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Updated: Jan 25, 2026

Models of Bone Metastasis
Published on: September 4, 2012
Postnatal ex vivo rat model for longitudinal bone growth investigations
Adamu Abdul Abubakar1,2, Sahar Mohammed Ibrahim1,3, Ahmed Khalaf Ali1,3
1Department of Companion Animal Medicine and Surgery Universiti Putra Malaysia Serdang Malaysia.
Insights
Long bone growth in rats is possible ex vivo, with significant increases in chondrocyte density influencing elongation. This study details growth rates and histological feasibility in young rats.
Area of Science:
- Skeletal biology
- Developmental biology
- Cell biology
Background:
- Chondrocytes in the growth plate (GP) are crucial for longitudinal bone growth.
- Chondrocyte volume increase is a key factor in understanding bone elongation mechanisms.
Purpose of the Study:
- To investigate ex vivo longitudinal bone growth in young rats.
- To determine the relationship between chondrocyte density and bone elongation.
- To assess the feasibility of histological analysis of growth plates without decalcification.
Main Methods:
- Utilized 45 Sprague-Dawley rat pups (7-15 days old) divided into nine age groups.
- Measured tibia and metatarsal bone lengths after 0, 24, 48, and 72 hours of ex vivo incubation.
- Determined growth plate lengths and chondrocyte densities via histology.
Main Results:
- Significant bone length differences observed after 72 hours of incubation across age groups.
- Histological sectioning was feasible without decalcification in specific age ranges.
- Chondrocyte density variations correlated with bone elongation.
Conclusions:
- Ex vivo tibia and metatarsal bone growth rates were 23.87% and 40.38%, respectively.
- Increased chondrocyte density along the growth plate significantly influences overall bone elongation.
- The study demonstrates the possibility of ex vivo bone growth analysis and histological examination in young rats.
Background:
Chondrocytes in the growth plate (GP) undergo increases in volume during different cascades of cell differentiation during longitudinal bone growth. The volume increase is reported to be the most significant variable in understanding the mechanism of long bone growth.
Methods:
Forty-five postnatal Sprague-Dawley rat pups, 7-15 days old were divided into nine age groups (P7-P15). Five pups were allocated to each group. The rats were sacrificed and tibia and metatarsal bones were harvested. Bone lengths were measured after 0, 24, 48, and 72 hours of ex vivo incubation. Histology of bones was carried out, and GP lengths and chondrocyte densities were determined.
Results:
There were significant differences in bone length among the age groups after 0 and 72 hours of incubation. Histological sectioning was possible in metatarsal bone from all age groups, and in tibia from 7- to 13-day-old rats. No significant differences in tibia and metatarsal GP lengths were seen among different age groups at 0 and 72 hours of incubation. Significant differences in chondrocyte densities along the epiphyseal GP of the bones between 0 and 72 hours of incubation were observed in most of the age groups.
Conclusion:
Ex vivo growth of tibia and metatarsal bones of rats aged 7-15 days old is possible, with percentage growth rates of 23.87 ± 0.80% and 40.38 ± 0.95% measured in tibia and metatarsal bone, respectively. Histological sectioning of bones was carried out without the need for decalcification in P7-P13 tibia and P7-P15 metatarsal bone. Increases in chondrocyte density along the GP influence overall bone elongation.
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