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1 Renal Service and Laboratory, Hospital Universitario, Instituto de Investigaciones Biomédicas (Fundacite-Zulia), Universidad del Zulia, Maracaibo 4001-A, Venezuela; and 2 Division of Nephrology and Hypertension, Department of Medicine, Physiology, and Biophysics, University of California, Irvine, California 92697
Several
studies have demonstrated that treatment with antioxidants improves
hypertension in spontaneously hypertensive rats (SHR). Because our
laboratory has shown that renal infiltration of immune cells plays a
role in the development of hypertension (Rodriguez-Iturbe B, Quiroz Y,
Nava M, Bonet L, Chavez M, Herrera-Acosta J, Johnson RJ, and Pons HA.
Am J Physiol Renal Physiol 282: F191-F201, 2002), we did the present studies to define whether the
antihypertensive effect of antioxidants was associated with an
improvement in renal inflammation. Melatonin was administered as an
antioxidant. For 6 wk, melatonin was added to the drinking water
(10 mg/100 ml) given to a group of SHR (SHR-Mel; n = 10), and we compared them with groups of untreated SHR
(n = 10) and Wistar-Kyoto (WKY) control rats
(n = 10). Hypertension became increasingly severe in
the SHR group [195 ± 14.3 (SD) mmHg at the end of the
experiment] and improved in the SHR-Mel group (149 ± 20.4 mmHg,
P < 0.001) in association with a 40-60%
reduction in the renal infiltration of lymphocytes, macrophages, and
angiotensin II-positive cells. Intracellular superoxide and renal
malondialdehyde content were reduced by melatonin treatment as was the
immunohistological expression of the 65-kDA DNA-binding subunit of
NF-
B. We conclude that melatonin treatment ameliorates hypertension
in SHR in association with a reduction in interstitial renal
inflammation. Decreased activation of NF-
B, likely resulting from a
reduction in local oxidative stress, may play a role in the suppression
of renal immune infiltration and, thereby, in the antihypertensive
effects of melatonin.
oxidative stress; salt-sensitive hypertension; immune infiltration; interstitial nephritis; nuclear factor-
B; angiotensin II
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