Comparative anatomy and metabolic profiles of brown and white adipose tissue in humans

Adipose tissue is a dynamic metabolic organ that plays a central role in energy homeostasis, endocrine signaling, and thermoregulation (Forner et al., 2009). Traditionally, adipose tissue has been classified into two major types: white adipose tissue (WAT), which primarily stores energy as triglycerides, and brown adipose tissue (BAT), which dissipates energy as heat through non-shivering thermogenesis. While WAT is widely distributed throughout the human body, BAT is more abundant in small mammals and infants but remains present and metabolically active in specific regions of adult humans. Recent molecular biology discoveries and imaging methods have reshaped the physiological status of BAT and recognized the presence of beige or brite adipocytes, which develop in WAT depots and display thermogenic potential. This led to renewed attention on adipose tissue plasticity and how it is relevant for metabolic health, obesity, and associated metabolic disorders. This narrative review compares the anatomical distribution, cellular morphology, developmental origins, and physiological functions of WAT and BAT in humans. It also summarizes imaging modalities used to identify metabolically active adipose tissue and discusses emerging concepts such as adipose browning, endocrine signaling, and therapeutic activation of thermogenic fat.

Authors

Institutions

Publication Details

Journal
Frontiers in Endocrinology
Published
2026-04-28
DOI
https://doi.org/10.3389/fendo.2026.1821542
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Comparative anatomy and metabolic profiles of brown and white adipose tissue in humans

Jesus Villarreal, Ancha Baranova
Frontiers in Endocrinology
Adipose Tissue and Metabolism
article

Comparative anatomy and metabolic profiles of brown and white adipose tissue in humans

Jesus Villarreal, Ancha Baranova
article en

Abstract

Adipose tissue is a dynamic metabolic organ that plays a central role in energy homeostasis, endocrine signaling, and thermoregulation (Forner et al., 2009). Traditionally, adipose tissue has been classified into two major types: white adipose tissue (WAT), which primarily stores energy as triglycerides, and brown adipose tissue (BAT), which dissipates energy as heat through non-shivering thermogenesis. While WAT is widely distributed throughout the human body, BAT is more abundant in small mammals and infants but remains present and metabolically active in specific regions of adult humans. Recent molecular biology discoveries and imaging methods have reshaped the physiological status of BAT and recognized the presence of beige or brite adipocytes, which develop in WAT depots and display thermogenic potential. This led to renewed attention on adipose tissue plasticity and how it is relevant for metabolic health, obesity, and associated metabolic disorders. This narrative review compares the anatomical distribution, cellular morphology, developmental origins, and physiological functions of WAT and BAT in humans. It also summarizes imaging modalities used to identify metabolically active adipose tissue and discusses emerging concepts such as adipose browning, endocrine signaling, and therapeutic activation of thermogenic fat.

Frontiers in EndocrinologyVol. 17
Texas A&M University – San Antonio (US), George Mason University (US), Research Centre for Medical Genetics (RU)
Openalex Percentile: Top 11%
Adipose Tissue and Metabolism
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.