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Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver
BACKGROUND: Nicotine is a major pharmacologically active substance in cigarette smoke. It is mainly metabolized in liver and causes devastating effects. Crocin is the chemical ingredient primarily responsible for the color of saffron. It has different pharmacological effects such as antioxidant and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593238/ https://www.ncbi.nlm.nih.gov/pubmed/26442615 http://dx.doi.org/10.4103/2008-7802.165203 |
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author | Jalili, Cyrus Tabatabaei, Hadis Kakaberiei, Seyran Roshankhah, Shiva Salahshoor, Mohammad Reza |
author_facet | Jalili, Cyrus Tabatabaei, Hadis Kakaberiei, Seyran Roshankhah, Shiva Salahshoor, Mohammad Reza |
author_sort | Jalili, Cyrus |
collection | PubMed |
description | BACKGROUND: Nicotine is a major pharmacologically active substance in cigarette smoke. It is mainly metabolized in liver and causes devastating effects. Crocin is the chemical ingredient primarily responsible for the color of saffron. It has different pharmacological effects such as antioxidant and anticancer. This study was designed to evaluate the protective role of crocin against nicotine on the liver of mice. METHODS: Forty-eight mice were equally divided into 8 groups; control (normal saline), nicotine (2.5 mg/kg), crocin (12.5, 25 and 50 mg/kg) and crocin plus nicotine treated groups. Saline, crocin, nicotine and crocin/nicotine (once a day) were intraperitoneally injected for 4 weeks. The liver weight and histology, aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), and serum nitric oxide levels have been studied. RESULTS: The results indicated that nicotine administration significantly decreased liver weight (48.37%) and increased the mean diameter of hepatocyte (239%), central hepatic vein (28.45%), liver enzymes level (ALP 29.43%, AST 21.81%, ALT 21.55%), and blood serum nitric oxide level (57.18%) compared to saline group (P < 0.05). However, crocin and crocin plus nicotine administration significantly boosted liver weight (49.54%) and decreased the mean diameter of hepatocyte (40.48%), central hepatic vein (15.44%), liver enzymes (ALP 22.02%, AST 19.05%, ALT 23.11%), and nitric oxide levels (35.80%) in all groups compared to nicotine group (percentages represent the maximum dose) (P < 0.05). CONCLUSIONS: Crocin showed its partly protective effect against nicotine-induced liver toxicity. |
format | Online Article Text |
id | pubmed-4593238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45932382015-10-06 Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver Jalili, Cyrus Tabatabaei, Hadis Kakaberiei, Seyran Roshankhah, Shiva Salahshoor, Mohammad Reza Int J Prev Med Original Article BACKGROUND: Nicotine is a major pharmacologically active substance in cigarette smoke. It is mainly metabolized in liver and causes devastating effects. Crocin is the chemical ingredient primarily responsible for the color of saffron. It has different pharmacological effects such as antioxidant and anticancer. This study was designed to evaluate the protective role of crocin against nicotine on the liver of mice. METHODS: Forty-eight mice were equally divided into 8 groups; control (normal saline), nicotine (2.5 mg/kg), crocin (12.5, 25 and 50 mg/kg) and crocin plus nicotine treated groups. Saline, crocin, nicotine and crocin/nicotine (once a day) were intraperitoneally injected for 4 weeks. The liver weight and histology, aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), and serum nitric oxide levels have been studied. RESULTS: The results indicated that nicotine administration significantly decreased liver weight (48.37%) and increased the mean diameter of hepatocyte (239%), central hepatic vein (28.45%), liver enzymes level (ALP 29.43%, AST 21.81%, ALT 21.55%), and blood serum nitric oxide level (57.18%) compared to saline group (P < 0.05). However, crocin and crocin plus nicotine administration significantly boosted liver weight (49.54%) and decreased the mean diameter of hepatocyte (40.48%), central hepatic vein (15.44%), liver enzymes (ALP 22.02%, AST 19.05%, ALT 23.11%), and nitric oxide levels (35.80%) in all groups compared to nicotine group (percentages represent the maximum dose) (P < 0.05). CONCLUSIONS: Crocin showed its partly protective effect against nicotine-induced liver toxicity. Medknow Publications & Media Pvt Ltd 2015-09-10 /pmc/articles/PMC4593238/ /pubmed/26442615 http://dx.doi.org/10.4103/2008-7802.165203 Text en Copyright: © 2015 Jalili C. http://creativecommons.org/licenses/by-nc-sa/3.0 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 author and source are credited. |
spellingShingle | Original Article Jalili, Cyrus Tabatabaei, Hadis Kakaberiei, Seyran Roshankhah, Shiva Salahshoor, Mohammad Reza Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver |
title | Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver |
title_full | Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver |
title_fullStr | Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver |
title_full_unstemmed | Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver |
title_short | Protective Role of Crocin Against Nicotine-induced Damages on Male Mice Liver |
title_sort | protective role of crocin against nicotine-induced damages on male mice liver |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593238/ https://www.ncbi.nlm.nih.gov/pubmed/26442615 http://dx.doi.org/10.4103/2008-7802.165203 |
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