| Literature DB >> 26805634 |
Elena Maneschi1, Ilaria Cellai1, Antonio Aversa2, Tommaso Mello3, Sandra Filippi4, Paolo Comeglio1, Daniele Bani5, Daniele Guasti5, Erica Sarchielli5, Giulia Salvatore1, Annamaria Morelli5, Benedetta Mazzanti5, Francesca Corcetto1, Chiara Corno1, Davide Francomano2, Andrea Galli3, Gabriella Barbara Vannelli5, Andrea Lenzi2, Edoardo Mannucci6, Mario Maggi1, Linda Vignozzi7.
Abstract
Development of metabolically healthy adipocytes within dysfunctional adipose tissue may represent an attractive way to counteract metabolic syndrome (MetS). In an experimental animal model of high fat diet (HFD)-induced MetS, in vivo, long- and short-term tadalafil treatments were able to reduce visceral adipose tissue (VAT) accumulation and hypertriglyceridemia, and to induce the expression in VAT of the brown fat-specific marker, uncoupling protein 1 (UCP1). VAT preadipocytes (PAD), isolated from the tadalafil-treated HFD rabbits, showed: i) a multilocular morphology; ii) an increased expression of brown fat-specific genes (such as UCP1 and CIDEA); iii) improved mitochondrial structure and dynamic and reduced superoxide production; iv) improved insulin sensitivity. Similar effects were obtained after in vitro tadalafil treatment in HFD rPAD. In conclusion, tadalafil counteracted HFD-associated VAT alterations, by restoring insulin-sensitivity and prompting preadipocytes differentiation towards a metabolically healthy phenotype.Entities:
Keywords: Insulin-resistance; Metabolic syndrome; PDE5; Tadalafil
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Year: 2016 PMID: 26805634 DOI: 10.1016/j.mce.2016.01.015
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102