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Taurine amplifies renal kallikrein and prevents salt-induced hypertension in Dahl rats.

AbstractOBJECTIVE:
To determine whether taurine reduces blood pressure by stimulating the renal kallikrein-kinin system.
METHODS:
The effects of taurine on blood pressure, urinary kallikrein activity and renal kallikrein gene expression were investigated in Dahl salt-sensitive (Dahl-S) rats. The specificity of the action of taurine was verified by comparison with the action of beta-alanine, a carboxylic analogue of taurine. The effect of co-administration of the specific bradykinin B2 receptor antagonist Hoe 140 was also examined.
RESULTS:
Administration of taurine (3% in drinking water) for 4 weeks retarded the development of salt (4% sodium chloride diet)-induced hypertension. Systolic blood pressure at the end of the experiment was significantly higher in control rats than in taurine-treated rats. Urinary sodium excretion was not decreased by the reduction in blood pressure. The heart weight:body weight ratio was significantly lower, and urinary volume and kallikrein excretion were significantly higher, in taurine-treated rats. Renal kallikrein gene expression at weeks 1 and 4 was higher in taurine-treated rats. Systolic blood pressure 3 and 4 weeks after the administration of beta-alanine was slightly, but not significantly, lower than that of untreated rats on a high-salt diet, and was accompanied by a significantly lower body weight. Urinary kallikrein excretion decreased with a high-salt diet regardless of beta-alanine administration. Continuous systemic administration of Hoe 140 did not cause any significant alteration in blood pressure in Dahl-S rats that received taurine with a high-salt diet. Taurine also showed a renoprotective effect, as judged by a reduction in proteinuria.
CONCLUSION:
These results suggest that taurine is an effective antihypertensive agent for salt-induced hypertension. Although taurine activated renal kallikrein, further studies are required to confirm the participation of activated kallikrein in the antihypertensive, cardioprotective and renoprotective effects of taurine.
AuthorsM Ideishi, S Miura, T Sakai, M Sasaguri, Y Misumi, K Arakawa
JournalJournal of hypertension (J Hypertens) Vol. 12 Issue 6 Pg. 653-61 (Jun 1994) ISSN: 0263-6352 [Print] England
PMID7963490 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • beta-Alanine
  • Taurine
  • Sodium Chloride
  • icatibant
  • Kallikreins
  • Bradykinin
Topics
  • Animals
  • Blood Pressure (drug effects)
  • Bradykinin (analogs & derivatives, pharmacology)
  • Gene Expression (drug effects)
  • Hypertension (prevention & control)
  • Kallikreins (biosynthesis, genetics, urine)
  • Kidney (drug effects, metabolism)
  • Male
  • Rats
  • Rats, Inbred Strains
  • Sodium Chloride (pharmacology)
  • Taurine (pharmacology)
  • beta-Alanine (pharmacology)

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