(Hypertension. 1995;26:705-710.)
© 1995 American Heart Association, Inc.
Articles |
From the Divisions of Clinical Pharmacology (C.M.S., H.H., A.J.J.W.) and Rheumatology (C.M.S., T.P.), Vanderbilt University School of Medicine, Nashville, Tenn.
Correspondence to Dr C. Michael Stein, Division of Clinical Pharmacology, Vanderbilt University School of Medicine, Medical Research Bldg, Room 546, Nashville, TN 37232-6602.
Abstract Hypertension and nephrotoxicity frequently
complicate treatment with cyclosporine; two suggested
mechanisms are increased sympathetic activity and altered vascular
reactivity. It is difficult to assess these mechanisms in patients
receiving cyclosporine after transplantation because of the
accompanying major physiological alterations.
Therefore, we studied 12 patients with rheumatoid arthritis
twicewhile they were taking and not taking
cyclosporine. We measured vascular response in the dorsal
hand vein using the linear variable differential transformer
technique. Cyclosporine treatment significantly attenuated
vasodilation induced by 60 ng/min isoproterenol (no
cyclosporine, 19.8±3.5% versus cyclosporine,
7.9±2.2%; P=.02) and prostaglandin
E1 at 1000 pg/min (no cyclosporine,
72.6±10.2% versus cyclosporine, 45.6±9.0%) and 2000
pg/min (no cyclosporine, 100.8±14.7% versus
cyclosporine, 68.6±8.0%; F=5.47, P=.047).
However, neither vascular response to phenylephrine or
nitroglycerin nor sympathetic activity assessed by
measurement of norepinephrine spillover with a
radioisotope dilution technique was affected by
cyclosporine (no cyclosporine,
516.1±47.9 ng/min versus cyclosporine, 476.6±51.8 ng/min;
P=.42). Cyclosporine impaired venodilation in
response to two agonists that act through adenylate cyclase
without altering
-agonistinduced venoconstriction or
sympathetic activity. Therefore, in humans impaired vasodilation rather
than sympathetic activation or enhanced vasoconstriction may be an
important mechanism for the alterations of vascular tone that occur
after long-term cyclosporine administration.
Key Words: vasodilation sympathetic nervous system vasoconstriction cyclosporine norepinephrine
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