Chronic Intranasal Insulin Does Not Affect Hepatic Lipids but Lowers Circulating BCAAs in Healthy Male Subjects

Context:Nonalcoholic fatty liver disease and elevated circulating branched-chain amino acids (BCAAs) are common characteristics of obesity and type 2 diabetes. In rodents, brain insulin signaling controls both hepatic triglyceride secretion and BCAA catabolism. Whether brain insulin signaling contro...

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Published inThe journal of clinical endocrinology and metabolism Vol. 102; no. 4; pp. 1325 - 1332
Main Authors Scherer, Thomas, Wolf, Peter, Smajis, Sabina, Gaggini, Melania, Hackl, Martina, Gastaldelli, Amalia, Klimek, Peter, Einwallner, Elisa, Marculescu, Rodrig, Luger, Anton, Fürnsinn, Clemens, Trattnig, Siegfried, Buettner, Christoph, Krššák, Martin, Krebs, Michael
Format Journal Article
LanguageEnglish
Published Washington, DC Endocrine Society 01.04.2017
Copyright Oxford University Press
Oxford University Press
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Summary:Context:Nonalcoholic fatty liver disease and elevated circulating branched-chain amino acids (BCAAs) are common characteristics of obesity and type 2 diabetes. In rodents, brain insulin signaling controls both hepatic triglyceride secretion and BCAA catabolism. Whether brain insulin signaling controls similar metabolic pathways in humans is unknown.Objective:Here we assessed if intranasal insulin, a method to preferentially deliver insulin to the central nervous system, is able to modulate hepatic lipid content and plasma BCAAs in humans.Design/Setting:We conducted a randomized, double-blind, placebo-controlled trial at the Medical University of Vienna.Participants/Intervention:We assessed if a chronic 4-week intranasal insulin treatment (40 IU, 4 times daily) reduces hepatic triglyceride content and circulating BCAAs in 20 healthy male volunteers.Main Outcome Measures:Hepatic lipid content was assessed noninvasively by 1H-magnetic resonance spectroscopy, and BCAAs were measured by gas chromatography mass spectrometry at defined time points during the study.Results:Chronic intranasal insulin treatment did not alter body weight, body mass index, and hepatic lipid content but reduced circulating BCAA levels.Conclusions:These findings support the notion that brain insulin controls BCAA metabolism in humans. Thus, brain insulin resistance could account at least in part for the elevated BCAA levels observed in the insulin-resistant state.Chronic intranasal insulin does not affect hepatic lipid content but lowers circulating branched-chain amino acid levels in nonobese male human subjects.
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Address all correspondence and requests for reprints to: Thomas Scherer, MD, Department of Medicine III, Division of Endocrinology and Metabolism, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria. E-mail: thomas.scherer@meduniwien.ac.at
ISSN:0021-972X
1945-7197
1945-7197
DOI:10.1210/jc.2016-3623