The Protective Role of Vitamin E against Oxidative Stress and Immunosuppression Induced by Non-Esterified Fatty Acids in Bovine Peripheral Blood Leukocytes

High levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a vitamin-E-supplemented diet reduces reactive oxygen species (ROS) levels in the blood and diminishes immunosuppression in the transition per...

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Published inAnimals (Basel) Vol. 14; no. 7; p. 1079
Main Authors Li, Cheng-Yan, Lin, Wei-Chen, Moonmanee, Tossapol, Chan, Jacky Peng-Wen, Wang, Chien-Kai
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 01.04.2024
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Abstract High levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a vitamin-E-supplemented diet reduces reactive oxygen species (ROS) levels in the blood and diminishes immunosuppression in the transition period. However, whether the restoration of immune cell function occurs through the direct action of vitamin E in cells is still a topic that requires further discussion. Therefore, in this experiment, we aimed to investigate the effect of NEFAs on peripheral blood leukocytes (PBLs) and whether vitamin E mitigates the impact of NEFAs. We employed three groups: (1) blank, (2) NEFA only, and (3) pre-culturing with vitamin E before NEFA treatment (VENEFA). In peripheral blood mononuclear cells (PBMCs), there were no differences in vitamin E content among the three groups. However, in the vitamin E pre-treatment group, the vitamin E levels of polymorphonuclear neutrophils (PMNs) were significantly higher than those in the other two groups. NEFA levels increased malondialdehyde (MDA) levels in PBMCs, but pre-treatment with vitamin E reduced accumulation of MDA levels. Regarding the expression of proinflammatory genes, NEFAs increased the expression of interleukin-1β in PBMCs and colony-stimulating factor 2 in PMNs. Vitamin E pre-treatment restored the increase in interleukin-1β levels caused by NEFAs in PBMCs. None of the groups affected the phagocytosis of PMNs. Few studies have confirmed that NEFAs cause oxidative stress in bovine PBLs. In summary, this study found that NEFAs induce oxidative stress in PBLs and alter the expression of inflammation-related genes; meanwhile, vitamin E can reduce some of the effects caused by NEFAs. This result may suggest that vitamin E can assist bovine PBLs in resisting the immune suppression caused by an NEB during the transition period.
AbstractList High levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a vitamin-E-supplemented diet reduces reactive oxygen species (ROS) levels in the blood and diminishes immunosuppression in the transition period. However, whether the restoration of immune cell function occurs through the direct action of vitamin E in cells is still a topic that requires further discussion. Therefore, in this experiment, we aimed to investigate the effect of NEFAs on peripheral blood leukocytes (PBLs) and whether vitamin E mitigates the impact of NEFAs. We employed three groups: (1) blank, (2) NEFA only, and (3) pre-culturing with vitamin E before NEFA treatment (VENEFA). In peripheral blood mononuclear cells (PBMCs), there were no differences in vitamin E content among the three groups. However, in the vitamin E pre-treatment group, the vitamin E levels of polymorphonuclear neutrophils (PMNs) were significantly higher than those in the other two groups. NEFA levels increased malondialdehyde (MDA) levels in PBMCs, but pre-treatment with vitamin E reduced accumulation of MDA levels. Regarding the expression of proinflammatory genes, NEFAs increased the expression of interleukin-1β in PBMCs and colony-stimulating factor 2 in PMNs. Vitamin E pre-treatment restored the increase in interleukin-1β levels caused by NEFAs in PBMCs. None of the groups affected the phagocytosis of PMNs. Few studies have confirmed that NEFAs cause oxidative stress in bovine PBLs. In summary, this study found that NEFAs induce oxidative stress in PBLs and alter the expression of inflammation-related genes; meanwhile, vitamin E can reduce some of the effects caused by NEFAs. This result may suggest that vitamin E can assist bovine PBLs in resisting the immune suppression caused by an NEB during the transition period.
High levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a vitamin-E-supplemented diet reduces reactive oxygen species (ROS) levels in the blood and diminishes immunosuppression in the transition period. However, whether the restoration of immune cell function occurs through the direct action of vitamin E in cells is still a topic that requires further discussion. Therefore, in this experiment, we aimed to investigate the effect of NEFAs on peripheral blood leukocytes (PBLs) and whether vitamin E mitigates the impact of NEFAs. We employed three groups: (1) blank, (2) NEFA only, and (3) pre-culturing with vitamin E before NEFA treatment (VENEFA). In peripheral blood mononuclear cells (PBMCs), there were no differences in vitamin E content among the three groups. However, in the vitamin E pre-treatment group, the vitamin E levels of polymorphonuclear neutrophils (PMNs) were significantly higher than those in the other two groups. NEFA levels increased malondialdehyde (MDA) levels in PBMCs, but pre-treatment with vitamin E reduced accumulation of MDA levels. Regarding the expression of proinflammatory genes, NEFAs increased the expression of interleukin-1β in PBMCs and colony-stimulating factor 2 in PMNs. Vitamin E pre-treatment restored the increase in interleukin-1β levels caused by NEFAs in PBMCs. None of the groups affected the phagocytosis of PMNs. Few studies have confirmed that NEFAs cause oxidative stress in bovine PBLs. In summary, this study found that NEFAs induce oxidative stress in PBLs and alter the expression of inflammation-related genes; meanwhile, vitamin E can reduce some of the effects caused by NEFAs. This result may suggest that vitamin E can assist bovine PBLs in resisting the immune suppression caused by an NEB during the transition period.High levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a vitamin-E-supplemented diet reduces reactive oxygen species (ROS) levels in the blood and diminishes immunosuppression in the transition period. However, whether the restoration of immune cell function occurs through the direct action of vitamin E in cells is still a topic that requires further discussion. Therefore, in this experiment, we aimed to investigate the effect of NEFAs on peripheral blood leukocytes (PBLs) and whether vitamin E mitigates the impact of NEFAs. We employed three groups: (1) blank, (2) NEFA only, and (3) pre-culturing with vitamin E before NEFA treatment (VENEFA). In peripheral blood mononuclear cells (PBMCs), there were no differences in vitamin E content among the three groups. However, in the vitamin E pre-treatment group, the vitamin E levels of polymorphonuclear neutrophils (PMNs) were significantly higher than those in the other two groups. NEFA levels increased malondialdehyde (MDA) levels in PBMCs, but pre-treatment with vitamin E reduced accumulation of MDA levels. Regarding the expression of proinflammatory genes, NEFAs increased the expression of interleukin-1β in PBMCs and colony-stimulating factor 2 in PMNs. Vitamin E pre-treatment restored the increase in interleukin-1β levels caused by NEFAs in PBMCs. None of the groups affected the phagocytosis of PMNs. Few studies have confirmed that NEFAs cause oxidative stress in bovine PBLs. In summary, this study found that NEFAs induce oxidative stress in PBLs and alter the expression of inflammation-related genes; meanwhile, vitamin E can reduce some of the effects caused by NEFAs. This result may suggest that vitamin E can assist bovine PBLs in resisting the immune suppression caused by an NEB during the transition period.
Simple SummaryDuring the transition period, dairy cows mobilize fat reserves to produce non-esterified fatty acids (NEFAs) as an additional energy source to meet the energy demands for fetal growth, calving, and lactation. However, high levels of serum NEFAs result in increased oxidative stress and disease incidence, and impairment of the immune function of leukocytes in cows. Vitamin E is a critical fat-soluble antioxidant that reduces the impact of oxidative stress on immune cells and enhances the functioning of immune cells during the transition period. In this in vitro study, peripheral blood leukocytes (PBLs) were isolated from dry cows to investigate the effects of high NEFA levels on bovine peripheral leukocytes and to explore the protective role of vitamin E through pre-treatment. The findings indicate that high levels of NEFA induce oxidative stress in PBLs and alterations in cytokine expression, while pre-treatment with vitamin E partially mitigates NEFA effects on bovine PBLs. This may suggest that a serious negative energy balance leads to oxidative stress on immune cells and induces changes in inflammation-related cytokines during cows’ transition period. Supplementation with vitamin E could diminish some of the impacts caused by the negative energy balance on immune cells.AbstractHigh levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a vitamin-E-supplemented diet reduces reactive oxygen species (ROS) levels in the blood and diminishes immunosuppression in the transition period. However, whether the restoration of immune cell function occurs through the direct action of vitamin E in cells is still a topic that requires further discussion. Therefore, in this experiment, we aimed to investigate the effect of NEFAs on peripheral blood leukocytes (PBLs) and whether vitamin E mitigates the impact of NEFAs. We employed three groups: (1) blank, (2) NEFA only, and (3) pre-culturing with vitamin E before NEFA treatment (VENEFA). In peripheral blood mononuclear cells (PBMCs), there were no differences in vitamin E content among the three groups. However, in the vitamin E pre-treatment group, the vitamin E levels of polymorphonuclear neutrophils (PMNs) were significantly higher than those in the other two groups. NEFA levels increased malondialdehyde (MDA) levels in PBMCs, but pre-treatment with vitamin E reduced accumulation of MDA levels. Regarding the expression of proinflammatory genes, NEFAs increased the expression of interleukin-1β in PBMCs and colony-stimulating factor 2 in PMNs. Vitamin E pre-treatment restored the increase in interleukin-1β levels caused by NEFAs in PBMCs. None of the groups affected the phagocytosis of PMNs. Few studies have confirmed that NEFAs cause oxidative stress in bovine PBLs. In summary, this study found that NEFAs induce oxidative stress in PBLs and alter the expression of inflammation-related genes; meanwhile, vitamin E can reduce some of the effects caused by NEFAs. This result may suggest that vitamin E can assist bovine PBLs in resisting the immune suppression caused by an NEB during the transition period.
During the transition period, dairy cows mobilize fat reserves to produce non-esterified fatty acids (NEFAs) as an additional energy source to meet the energy demands for fetal growth, calving, and lactation. However, high levels of serum NEFAs result in increased oxidative stress and disease incidence, and impairment of the immune function of leukocytes in cows. Vitamin E is a critical fat-soluble antioxidant that reduces the impact of oxidative stress on immune cells and enhances the functioning of immune cells during the transition period. In this in vitro study, peripheral blood leukocytes (PBLs) were isolated from dry cows to investigate the effects of high NEFA levels on bovine peripheral leukocytes and to explore the protective role of vitamin E through pre-treatment. The findings indicate that high levels of NEFA induce oxidative stress in PBLs and alterations in cytokine expression, while pre-treatment with vitamin E partially mitigates NEFA effects on bovine PBLs. This may suggest that a serious negative energy balance leads to oxidative stress on immune cells and induces changes in inflammation-related cytokines during cows’ transition period. Supplementation with vitamin E could diminish some of the impacts caused by the negative energy balance on immune cells. High levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a vitamin-E-supplemented diet reduces reactive oxygen species (ROS) levels in the blood and diminishes immunosuppression in the transition period. However, whether the restoration of immune cell function occurs through the direct action of vitamin E in cells is still a topic that requires further discussion. Therefore, in this experiment, we aimed to investigate the effect of NEFAs on peripheral blood leukocytes (PBLs) and whether vitamin E mitigates the impact of NEFAs. We employed three groups: (1) blank, (2) NEFA only, and (3) pre-culturing with vitamin E before NEFA treatment (VENEFA). In peripheral blood mononuclear cells (PBMCs), there were no differences in vitamin E content among the three groups. However, in the vitamin E pre-treatment group, the vitamin E levels of polymorphonuclear neutrophils (PMNs) were significantly higher than those in the other two groups. NEFA levels increased malondialdehyde (MDA) levels in PBMCs, but pre-treatment with vitamin E reduced accumulation of MDA levels. Regarding the expression of proinflammatory genes, NEFAs increased the expression of interleukin-1β in PBMCs and colony-stimulating factor 2 in PMNs. Vitamin E pre-treatment restored the increase in interleukin-1β levels caused by NEFAs in PBMCs. None of the groups affected the phagocytosis of PMNs. Few studies have confirmed that NEFAs cause oxidative stress in bovine PBLs. In summary, this study found that NEFAs induce oxidative stress in PBLs and alter the expression of inflammation-related genes; meanwhile, vitamin E can reduce some of the effects caused by NEFAs. This result may suggest that vitamin E can assist bovine PBLs in resisting the immune suppression caused by an NEB during the transition period.
During the transition period, dairy cows mobilize fat reserves to produce non-esterified fatty acids (NEFAs) as an additional energy source to meet the energy demands for fetal growth, calving, and lactation. However, high levels of serum NEFAs result in increased oxidative stress and disease incidence, and impairment of the immune function of leukocytes in cows. Vitamin E is a critical fat-soluble antioxidant that reduces the impact of oxidative stress on immune cells and enhances the functioning of immune cells during the transition period. In this in vitro study, peripheral blood leukocytes (PBLs) were isolated from dry cows to investigate the effects of high NEFA levels on bovine peripheral leukocytes and to explore the protective role of vitamin E through pre-treatment. The findings indicate that high levels of NEFA induce oxidative stress in PBLs and alterations in cytokine expression, while pre-treatment with vitamin E partially mitigates NEFA effects on bovine PBLs. This may suggest that a serious negative energy balance leads to oxidative stress on immune cells and induces changes in inflammation-related cytokines during cows’ transition period. Supplementation with vitamin E could diminish some of the impacts caused by the negative energy balance on immune cells.
Audience Academic
Author Wang, Chien-Kai
Lin, Wei-Chen
Chan, Jacky Peng-Wen
Li, Cheng-Yan
Moonmanee, Tossapol
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Keywords negative energy balance (NEB)
non-esterified fatty acids (NEFA)
peripheral blood leukocytes
transition period
vitamin E
oxidative stress
pro-inflammatory
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Snippet High levels of non-esterified fatty acids (NEFAs) during the transition period lead to increased oxidative stress and immunosuppression in cows. Feeding them a...
During the transition period, dairy cows mobilize fat reserves to produce non-esterified fatty acids (NEFAs) as an additional energy source to meet the energy...
Simple SummaryDuring the transition period, dairy cows mobilize fat reserves to produce non-esterified fatty acids (NEFAs) as an additional energy source to...
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StartPage 1079
SubjectTerms Blood
cattle
colony-stimulating factors
Cytokines
Dairy cattle
diet
Disease susceptibility
Ethylenediaminetetraacetic acid
Fatty acids
Granulocytes
Health risk assessment
Health risks
immunosuppression
Immunotherapy
Leukocytes
malondialdehyde
negative energy balance (NEB)
Neutrophils
non-esterified fatty acids (NEFA)
Oxidative stress
Penicillin
peripheral blood leukocytes
phagocytosis
Plasma
pro-inflammatory
protective effect
reactive oxygen species
Selenium
Vitamin E
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Title The Protective Role of Vitamin E against Oxidative Stress and Immunosuppression Induced by Non-Esterified Fatty Acids in Bovine Peripheral Blood Leukocytes
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Volume 14
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