Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats

Introduction: Metabolomic analyses have become paramount in unveiling the therapeutic capacities of bioactive agents. Dabai pulp oil (DPO) has emerged as a prospective agent against hypercholesterolemia. This investigation delineates the metabolic imprints of DPO’s therapeutic actions using 1H NMR-b...

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Main Authors: Abdul Kadir, Noor Atiqah Aizan, Azlan, Azrina, Abdul Mutalib, Maisarah
Format: Article
Language:English
Published: Universiti Putra Malaysia 2024
Online Access:http://psasir.upm.edu.my/id/eprint/111522/1/MJMHS_0879.pdf
http://psasir.upm.edu.my/id/eprint/111522/
https://medic.upm.edu.my/upload/dokumen/2024052916594419_MJMHS_0879.pdf
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spelling my.upm.eprints.1115222024-07-29T08:22:11Z http://psasir.upm.edu.my/id/eprint/111522/ Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats Abdul Kadir, Noor Atiqah Aizan Azlan, Azrina Abdul Mutalib, Maisarah Introduction: Metabolomic analyses have become paramount in unveiling the therapeutic capacities of bioactive agents. Dabai pulp oil (DPO) has emerged as a prospective agent against hypercholesterolemia. This investigation delineates the metabolic imprints of DPO’s therapeutic actions using 1H NMR-based urinary metabolomic profiling. Methods: Male Sprague-Dawley rats were first exposed to a high-cholesterol regimen to simulate hypercholesterolemia. Following this induction, they were transitioned to a DPO-infused diet. The ensuing metabolic variations were tracked using 1H NMR-based urinary metabolomic analysis. Results: The metabolic landscape displayed discernible shifts post-DPO administration, underlining its therapeutic potential. There was a marked decrement in the concentrations of pivotal metabolites such as creatinine, succinate, pyruvate, acetate, TMAO, and choline (p<0.05). Notably, an augmented taurine concentration after DPO administration spotlighted the oil’s antioxidative and anti-inflammatory prowess (p<0.05). These observations underscore DPO’s proficiency in rectifying metabolic aberrations inherent to hypercholesterolemia, particularly affecting energy transduction and cardiovascular function. Conclusion: This empirical evidence bolsters the notion that DPO harbours potent therapeutic virtues for hypercholesterolemia amelioration. Nevertheless, in-depth explorations are quintessential to decoding its holistic therapeutic pathways, fortifying its role in future targeted interventions. Universiti Putra Malaysia 2024-05 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/111522/1/MJMHS_0879.pdf Abdul Kadir, Noor Atiqah Aizan and Azlan, Azrina and Abdul Mutalib, Maisarah (2024) Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats. Malaysian Journal of Medicine and Health Sciences, 20 (3). pp. 142-149. ISSN 16758544; EISSN: 26369346 https://medic.upm.edu.my/upload/dokumen/2024052916594419_MJMHS_0879.pdf 10.47836/mjmhs.20.3.20
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Introduction: Metabolomic analyses have become paramount in unveiling the therapeutic capacities of bioactive agents. Dabai pulp oil (DPO) has emerged as a prospective agent against hypercholesterolemia. This investigation delineates the metabolic imprints of DPO’s therapeutic actions using 1H NMR-based urinary metabolomic profiling. Methods: Male Sprague-Dawley rats were first exposed to a high-cholesterol regimen to simulate hypercholesterolemia. Following this induction, they were transitioned to a DPO-infused diet. The ensuing metabolic variations were tracked using 1H NMR-based urinary metabolomic analysis. Results: The metabolic landscape displayed discernible shifts post-DPO administration, underlining its therapeutic potential. There was a marked decrement in the concentrations of pivotal metabolites such as creatinine, succinate, pyruvate, acetate, TMAO, and choline (p<0.05). Notably, an augmented taurine concentration after DPO administration spotlighted the oil’s antioxidative and anti-inflammatory prowess (p<0.05). These observations underscore DPO’s proficiency in rectifying metabolic aberrations inherent to hypercholesterolemia, particularly affecting energy transduction and cardiovascular function. Conclusion: This empirical evidence bolsters the notion that DPO harbours potent therapeutic virtues for hypercholesterolemia amelioration. Nevertheless, in-depth explorations are quintessential to decoding its holistic therapeutic pathways, fortifying its role in future targeted interventions.
format Article
author Abdul Kadir, Noor Atiqah Aizan
Azlan, Azrina
Abdul Mutalib, Maisarah
spellingShingle Abdul Kadir, Noor Atiqah Aizan
Azlan, Azrina
Abdul Mutalib, Maisarah
Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats
author_facet Abdul Kadir, Noor Atiqah Aizan
Azlan, Azrina
Abdul Mutalib, Maisarah
author_sort Abdul Kadir, Noor Atiqah Aizan
title Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats
title_short Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats
title_full Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats
title_fullStr Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats
title_full_unstemmed Metabolite alteration associated with Dabai pulp oil supplementation in hypercholesterolemic rats
title_sort metabolite alteration associated with dabai pulp oil supplementation in hypercholesterolemic rats
publisher Universiti Putra Malaysia
publishDate 2024
url http://psasir.upm.edu.my/id/eprint/111522/1/MJMHS_0879.pdf
http://psasir.upm.edu.my/id/eprint/111522/
https://medic.upm.edu.my/upload/dokumen/2024052916594419_MJMHS_0879.pdf
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