Abstract:
:Administration of cyclosporine (CS) as an immunosuppressive agent in clinical transplantation is associated with multiple side effects including nephrotoxicity and hypertension. These two effects could be related in that the renal changes may be secondary to alterations in organ blood flow. The present studies investigate the ability of CS to augment contractile responsiveness in blood vessels from normotensive rats. Isometric force generation was measured in isolated tail arteries and portal veins. CS (8.3 X 10(-6)M) potentiated tail artery contractile responses to sympathetic nerve stimulation, exogenous norepinephrine, and increases in extracellular potassium concentration. Portal veins undergo spontaneous contractions which are related to the firing of calcium-driven action potentials in the smooth muscle cells. CS significantly increased the frequency of these spontaneous contractile events. These results suggest that components of CS toxicity may involve a direct action on vascular smooth muscle and/or on vascular adrenergic neurotransmission.
journal_name
Life Scijournal_title
Life sciencesauthors
Lamb FS,Webb RCdoi
10.1016/0024-3205(87)90080-4subject
Has Abstractpub_date
1987-06-29 00:00:00pages
2571-8issue
26eissn
0024-3205issn
1879-0631pii
0024-3205(87)90080-4journal_volume
40pub_type
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