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Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet

BACKGROUND: Lipotropic molecules are effective therapeutic targets to counteract non-alcoholic fatty liver disease (NAFLD). Lipotropic compounds are capable of removing fat from the liver and/or manage the reduction of the synthesis or deposition of lipids in the liver. The objective of this study w...

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Autores principales: Nnanga, Leila Sandra, Ambamba, Bruno Dupon Akamba, Ella, Fils Armand, Mandob, Damaris Enyegue, Ngondi, Judith Laure
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047370/
https://www.ncbi.nlm.nih.gov/pubmed/35484544
http://dx.doi.org/10.1186/s12906-022-03602-4
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author Nnanga, Leila Sandra
Ambamba, Bruno Dupon Akamba
Ella, Fils Armand
Mandob, Damaris Enyegue
Ngondi, Judith Laure
author_facet Nnanga, Leila Sandra
Ambamba, Bruno Dupon Akamba
Ella, Fils Armand
Mandob, Damaris Enyegue
Ngondi, Judith Laure
author_sort Nnanga, Leila Sandra
collection PubMed
description BACKGROUND: Lipotropic molecules are effective therapeutic targets to counteract non-alcoholic fatty liver disease (NAFLD). Lipotropic compounds are capable of removing fat from the liver and/or manage the reduction of the synthesis or deposition of lipids in the liver. The objective of this study was to evaluate the lipotropic effects of the aqueous extract of leaves of Vernonia guineensis (AEVG) on rats fed high fat diet. METHODS: Twenty male rats with an average mass of 235 g were allow acclimatize for seven days, following which they were divided into four groups of five animals each. The test group was treated with high fat diet (HFD) and AEVG at 400 mg/kgBW, while positive control group received HFD and Fenofibrate at 100 mg/kgBW. The normal control group received a normal diet; and the negative control group received HFD. After 14 days of treatment, animals were sacrificed, blood and organs (liver, heart and kidneys), as well as the faeces were collected for the preparation of plasma and homogenates respectively. Some markers of lipid profil (total cholesterol, triglycerides, HDL-c, LDL-c,) and markers of toxicity (AST, ALT, γ-GT, creatinine) were evaluated. RESULTS: The results obtained showed that a HFD at the hepatic level led to the accumulation of lipids (triglycerides (TG) and total cholesterol (TC)) and had adverse effects on hepatic function by promoting cytolysis. At the plasma level, HFD induced hyperlipidemia. Administration of AEVG at 400 mg/kgBW improved the blood lipid profile and reduced the storage of TG and cholesterol in the liver. AEVG also promoted fecal cholesterol excretion and reduced atherogenic indices which include Total Cholesterol/High-Density Lipoprotein cholesterol (TC/HDL-c) and Low-Density Lipoprotein cholesterol/High-Density Lipoprotein cholesterol (LDL-c/HDL-c). The extract exhibited hepato-protective activity (anticholestasis) and improved glomerular filtration. CONCLUSION: These findings suggest that AEVG possesses lipotropic effects confirming its probable use in the management of non-alcoholic fatty liver disease and its cardiometabolic complications. This virtue could be exploited for local pharmaceutical development.
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spelling pubmed-90473702022-04-29 Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet Nnanga, Leila Sandra Ambamba, Bruno Dupon Akamba Ella, Fils Armand Mandob, Damaris Enyegue Ngondi, Judith Laure BMC Complement Med Ther Research BACKGROUND: Lipotropic molecules are effective therapeutic targets to counteract non-alcoholic fatty liver disease (NAFLD). Lipotropic compounds are capable of removing fat from the liver and/or manage the reduction of the synthesis or deposition of lipids in the liver. The objective of this study was to evaluate the lipotropic effects of the aqueous extract of leaves of Vernonia guineensis (AEVG) on rats fed high fat diet. METHODS: Twenty male rats with an average mass of 235 g were allow acclimatize for seven days, following which they were divided into four groups of five animals each. The test group was treated with high fat diet (HFD) and AEVG at 400 mg/kgBW, while positive control group received HFD and Fenofibrate at 100 mg/kgBW. The normal control group received a normal diet; and the negative control group received HFD. After 14 days of treatment, animals were sacrificed, blood and organs (liver, heart and kidneys), as well as the faeces were collected for the preparation of plasma and homogenates respectively. Some markers of lipid profil (total cholesterol, triglycerides, HDL-c, LDL-c,) and markers of toxicity (AST, ALT, γ-GT, creatinine) were evaluated. RESULTS: The results obtained showed that a HFD at the hepatic level led to the accumulation of lipids (triglycerides (TG) and total cholesterol (TC)) and had adverse effects on hepatic function by promoting cytolysis. At the plasma level, HFD induced hyperlipidemia. Administration of AEVG at 400 mg/kgBW improved the blood lipid profile and reduced the storage of TG and cholesterol in the liver. AEVG also promoted fecal cholesterol excretion and reduced atherogenic indices which include Total Cholesterol/High-Density Lipoprotein cholesterol (TC/HDL-c) and Low-Density Lipoprotein cholesterol/High-Density Lipoprotein cholesterol (LDL-c/HDL-c). The extract exhibited hepato-protective activity (anticholestasis) and improved glomerular filtration. CONCLUSION: These findings suggest that AEVG possesses lipotropic effects confirming its probable use in the management of non-alcoholic fatty liver disease and its cardiometabolic complications. This virtue could be exploited for local pharmaceutical development. BioMed Central 2022-04-28 /pmc/articles/PMC9047370/ /pubmed/35484544 http://dx.doi.org/10.1186/s12906-022-03602-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Nnanga, Leila Sandra
Ambamba, Bruno Dupon Akamba
Ella, Fils Armand
Mandob, Damaris Enyegue
Ngondi, Judith Laure
Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet
title Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet
title_full Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet
title_fullStr Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet
title_full_unstemmed Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet
title_short Lipotropic activities of aqueous extract of Vernonia guineensis Benth. in Wistar rats fed high fat diet
title_sort lipotropic activities of aqueous extract of vernonia guineensis benth. in wistar rats fed high fat diet
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047370/
https://www.ncbi.nlm.nih.gov/pubmed/35484544
http://dx.doi.org/10.1186/s12906-022-03602-4
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