www.ncbi.nlm.nih.gov/pubmed/23671826
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