In mammals, release from growth-inhibiting conditions results in catch-up g
rowth. To explain this phenomenon, we proposed the following model: 1) The
normal senescent decline in growth plate function depends not on age per se
, but on the cumulative number of replications that growth plate chondrocyt
es have undergone. 2) Conditions that suppress growth plate chondrocyte pro
liferation therefore slow senescence. 3) After transient growth inhibition,
growth plates are thus less senescent and hence show a greater growth rate
than expected for acre, resulting in catch-up growth. To test this model,
we administered dexamethasone to growing rabbits to suppress linear growth.
After stopping dexamethasone, catch-Lip growth occurred. In distal femoral
growth plates of untreated controls, we observed a senescent decline in th
e growth rate and in the heights of the proliferative zone, hypertrophic zo
ne, and total growth plate. During the period of catch-up growth, in the an
imals previously treated with dexamethasone, the senescent decline in all t
hese variables was delayed. Prior treatment with dexamethasone also delayed
epiphyseal fusion, These findings support our model that linear catch-up g
rowth is caused, at least in part, by a delay in growth plate senescence.