Transforming growth factor-beta(1) (TGF-beta(1)) mRNA is induced from
5 h to 3 days following hypoxic-ischaemic brain injury. Cell death als
o develops during this time suggesting that extracellular accumulation
of this peptide may be involved in the processes that regulate cell l
oss. We examined the effect of rhTGF-beta(1), (0, 2.5, 10, 50 ng) inje
cted into the cerebral lateral ventricle of rats 2 h after severe hypo
xic-ischaemic brain injury. Histological outcome and B-4-isolectin his
tochemistry were assessed 5 and 2 days, respectively following hypoxia
. Treatment with 10 ng TGF-beta(1) reduced the microglia reaction (p<0
.05), the magnitude of neuronal loss (p<0.01) and the area of cortical
infarction (p<0.05). Exogenous TGF-beta(1) given soon after hypoxic-i
schaemic brain injury may have therapeutic potential and act by inhibi
ting the microglial reaction.