Key result
17 beta-estradiol reduced cholesterol accumulation to one seventh in the undamaged upper abdominal aorta (P=0.001), but this antiatherogenic effect was abolished by balloon catheter injury.
Why the study?
Does 17 beta-estradiol prevent aortic cholesterol accumulation in ovariectomized, cholesterol-clamped rabbits with and without endothelial injury?
Does 17 beta-estradiol prevent aortic cholesterol accumulation in ovariectomized, cholesterol-clamped rabbits with and without endothelial injury?
The antiatherogenic effect of estrogen on the arterial wall is abolished by balloon catheter injury, suggesting an intact endothelium is crucial for its protective effects.
Intact endothelium may be required for estrogen vascular protection; hypothesis-generating for endothelial injury effects in atherosclerosis.
The purpose of this study was to investigate the importance of an intact endothelial cell layer for the direct antiatherogenic effect of estrogen on the arterial wall. Thirty rabbits were bilaterally ovariectomized and subjected to mechanical injury of the endothelium by balloon catheterization of the upper thoracic aorta. Immediately after the operation, treatment was initiated with either 17 beta-estradiol or placebo given intramuscularly. All rabbits were clamped at a similar plasma cholesterol level from 1 week before the operation until the experiment was terminated 13 weeks later. In the undamaged aorta, ie, the aortic arch, the lower thoracic aorta, and the upper abdominal aorta, the estrogen-treated rabbits had one third (P = .06), one sixth (P = .002), and one seventh (P = .001), respectively, the accumulation of cholesterol of the placebo-treated rabbits. In the upper thoracic aorta that had been subjected to mechanical injury of the endothelium, however, aortic cholesterol accumulation was not significantly different between the two groups. Similar results were obtained by histological evaluation of the aortic tissues. Immunohistochemical staining with antibodies against macrophages, smooth muscle cells, and T lymphocytes revealed no significant differences in the intimal distribution of cells between estrogen- and placebo-treated rabbits, except for a higher number of T lymphocytes per unit intimal area of the undamaged aortic arch (P < .0005) in the estrogen-treated-rabbits than the placebo-treated rabbits. This is the first study to demonstrate that the antiatherogenic effect of estrogen is abolished by balloon catheter injury in cholesterol-clamped rabbits. These results may indicate that an intact endothelial cell layer is crucial for the direct antiatherogenic effect of estrogen on the arterial wall.
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Holm et al. (1997) studied Atherosclerosis (n=30). 17 beta-estradiol vs. placebo was evaluated on Aortic cholesterol accumulation. 17 beta-estradiol reduced cholesterol accumulation to one seventh in the undamaged upper abdominal aorta (P=0.001), but this antiatherogenic effect was abolished by balloon catheter injury.
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