4.6 Article

Hypertension Enhances Advanced Atherosclerosis and Induces Cardiac Death in Watanabe Heritable Hyperlipidemic Rabbits

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 188, Issue 12, Pages 2936-2947

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajpath.2018.08.007

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Funding

  1. National Key Research and Development Program of China [2016YFE0126000]
  2. National Natural Science Foundation of China [81570392, 81770457]
  3. JSPS KAKENHI [15H04718]
  4. JSPS-CAS under the Japan China Research Cooperative Program
  5. Natural Science Foundation of Shaanxi Province [2017JZ028]
  6. NIH [R01HL117491, R01HL129778]

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Hypertension is a major risk factor for the development of atherosclerosis. Cardiovascular risk has been reported to be significantly increased in hyperlipidemic patients with hypertension. However, it is not clear whether hypertension can directly destabilize plaques, thereby enhancing cardiovascular events. To examine whether hypertension enhances the development of atherosclerosis and increases plaque vulnerability, we generated hypertensive Watanabe heritable hyperlipidemic (WHHL) rabbits by surgical removal of one kidney and partial ligation of the other renal artery and compared the nature of aortic and coronary atherosclerosis in hypertensive WHHL rabbits with normotensive WHHL rabbits. All hypertensive WHHL rabbits died from 34 to 56 weeks after surgery, whereas no normotensive WHHL rabbits died. Pathologic examinations revealed that hypertensive WHHL rabbits showed different degrees of myocardial infarction caused by severe coronary stenosis along with myocardial hypertrophy. Furthermore, aortic lesions in hypertensive WHHL rabbits exhibited a higher frequency of intraplaque hemorrhage and vulnerable plaques than those in normotensive WHHL rabbits. These results indicate that hypertension induced by the surgical removal of one kidney and partial ligation of the other renal artery method in WHHL rabbits may not only enhance the development of atherosclerosis but also destabilize the plaques, increasing cardiac death.

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