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Dihydrodehydrodiisoeugenol enhances adipocyte differentiation and decreases lipolysis in murine and human cells
Author(s) -
Nehrenheim Katja,
Meyer Imke,
Brenden Heidi,
Vielhaber Gabriele,
Krutmann Jean,
GretherBeck Susanne
Publication year - 2013
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/exd.12218
Subject(s) - medicine , lipolysis , endocrinology , adipocyte , adiponectin , adipogenesis , chemistry , adipose tissue , peroxisome proliferator activated receptor , perilipin , lipodystrophy , receptor , biology , insulin resistance , insulin , immunology , human immunodeficiency virus (hiv) , antiretroviral therapy , viral load
Loss of subcutaneous fat is a hallmark of ageing usually starting in the face. Attempts to ameliorate cosmetically the appearance of subcutaneous fat loss have been of limited success as they fail to rebuild the missing subcutaneous tissue. Ageing‐driven loss of subcutaneous fat results from (i) the reduced capacity of pre‐adipocytes to differentiate into adipocytes and (ii) the fact that adipocytes of the elderly secrete increased amounts of TNF α, that in turn enhances lipolysis, inhibits pre‐adipocyte differentiation and induces dedifferentiation of adipocytes. The neolignan dihydrodehydrodiisoeugenol ( DDE ) caused a 30% increase in lipid accumulation in murine 3 T 3‐L1 cells. This effect was accompanied by an induction of the differentiation‐associated transcription factors peroxisome proliferator‐activated receptorγ ( PPAR γ2), CAAT /enhancer‐binding protein α ( C / EBP α), fatty acid binding protein 4 and adiponectin, and a loss of the pre‐adipocyte marker P ref1. In addition, DDE diminished both basal and TNF α‐induced lipolysis. Similar results were obtained in human subcutaneous (hsc) pre‐adipocytes cultured in an age‐adapted hormone mix with reduced levels of insulin and dexamethasone. In this system, DDE significantly increased lipid accumulation by 71% and 94% and was associated with an induction of PPAR γ2 and adiponectin m RNA expression. DDE also reduced basal lipolysis in mature hsc adipocytes. DDE acted as a partial PPAR γ agonist because (i) DDE displaced PPAR γ ligand from the human PPAR ligand‐binding site, (ii) DDE ‐induced lipid accumulation and (iii) DDE ‐induced adiponectin secretion could be overcome by the addition of PPAR γ antagonists. Taken together, these studies identify DDE as a compound well suited to prevent and reverse loss of subcutaneous fat.