Dj. Heal et al., QUANTIFICATION OF PRESYNAPTIC ALPHA(2)-ADRENOCEPTORS IN RAT-BRAIN AFTER SHORT-TERM DSP-4 LESIONING, European journal of pharmacology, 249(1), 1993, pp. 37-41
The relative numbers of pre- and postsynaptic alpha2-adrenoceptors wer
e determined in various rat brain regions after short-term DSP-4 (N-(2
-chloroethyl)-N-ethyl-2-bromobenzylamine) lesioning. For these studies
, rats pretreated with zimeldine (10 mg/kg i.p.) were injected with DS
P-4 (100 mg/kg i.p.) and were killed either 3 or 15 days later. At the
3 day time-point, DSP-4 treatment produced marked reductions in the n
oradrenaline content of the cortex (93%), hippocampus (89%), hypothala
mus (83%) and cerebellum (92%) with no change in the levels of dopamin
e or 5-HT. This treatment also decreased the number of alpha2-adrenoce
ptors labelled with [H-3]idazoxan in the cortex (20%), hippocampus (18
%), cerebellum (24%) and hypothalamus (39%). Fifteen days after DSP-4
lesioning, the marked reductions of noradrenaline were sustained in th
e cortex, hippocampus and cerebellum, but there was a considerable rev
ersal of the effect of DSP-4 in the hypothalamus. At this time-point,
the decrease in a2-adrenoceptors was attenuated in cortex (4%) and cer
ebellum (0%) and their number was increased in hippocampus (8%) and hy
pothalamus (7%). Together, the data argue that presynaPtic alpha2-adre
noceptors comprise approximately 20% of the total alpha2-adrenoceptor
population in the cortex, hippocampus and cerebellum, but about 40% of
it in the hypothalamus. Furthermore, they also demonstrate that altho
ugh the number of presynaptic alpha2-adrenoceptors in rat brain can be
determined by the reduction of radioligand-receptor binding shortly a
fter DSP-4 lesioning, this effect is rapidly masked by receptor prolif
eration in response to noradrenergic denervation.