Vitamin E slows the progression of hypercholesterolemia-induced oxidative stress in heart, liver and kidney
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Updated: May 21, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Kailash Prasad1, Erick D McNair, A Mabood Qureshi
1Department of Physiology, College of medicine, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada. k.prasad@usask.ca
Insights
Vitamin E reduces oxidative stress in the heart, liver, and kidney caused by high cholesterol. This effect is linked to the duration of hypercholesterolemia, with the heart being most susceptible.
Area of Science:
- Biochemistry
- Cardiovascular Biology
- Nephrology
Background:
- Hypercholesterolemia is a known risk factor for cardiovascular disease.
- Oxidative stress plays a critical role in the pathogenesis of hypercholesterolemia-related organ damage.
- The impact of hypercholesterolemia on oxidative stress in multiple organs and the potential protective effects of vitamin E require further investigation.
Purpose of the Study:
- To compare the levels of oxidative stress in the heart, liver, and kidney of rabbits with hypercholesterolemia.
- To determine if the observed oxidative stress is dependent on the duration of hypercholesterolemia.
- To evaluate the efficacy of vitamin E in mitigating hypercholesterolemia-induced oxidative stress in these organs.
Main Methods:
- Rabbits were fed a cholesterol-rich diet for varying durations, with one group receiving vitamin E supplementation.
- Total cholesterol levels were measured in blood samples.
- Oxidative stress markers, including malondialdehyde (MDA) and chemiluminescence (CL), were assessed in heart, liver, and kidney tissues.
Main Results:
- Hypercholesterolemia significantly increased malondialdehyde (MDA) levels in the heart, liver, and kidney, with the heart showing the most substantial increase.
- The elevation in MDA levels was positively correlated with the duration of the cholesterol-rich diet.
- Vitamin E supplementation reduced MDA levels in all investigated organs without affecting total cholesterol levels.
Conclusions:
- Hypercholesterolemia induces significant oxidative stress in the heart, liver, and kidney, with varying susceptibility among organs.
- The progression of oxidative stress is directly related to the duration of hypercholesterolemia.
- Vitamin E effectively attenuates the development of oxidative stress in these organs, highlighting its potential therapeutic role.
Abstract:
Vitamin E suppresses the hypercholesterolemia-induced oxidative stress in the heart. The objectives were to investigate if: (a) hypercholesterolemia-induced oxidative stress is similar in heart, liver, and kidney, and is dependent upon duration of hypercholesterolemia; and (b) vitamin E slows the progression of oxidative stress in these organs. The rabbits were assigned to 4 groups: I, regular diet (2 months); II, 0.25 % cholesterol diet (2 months); III, 0.25 % cholesterol diet (4 months); and IV, 0.25 % cholesterol diet (2 months) followed by 0.25 % cholesterol diet plus vitamin E (2 months). Blood samples were collected before and at the end of protocol for the measurement of total cholesterol (TC). Hearts, livers, and kidneys were removed at the end of the protocol under anesthesia for the measurement of oxidative parameters, malondialdehyde (MDA), and chemiluminescence (CL). The basal MDA levels in the heart, liver, and kidney of rabbits in Group I were similar, but increased to 14.65-, 3.18-, and 10.35-fold, respectively, with hypercholesterolemia. The increases in MDA levels were dependent upon the duration of hypercholesterolemia. Vitamin E did not alter the TC levels, but reduced the MDA levels in all organs. Hypercholesterolemia and vitamin E had variable effects on CL activity. In conclusion, (i) hypercholesterolemia induces oxidative stress in heart, liver, and kidney, the heart being the most and the liver the least susceptible to oxidative stress; (ii) oxidative stress is positively associated with duration of hypercholesterolemia; and (iii) vitamin E slows the progression of oxidative stress in these organs.
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