QUANTIFICATION OF PRESYNAPTIC ALPHA(2)-ADRENOCEPTORS IN RAT-BRAIN AFTER SHORT-TERM DSP-4 LESIONING

Citation
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
Citations number
19
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00142999
Volume
249
Issue
1
Year of publication
1993
Pages
37 - 41
Database
ISI
SICI code
0014-2999(1993)249:1<37:QOPAIR>2.0.ZU;2-D
Abstract
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.