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Isolation and Culturing of Primary Murine Adipocytes from Lean and Obese Mice
Published on: January 24, 2025
Age-associated adaptations in murine adipose tissues
Bianca Hemmeryckx1, Dirk Loeckx, Tom Dresselaers
1Center for Molecular and Vascular Biology, Katholieke Universiteit Leuven, Leuven, Belgium.
Endocrine Journal
|August 6, 2010
Summary
Aging male mice show a biphasic fat mass pattern, increasing by 12 months and decreasing by 24 months. This study details age-related changes in subcutaneous (SC) and gonadal (GON) adipose tissue composition and insulin sensitivity.
Area of Science:
- Metabolic research
- Aging studies
- Obesity research
Background:
- Ageing correlates with increased visceral obesity in humans.
- C57Bl/6 mice are common models for obesity and metabolism research.
- Limited data exists on age-related adipose tissue changes in C57Bl/6 mice.
Purpose of the Study:
- To investigate age-associated changes in subcutaneous (SC) and gonadal (GON) adipose tissue in male C57Bl/6 mice.
- To analyze body weight, fat mass, adipocyte size, blood vessel size, and insulin sensitivity across different ages.
Main Methods:
- Male C57Bl/6 mice were studied at 10 weeks, 12 months, and 24 months of age.
- Measurements included total body weight, SC and GON fat mass, adipocyte and blood vessel size.
- Plasma leptin, insulin, and glucose levels were analyzed to assess metabolic status.
Main Results:
- Body weight and SC/GON fat mass increased from 10 weeks to 12 months, then decreased by 24 months.
- Adipocyte and blood vessel sizes followed a similar biphasic pattern.
- Insulin sensitivity improved with age, indicated by lower insulin and glucose levels in older mice.
- Plasma leptin levels positively correlated with body weight and fat mass.
Conclusions:
- Male C57Bl/6 mice exhibit a biphasic pattern of body weight and adipose tissue changes during aging.
- Age-related alterations in fat depots are accompanied by improved insulin sensitivity.
- These findings provide insights into the aging process and metabolic changes in a key mouse model.

