Co-administration of berberine and plant stanols synergistically reduces plasma cholesterol in rats

Abstract The objective of the present study was to determine the beneficial effects and the safety of oral administration of the combination of berberine (BBR) and plant stanols (PS) on plasma lipid profiles in male Sprague–Dawley rats. Four groups of animals were fed a cornstarch–casein–sucrose-bas...

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Published inAtherosclerosis Vol. 201; no. 1; pp. 101 - 107
Main Authors Jia, Xiaoming, Chen, Yanfeng, Zidichouski, Jeffrey, Zhang, Junzeng, Sun, Changhao, Wang, Yanwen
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ireland Ltd 01.11.2008
Elsevier
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Abstract Abstract The objective of the present study was to determine the beneficial effects and the safety of oral administration of the combination of berberine (BBR) and plant stanols (PS) on plasma lipid profiles in male Sprague–Dawley rats. Four groups of animals were fed a cornstarch–casein–sucrose-based high-cholesterol (2%, w:w) and high-fat (27.5%) diet. Three treatment groups were supplemented with either BBR (100 mg kg−1 body weight d−1 ), PS (1% in diet, w:w), or the combination of both (BBRPS). After 6 wk, animals were sacrificed and followed immediately with the collection of blood and organ samples. Lipid analysis revealed that PS lowered plasma total cholesterol (T-C) by 18% ( p = 0.067) and non-HDL-cholesterol (non-HDL-C) by 29% ( p = 0.013) as compared with the control, while BBR had no effect on both T-C and non-HDL-C. The combination treatment of BBRPS reduced plasma T-C by 41% ( p = 0.0002) and non-HDL-C by 59% ( p < 0.0001) compared to the control group. BBR reduced plasma TG levels by 31% at a marginal significance relative to the control ( p = 0.054), whereas PS had no effect. BBRPS showed an additive effect of BBR and PS on plasma TAG. PS and BBRPS both decreased liver cholesterol ( p = 0.0027 and 0.0002, respectively). BBR and PS, either alone or in combination, did not show any toxic effects as assessed by plasma concentration of hepatic biochemical parameters. These results demonstrate that BBR and PS, when combined, synergistically lower plasma cholesterol levels and significantly reduce liver cholesterol, without the observation of any toxic effects.
AbstractList The objective of the present study was to determine the beneficial effects and the safety of oral administration of the combination of berberine (BBR) and plant stanols (PS) on plasma lipid profiles in male Sprague–Dawley rats. Four groups of animals were fed a cornstarch–casein–sucrose-based high-cholesterol (2%, w:w) and high-fat (27.5%) diet. Three treatment groups were supplemented with either BBR (100 mg kg −1 body weight d −1), PS (1% in diet, w:w), or the combination of both (BBRPS). After 6 wk, animals were sacrificed and followed immediately with the collection of blood and organ samples. Lipid analysis revealed that PS lowered plasma total cholesterol (T-C) by 18% ( p = 0.067) and non-HDL-cholesterol (non-HDL-C) by 29% ( p = 0.013) as compared with the control, while BBR had no effect on both T-C and non-HDL-C. The combination treatment of BBRPS reduced plasma T-C by 41% ( p = 0.0002) and non-HDL-C by 59% ( p < 0.0001) compared to the control group. BBR reduced plasma TG levels by 31% at a marginal significance relative to the control ( p = 0.054), whereas PS had no effect. BBRPS showed an additive effect of BBR and PS on plasma TAG. PS and BBRPS both decreased liver cholesterol ( p = 0.0027 and 0.0002, respectively). BBR and PS, either alone or in combination, did not show any toxic effects as assessed by plasma concentration of hepatic biochemical parameters. These results demonstrate that BBR and PS, when combined, synergistically lower plasma cholesterol levels and significantly reduce liver cholesterol, without the observation of any toxic effects.
The objective of the present study was to determine the beneficial effects and the safety of oral administration of the combination of berberine (BBR) and plant stanols (PS) on plasma lipid profiles in male Sprague-Dawley rats. Four groups of animals were fed a cornstarch-casein-sucrose-based high-cholesterol (2%, w:w) and high-fat (27.5%) diet. Three treatment groups were supplemented with either BBR (100mgkg(-1)bodyweightd(-1)), PS (1% in diet, w:w), or the combination of both (BBRPS). After 6 wk, animals were sacrificed and followed immediately with the collection of blood and organ samples. Lipid analysis revealed that PS lowered plasma total cholesterol (T-C) by 18% (p=0.067) and non-HDL-cholesterol (non-HDL-C) by 29% (p=0.013) as compared with the control, while BBR had no effect on both T-C and non-HDL-C. The combination treatment of BBRPS reduced plasma T-C by 41% (p=0.0002) and non-HDL-C by 59% (p<0.0001) compared to the control group. BBR reduced plasma TG levels by 31% at a marginal significance relative to the control (p=0.054), whereas PS had no effect. BBRPS showed an additive effect of BBR and PS on plasma TAG. PS and BBRPS both decreased liver cholesterol (p=0.0027 and 0.0002, respectively). BBR and PS, either alone or in combination, did not show any toxic effects as assessed by plasma concentration of hepatic biochemical parameters. These results demonstrate that BBR and PS, when combined, synergistically lower plasma cholesterol levels and significantly reduce liver cholesterol, without the observation of any toxic effects.
Abstract The objective of the present study was to determine the beneficial effects and the safety of oral administration of the combination of berberine (BBR) and plant stanols (PS) on plasma lipid profiles in male Sprague–Dawley rats. Four groups of animals were fed a cornstarch–casein–sucrose-based high-cholesterol (2%, w:w) and high-fat (27.5%) diet. Three treatment groups were supplemented with either BBR (100 mg kg−1 body weight d−1 ), PS (1% in diet, w:w), or the combination of both (BBRPS). After 6 wk, animals were sacrificed and followed immediately with the collection of blood and organ samples. Lipid analysis revealed that PS lowered plasma total cholesterol (T-C) by 18% ( p = 0.067) and non-HDL-cholesterol (non-HDL-C) by 29% ( p = 0.013) as compared with the control, while BBR had no effect on both T-C and non-HDL-C. The combination treatment of BBRPS reduced plasma T-C by 41% ( p = 0.0002) and non-HDL-C by 59% ( p < 0.0001) compared to the control group. BBR reduced plasma TG levels by 31% at a marginal significance relative to the control ( p = 0.054), whereas PS had no effect. BBRPS showed an additive effect of BBR and PS on plasma TAG. PS and BBRPS both decreased liver cholesterol ( p = 0.0027 and 0.0002, respectively). BBR and PS, either alone or in combination, did not show any toxic effects as assessed by plasma concentration of hepatic biochemical parameters. These results demonstrate that BBR and PS, when combined, synergistically lower plasma cholesterol levels and significantly reduce liver cholesterol, without the observation of any toxic effects.
Author Sun, Changhao
Wang, Yanwen
Chen, Yanfeng
Zidichouski, Jeffrey
Jia, Xiaoming
Zhang, Junzeng
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Issue 1
Keywords triacylglycerides
PS
LDL-C
Toxicity
HDL-cholesterol
T-C
acetyl-CoA carboxylase
AMP-activated protein kinase
berberine chloride
total cholesterol
Plasma triacylglyceride
body weight
HDL-C
LDL-cholesterol
BBR
BBRPS
BW
non-HDL-C
Liver cholesterol
ACC
Berberine
Plasma cholesterol
non-HDL-cholesterol (VLDL-cholesterol + intermediate density lipoprotein cholesterol + LDL-cholesterol)
Rats
combination of BBR and plant stanols
control
CT
AMPK
TAG
plant stanols
Plant stanols
Rat
Digestive system
Liver
Rodentia
Lipids
Cardiovascular disease
Cholesterol
Vascular disease
Vertebrata
Mammalia
Animal
Atherosclerosis
Language English
License CC BY 4.0
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PMID 18430428
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Snippet Abstract The objective of the present study was to determine the beneficial effects and the safety of oral administration of the combination of berberine (BBR)...
The objective of the present study was to determine the beneficial effects and the safety of oral administration of the combination of berberine (BBR) and...
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SubjectTerms Administration, Oral
Animals
Anticholesteremic Agents - administration & dosage
Atherosclerosis (general aspects, experimental research)
Berberine
Berberine - administration & dosage
Biological and medical sciences
Blood and lymphatic vessels
Cardiology. Vascular system
Cardiovascular
Cholesterol - blood
Coronary heart disease
Diet, Atherogenic
Drug Therapy, Combination
Heart
Lipoproteins - blood
Liver cholesterol
Male
Medical sciences
Phytosterols - administration & dosage
Plant stanols
Plasma cholesterol
Plasma triacylglyceride
Rats
Rats, Sprague-Dawley
Sitosterols - administration & dosage
Toxicity
Triglycerides - blood
Title Co-administration of berberine and plant stanols synergistically reduces plasma cholesterol in rats
URI https://www.clinicalkey.es/playcontent/1-s2.0-S002191500800172X
https://dx.doi.org/10.1016/j.atherosclerosis.2008.03.008
https://www.ncbi.nlm.nih.gov/pubmed/18430428
Volume 201
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