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Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats
Aging is a progressive process which is associated with liver dysfunction and it is due to oxidative stress, inflammation, and cell apoptosis. Long-term D-galactose (D-gal) administration is able to develop an aging model in animals. Crocin as a major active ingredient in saffron has shown anti-infl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Shaheed Beheshti University of Medical Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757971/ https://www.ncbi.nlm.nih.gov/pubmed/33680043 http://dx.doi.org/10.22037/ijpr.2019.15022.12825 |
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author | Omidkhoda, Seyedeh Farzaneh Mehri, Soghra Heidari, Somaye Hosseinzadeh, Hossein |
author_facet | Omidkhoda, Seyedeh Farzaneh Mehri, Soghra Heidari, Somaye Hosseinzadeh, Hossein |
author_sort | Omidkhoda, Seyedeh Farzaneh |
collection | PubMed |
description | Aging is a progressive process which is associated with liver dysfunction and it is due to oxidative stress, inflammation, and cell apoptosis. Long-term D-galactose (D-gal) administration is able to develop an aging model in animals. Crocin as a major active ingredient in saffron has shown anti-inflammatory and hepatoprotective effects via its antioxidant capacity. Thus, the aim of the present study was the assessment of crocin effects on hepatic and metabolic disorders induced by D-gal in rats. Aging model was induced in rats by 56-day administration of D-gal (400 mg/kg/day subcutaneously). Protective effects of different doses of crocin (7.5, 15 and 30 mg/kg/day) in concomitant with D-gal administration were evaluated. Malondialdehyde (MDA) and reduced glutathione (GSH) amounts were measured by means of their reaction, respectively, with thiobarbituric acid and 5,5′-Dithiobis (2-nitrobenzoic acid) (DTNB) under a specific condition. Cyclooxygenase-2 (COX-2), β-galactosidase, induced nitric oxide synthase (iNOS), and carboxymethyllysine (CML) levels were determined by western blotting method. Additionally, the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) were measured in serum. D-gal administration significantly elevated ALT, AST, ALP levels, which were markedly inhibited by crocin administration. Crocin suppressed the overgeneration of lipid peroxidation products such as MDA. iNOS was elevated by D-gal administration and was returned to the normal extent by crocin. Therefore, Crocin as a powerful antioxidant and radical scavenger, totally exhibited hepatoprotective effects against D-gal-induced toxicity in rats. |
format | Online Article Text |
id | pubmed-7757971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Shaheed Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-77579712021-03-05 Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats Omidkhoda, Seyedeh Farzaneh Mehri, Soghra Heidari, Somaye Hosseinzadeh, Hossein Iran J Pharm Res Original Article Aging is a progressive process which is associated with liver dysfunction and it is due to oxidative stress, inflammation, and cell apoptosis. Long-term D-galactose (D-gal) administration is able to develop an aging model in animals. Crocin as a major active ingredient in saffron has shown anti-inflammatory and hepatoprotective effects via its antioxidant capacity. Thus, the aim of the present study was the assessment of crocin effects on hepatic and metabolic disorders induced by D-gal in rats. Aging model was induced in rats by 56-day administration of D-gal (400 mg/kg/day subcutaneously). Protective effects of different doses of crocin (7.5, 15 and 30 mg/kg/day) in concomitant with D-gal administration were evaluated. Malondialdehyde (MDA) and reduced glutathione (GSH) amounts were measured by means of their reaction, respectively, with thiobarbituric acid and 5,5′-Dithiobis (2-nitrobenzoic acid) (DTNB) under a specific condition. Cyclooxygenase-2 (COX-2), β-galactosidase, induced nitric oxide synthase (iNOS), and carboxymethyllysine (CML) levels were determined by western blotting method. Additionally, the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) were measured in serum. D-gal administration significantly elevated ALT, AST, ALP levels, which were markedly inhibited by crocin administration. Crocin suppressed the overgeneration of lipid peroxidation products such as MDA. iNOS was elevated by D-gal administration and was returned to the normal extent by crocin. Therefore, Crocin as a powerful antioxidant and radical scavenger, totally exhibited hepatoprotective effects against D-gal-induced toxicity in rats. Shaheed Beheshti University of Medical Sciences 2020 /pmc/articles/PMC7757971/ /pubmed/33680043 http://dx.doi.org/10.22037/ijpr.2019.15022.12825 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Omidkhoda, Seyedeh Farzaneh Mehri, Soghra Heidari, Somaye Hosseinzadeh, Hossein Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats |
title | Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats |
title_full | Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats |
title_fullStr | Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats |
title_full_unstemmed | Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats |
title_short | Protective Effects of Crocin Against Hepatic Damages in D-galactose Aging Model in Rats |
title_sort | protective effects of crocin against hepatic damages in d-galactose aging model in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757971/ https://www.ncbi.nlm.nih.gov/pubmed/33680043 http://dx.doi.org/10.22037/ijpr.2019.15022.12825 |
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