Literature DB >> 1773499

Overview: studies on spontaneous hypertension-development from animal models toward man.

Y Yamori1.   

Abstract

The development of genetic rat models for research on hypertension, stroke and other cardiovascular diseases (CVD) such as spontaneously hypertensive rats (SHR) and stroke-prone SHR (SHRSP) have contributed not only to the elucidation of the pathogenesis of hypertension-related CVD but also to their prediction and prevention. Since both genetic and environmental factors are involved in the pathogenesis of CVD as extensively studied so far on these models, the detection of the early pathogenic mechanisms related to the genetic factors and the control of environmental factors such as dietary improvement are useful as predictive and preventive measures against CVD. Sympathetic overresponsiveness, early development of cardiovascular hypertrophy, increased salt sensitivity and membrane or transport abnormalities in vascular smooth muscle cells (VSMC) from SHR and SHRSP, possibly related to the pathogenesis of hypertension, are so far regarded as predictors for hypertension partly applicable to human hypertension. Genetic pathogenic mechanisms of stroke in SHRSP which have been proven to be greatly influenced also by dietary factors are hypertension-induced VSMC degeneration and necrosis of intracerebral arteries due to local nutritional disturbance. One of predictors of stroke related to the pathogenic mechanisms is reduction of regional cerebral blood flow. On the other hand, the control of environmental factors, especially nutrition and diets such as intakes of animal and vegetable proteins, some amino acids and fatty acids, potassium, calcium, magnesium, dietary fibers, etc., have been experimentally demonstrated to be effective for the prevention of CVD in these genetic models, and the applicability of these experimental findings to the CVD prevention in man is now supported from our world-wide epidemiological studies (WHO CARDIAC Study).

Entities:  

Mesh:

Year:  1991        PMID: 1773499     DOI: 10.3109/10641969109042066

Source DB:  PubMed          Journal:  Clin Exp Hypertens A        ISSN: 0730-0077


  11 in total

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Review 2.  Rodent Models of Vascular Cognitive Impairment.

Authors:  Yi Yang; Shihoko Kimura-Ohba; Jeffrey Thompson; Gary A Rosenberg
Journal:  Transl Stroke Res       Date:  2016-08-08       Impact factor: 6.829

3.  Effect of hypertension and carotid occlusion on brain parenchymal arteriole structure and reactivity.

Authors:  Julie G Sweet; Siu-Lung Chan; Marilyn J Cipolla
Journal:  J Appl Physiol (1985)       Date:  2015-08-20

4.  Nutritional prevention on hypertension, cerebral hemodynamics and thrombosis in stroke-prone spontaneously hypertensive rats.

Authors:  Takanori Noguchi; Katsumi Ikeda; Yasuto Sasaki; Yukio Yamori
Journal:  Cell Mol Neurobiol       Date:  2004-10       Impact factor: 5.046

5.  Substrain differences, gender, and age of spontaneously hypertensive rats critically determine infarct size produced by distal middle cerebral artery occlusion.

Authors:  Hitonori Takaba; Kenji Fukuda; Hiroshi Yao
Journal:  Cell Mol Neurobiol       Date:  2004-10       Impact factor: 5.046

Review 6.  Application of genome editing technologies in rats for human disease models.

Authors:  Kazuto Yoshimi; Tomoji Mashimo
Journal:  J Hum Genet       Date:  2017-11-20       Impact factor: 3.172

Review 7.  Rodent Models of Vascular Cognitive Impairment.

Authors:  Qing-Zhang Tuo; Jin-Jun Zou; Peng Lei
Journal:  J Mol Neurosci       Date:  2020-10-27       Impact factor: 3.444

Review 8.  Nitric oxide and coronary vascular endothelium adaptations in hypertension.

Authors:  Andrew S Levy; Justin C S Chung; Jeffrey T Kroetsch; James W E Rush
Journal:  Vasc Health Risk Manag       Date:  2009-12-29

9.  Assessment of oxidative stress and antioxidant property using electron spin resonance (ESR) spectroscopy.

Authors:  Masaichi-Chang-Il Lee
Journal:  J Clin Biochem Nutr       Date:  2012-12-28       Impact factor: 3.114

10.  Allele-specific genome editing and correction of disease-associated phenotypes in rats using the CRISPR-Cas platform.

Authors:  K Yoshimi; T Kaneko; B Voigt; T Mashimo
Journal:  Nat Commun       Date:  2014-06-26       Impact factor: 14.919

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