M.Sc. Xiumin Wu's dissertation of
Arterial Function in Experimental Hypertension. Influence of Dietary Potassium
will be presented for public discussion on 2nd June 2000 at 12 o'clock in the small
auditorium of Building B, Medical School of the University of Tampere,
Medisiinarinkatu 3, Tampere.
The opponent is professor Peter A. Doris (University of Texas).
The chairman is professor Pauli Ylitalo.
Wu was born in Beijing, China, 29.12.1957. She graduated as
M.Sc. in 1988 (Zhejiang Traditional Chinese Medical University). Wu has served
as researcher fellow and teaching lecturer in Department of
pharmaceutical and New drug developing Centre Liaoning TCM University (Shengyang, China)
years 1982-1986, researcher fellow and MS student in pharmacophore
Department Zhejiang Traditional Chinese Medicine (TCM) University (Hangzhou, China)
years 1986-1988, researcher fellow and group leader in R & D Department
Guangshen Medical Co. Ltd of State Medical Bureau (Shenzhen, China) years 1988-1990,
researcher fellow and Manager in R & D Department Fangda
Medical Co. Ltd. (Shenzhen, China) years 1990-1992, PhD. Student
in Department of Pharmacology University of Tampere (Tampere, Finland) years 1992-1997 and
chemist in developing department of Wallac Oy (Turku, Finland) since year 1998.
Wu's dissertation is published in publication series Acta Universitatis Tamperensis;
749, University of Tampere, Tampere 2000. ISBN 951-44-4821-9, ISSN 1455-1616.
Acta Electronica Universitatis Tamperensis; 35, University of Tampere 2000.
ISBN 951-44-4822-7, ISSN 1456-954X.
Distribution: Granum or University of
Tampere Sales Office, P.O.Box 617, 33101 Tampere, tel. +358 3 215 6055,
Information: Xiumin Wu, (02) 267 8593 (office), 318 1683 (home),
This study was designed to examine arterial function in three different models of experimental
hypertension, and study the influences of Whey supplementation, increased dietary K+ intake, and
regular physical exercise on the control of arterial tone in experimental hypertension.
The major findings and conclusions are:
1. Experimental models of genetic, mineralocorticoid-NaCl-induced, and obesity-related
hypertension were associated with attenuated arterial dilatation. The defect of
endothelium-mediated relaxation most likely resulted from impaired endothelium-dependent
hyperpolarization of vascular smooth muscle in these hypertensive models, whereas the
endothelial L-arginine-NO pathway appeared to be preserved. The function of voltage-dependent
Ca2+ channels, as evaluated by enhanced inhibitory effect of nifedipine on the arterial
contractions, was abnormal in smooth muscle of SHR and DOC-treated animals, while such an
abnormality was not observed in obesity-related hypertension.
2. Supplementation with Whey and a comparable dose of K+ similarly opposed the development
of experimental genetic hypertension, an effect which was associated with improved arterial
dilatory properties. Supplementation with Whey had a protective effect on endothelium-mediated
control of arterial tone in experimental DOC-NaCl hypertension even in the absence of a
significant effect on blood pressure. Both supplements augmented the hyperpolarization-related
component of arterial relaxation, increased the sensitivity of smooth muscle to NO, and
decreased the production of vasoconstrictor prostanoids. Altogether the beneficial effects
of the Whey diet could be attributed to increased intake of K+ in SHR and DOC.
3. The antihypertensive effect of long-term exercise in experimental obesity-related
hypertension was associated with improved vasodilation. This was expressed as enhanced
relaxation via endogenous and exogenous NO, and increased endothelial PGI2 production.
The improved control of arterial tone after training could be attributed to the alleviation
of hyperlipidemia and insulin resistance, whereas hyperinsulinaemia per se remained unaffected.
4. The sensitivity of NOS to induction by IL-1ß was higher in arterial smooth muscle of the
OZR than the lean controls. Thus, this model of hyperinsuli-naemia was not associated with
reduced sensitivity of smooth muscle NOS to induction by IL-1ß. Regular exercise did not
change plasma insulin concentrations, but it enhanced the action of insulin in both rats
strains as reflected by reduced blood glucose, and increased the sensitivity of smooth
muscle NOS to induction by IL-1ß.
5. In the absence of preceding myocardial hypertrophy the long-term exercise-induced workload
was not deleterious to the heart in experimental OZR, since no changes in plasma and tissue
atrial natriuretic peptide were detected.
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