Plants and their components are the only source of most drugs which comprise of distinct groups such as antispasmodics, emetics, anticancer and antimicrobials. Plants capable of improving health conditions and treating diseases have been identified and used since human existence. A wide variety of compound synthesized from plants participate in biological roles such as defense against predators. This study examined the protective effect of Aframomunchrysanthum seed aqueous extract against acetaminophen-induced liver toxicity in rats. A suspension of 750 mg/kg acetaminophen was administered once every 72 hours to induce toxicity in the rats. This was followed by oral administration of the plant extract (500, 1000 and 2000 mg/kg) body weight and 100 mg/kg of silymarine. For ten days. Eighteen hours after the last dosage, blood sample was collected for biochemical analysis. The result showed significant (p < 0.05) increase in the activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) as well as the concentrations of albumin (ALB) and total bilirubin (T. B) levels in rats administered with acetaminophen only. The levels of these parameters were significantly (p < 0.05) decreased in the groups pretreated with the extract.
| Published in | Advances in Biochemistry (Volume 7, Issue 1) |
| DOI | 10.11648/j.ab.20190701.11 |
| Page(s) | 1-4 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2024. Published by Science Publishing Group |
Aframomun Chrysanthum, Silymarine, Hepatoprotective
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APA Style
Nwachoko Ndidi, Essien Eka Bassey, Ayalogu Edward Obiozo. (2019). Effects of Aframomun Chrysanthum Seed Aqueous Extract Against Acetaminophen-induced Liver Toxicity in Rats. Advances in Biochemistry, 7(1), 1-4. https://doi.org/10.11648/j.ab.20190701.11
ACS Style
Nwachoko Ndidi; Essien Eka Bassey; Ayalogu Edward Obiozo. Effects of Aframomun Chrysanthum Seed Aqueous Extract Against Acetaminophen-induced Liver Toxicity in Rats. Adv. Biochem. 2019, 7(1), 1-4. doi: 10.11648/j.ab.20190701.11
AMA Style
Nwachoko Ndidi, Essien Eka Bassey, Ayalogu Edward Obiozo. Effects of Aframomun Chrysanthum Seed Aqueous Extract Against Acetaminophen-induced Liver Toxicity in Rats. Adv Biochem. 2019;7(1):1-4. doi: 10.11648/j.ab.20190701.11
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Download@article{10.11648/j.ab.20190701.11,
author = {Nwachoko Ndidi and Essien Eka Bassey and Ayalogu Edward Obiozo},
title = {Effects of Aframomun Chrysanthum Seed Aqueous Extract Against Acetaminophen-induced Liver Toxicity in Rats},
journal = {Advances in Biochemistry},
volume = {7},
number = {1},
pages = {1-4},
doi = {10.11648/j.ab.20190701.11},
url = {https://doi.org/10.11648/j.ab.20190701.11},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ab.20190701.11},
abstract = {Plants and their components are the only source of most drugs which comprise of distinct groups such as antispasmodics, emetics, anticancer and antimicrobials. Plants capable of improving health conditions and treating diseases have been identified and used since human existence. A wide variety of compound synthesized from plants participate in biological roles such as defense against predators. This study examined the protective effect of Aframomunchrysanthum seed aqueous extract against acetaminophen-induced liver toxicity in rats. A suspension of 750 mg/kg acetaminophen was administered once every 72 hours to induce toxicity in the rats. This was followed by oral administration of the plant extract (500, 1000 and 2000 mg/kg) body weight and 100 mg/kg of silymarine. For ten days. Eighteen hours after the last dosage, blood sample was collected for biochemical analysis. The result showed significant (p < 0.05) increase in the activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) as well as the concentrations of albumin (ALB) and total bilirubin (T. B) levels in rats administered with acetaminophen only. The levels of these parameters were significantly (p < 0.05) decreased in the groups pretreated with the extract.},
year = {2019}
}
TY - JOUR T1 - Effects of Aframomun Chrysanthum Seed Aqueous Extract Against Acetaminophen-induced Liver Toxicity in Rats AU - Nwachoko Ndidi AU - Essien Eka Bassey AU - Ayalogu Edward Obiozo Y1 - 2019/06/05 PY - 2019 N1 - https://doi.org/10.11648/j.ab.20190701.11 DO - 10.11648/j.ab.20190701.11 T2 - Advances in Biochemistry JF - Advances in Biochemistry JO - Advances in Biochemistry SP - 1 EP - 4 PB - Science Publishing Group SN - 2329-0862 UR - https://doi.org/10.11648/j.ab.20190701.11 AB - Plants and their components are the only source of most drugs which comprise of distinct groups such as antispasmodics, emetics, anticancer and antimicrobials. Plants capable of improving health conditions and treating diseases have been identified and used since human existence. A wide variety of compound synthesized from plants participate in biological roles such as defense against predators. This study examined the protective effect of Aframomunchrysanthum seed aqueous extract against acetaminophen-induced liver toxicity in rats. A suspension of 750 mg/kg acetaminophen was administered once every 72 hours to induce toxicity in the rats. This was followed by oral administration of the plant extract (500, 1000 and 2000 mg/kg) body weight and 100 mg/kg of silymarine. For ten days. Eighteen hours after the last dosage, blood sample was collected for biochemical analysis. The result showed significant (p < 0.05) increase in the activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) as well as the concentrations of albumin (ALB) and total bilirubin (T. B) levels in rats administered with acetaminophen only. The levels of these parameters were significantly (p < 0.05) decreased in the groups pretreated with the extract. VL - 7 IS - 1 ER -
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