Circulation Research, Vol 49, 518-524, Copyright © 1981 by American Heart Association
ARTICLES |
J Black, B Waeber, MR Bresnahan, I Gavras and H Gavras
We studied the effects on blood pressure and heart rate of two different phenylethanolamine N-methyltransferase (PNMT) inhibitors in normotensive, in two-kidney renal hypertensive, and in deoxycorticosterone-salt (DOC-salt) hypertensive rats. One compound (SK&F 64139) blocks the conversion of norepinephrine to epinephrine in both the central and the peripheral nervous system, whereas the other (SK&F 29661) does not cross the blood-brain barrier and therefore is active mostly in the adrenal glands. In the rats given SK&F 29661, practically no acute blood pressure changes were in the adrenal glands. In the rats given SK&F 64139 induced only a minor blood pressure and heart rate response in normotensive and two-kidney renal hypertensive rats. However, in DOC-salt hypertensive rats, it reduced arterial pressure to approximately normal levels and concomitantly slowed pulse rate. There was a close correlation between the magnitude of the blood pressure response observed in all SK&F 64139-treated animals and the control plasma norepinephrine (4 = -0.795, P less than 0.001) and epinephrine (r = -0.789, P less than 0.001) levels. These results suggest an important role for central epinephrine in regulating the peripheral sympathoadrenomedullary and the baroreceptor reflex activity, particularly when the maintenance of the high blood pressure is not renin-dependent.
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G. Koike, H. J. Jacob, J. E. Krieger, C. Szpirer, M. R. Hoehe, M. Horiuchi, and V. J. Dzau Investigation of the Phenylethanolamine N-Methyltransferase Gene as a Candidate Gene for Hypertension Hypertension, October 1, 1995; 26(4): 595 - 601. [Abstract] [Full Text] |
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