Title of article :
Loss of nocturnal dipping of blood pressure and heart rate in obesity-induced hypertension in rabbits
Author/Authors :
Vladan Antic، نويسنده , , Bruce N. Van Vliet، نويسنده , , Jean-Pierre Montani، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Abstract :
We have investigated in rabbits whether overfeeding and weight gain, which lead to hypertension, are associated with changes in circadian rhythm of blood pressure (BP) and heart rate, and whether the sympathetic nervous system is involved in these changes.
In adult male rabbits, mean arterial pressure (MAP) and heart rate (HR) were monitored by telemetry 22 h a day. Daily MAP and HR records were divided into four equal intervals and used to calculate day–night differences. After a 1-week control period, animals were switched to a high-fat (HFD) ad libitum diet for 8 weeks. HFD increased whole day MAP and HR, and rapidly abolished the normal diurnal rhythm of MAP and HR. Since HFD abolished the nocturnal dip in MAP, but had little effect on daytime values, the loss of dipping appears to account for most of the hypertension in this model of obesity.
In a separate set of rabbits, α- and β-adrenergic blockade (terazosin+propranolol) prevented HFD-induced hypertension and attenuated the increase in HR by more than half. Adrenergic blockade alone abolished the diurnal rhythm of MAP, chiefly by preventing daytime elevation of MAP. The addition of HFD ad libitum did not further modify daily MAP or its circadian pattern. The diurnal rhythm of HR was relatively unaffected by α+β blockade alone, but was abolished after switching to HFD.
In conclusion, rabbits fed an HFD ad libitum develop hypertension and tachycardia associated with a loss of the normal diurnal rhythm of MAP and HR. The hypertension appears to be sympathetically mediated.
Keywords :
hypertension , obesity , sympathetic activity , rabbits , High-fat diet , Non-dipping
Journal title :
Autonomic Neuroscience: Basic and Clinical
Journal title :
Autonomic Neuroscience: Basic and Clinical