Salt-induced hypertension in normotensive spontaneously hypertensive rats.

Academic Article


  • Lifetime treatment with oral captopril prevents the development of hypertension in spontaneously hypertensive rats (SHR). We tested the hypothesis that this treatment also prevents the hypertensive response that occurs when untreated NaCl-sensitive SHR are placed on a high NaCl diet. Female SHR were continuously treated with oral captopril before conception and throughout lactation, and the offspring were similarly treated with oral captopril throughout life. At 6 weeks of age, treated male SHR were placed on an 8% (or remained on a 1%) NaCl diet, and systolic arterial pressure, heart rate, and body weight were monitored for 2 weeks. The 8% NaCl diet caused a rapid increase in arterial pressure in the lifetime captopril-treated rats, and 18 days after the initiation of the diet, the mean arterial pressure of this group was 136 +/- 7 mm Hg compared with 100 +/- 2 mm Hg in the 1% NaCl diet rats. The results of a second experiment confirmed the hypertensive effect of the high NaCl diet in lifetime captopril-treated SHR and demonstrated that after 18 days on the diet the dietary NaCl-induced hypertensive response was greater in magnitude in lifetime captopril-treated compared with untreated SHR. The results also demonstrated that lifetime captopril-treated Wistar-Kyoto rats, which are normotensive irrespective of captopril treatment, display no significant increase in arterial pressure when given a high NaCl diet. A third experiment demonstrated that rapidly progressing NaCl sensitivity is also present in female lifetime captopril-treated SHR.(ABSTRACT TRUNCATED AT 250 WORDS)
  • Authors

    Published In

  • Hypertension  Journal
  • Keywords

  • Aging, Animals, Blood Pressure, Captopril, Diet, Sodium-Restricted, Drug Administration Schedule, Female, Hypertension, Male, Rats, Rats, Inbred SHR, Rats, Inbred WKY, Sodium Chloride, Time Factors
  • Digital Object Identifier (doi)

    Pubmed Id

  • 11665461
  • Author List

  • Wyss JM; Roysommuti S; King K; Kadisha I; Regan CP; Berecek KH
  • Start Page

  • 791
  • End Page

  • 796
  • Volume

  • 23
  • Issue

  • 6 Pt 1