Comparative Assessment of Beeswax Alcohol and Coenzyme Q10 (CoQ10) to Prevent Liver Aging, Organ Damage, and Oxidative Stress in Hyperlipidemic Zebrafish Exposed to D-Galactose: A 12-Week Dietary Intervention

The current study was designed to compare in vivo efficacy between beeswax alcohol (BWA) and coenzyme Q<sub>10</sub> (CoQ<sub>10</sub>) to treat fatty liver changes, oxidative stress, and damages in major organs of zebrafish by 12 weeks with high-cholesterol (HC) and galactose (Gal) supplementation. At week 12, the HC control and HC+Gal control groups showed 96% and 92% survivability, respectively, while co-supplementation of the 0.5% BWA and 1.0% BWA groups exhibited 96% and 100% survivability. However, co-supplementation of the 0.5% CoQ<sub>10</sub> and 1.0% CoQ<sub>10</sub> groups revealed the lowest survivability, around 92% and 89%, respectively. The 0.5% BWA and 1.0% BWA groups showed 21% (<i>p</i> < 0.001) and 41% (<i>p</i> < 0.001), respectively, lower total cholesterol (TC) than the HC+Gal control, while the 1.0% CoQ<sub>10</sub> group showed only 15% lower TC than the control. Interestingly, the 0.5% BWA and 1.0% BWA groups showed 22% (<i>p</i> < 0.001) and 38% (<i>p</i> < 0.001), respectively, lower triglyceride (TG) than the HC+Gal control. However, both the 0.5% CoQ<sub>10</sub> and 1.0% CoQ<sub>10</sub> groups showed similar TG levels as the control, suggesting that CoQ<sub>10</sub> supplementation had no effect on lowering serum TG. The 1.0% BWA group showed the highest plasma HDL-C and HDL-C/TC (%) up to 3.2-fold and 5.5-fold, respectively, higher than those of the HC+Gal control, while the 1.0% CoQ<sub>10</sub> group showed 2.4-fold and 2.8-fold higher plasma HDL-C and HDL-C/TC (%), respectively, than the control. The plasma aspartate transaminase (AST) and alanine transaminase (ALT) levels were lowest in the 1.0% BWA group, 51% and 72%, respectively, lower than HC+Gal control, suggesting the lowest extent of hepatic damage. In hepatic tissue, neutrophil infiltration and interleukin (IL)-6 production were the lowest in the 1.0% BWA group, around 67% and 85%, respectively, lower than the HC+Gal control. Fatty liver change, cellular apoptosis, and cell senescence in hepatic tissue were remarkably lowered in the 1.0% BWA group, while the CoQ<sub>10</sub> group showed much less effect than the BWA group. In kidney, ovary, and testis tissue, the 1.0% BWA group showed the lowest production of reactive oxygen species, the extent of cellular senescence, and cellular apoptosis with the healthiest cell morphology. In conclusion, supplementation of BWA remarkably protected the liver, kidney, ovary, and testis from oxidative damage by cholesterol and galactose consumption, with the least serum AST and ALT levels, inflammatory parameters, and senescence markers.

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Publication Details

Journal
Pharmaceuticals
Published
2024-09-23
DOI
https://doi.org/10.3390/ph17091250
Citations
6
Primary Topic
Coenzyme Q10 studies and effects
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article
Field-Weighted Citation Impact
1.40
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article

Comparative Assessment of Beeswax Alcohol and Coenzyme Q10 (CoQ10) to Prevent Liver Aging, Organ Damage, and Oxidative Stress in Hyperlipidemic Zebrafish Exposed to D-Galactose: A 12-Week Dietary Intervention

Yunki Lee, Kyung‐Hyun Cho, Ashutosh Bahuguna, Ji-Eun Kim et al.
6 citations
Pharmaceuticals
Coenzyme Q10 studies and effects
1.40
article

Comparative Assessment of Beeswax Alcohol and Coenzyme Q10 (CoQ10) to Prevent Liver Aging, Organ Damage, and Oxidative Stress in Hyperlipidemic Zebrafish Exposed to D-Galactose: A 12-Week Dietary Intervention

Yunki Lee, Kyung‐Hyun Cho, Ashutosh Bahuguna, Ji-Eun Kim, Sang‐Hyuk Lee
article en
6 citations

Abstract

The current study was designed to compare in vivo efficacy between beeswax alcohol (BWA) and coenzyme Q<sub>10</sub> (CoQ<sub>10</sub>) to treat fatty liver changes, oxidative stress, and damages in major organs of zebrafish by 12 weeks with high-cholesterol (HC) and galactose (Gal) supplementation. At week 12, the HC control and HC+Gal control groups showed 96% and 92% survivability, respectively, while co-supplementation of the 0.5% BWA and 1.0% BWA groups exhibited 96% and 100% survivability. However, co-supplementation of the 0.5% CoQ<sub>10</sub> and 1.0% CoQ<sub>10</sub> groups revealed the lowest survivability, around 92% and 89%, respectively. The 0.5% BWA and 1.0% BWA groups showed 21% (<i>p</i> < 0.001) and 41% (<i>p</i> < 0.001), respectively, lower total cholesterol (TC) than the HC+Gal control, while the 1.0% CoQ<sub>10</sub> group showed only 15% lower TC than the control. Interestingly, the 0.5% BWA and 1.0% BWA groups showed 22% (<i>p</i> < 0.001) and 38% (<i>p</i> < 0.001), respectively, lower triglyceride (TG) than the HC+Gal control. However, both the 0.5% CoQ<sub>10</sub> and 1.0% CoQ<sub>10</sub> groups showed similar TG levels as the control, suggesting that CoQ<sub>10</sub> supplementation had no effect on lowering serum TG. The 1.0% BWA group showed the highest plasma HDL-C and HDL-C/TC (%) up to 3.2-fold and 5.5-fold, respectively, higher than those of the HC+Gal control, while the 1.0% CoQ<sub>10</sub> group showed 2.4-fold and 2.8-fold higher plasma HDL-C and HDL-C/TC (%), respectively, than the control. The plasma aspartate transaminase (AST) and alanine transaminase (ALT) levels were lowest in the 1.0% BWA group, 51% and 72%, respectively, lower than HC+Gal control, suggesting the lowest extent of hepatic damage. In hepatic tissue, neutrophil infiltration and interleukin (IL)-6 production were the lowest in the 1.0% BWA group, around 67% and 85%, respectively, lower than the HC+Gal control. Fatty liver change, cellular apoptosis, and cell senescence in hepatic tissue were remarkably lowered in the 1.0% BWA group, while the CoQ<sub>10</sub> group showed much less effect than the BWA group. In kidney, ovary, and testis tissue, the 1.0% BWA group showed the lowest production of reactive oxygen species, the extent of cellular senescence, and cellular apoptosis with the healthiest cell morphology. In conclusion, supplementation of BWA remarkably protected the liver, kidney, ovary, and testis from oxidative damage by cholesterol and galactose consumption, with the least serum AST and ALT levels, inflammatory parameters, and senescence markers.

PharmaceuticalsVol. 17(9)
Openalex Percentile: Top 19%
Coenzyme Q10 studies and effects
1.40
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