Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms
Inflammation and oxidative stress have been considered the major contributor in developing chronic diseases including cancer, atherosclerosis, diabetes, neurodegenerative diseases, arthritis and obesity. A number of dietary and nutraceuticals interventions to attenuate inflammation- and oxidat...
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my-upm-ir.855342021-12-14T07:13:56Z Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms 2018-11 Ranneh, Yazan Inflammation and oxidative stress have been considered the major contributor in developing chronic diseases including cancer, atherosclerosis, diabetes, neurodegenerative diseases, arthritis and obesity. A number of dietary and nutraceuticals interventions to attenuate inflammation- and oxidative stress-related diseases target pro-inflammatory mediators, reactive oxygen species, transcription factors including nuclear factor-kappa B (NF-κB), and nuclear factor erythroid 2- releated factor 2 (Nrf-2) and specific regulatory transcription proteins including P38- mitogen activated protein kinases (P38-MAPK) and high mobility group box-1 protein (HMGB-1) and. Stingless bee honey (SBH) has been recently found to be rich in bioactive compounds especially, polyphenols more than honey-made by normal bee. The unique body size of stingless bee helps her stretch itself inside a plenty number of flowers which increase the diversity of collected polyphenols and preserve them from degradation. In this study, SBH had a higher phenolic content than other types of normal honey and there were fifteen phenolic compounds identified using LCMS/ MS. The richness of SBH in phenolic compounds were also manifested with high and significant total antioxidant capacity measured by DPPH, ABTS and ORAC assays. The significant statistical correlation between polyphenols content and antioxidant results confirmed the biological actions of SBH against free radicals. Subsequently, a model of chronic subclinical systemic inflammation was developed by injecting male rats with 1 mg/kg of lipopolysaccharide thrice per week for 28 days. The results demonstrated an elevation in C-reactive protein, IL-6, TNF-α and lymphocyte along with inflammatory changes in the histological features of heart, lung, kidney and liver tissues. Then, the ability of SBH to mitigate inflammation and oxidative stress was studied in two separate experiments; systemic acute inflammation and chronic subclinical systemic inflammation. In the first experiment, SBH was supplemented at two different doses (4.6 and 9.3 g/kg/day) for seven days prior to induce systemic acute inflammation by injecting male rat with 5 mg/kg LPS. In the second experiment, SBH was supplemented for 30 days at two different doses (4.6 and 9.3 g/kg/day) concurrently with 1 mg/kg of LPS injection thrice per week for 28 days to induce chronic subclinical systemic inflammation. In both experiments, SBH demonstrated a significant reduction in pro-inflammatory mediators and oxidative stress. Regulating the protein levels of NF-κB, p38-MAPK, HMGB-1 and activating Nrf-2 in SBH treated group unveiled partially the mechanism of SBH against inflammation and oxidative stress. The histopathological examination of both studies revealed that SBH exceled a reduction in the pathology of heart, lung, kidney and liver. These biological activates of SBH could be due to the synergistic actions of polyphenols and it also provides a novel insight into the possible mechanism behind the preventive actions of SBH on the emergence of inflammation and oxidative markers in rats with LPS-induced inflammation. Collectively, the results presented in this thesis suggest that SBH can mitigate and prevent systemic acute inflammation and chronic subclinical systemic inflammation along with oxidative stress via regulating NF-κB, P38-MAPK, HMGB-1 and Nrf-2. SBH is expected to be a useful natural supplement for alleviating and preventing oxidative stress and chronic inflammationrelated diseases. Oxidative Stress Inflammation Apitherapy 2018-11 Thesis http://psasir.upm.edu.my/id/eprint/85534/ http://psasir.upm.edu.my/id/eprint/85534/1/FPSK%28p%29%202019%2016%20ir.pdf text en public doctoral Universiti Putra Malaysia Oxidative Stress Inflammation Apitherapy Md Akim, Abdah |
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Md Akim, Abdah |
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Oxidative Stress Inflammation Apitherapy |
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Oxidative Stress Inflammation Apitherapy Ranneh, Yazan Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms |
description |
Inflammation and oxidative stress have been considered the major contributor in
developing chronic diseases including cancer, atherosclerosis, diabetes,
neurodegenerative diseases, arthritis and obesity. A number of dietary and
nutraceuticals interventions to attenuate inflammation- and oxidative stress-related
diseases target pro-inflammatory mediators, reactive oxygen species, transcription
factors including nuclear factor-kappa B (NF-κB), and nuclear factor erythroid 2-
releated factor 2 (Nrf-2) and specific regulatory transcription proteins including P38-
mitogen activated protein kinases (P38-MAPK) and high mobility group box-1 protein
(HMGB-1) and. Stingless bee honey (SBH) has been recently found to be rich in
bioactive compounds especially, polyphenols more than honey-made by normal bee.
The unique body size of stingless bee helps her stretch itself inside a plenty number
of flowers which increase the diversity of collected polyphenols and preserve them
from degradation. In this study, SBH had a higher phenolic content than other types
of normal honey and there were fifteen phenolic compounds identified using LCMS/
MS. The richness of SBH in phenolic compounds were also manifested with high
and significant total antioxidant capacity measured by DPPH, ABTS and ORAC
assays. The significant statistical correlation between polyphenols content and antioxidant
results confirmed the biological actions of SBH against free radicals.
Subsequently, a model of chronic subclinical systemic inflammation was developed
by injecting male rats with 1 mg/kg of lipopolysaccharide thrice per week for 28 days.
The results demonstrated an elevation in C-reactive protein, IL-6, TNF-α and
lymphocyte along with inflammatory changes in the histological features of heart,
lung, kidney and liver tissues. Then, the ability of SBH to mitigate inflammation and
oxidative stress was studied in two separate experiments; systemic acute inflammation
and chronic subclinical systemic inflammation. In the first experiment, SBH was
supplemented at two different doses (4.6 and 9.3 g/kg/day) for seven days prior to induce systemic acute inflammation by injecting male rat with 5 mg/kg LPS. In the
second experiment, SBH was supplemented for 30 days at two different doses (4.6
and 9.3 g/kg/day) concurrently with 1 mg/kg of LPS injection thrice per week for 28
days to induce chronic subclinical systemic inflammation. In both experiments, SBH
demonstrated a significant reduction in pro-inflammatory mediators and oxidative
stress. Regulating the protein levels of NF-κB, p38-MAPK, HMGB-1 and activating
Nrf-2 in SBH treated group unveiled partially the mechanism of SBH against
inflammation and oxidative stress. The histopathological examination of both studies
revealed that SBH exceled a reduction in the pathology of heart, lung, kidney and
liver. These biological activates of SBH could be due to the synergistic actions of
polyphenols and it also provides a novel insight into the possible mechanism behind
the preventive actions of SBH on the emergence of inflammation and oxidative
markers in rats with LPS-induced inflammation. Collectively, the results presented in
this thesis suggest that SBH can mitigate and prevent systemic acute inflammation and
chronic subclinical systemic inflammation along with oxidative stress via regulating
NF-κB, P38-MAPK, HMGB-1 and Nrf-2. SBH is expected to be a useful natural
supplement for alleviating and preventing oxidative stress and chronic inflammationrelated
diseases. |
format |
Thesis |
qualification_level |
Doctorate |
author |
Ranneh, Yazan |
author_facet |
Ranneh, Yazan |
author_sort |
Ranneh, Yazan |
title |
Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms |
title_short |
Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms |
title_full |
Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms |
title_fullStr |
Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms |
title_full_unstemmed |
Ameliorative activities of Malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress In vivo and its underlying mechanisms |
title_sort |
ameliorative activities of malaysian stingless bee honey on lipopolysaccharide-induced inflammation and oxidative stress in vivo and its underlying mechanisms |
granting_institution |
Universiti Putra Malaysia |
publishDate |
2018 |
url |
http://psasir.upm.edu.my/id/eprint/85534/1/FPSK%28p%29%202019%2016%20ir.pdf |
_version_ |
1747813554612862976 |