Related Experiment Video
Updated: Aug 17, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Oxidized lipoproteins inhibit endothelium-dependent vasodilation. Effects of pressure and high-density lipoprotein
J Galle1, M Ochslen, P Schollmeyer
1Department of Medicine, University Hospital of Freiburg, Germany.
Insights
High blood pressure and oxidized LDLs impair blood vessel dilation. However, high-density lipoproteins (HDLs) protect against this damage, preserving endothelial function under elevated pressure.
Area of Science:
- Cardiovascular Physiology
- Endothelial Function
- Lipoprotein Metabolism
Background:
- Hypertension and low-density lipoproteins (LDLs) are known to impair endothelium-dependent vasodilation.
- The interaction between elevated transmural pressure and LDLs on endothelial function requires further investigation.
- High-density lipoproteins (HDLs) are recognized for their protective role in cardiovascular health.
Purpose of the Study:
- To investigate the effect of high transmural pressure on the interaction between low-density lipoproteins (LDLs) and endothelium-dependent dilation in vitro.
- To determine if high-density lipoproteins (HDLs) can preserve endothelial function under conditions of elevated pressure and LDL exposure.
- To examine the mechanism by which oxidized LDLs attenuate dilations under high pressure.
Main Methods:
- Rabbit renal arteries were isolated and subjected to varying transmural pressures (30 vs. 100 mm Hg).
- Arteries were perfused with native or oxidized LDLs and stimulated with acetylcholine to assess endothelium-dependent dilation.
- Endothelium-independent dilation was measured using glyceroltrinitrate; lipoprotein infiltration was visualized using Sudan III staining.
Main Results:
- High transmural pressure did not affect acetylcholine-induced dilation under low-pressure conditions.
- Oxidized LDLs, but not native LDLs, attenuated endothelium-dependent dilations under high-pressure conditions.
- HDLs prevented the attenuation of dilations by oxidized LDLs and inhibited lipoprotein infiltration into the vessel wall.
Conclusions:
- Elevated transmural pressure potentiates the detrimental effects of oxidized LDLs on endothelial function.
- HDLs exert a protective effect by preserving endothelial dilatory responses and preventing LDL infiltration.
- These findings highlight the critical role of HDL in mitigating vascular damage associated with hypertension and dyslipidemia.
Abstract:
Hypertension and atherogenic low-density lipoproteins cause attenuation of endothelium-dependent dilations in vivo. We investigated a potential interference of high transmural pressure with the effects of low-density lipoproteins on endothelium-dependent dilation in vitro. Furthermore, we determined whether high-density lipoproteins preserve endothelial function. Endothelium-intact rabbit renal arteries were isolated, placed in an organ bath, perfused intraluminally with Tyrode's solution, and exposed to different degrees of transmural pressure and native or oxidized low-density lipoproteins. In preconstricted arteries perfused under low-pressure conditions (30 mm Hg), acetylcholine dose dependently elicited endothelium-dependent dilations that were not altered by increasing the perfusion pressure to 100 mm Hg for 90 minutes (high-pressure conditions). Incubation of the arteries with native or oxidized low-density lipoproteins (0.2 and 1 mg/mL for 60 minutes, respectively) under low-pressure conditions did not attenuate acetylcholine-induced dilations. However, under high-pressure conditions dilations were dose dependently attenuated by oxidized but not by native low-density lipoproteins. Endothelium-independent dilations to glyceroltrinitrate (0.001 to 3 mumol/L) were not affected. Preincubation of the segments with high-density lipoproteins (0.5 mg/mL, 30 minutes) prevented attenuation of dilator responses. The attenuation of endothelium-dependent dilations by oxidized low-density lipoproteins under high-pressure conditions was accompanied by a transmural, dose-dependent infiltration of the vessel wall with lipoprotein, as detected by light microscopy of cryostat sections stained with Sudan III. This infiltration was prevented by high-density lipoprotein. Under low-pressure conditions no lipoprotein infiltration was visible. In segments incubated with native low-density lipoprotein, no lipoprotein infiltration was detectable.(ABSTRACT TRUNCATED AT 250 WORDS)
Related Concept Videos
Lipid-derived Compounds in the Human Body
Fat-soluble Vitamins
Fat-soluble vitamins, including vitamins A, D, E, and K, are required in minimal quantities, but their deficiencies can lead to severely abnormal physiological conditions. For example, vitamin A deficiency can cause night blindness, dry skin, delayed...
Lipid-Lowering Drugs: Statins and Miscellaneous Agents
Cholesterol: Significance and Regulation
Considering cholesterol and...
Coronary Artery Disease II: Pathophysiology
Atherosclerosis I: Introduction
Peripheral Artery Disease I: Introduction

