| dc.contributor.author | Alvandi, Mahdi | en_US |
| dc.contributor.author | Dastan, Dara | en_US |
| dc.contributor.author | Soleimani Asl, Sara | en_US |
| dc.contributor.author | Nili-Ahmadabadi*, Amir | en_US |
| dc.date.accessioned | 1399-07-08T22:08:45Z | fa_IR |
| dc.date.accessioned | 2020-09-29T22:08:45Z | |
| dc.date.available | 1399-07-08T22:08:45Z | fa_IR |
| dc.date.available | 2020-09-29T22:08:45Z | |
| dc.date.issued | 2020-04-01 | en_US |
| dc.date.issued | 1399-01-13 | fa_IR |
| dc.date.submitted | 2019-12-01 | en_US |
| dc.date.submitted | 1398-09-10 | fa_IR |
| dc.identifier.citation | Alvandi, Mahdi, Dastan, Dara, Soleimani Asl, Sara, Nili-Ahmadabadi*, Amir. (2020). The Role of Allium saralicum Extract on Prevention of Acetaminophen-Induced Hepatic Failure: an Experimental Study. Research Journal of Pharmacognosy, 7(2), 43-51. doi: 10.22127/rjp.2020.207706.1533 | en_US |
| dc.identifier.issn | 2345-4458 | |
| dc.identifier.issn | 2345-5977 | |
| dc.identifier.uri | https://dx.doi.org/10.22127/rjp.2020.207706.1533 | |
| dc.identifier.uri | http://www.rjpharmacognosy.ir/article_103488.html | |
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/126035 | |
| dc.description.abstract | <strong>Background and objectives:</strong> Acetaminophen (APAP) is a common analgesic medicine whose overdose leads to severe hepatic dysfunction. Due to the known antioxidant properties of <em>Allium</em>species, the present study aimed to evaluate the protective effects of <em>Allium</em><em> saralicum </em>plant on APAP induced liver toxicity.<strong> Methods:</strong> The hydro-alcoholic extract of <em>A.</em><em> saralicum </em>was prepared by maceration and ultrasonic methods. Forty-two rats in seven groups were treated by gavage as follows: groups 1 and 2 received normal saline, groups 3 received 400 mg/kg of <em>A.</em><em> saralicum </em>hydro-alcoholic extract, and the groups 4-7 were treated with 50, 100, 200 and 400 mg/kg of <em>A.</em><em> saralicum </em>extract, respectively. After two consecutive weeks, the therapeutic groups, as well as the positive control (APAP) group, were administered a single dose of APAP (2 g/kg). After 48 hours, the animals were anesthetized, and blood and liver samples were collected for histological and biochemical examinations.<strong>Results:</strong> Our findings indicated that APAP caused a significant rise in ALT (p<0.001), AST (p<0.001), ALP (p<0.001) and LDH (p<0.001) serum levels, total and direct bilirubin (p<0.001), hepatic lipid peroxidation (LPO; p<0.001) and nitric oxide (NO; p<0.001). In addition, APAP let to the decreasing of the total antioxidant capacity (TAC; p< 0.001), total thiol molecules (TTM; p<0.001), and structural changes in the hepatic tissue. Following administration of<em>A.</em><em> saralicum </em>extract, a remarkable improvement was observed in the functional and oxidative stress indices of liver tissue alongside histopathologic alterations.<strong> Conclusion:</strong> Our results showed that <em>A.</em><em> saralicum </em>extractsignificantly improved APAP-induced hepatic failure through inhibition of oxidative/nitrosative stress. | en_US |
| dc.format.extent | 605 | |
| dc.format.mimetype | application/pdf | |
| dc.language | English | |
| dc.language.iso | en_US | |
| dc.publisher | - The Iranian Society of Pharmacognosy
- Shahid Beheshti University of Medical Sciences | en_US |
| dc.relation.ispartof | Research Journal of Pharmacognosy | en_US |
| dc.relation.isversionof | https://dx.doi.org/10.22127/rjp.2020.207706.1533 | |
| dc.subject | Acetaminophen | en_US |
| dc.subject | Allium saralicum | en_US |
| dc.subject | hepatotoxicity | en_US |
| dc.subject | oxidative stress | en_US |
| dc.subject | Hepatotoxicity | en_US |
| dc.title | The Role of Allium saralicum Extract on Prevention of Acetaminophen-Induced Hepatic Failure: an Experimental Study | en_US |
| dc.type | Text | en_US |
| dc.type | Original paper | en_US |
| dc.contributor.department | Medicinal Plants and Natural Products Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Pharmacology and Toxicology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran. | en_US |
| dc.contributor.department | Medicinal Plants and Natural Products Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.Department of Pharmacognosy, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran. | en_US |
| dc.contributor.department | Anatomy Department, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. | en_US |
| dc.contributor.department | Medicinal Plants and Natural Products Research Center, Hamadan University of Medical Sciences, Hamadan, Iran. Department of Pharmacology and Toxicology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran. | en_US |
| dc.citation.volume | 7 | |
| dc.citation.issue | 2 | |
| dc.citation.spage | 43 | |
| dc.citation.epage | 51 | |
| nlai.contributor.orcid | 0000-0001-6779-6099 | |
| nlai.contributor.orcid | 0000-0002-7838-9090 | |