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Veterans Affairs Medical Center and Tulane University School of Medicine, New Orleans, Louisiana 70112-1262; the Department of Pathology, Amgen, Inc. (C.L.F.), Thousand Oaks, California 91320-1789; and Geriatric Research Educational and Clinical Center (GRECC), Veterans Administration Medical Center-St. Louis (W.A.B.) and the Division of Geriatrics, Department of Internal Medicine, Saint Louis University School of Medicine (W.A.B.), Saint Louis, Missouri 63106
Address all correspondence and requests for reprints to: Lawrence M. Maness, Ph.D., Veterans Affairs Medical Center, Research Service, 1601 Perdido Street, New Orleans, Louisiana 70112-1262. E-mail: lmaness{at}mailhost.tcs.tulane.edu
The fate of the metabolic regulatory protein leptin was studied after intracerebroventricular (icv) administration into the lateral ventricle of the brain. In the brain, a mean of 72% of the recovered radioiodinated leptin was intact. Efflux from the brain for leptin occurred with the reabsorption of the cerebrospinal fluid into the blood. Leptin appearing in the blood was 71% intact over the course of the study. The amount of leptin in the blood rose slowly, and 20 min after icv injection equaled or exceeded levels previously seen 20 min after iv administration. Autoradiography showed the slow disappearance of leptin from the ventricular system over time. The degree of periventricular penetration of radiolabeled leptin also was determined. By 30 min, leptin was detected 600 µm from the midline, but computer-assisted image analysis showed that the amount of radioactivity had fallen to half the midline value by 300 µm. The concentration of leptin within the arcuate nucleus, previously observed after iv administration, was not seen after icv injection. High concentrations of leptin were found at the choroid plexus, suggesting the presence of leptin receptors on the brain side of the blood-cerebrospinal fluid barrier and within the lumen of the middle cerebral arteries.
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