Impaired atrial M(2)-cholinoceptor function in obesity-related hypertension

Hypertension. 1999 Nov;34(5):1066-72. doi: 10.1161/01.hyp.34.5.1066.

Abstract

The aim of this study was to investigate the activity of the parasympathetic limb of the baroreflex arch in a canine model of obesity-related hypertension. Twelve male beagle dogs were randomized into 2 groups. Six dogs were fed with normal canine food and 6 were submitted to a 10-week high-fat diet (HFD). We have evaluated the consequences of HFD on heart rate (HR) and blood pressure (BP) circadian cycles and methylscopolamine dose-response curves. Binding of [(3)H]-AF-DX 384 and adenylyl cyclase activity were investigated to determine the density and functionality of M(2)-cholinoceptors on right atrial membranes from control and HFD dogs. HFD induced a significant increase in body weight (15+/-1 vs 12+/-1 kg), systolic BP (161+/-5 vs 145+/-4 mm Hg), diastolic BP (92+/-3 vs 79+/-2 mm Hg), and HR (96+/-4 vs 81+/-3 bpm). Circadian rhythms of HR and BP observed in the baseline period were abolished after 9 weeks of HFD. After propranolol (1 mg/kg) pretreatment, the dose of methylscopolamine able to induce 50% maximum tachycardia was significantly increased after 9 weeks of HFD (7.4+/-0.3 vs 4.7+/-0.1 microg/kg). In the control group, the experimental period failed to modify these parameters. The numbers of M(2)-cholinoceptors measured in right atrial membranes were significantly lower in HFD than in control groups (54+/-6 vs 27+/-6 fmol/mg protein). The ability of carbachol to inhibit isoproterenol-stimulated adenylyl cyclase activity was significantly lower in HFD than in control groups (IC(50)=47+/-12 vs 6.4+/-1.4 micromol/L). However, the basal activity of adenylyl cyclase was unchanged by HFD. HFD decreases M(2)-cholinoceptor number and function in cardiomyocytes. This could explain the abolition of circadian rhythm of HR and the changes in chronotropic effect brought about by methylscopolamine.

MeSH terms

  • Adenylyl Cyclases / metabolism
  • Animals
  • Blood Pressure
  • Body Weight
  • Dogs
  • Dose-Response Relationship, Drug
  • Heart Atria / physiopathology*
  • Hypertension / physiopathology*
  • Male
  • N-Methylscopolamine / pharmacology
  • Obesity / physiopathology*
  • Pirenzepine / analogs & derivatives
  • Pirenzepine / metabolism
  • Receptor, Muscarinic M2
  • Receptors, Muscarinic / physiology*

Substances

  • Receptor, Muscarinic M2
  • Receptors, Muscarinic
  • AFDX 384
  • Pirenzepine
  • Adenylyl Cyclases
  • N-Methylscopolamine