Literature DB >> 3579601

Effect of selenium on blood pressure, urinary sodium excretion and plasma aldosterone in cadmium-treated male rats.

S Nishiyama, K Nakamura, Y Konishi.   

Abstract

The present study was carried out to help elucidate the possible mechanisms underlying the effect of Cd and the interaction of Se with Cd on blood pressure. Male Wistar rats were divided into four groups: control, Cd-treated, Se-treated, Se-and Cd-treated. Cd and Se were administered at doses of 1.0 mg/kg body weight by subcutaneous injection of aqueous solutions of CdCl2 X 2 X 1/2 H2O and Na2SeO3, respectively. Injections were made either alone or in the Cd + Se treated group, simultaneously at 12-h intervals for 7 consecutive days. All animals were then maintained without further treatment for an additional period of 18 days. Treatment with Cd and Se separately lowered the blood pressure on days 3 and 8, but these levels increased and were significantly higher than that in control rats by day 26. Plasma aldosterone concentrations increased and urinary Na excretion decreased from day 1 to 3 in rats treated with Cd and Se separately. Thereafter, increased water retention precedes the onset of increased blood pressure. From these findings, we suggest that in rats treated with Cd and Se separately the increase in plasma aldosterone is a main factor for decreased urinary Na excretion and increased retention of water, and these factors may be associated with an increase in blood pressure. The treatment with Cd and Se simultaneously decreased urinary Na excretion and increased the plasma aldosterone concentration and water retention before the onset of increased blood pressure.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1987        PMID: 3579601     DOI: 10.1007/bf00295091

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  22 in total

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Authors:  A J VANDER
Journal:  Am J Physiol       Date:  1962-12

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Authors:  H A SCHROEDER; W H VINTON
Journal:  Am J Physiol       Date:  1962-03

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Journal:  Am J Med       Date:  1972-05       Impact factor: 4.965

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Authors:  S J Kopp; T Glonek; H M Perry; M Erlanger; E F Perry
Journal:  Science       Date:  1982-08-27       Impact factor: 47.728

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Authors:  T A Gasiewicz; J C Smith
Journal:  Chem Biol Interact       Date:  1978-11       Impact factor: 5.192

6.  Cardiac physiologic and tissue metabolic changes following chronic low-level cadmium and cadmium plus lead ingestion in the rat.

Authors:  S J Kopp; H M Perry; E F Perry; M Erlanger
Journal:  Toxicol Appl Pharmacol       Date:  1983-06-15       Impact factor: 4.219

7.  Blood pressure and urinary sodium and potassium excretion in cadmium-treated male rats.

Authors:  S Nishiyama; K Nakamura; Y Konishi
Journal:  Environ Res       Date:  1986-08       Impact factor: 6.498

8.  Effect of cadmium on arterial blood pressure and lipid metabolism in rats.

Authors:  B Barański; J Opacka; T Wrońska-Nofer; M Trzcinka-Ochocka; K Sitarek
Journal:  Toxicol Lett       Date:  1983-09       Impact factor: 4.372

9.  Effects of cadmium on glutathione peroxidase, superoxide dismutase, and lipid peroxidation in the rat heart: a possible mechanism of cadmium cardiotoxicity.

Authors:  I S Jamall; J C Smith
Journal:  Toxicol Appl Pharmacol       Date:  1985-08       Impact factor: 4.219

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Authors:  H M Perry; M Erlanger; E F Perry
Journal:  Am J Physiol       Date:  1977-02
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  2 in total

1.  Effect of cadmium (CdCl2) on cell proliferation and production of EDRF (endothelium-derived relaxing factor) by cultured human umbilical arterial endothelial cells.

Authors:  T Kishimoto; T Oguri; M Ohno; K Matsubara; K Yamamoto; M Tada
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

2.  Increase in number of Weibel-Palade bodies and endothelin-1 release from endothelial cells in the cadmium-treated rat thoracic aorta.

Authors:  Y Doi; T Ozaka; H Fukushige; H Furukawa; M Yoshizuka; S Fujimoto
Journal:  Virchows Arch       Date:  1996-08       Impact factor: 4.064

  2 in total

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