Sino-aortic denervation augments the increase in blood pressure seen during paradoxical sleep in the rat.

Using a computer assisted telemetric system, we have re-examined the effect of sino-aortic denervation (SAD) on the changes in arterial blood pressure (AP) and heart rate (HR) during sleep in the rat suitably recovered from the operation. Eight 1 hourly polygraphic recordings were performed 4 weeks after the initial SAD surgery. In the SAD rats, the increase in AP during paradoxical sleep (PS) was much larger than that in sham-operated rats. HR in the SAD rats increased on-going from slow-wave sleep to PS, but it showed no change in sham-operated rats. The present study suggests that chronic SAD causes the enhanced AP increase during PS concomitantly with the persistent hypertension and tachycardia across sleep-wake states.

Role of the liver in long-term control of drinking behavior, Na+ balance, and arterial pressure in Dahl rats.

The role of postabsorptive mechanisms in long-term control of drinking behavior, Na+ balance, and arterial pressure was examined in Dahl salt-sensitive (DS) and salt-resistant (DR) rats. NaCl (0.15 M) was infused (0.5 ml/h) into either the inferior vena cava (IVC) or the portal vein (PV) for 7 days, and then 1.5 M NaCl was infused for 10 days. During 1.5 M infusion, the IVC group retained more Na+ than the PV group. Furthermore, in DS rats, mean arterial pressure was higher in the IVC group than in the PV group. Regardless of the strain and infusion route, 1.5 M infusion had no effect on volume of daily saline consumption. However, when the data for light and dark periods were analyzed separately, dark period saline consumption in the PV group was decreased by 1.5 M infusion but was not changed in the IVC group. These results indicate that, in Dahl rats, the postabsorptive mechanism plays a significant role in controlling long-term saline drinking behavior and Na+ balance and has a significant role in controlling arterial pressure in DS, but not DR, rats.

Effect of a chronic high-salt diet on whole-body and organ sodium contents of Dahl rats.

OBJECTIVE: To evaluate whether a high-salt diet causes retention of Na in Dahl rats. DESIGN: To compare the whole-body and organ (liver, spleen, kidney, heart, lung, femur, submaxillary gland and muscle) Na contents in Dahl salt-sensitive rats and Dahl salt-resistant rats. METHODS: Rats aged 6-10 weeks of both strains were fed a normal-salt (0.4% NaCl) or a high-salt (8% NaCl) diet. The whole-body and organs were then ashed and their respective Na contents determined. RESULTS: Salt-resistant rats fed the normal-salt diet had a higher whole-body Na content than did salt-sensitive rats. The high-salt diet increased the whole-body Na content of salt-sensitive rats significantly, but it did not increase that of salt-resistant rats. The high-salt diet caused a significant increase in the organ weight: body weight ratio for all organs of the salt-sensitive rats, except the submaxillary gland, but had no effect on the ratios for salt-resistant rats, apart from that for the kidney. The kidney, submaxillary gland and muscle Na concentrations were greater in salt-sensitive rats than they were in salt-resistant rats. Nonetheless, regardless of strain, the high-salt diet had no effect on organ and plasma Na concentrations. The high-salt diet increased the organ weights (liver, spleen, kidney, heart and lung) and the organ Na contents per kg body weight significantly for salt-sensitive rats but not for salt-resistant rats. CONCLUSIONS: A high-salt diet caused Na retention in salt-sensitive rats only and this was partially due to enlargement of the organs.