Related Experiment Video
Updated: Oct 18, 2026

Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro
Published on: March 17, 2023
Decreased expression and function of adipocyte hormone-sensitive lipase in subcutaneous fat cells of obese subjects
V Large1, S Reynisdottir, D Langin
1Department of Medicine, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden.
Abstract:
Decreased lipolytic effect of catecholamines in adipose tissue has repeatedly been demonstrated in obesity and may be a cause of excess accumulation of body fat. However, the mechanisms behind this lipolysis defect are unclear. The role of hormone-sensitive lipase was examined using abdominal subcutaneous adipocytes from 34 obese drug-free and otherwise healthy males or females and 14 non-obese control subjects. The enzyme catalyzes the rate-limiting step of the lipolysis pathway. The maximum lipolytic capacity of fat cells was significantly decreased in obesity when measured using either a non-selective beta-adrenergic receptor agonist (isoprenaline) or a phosphodiesterase resistant cyclic AMP analogue (dibutyryl cyclic AMP). Likewise, enzyme activity, protein expression, and mRNA of hormone-sensitive lipase were significantly decreased in adipocytes of obese subjects. The findings were not influenced by age or gender. The data suggest that a decreased expression of hormone-sensitive lipase in subcutaneous fat cells, which in turn causes decreased enzyme function and impaired lipolytic capacity of adipocytes, is present in obesity. Impaired expression of the hormone-sensitive lipase gene might at least in part explain the enzyme defect.
Insights
Obesity is linked to reduced fat breakdown due to lower hormone-sensitive lipase (HSL) expression in fat cells. This impaired HSL function contributes to excess body fat accumulation.
Area of Science:
- Metabolism and Endocrinology
- Adipose Tissue Biology
- Obesity Pathophysiology
Background:
- Reduced lipolytic response to catecholamines is observed in obesity, but underlying mechanisms remain unclear.
- Hormone-sensitive lipase (HSL) is crucial, catalyzing the rate-limiting step in fat breakdown.
- Understanding HSL's role in obesity is vital for addressing excess body fat accumulation.
Purpose of the Study:
- To investigate the role and expression of hormone-sensitive lipase (HSL) in the lipolysis defect associated with obesity.
- To determine if decreased HSL enzyme activity, protein, or mRNA levels contribute to impaired fat cell function in obese individuals.
Main Methods:
- Analysis of abdominal subcutaneous adipocytes from 34 obese and 14 non-obese healthy subjects.
- Measurement of maximum lipolytic capacity using beta-adrenergic receptor agonist and cyclic AMP analogue.
- Quantification of hormone-sensitive lipase (HSL) enzyme activity, protein expression, and mRNA levels.
Main Results:
- Obese subjects exhibited significantly decreased maximum lipolytic capacity in fat cells.
- Hormone-sensitive lipase (HSL) enzyme activity, protein expression, and mRNA levels were significantly reduced in adipocytes of obese individuals.
- These findings were consistent across different ages and genders.
Conclusions:
- Decreased expression of hormone-sensitive lipase (HSL) in subcutaneous fat cells is a key feature of obesity.
- Impaired HSL expression leads to reduced enzyme function and diminished lipolytic capacity of adipocytes.
- Reduced HSL gene expression may partially explain the lipolysis defect observed in obesity.
More Related Videos
10:40Characterization of Adipocyte-Derived Extracellular Vesicle Secretion Using a CD63-GFP Reporter Mouse Model In Vivo and In Vitro
Published on: December 5, 2025
06:08Semi-Automated Isolation of the Stromal Vascular Fraction from Murine White Adipose Tissue Using a Tissue Dissociator
Published on: May 19, 2023
Related Concept Videos
Obesity
Pharmacokinetics in Obese Patients: Drug Absorption and Distribution
Cholesterol: Significance and Regulation
Considering cholesterol and...
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion