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Related Concept Videos

Bone Remodeling01:40

Bone Remodeling

Bone remodeling is a continuous and balanced process of bone resorption by osteoclasts and bone formation by osteoblasts. In adults, it helps maintain bone mass and calcium homeostasis. While mechanical stress can stimulate turnover as part of the normal maintenance and reparative process, several hormones also regulate bone remodeling.
Osteoclasts in Bone Remodeling01:31

Osteoclasts in Bone Remodeling

Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during bone...
Bone Disorders01:29

Bone Disorders

Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...

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Related Experiment Video

Updated: Jun 22, 2026

Mechanism of Regulation of Adipocyte Numbers in Adult Organisms Through Differentiation and Apoptosis Homeostasis
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Adipose Tissue Denervation Blunted the Decrease in Bone Formation Promoted by Obesity in Rats.

Milene Subtil Ormanji1, Maria Victória Lazarini Melo1, Renata Meca1

  • 1Nephrology Division, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.

Nutrients
|August 26, 2023
PubMed
Summary
This summary is machine-generated.

Denerving white adipose tissue improved bone formation in obese rats. This suggests the adipose tissue-brain-bone axis, particularly neuropeptide Y, plays a key role in obesity-related bone metabolism changes.

Keywords:
bone histomorphometrybone–fatbone–nervous system interactionsneuropeptide Y

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Area of Science:

  • Endocrinology
  • Bone Biology
  • Neuroscience

Background:

  • Obesity's impact on bone metabolism is debated, with conflicting reports on its effects.
  • The central nervous system influences bone remodeling via cytokines, hormones, and neuromodulators.

Purpose of the Study:

  • To investigate the effects of bilateral retroperitoneal white adipose tissue (rWAT) denervation (Dnx) on bone metabolism and remodeling in obese rats.
  • To elucidate the role of the adipose tissue-brain-bone axis in obesity-induced bone alterations.

Main Methods:

  • Male Wistar rats were fed a high-fat diet (HFD) or standard diet (SD) for 18 weeks.
  • rWAT denervation (Dnx) or sham surgery was performed at week 14.
  • Analysis included biochemical, hormonal, bone histomorphometry, and tissue gene/protein expression.

Main Results:

  • HFD-fed rats exhibited reduced bone formation, elevated serum/bone leptin and FGF23, increased neuropeptide Y (NPY) in serum and hypothalamus, and decreased vitamin D and PTH.
  • rWAT Dnx restored bone formation markers and histomorphometry in obese rats.
  • Serum and hypothalamic NPY levels decreased post-Dnx without affecting leptin.

Conclusions:

  • Denervation of rWAT enhances bone formation in obese rats.
  • This improvement is primarily mediated by reduced neurohormonal actions of NPY.
  • The study highlights the significance of the adipose tissue-brain-bone axis in regulating bone metabolism during obesity.