The Metabolic Effects of the Acetic and Propionic Acid Analogs of Thyroxine

نویسنده

  • Eli Lilly
چکیده

Within the last six years the identification of several new substances with thyroid hormone-like activity has led to a re-evaluation of the physiological role of thyroxine and of its analogs and derivatives. Since its isolation in 1915 (1) thyroxine was considered the most biologically potent of all simple thyroactive materials until the discovery by Gross and Pitt-Rivers (2) and by Roche, Lissitzky and Michel (3) that 3,5,3'-triiodo-L-thyronine (trit) was four to five times more effective in both animals and man. The acetic acid analogs of thyroxine and trit have been actively investigated since 1953 (4). Thibault and Pitt-Rivers (5-7) described a unique action of these compounds in that they produced an increased oxygen consumption in vitro without previous injection into animals. The maximum effects were reached in 15 minutes and disappeared after 90 minutes. A single injection of these drugs into thyroidectomized rats increased oxygen consumption within two hours. Although these studies have not been confirmed (8, 9), they resulted in the postulate that this might be the form of the thyroid hormone utilized at the tissue level. This suggestion became even more attractive when these substances were isolated from tissues and homogenates (10-17). Other studies in man have suggested a dissociation of responses to those drugs (18-25). In patients with hypothyroidism, (19, 21) it was noted that on small doses of the acetic acid analogs the serum cholesterol level fell, the nitrogen and

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تاریخ انتشار 2013