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Current Clinical Status of Lipid-Mobilizer Hormone
CHRIS J. D. ZARAFONETIS, M.D.;
JOSEPH SEIFTER, M.D.;
DAVID H. BAEDER, Ph.D.;
JOHN P. KALAS, M.D.
AMA Arch Intern Med. 1959;104(6):974-981.
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A number of studies dealing with a lipidmobilizing hormone (LM) have been reported from these experimental and clinical laboratories.1-18 This substance was discovered, in 1954, by Seifter and Baeder.1 These investigators, working with rats and dogs, demonstrated a lipemia-clearing effect with hyaluronidase, with hyaluronate, and with deoxycorticosterone. At the same time, they found that the lipemia-clearing effect of these substances could be inhibited by the administration of cortisone or by stress (cold exposure) and by nephrosis. Studies in connection with the latter findings led to the discovery of LM in the plasma of several animal species, including man.2 Other experiments by Seifter and Baeder revealed that the pituitary was essential for the release of LM.3 More recently, LM was recovered from the posterior pituitary of hogs,4 denoting that this hormone is either produced or stored at that site. LM is dialyzable; it has been crystallized and appears to be
. . . [Full Text PDF of this Article]
Author Affiliations
Philadelphia; Radnor, Pa.; Philadelphia
From the Department of Medicine, Temple University School of Medicine, Philadelphia, and the Wyeth Institute for Medical Research, Radnor, Pa.; Professor of Clinical and Research Medicine (Dr. Zarafonetis); Director, Wyeth Institute for Medical Research (Dr. Seifter); Pharmacologist, Wyeth Institute for Medical Research (Dr. Baeder), and Research Fellow in Medicine (Dr. Kalas).
Footnotes
Received for publication July 6, 1959.
Read before the Section on Internal Medicine at the 108th Annual Meeting of the American Medical Association, Atlantic City, June 11, 1959.
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