Table 3

Effect of CEC and (+)-niguldipine on [3H]prazosin binding in rat arteries before and after chemical sympathectomy3-a

Intact RatsSympathectomized Rats
ControlCEC(+)-NiguldipineControlCEC(+)-Niguldipine
fmol/mg protein fmol/mg protein
Thoracic aorta24.3  ± 2.50.80  ± 0.6* 18.5  ± 3.023.2  ± 6.51.9  ± 0.8* 23.1  ± 5.6
Carotid artery20.3  ± 4.70.05  ± 1.9* 24.3  ± 1.830.0  ± 6.82.03  ± 1.6* 32.9  ± 4.3
Mammary artery13.0  ± 5.01.1  ± 2.2* 6.4  ± 1.6* N.A.N.A.N.A.
Renal artery15.5  ± 3.52.8  ± 2.3* 8.1  ± 0.5* N.A.N.AN.A
Femoral artery12.4  ± 1.91.6  ± 1.8* 7.6  ± 1.1* 9.2  ± 2.2 1.2  ± 0.9* 15.0  ± 6.3
Mesenteric arteries
 Superior25.5  ± 2.25.2  ± 1.5* 24.3  ± 1.715.0  ± 1.6 1.1  ± 0.9* 16.4  ± 6.9
 Small (first order branch)46.8  ± 2.527.9  ± 7.1* 10.9  ± 5.2* 28.1  ± 7.6 6.6  ± 3.2* 18.1  ± 4.2*
 Resistance-sized (third order branch)28.4  ± 4.820.0  ± 4.86.8  ± 2.4* 45.3  ± 14.78.6  ± 3.6* 20.4  ± 5.3*
  • 3-a Specific binding observed in the presence of 300 pM [3H]prazosin in control conditions, after pretreatment with CEC (100 μM, 30 min) or in the presence of (+)-niguldipine (30 nM) is shown for arteries of intact rats and of rats that had been chemically sympathectomized with 6-hydroxydopamine. Mean ± S.E.M. (n = 12). N.A., not available.

  • †,* the difference is statistically significant (P < .05) from intact rats or control values, respectively.