Reduced Regional and Global Cerebral Blood Flow During Fenoldopam-Induced Hypotension in Volunteers

Dopamine has a wide spectrum of receptor and pharmacologic actions that may affect cerebral blood flow (CBF). A new, selective dopamine-1 agonist, fenoldopam, is a potent systemic vasodilator with moderate &agr;2-receptor affinity. However, the effects of fenoldopam on the cerebral circulation are undefined. We therefore hypothesized that infusion of fenoldopam would decrease mean arterial blood pressure (MAP) and might concurrently decrease CBF via vascular &agr;2-adrenoreceptor activation in awake volunteers. We studied nine healthy normotensive subjects, using positron emission tomography to measure CBF in multiple cortical and subcortical regions of interest. In addition, bioimpedance cardiac output and middle cerebral artery blood flow velocity were determined during fenoldopam-induced hypotension. Three men and four women, aged 25–43 yr, completed the study. Fenoldopam infused at 1.3 ± 0.4 &mgr;g · kg−1 · min−1 (mean ± sd) reduced MAP 16% from baseline: from 94 (89–100) mm Hg (mean [95% confidence interval]) to 79 [74–85] mm Hg (P < 0.0001). During the fenoldopam infusion, both cardiac output (+39%), and heart rate (+45%) increased significantly, whereas global CBF decreased from baseline, 45.6 [35.6–58.5] mL · 100 g−1 · min−1, to 37.7 [33.9–42.0] mL · 100 g−1 · min−1 (P < 0.0001). Despite restoration of baseline MAP with a concurrent infusion of phenylephrine, global CBF remained decreased relative to baseline values at 37.9 [34.0–42.3] mL · 100 gm−1 · min−1 (P < 0.0001). Changes in middle cerebral artery velocity did not correlate with positron emission tomography-measured changes of CBF induced by fenoldopam, with or without concurrent phenylephrine.

[1]  K. Lawson,et al.  Cardiovascular characterization of DA-1 and DA-2 dopamine receptor agonists in anesthetized rats. , 1987, Clinical and experimental hypertension. Part A, Theory and practice.

[2]  S. Gelman,et al.  Transcranial Doppler and rCBF compared in carotid endarterectomy. , 1986, Stroke.

[3]  H Iida,et al.  Mechanisms of Dexmedetomidine-Induced Cerebrovascular Effects in Canine In Vivo Experiments , 1995, Anesthesia and analgesia.

[4]  R. P. Wray CRYOPROBE LEAKAGE OF NITROUS OXIDE INTO OPERATING ROOM AIR , 1979 .

[5]  R. Patterson,et al.  The Minnesota impedance cardiograph- theory and applications. , 1974, Biomedical engineering.

[6]  C. Iadecola Neurogenic control of the cerebral microcirculation: is dopamine minding the store? , 1998, Nature Neuroscience.

[7]  P. Patel,et al.  The cerebral pressure-flow relationship during 1.0 MAC isoflurane anesthesia in the rabbit: the effect of different vasopressors. , 1990, Anesthesiology.

[8]  M. L. Marsh,et al.  Changes in neurologic status and intracranial pressure associated with sodium nitroprusside administration. , 1979, Anesthesiology.

[9]  W. K. Luk,et al.  Adaptive, segmented attenuation correction for whole-body PET imaging , 1996 .

[10]  K. Minneman Alpha 1-adrenergic receptor subtypes, inositol phosphates, and sources of cell Ca2+. , 1988, Pharmacological reviews.

[11]  J. Kirsch,et al.  α2-Adrenergic agonist effects on normocapnic and hypercapnic cerebral blood flow in the dog are anesthetic dependent , 1994 .

[12]  Mental Disease,et al.  Brain imaging and brain function , 1985 .

[13]  R. Weinshilboum,et al.  The sixth report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure. , 1997, Archives of internal medicine.

[14]  M. Zornow,et al.  Dexmedetomidine, an α2‐Adrenergic Agonist, Decreases Cerebral Blood Flow in the Isoflurane‐Anesthetized Dog , 1990, Anesthesia and analgesia.

[15]  N. Toda Alpha adrenergic receptor subtypes in human, monkey and dog cerebral arteries. , 1983, The Journal of pharmacology and experimental therapeutics.

[16]  K. Herholz Signal sources in PET. , 1997, Advances in experimental medicine and biology.

[17]  Yuko Sato,et al.  Regulation of regional cerebral blood flow by cholinergic fibers originating in the basal forebrain , 1992, Neuroscience Research.

[18]  B. McGrath,et al.  Beneficial effects of fenoldopam on systemic and regional hemodynamics in rabbits with congestive heart failure. , 1988, Journal of cardiovascular pharmacology.

[19]  W. Frishman,et al.  Fenoldopam: A New Dopamine Agonist for the Treatment of Hypertensive Urgencies and Emergencies , 1998, Journal of clinical pharmacology.

[20]  D C Jeutter,et al.  Determination of cardiac output using ensemble-averaged impedance cardiograms. , 1985, Journal of applied physiology.

[21]  J. Kirsch,et al.  α2-ADRENERGIC AGONIST EFFECTS ON NORMOCAPNIC AND HYPERCAPNIC CEREBRAL BLOOD FLOW IN THE DOG ARE ANESTHETIC-DEPENDENT , 1994 .

[22]  R A Koeppe,et al.  Performance Comparison of Parameter Estimation Techniques for the Quantitation of Local Cerebral Blood Flow by Dynamic Positron Computed Tomography , 1985, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[23]  Ulrich Dirnagl,et al.  Optical Imaging of Brain Function and Metabolism 2 , 1997, Advances in Experimental Medicine and Biology.

[24]  S. Garwood,et al.  Perioperative renal preservation: Dopexamine and fenoldopam— New agents to augment renal performance , 1998 .

[25]  S. Sudikoff,et al.  Techniques for measuring cerebral blood flow in children. , 1998, Current opinion in pediatrics.

[26]  R. Koehler,et al.  Intraventricular Dexmedetomidine Decreases Cerebral Blood Flow During Normoxia and Hypoxia in Dogs , 1997, Anesthesia and analgesia.

[27]  R. Lewis,et al.  Guidelines for clinical investigator involvement in industry-sponsored clinical trials. SAEM Research Committee. , 1995, Academic emergency medicine : official journal of the Society for Academic Emergency Medicine.

[28]  P. Goldman-Rakic,et al.  Dopaminergic regulation of cerebral cortical microcirculation , 1998, Nature Neuroscience.

[29]  T. Sloan,et al.  Neurologic monitoring. , 1988, Critical care clinics.

[30]  B. Clyde,et al.  The relationship of blood velocity as measured by transcranial doppler ultrasonography to cerebral blood flow as determined by stable xenon computed tomographic studies after aneurysmal subarachnoid hemorrhage. , 1996, Neurosurgery.

[31]  Detection The sixth report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC VI) , 1997 .

[32]  M. Raichle Positron Emission Tomography with Oxygen-15 Radiopharmaceuticals , 1986 .

[33]  C. Grant,et al.  A comparison of the effects of norepinephrine, epinephrine, and dopamine on cerebral blood flow and oxygen utilisation. , 1998, Acta neurochirurgica. Supplement.

[34]  F. Amenta,et al.  Autoradiographic localization of vascular dopamine receptors. , 1990, American journal of hypertension.

[35]  B. K. Hartman,et al.  Central noradrenergic regulation of cerebral blood flow and vascular permeability. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[36]  E. Panacek,et al.  Randomized, Prospective Trial of Fenoldopam vs Sodium Nitroprusside in the Treatment of Acute Severe Hypertension , 1995 .

[37]  S. Oparil,et al.  Fenoldopam: a new parenteral antihypertensive: consensus roundtable on the management of perioperative hypertension and hypertensive crises. , 1999, American journal of hypertension.