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Nitric oxide and preglomerular vascular lesions in lyon spontaneously hypertensive rats.

Abstract
Accumulation of Sudan black-stainable (SB+) lipids is a hallmark of the focal inflammato-proliferative lesions that develop along preglomerular vessels in N G-nitro-L-arginine methyl ester (L-NAME) and angiotensin II hypertensive rats. We extended our findings to genetically hypertensive Lyon (LH) rats aged 14 and 30 weeks and to age-matched normotensive (LN) rats. Vessels were isolated by HCl maceration. Despite high systolic blood pressure (SBP), hypercholesterolaemia, albuminuria and increased interlobular and afferent arteriolar media thickness, SB+ lesions were rarely found in LH rats, regardless of age. To probe nitric oxide as a potential source of vascular protection, 14-week-old LN and LH rats received L-NAME for 10 days (20 mg kg-1 day-1, per os), which increased SBP to 174 +/- 5 and to >200 mmHg, respectively. It induced formation of focal SB+ lesions less frequently in LN than LH rats, in which they affected 39 +/- 7, 44 +/- 5 and 15 +/- 5% of arcuate arterial branches, interlobular arteries and afferent arterioles, respectively. Immunoreactive endothelin-1 was found to accumulate at the level of SB+ lesions. Co-administered with L-NAME, hydralazine (15 mg kg-1 day-1, per os) limited SBP rise to approximately 10 mmHg in both LN and LH rats. As a result, SB+ lesions were rare in LN rats, but were frequent in LH rats. In conclusion, preglomerular SB+ lesions are spontaneously lacking in LH rats. Endogenous nitric oxide production provides protection against vascular barotrauma. Endothelin-1 likely plays an autocrine/paracrine role in vascular lesion formation.
AuthorsD Casellas, N Bouriquet, A Artuso
JournalActa physiologica Scandinavica (Acta Physiol Scand) Vol. 168 Issue 1 Pg. 133-8 (Jan 2000) ISSN: 0001-6772 [Print] England
PMID10691791 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antihypertensive Agents
  • Azo Compounds
  • Coloring Agents
  • Drug Combinations
  • Enzyme Inhibitors
  • Naphthalenes
  • Hydralazine
  • Nitric Oxide
  • Sudan Black B
  • NG-Nitroarginine Methyl Ester
Topics
  • Aging (physiology)
  • Animals
  • Antihypertensive Agents (pharmacology)
  • Azo Compounds
  • Coloring Agents
  • Drug Combinations
  • Enzyme Inhibitors (pharmacology)
  • Hydralazine (pharmacology)
  • Hypertension (complications)
  • Kidney Glomerulus (blood supply)
  • NG-Nitroarginine Methyl Ester (pharmacology)
  • Naphthalenes
  • Nitric Oxide (physiology)
  • Rats
  • Rats, Inbred SHR (anatomy & histology)
  • Vascular Diseases (etiology, pathology)

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