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Research Article Free access | 10.1172/JCI109119

The Nature of the Immunoreactive Lipotropins in Human Plasma and Tissue Extracts

Koshi Tanaka, Wendell E. Nicholson, and David N. Orth

Department of Medicine and Cancer Research Center, Vanderbilt University Medical Center, Nashville, Tennessee 37232

Find articles by Tanaka, K. in: JCI | PubMed | Google Scholar

Department of Medicine and Cancer Research Center, Vanderbilt University Medical Center, Nashville, Tennessee 37232

Find articles by Nicholson, W. in: JCI | PubMed | Google Scholar

Department of Medicine and Cancer Research Center, Vanderbilt University Medical Center, Nashville, Tennessee 37232

Find articles by Orth, D. in: JCI | PubMed | Google Scholar

Published July 1, 1978 - More info

Published in Volume 62, Issue 1 on July 1, 1978
J Clin Invest. 1978;62(1):94–104. https://doi.org/10.1172/JCI109119.
© 1978 The American Society for Clinical Investigation
Published July 1, 1978 - Version history
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Abstract

This study was designed to establish definitively the nature of immunoreactive lipotropin (IR-LPH) in human plasma and tissue extracts. Using gel filtration, gel filtration under denaturing conditions, cationic exchange chromatography, immunoprecipitation, and radioimmunoassay, we have studied normal and tumorous human pituitaries, ectopic ACTH- and LPH-secreting tumors, plasma from normal subjects before and after dexamethasone administration, and plasma from patients with primary adrenal insufficiency and pituitary and nonpituitary ACTH- and LPH-secreting tumors. Except in the plasma and tumors of occasional patients with ectopic ACTH syndrome, the smallest IR-LPH appears to be λ-lipotropin (λLPH), which is often the predominant and occasionally the only IR-LPH present. The other major peptide appears to be βLPH, a 91-amino acid molecule that contains λLPH as its 1-58 sequence. Larger immunoreactive materials were observed in some specimens, but the “big” LPH in one plasma was shown to be λLPH bound to IgG.

The weak melanocyte-stimulating activity of LPH suggests that ACTH may be the principal pigmentary hormone in man. The fact that λLPH, rather than βLPH, is the predominant form in plasma suggests that the enkephalin-endorphin opiate peptides, which are contained in the “missing” 59-91 sequence from the βLPH precursor of λLPH, may be secreted in parallel with ACTH under both physiological and pathological conditions in man.

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