Running exercise |
6 to 12 km/day |
Hamster |
Increased proteoglycan content |
[26] |
Running exercise |
15 km over 28 days |
Rat OA induced by ACLT |
Reduced apoptosis and chondral erosions |
[50] |
Running exercise |
Varied age, 15 months exercise |
Rabbit |
Improved collagen organisation in young and reversed OA in older animals |
[54] |
Increased loading |
Increased loading following 8 weeks of splinting |
Rabbit |
Increased maturation of tissue and increased collagen content |
[55] |
Conditioning exercise |
Increased workload by 30% |
Foals |
Reduced cartilage degeneration index |
[56] |
Running exercise |
4 km/day, uphill, 15 weeks |
Beagle dogs |
Increased proteoglycan content and cartilage thickness |
[53] |
Cyclic pressure-induced strain |
0.3 Hz, 6 hours |
Human and monolayer |
Increased aggrecan gene expression |
[58] |
Hydrostatic pressure |
5 and 10 MPa at 1 Hz for durations of 4 h per day for 4 days |
Human monolayer |
Increased aggrecan and collagen type II gene expression |
[59] |
Dynamic compression |
3% at 0.01 to 1 Hz, 43 days |
Bovine and agarose |
Increased proteoglycan and collagen synthesis |
[63] |
Dynamic compression |
15%, 1 Hz, 48 hours |
Bovine and agarose |
Increased cell proliferation and proteoglycan synthesis and reduced nitrite release |
[60, 61] |
Dynamic compression |
10% at 1 Hz, 3 × 1 hr on, 1 hr off, 5 days/week for 21 days |
Bovine and agarose |
Increased equilibrium aggregate modulus, sGAG and collagen synthesis |
[62] |
Dynamic compression |
1 MPa, repeated 2 and 4 sec, 1.5 hour |
Bovine and explants |
Increased proteoglycan synthesis |
[64] |
Cyclic compression |
1 MPa, 0.5 Hz, 3 days |
Bovine and explants |
Increased proteoglycan synthesis |
[70] |