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Chronic central nervous system MC3/4R blockade attenuates hypertension induced by nitric oxide synthase inhibition but not by angiotensin II infusion.
da Silva, Alexandre A; do Carmo, Jussara M; Dubinion, John H; Bassi, Mirian; Mokhtarpouriani, Kasra; Hamza, Shereen M; Hall, John E.
Affiliation
  • da Silva AA; From the Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Center of Excellence in Cardiovascular-Renal Research, University of Mississippi Medical Center, Jackson. asilva@umc.edu.
  • do Carmo JM; From the Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Center of Excellence in Cardiovascular-Renal Research, University of Mississippi Medical Center, Jackson.
  • Dubinion JH; From the Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Center of Excellence in Cardiovascular-Renal Research, University of Mississippi Medical Center, Jackson.
  • Bassi M; From the Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Center of Excellence in Cardiovascular-Renal Research, University of Mississippi Medical Center, Jackson.
  • Mokhtarpouriani K; From the Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Center of Excellence in Cardiovascular-Renal Research, University of Mississippi Medical Center, Jackson.
  • Hamza SM; From the Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Center of Excellence in Cardiovascular-Renal Research, University of Mississippi Medical Center, Jackson.
  • Hall JE; From the Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Center of Excellence in Cardiovascular-Renal Research, University of Mississippi Medical Center, Jackson.
Hypertension ; 65(1): 171-7, 2015 Jan.
Article in En | MEDLINE | ID: mdl-25287400
ABSTRACT
We examined whether central melanocortin 3 and 4 receptor (MC3/4R) blockade attenuates the blood pressure (BP) responses to chronic L-NAME or angiotensin II (Ang II) infusion in Sprague-Dawley rats implanted with telemetry transmitters, venous catheters, and intracerebroventricular cannula into the lateral ventricle. After 5 days of control measurements, L-NAME (10 µg/kg/min IV, groups 1 and 2) or Ang II (10 ng/kg/min IV, groups 3 and 4) were infused for 24 days, and starting on day 7 of L-NAME or Ang II infusion, the MC3/4R antagonist SHU-9119 (24 nmol/d, n=6/group; groups 1 and 3) or vehicle (saline 0.5 µL/h, n=6/group; groups 2 and 4) was infused intracerebroventricularly for 10 days. A control normotensive group also received SHU-9119 for 10 days (n=5). L-NAME and Ang II increased BP by 40±3 and 56±5 mm Hg, respectively, although heart rate was slightly reduced. MC3/4R blockade doubled food intake and reduced heart rate (≈40 to ≈50 bpm) in all groups. MC3/4R blockade caused only a small reduction in BP in normotensive group (4 mm Hg) and no change in rats receiving Ang II, although markedly reducing BP by 21±4 mm Hg in L-NAME-treated rats. After SHU-9119 infusion was stopped, food intake, heart rate, and BP gradually returned to values observed before SHU-9119 infusion was started. Ganglionic blockade at the end of L-NAME or Ang II infusion caused similar BP reduction in both groups. These results suggest that the brain MC3/4R contributes, at least in part, to the hypertension induced by chronic L-NAME infusion but not by Ang II.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Pressure / Angiotensin II / Central Nervous System / Nitric Oxide Synthase / Receptor, Melanocortin, Type 3 / Receptor, Melanocortin, Type 4 / Hypertension Limits: Animals Language: En Journal: Hypertension Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Pressure / Angiotensin II / Central Nervous System / Nitric Oxide Synthase / Receptor, Melanocortin, Type 3 / Receptor, Melanocortin, Type 4 / Hypertension Limits: Animals Language: En Journal: Hypertension Year: 2015 Document type: Article
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