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Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats
Context: γ-Linolenic acid (GLA) is an important constituent of anti-ageing supplements. Objective: The current study investigates the anti-ageing effect of GLA in Sprague-Dawley rats. Materials and methods: GLA (0.1, 0.2, 0.4, 2, 10, 20 and 24 μM) was initially evaluated for its effect on the format...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012036/ https://www.ncbi.nlm.nih.gov/pubmed/28545346 http://dx.doi.org/10.1080/13880209.2017.1331363 |
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author | Khan, Shahab Ali Haider, Ali Mahmood, Wajahat Roome, Talat Abbas, Ghulam |
author_facet | Khan, Shahab Ali Haider, Ali Mahmood, Wajahat Roome, Talat Abbas, Ghulam |
author_sort | Khan, Shahab Ali |
collection | PubMed |
description | Context: γ-Linolenic acid (GLA) is an important constituent of anti-ageing supplements. Objective: The current study investigates the anti-ageing effect of GLA in Sprague-Dawley rats. Materials and methods: GLA (0.1, 0.2, 0.4, 2, 10, 20 and 24 μM) was initially evaluated for its effect on the formation of advanced glycation end products (AGEs) in vitro. For in vivo assessment (1, 5 or 15 mg/kg), the rat model of accelerated ageing was developed using d-fructose (1000 mg/kg (i.p.) plus 10% in drinking water for 40 days). Morris water maze was used to evaluate impairment in learning and memory. The blood of treated animals was used to measure glycosylated haemoglobin (HbA1c) levels. The interaction of GLA with active residues of receptor of AGE (RAGE) was analyzed using AutoDock Vina. Results: Our data showed that GLA inhibited the production of AGEs (IC(50) = 1.12 ± 0.05 μM). However, this effect was more significant at lower tested doses. A similar pattern was also observed in in vivo experiments, where the effect of fructose was reversed by GLA only at lowest tested dose of 1 mg/kg. The HbA1c levels also revealed significant reduction at lower doses (1 and 5 mg/kg). The in silico data exhibited promising interaction of GLA with active residues (Try72, Arg77 and Gln67) of RAGE. Conclusion: The GLA, at lower doses, possesses therapeutic potential against glycation-induced memory decline. |
format | Online Article Text |
id | pubmed-7012036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-70120362020-02-24 Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats Khan, Shahab Ali Haider, Ali Mahmood, Wajahat Roome, Talat Abbas, Ghulam Pharm Biol Original Article Context: γ-Linolenic acid (GLA) is an important constituent of anti-ageing supplements. Objective: The current study investigates the anti-ageing effect of GLA in Sprague-Dawley rats. Materials and methods: GLA (0.1, 0.2, 0.4, 2, 10, 20 and 24 μM) was initially evaluated for its effect on the formation of advanced glycation end products (AGEs) in vitro. For in vivo assessment (1, 5 or 15 mg/kg), the rat model of accelerated ageing was developed using d-fructose (1000 mg/kg (i.p.) plus 10% in drinking water for 40 days). Morris water maze was used to evaluate impairment in learning and memory. The blood of treated animals was used to measure glycosylated haemoglobin (HbA1c) levels. The interaction of GLA with active residues of receptor of AGE (RAGE) was analyzed using AutoDock Vina. Results: Our data showed that GLA inhibited the production of AGEs (IC(50) = 1.12 ± 0.05 μM). However, this effect was more significant at lower tested doses. A similar pattern was also observed in in vivo experiments, where the effect of fructose was reversed by GLA only at lowest tested dose of 1 mg/kg. The HbA1c levels also revealed significant reduction at lower doses (1 and 5 mg/kg). The in silico data exhibited promising interaction of GLA with active residues (Try72, Arg77 and Gln67) of RAGE. Conclusion: The GLA, at lower doses, possesses therapeutic potential against glycation-induced memory decline. Taylor & Francis 2017-05-26 /pmc/articles/PMC7012036/ /pubmed/28545346 http://dx.doi.org/10.1080/13880209.2017.1331363 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Khan, Shahab Ali Haider, Ali Mahmood, Wajahat Roome, Talat Abbas, Ghulam Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats |
title | Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats |
title_full | Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats |
title_fullStr | Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats |
title_full_unstemmed | Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats |
title_short | Gamma-linolenic acid ameliorated glycation-induced memory impairment in rats |
title_sort | gamma-linolenic acid ameliorated glycation-induced memory impairment in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012036/ https://www.ncbi.nlm.nih.gov/pubmed/28545346 http://dx.doi.org/10.1080/13880209.2017.1331363 |
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