| Literature DB >> 32402266 |
Inês Mahú1, Andreia Barateiro2, Eva Rial-Pensado3, Noelia Martinéz-Sánchez4, Sandra H Vaz5, Pedro M S D Cal6, Benjamin Jenkins7, Tiago Rodrigues6, Carlos Cordeiro8, Miguel F Costa9, Raquel Mendes1, Elsa Seixas1, Mafalda M A Pereira1, Nadiya Kubasova1, Vitka Gres1, Imogen Morris1, Carolina Temporão1, Marta Olivares10, Yolanda Sanz10, Albert Koulman7, Francisco Corzana11, Ana M Sebastião5, Miguel López3, Gonçalo J L Bernardes12, Ana I Domingos13.
Abstract
Anti-obesity drugs in the amphetamine (AMPH) class act in the brain to reduce appetite and increase locomotion. They are also characterized by adverse cardiovascular effects with origin that, despite absence of any in vivo evidence, is attributed to a direct sympathomimetic action in the heart. Here, we show that the cardiac side effects of AMPH originate from the brain and can be circumvented by PEGylation (PEGyAMPH) to exclude its central action. PEGyAMPH does not enter the brain and facilitates SNS activity via theβ2-adrenoceptor, protecting mice against obesity by increasing lipolysis and thermogenesis, coupled to higher heat dissipation, which acts as an energy sink to increase energy expenditure without altering food intake or locomotor activity. Thus, we provide proof-of-principle for a novel class of exclusively peripheral anti-obesity sympathofacilitators that are devoid of any cardiovascular and brain-related side effects.Entities:
Keywords: amphetamine; heat dissipation; lipolysis; obesity; sympathetic-nervous-system; sympathofacilitators; sympathomimetics; tachycardia; thermogenesis; thermoregulation
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Year: 2020 PMID: 32402266 PMCID: PMC7671941 DOI: 10.1016/j.cmet.2020.04.013
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287