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A carnosine analog mitigates metabolic disorders of obesity by reducing carbonyl stress
Ethan J. Anderson, … , Marina Carini, Giancarlo Aldini
Ethan J. Anderson, … , Marina Carini, Giancarlo Aldini
Published September 18, 2018
Citation Information: J Clin Invest. 2018;128(12):5280-5293. https://doi.org/10.1172/JCI94307.
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Research Article Endocrinology Metabolism

A carnosine analog mitigates metabolic disorders of obesity by reducing carbonyl stress

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Abstract

Sugar- and lipid-derived aldehydes are reactive carbonyl species (RCS) frequently used as surrogate markers of oxidative stress in obesity. A pathogenic role for RCS in metabolic diseases of obesity remains controversial, however, partly because of their highly diffuse and broad reactivity and the lack of specific RCS-scavenging therapies. Naturally occurring histidine dipeptides (e.g., anserine and carnosine) show RCS reactivity, but their therapeutic potential in humans is limited by serum carnosinases. Here, we present the rational design, characterization, and pharmacological evaluation of carnosinol, i.e., (2S)-2-(3-amino propanoylamino)-3-(1H-imidazol-5-yl)propanol, a derivative of carnosine with high oral bioavailability that is resistant to carnosinases. Carnosinol displayed a suitable ADMET (absorption, distribution, metabolism, excretion, and toxicity) profile and was determined to have the greatest potency and selectivity toward α,β-unsaturated aldehydes (e.g., 4-hydroxynonenal, HNE, ACR) among all others reported thus far. In rodent models of diet-induced obesity and metabolic syndrome, carnosinol dose-dependently attenuated HNE adduct formation in liver and skeletal muscle, while simultaneously mitigating inflammation, dyslipidemia, insulin resistance, and steatohepatitis. These improvements in metabolic parameters with carnosinol were not due to changes in energy expenditure, physical activity, adiposity, or body weight. Collectively, our findings illustrate a pathogenic role for RCS in obesity-related metabolic disorders and provide validation for a promising new class of carbonyl-scavenging therapeutic compounds rationally derived from carnosine.

Authors

Ethan J. Anderson, Giulio Vistoli, Lalage A. Katunga, Katsuhiko Funai, Luca Regazzoni, T. Blake Monroe, Ettore Gilardoni, Luca Cannizzaro, Mara Colzani, Danilo De Maddis, Giuseppe Rossoni, Renato Canevotti, Stefania Gagliardi, Marina Carini, Giancarlo Aldini

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Figure 1

In silico models and biochemistry of carnosinol metabolism.

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In silico models and biochemistry of carnosinol metabolism.
(A) Structur...
(A) Structure-activity relationships for l-carnosine and comparison with carnosinol. (B) Putative complex between carnosinol and CN1, highlighting the missing ion pair with Arg350 when compared with the corresponding complex for l-carnosine. (C) Putative complex between carnosinol and hPepT1, revealing that the inserted hydroxyl group elicits H-bonds similar to those already observed for l-carnosine.

Copyright © 2023 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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