Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1782269328076308480 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3652539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT azadnahid neuroprotectiveeffectsofcarnosicacidinanexperimentalmodelofalzheimersdiseaseinrats AT rasoolijazihoma neuroprotectiveeffectsofcarnosicacidinanexperimentalmodelofalzheimersdiseaseinrats AT joghataiemohammadtaghi neuroprotectiveeffectsofcarnosicacidinanexperimentalmodelofalzheimersdiseaseinrats AT soleimanisara neuroprotectiveeffectsofcarnosicacidinanexperimentalmodelofalzheimersdiseaseinrats |