Td. Schmanke et al., A CRITICAL PERIOD FOR REDUCED BRAIN VULNERABILITY TO DEVELOPMENTAL INJURY II - VOLUMETRIC STUDY OF THE NEOCORTEX AND THALAMUS IN CATS, Developmental brain research, 105(2), 1998, pp. 325-337
Groups of young adult cats with a left hemineodecortication at postnat
al (P) ages (in days) 5-15 (P10), 30 (P30), 60 (P60), 90 (P90), 120 (P
120) and in adulthood, were used to measure the volume of the thalamus
, bilaterally, and of the remaining neocortex (right hemisphere). The
same subjects were employed for the behavioral studies reported in the
preceding paper. There was a bilateral, age-dependent, thalamic volum
e decrease. Ipsilateral to the resection, the thalamic shrinkage was t
he largest for the adult-lesioned cats (by 56.7%) and it was the small
est for the P30 group (43.3%), with a tendency towards a greater atrop
hy as the age at lesion increased. A similar pattern of atrophy was se
en for the contralateral thalamus but the volume reduction was much le
ss pronounced such that it was significant only for the four older age
-at-lesion groups (ranging from 18.2% to 11.2% for the P120 and P90 gr
oups respectively). Once again, the shrinkage was the smallest for the
P30 group (5.3%). The remaining neocortex also shrunk in these animal
s, but the volume decrease was significant only for the adult-lesioned
(17.8%) and the P120 group (15.4%), while the P30 group had practical
ly no shrinkage (2.4%). The frontal cortex had no atrophy or it was mi
nimal but the shrinkage gradually increased caudally such that all les
ioned groups had some size reduction of the occipital cortex. The pres
ent results, together with the main conclusion of the preceding paper,
indicate that there is a critical maturation period (CMP) of reduced
forebrain vulnerability to neocortical injury which, in cats, tends to
end between 30 to 60 days postnatally. The implications for developme
ntal brain damage in other higher mammal species as well as the possib
le morphological ontogenetical underpinnings of this period are discus
sed. (C) 1998 Elsevier Science B.V.