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Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals

BACKGROUND: To search for new sources of safe and inexpensive antioxidant agents which can be used to treat various oxidative stress - related diseases, the phenolic contents of leaf of Tetracarpidium conophorum were characterized and its effect on pro-oxidant induced oxidative stress in rat’s genit...

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Autores principales: Akomolafe, Seun F, Oboh, Ganiyu, Akindahunsi, Afolabi A, Afolayan, Anthony J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364579/
https://www.ncbi.nlm.nih.gov/pubmed/25880567
http://dx.doi.org/10.1186/s12906-015-0547-1
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author Akomolafe, Seun F
Oboh, Ganiyu
Akindahunsi, Afolabi A
Afolayan, Anthony J
author_facet Akomolafe, Seun F
Oboh, Ganiyu
Akindahunsi, Afolabi A
Afolayan, Anthony J
author_sort Akomolafe, Seun F
collection PubMed
description BACKGROUND: To search for new sources of safe and inexpensive antioxidant agents which can be used to treat various oxidative stress - related diseases, the phenolic contents of leaf of Tetracarpidium conophorum were characterized and its effect on pro-oxidant induced oxidative stress in rat’s genitals for the first time was investigated. METHODS: The aqueous extract of the plant was prepared, the antioxidant activities of the extract were then evaluated using spectrophotometric method. RESULTS: The result revealed that the introduction of aqueous extract of the plant caused significant concentration-dependent decrease (P < 0.05) in the MDA content of the Fe(2+) -stressed testes and penis homogenates. The least MDA production occurred at the highest concentration of the extract (0.625 mg/mL). However, characterization of the extract with HPLC revealed that its major constituents were gallic acid, catechin, chlorogenic acid, caffeic acid, coumarin, rutin, quercitrin, quercetin, kaempferol and luteolin. Also, the result revealed that the ABTS* scavenging ability of the extract was 4.60 mmol/100 g while its vitamin C content was 23.49 mg/g which indicated that the plant is very rich in vitamin C. Furthermore, the extract scavenged DPPH, NO, OH* radicals and chelated Fe(2+) in a dose-dependent manner. CONCLUSION: The inhibitory effect of Tetracarpidium conophorum leaves could be attributed to the high levels of quercitrin, quercetin and luteolin and the mechanism through which these compounds possibly do this, could be by their radical scavenging abilities.
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spelling pubmed-43645792015-03-19 Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals Akomolafe, Seun F Oboh, Ganiyu Akindahunsi, Afolabi A Afolayan, Anthony J BMC Complement Altern Med Research Article BACKGROUND: To search for new sources of safe and inexpensive antioxidant agents which can be used to treat various oxidative stress - related diseases, the phenolic contents of leaf of Tetracarpidium conophorum were characterized and its effect on pro-oxidant induced oxidative stress in rat’s genitals for the first time was investigated. METHODS: The aqueous extract of the plant was prepared, the antioxidant activities of the extract were then evaluated using spectrophotometric method. RESULTS: The result revealed that the introduction of aqueous extract of the plant caused significant concentration-dependent decrease (P < 0.05) in the MDA content of the Fe(2+) -stressed testes and penis homogenates. The least MDA production occurred at the highest concentration of the extract (0.625 mg/mL). However, characterization of the extract with HPLC revealed that its major constituents were gallic acid, catechin, chlorogenic acid, caffeic acid, coumarin, rutin, quercitrin, quercetin, kaempferol and luteolin. Also, the result revealed that the ABTS* scavenging ability of the extract was 4.60 mmol/100 g while its vitamin C content was 23.49 mg/g which indicated that the plant is very rich in vitamin C. Furthermore, the extract scavenged DPPH, NO, OH* radicals and chelated Fe(2+) in a dose-dependent manner. CONCLUSION: The inhibitory effect of Tetracarpidium conophorum leaves could be attributed to the high levels of quercitrin, quercetin and luteolin and the mechanism through which these compounds possibly do this, could be by their radical scavenging abilities. BioMed Central 2015-03-12 /pmc/articles/PMC4364579/ /pubmed/25880567 http://dx.doi.org/10.1186/s12906-015-0547-1 Text en © Akomolafe et al.; licensee BioMed Central. 2015 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Akomolafe, Seun F
Oboh, Ganiyu
Akindahunsi, Afolabi A
Afolayan, Anthony J
Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals
title Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals
title_full Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals
title_fullStr Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals
title_full_unstemmed Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals
title_short Tetracarpidium conophorum (Mull.Arg) Hutch & Dalziel inhibits FeSO(4) -induced lipid peroxidation in rat’s genitals
title_sort tetracarpidium conophorum (mull.arg) hutch & dalziel inhibits feso(4) -induced lipid peroxidation in rat’s genitals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364579/
https://www.ncbi.nlm.nih.gov/pubmed/25880567
http://dx.doi.org/10.1186/s12906-015-0547-1
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