TY - JOUR
T1 - Differential long-term effect of AF64A on [3H]ACh synthesis and release in rat hippocampal synaptosomes
AU - Pittel, Zipora
AU - Cohen, Sasson
AU - Fisher, Abraham
AU - Heldman, Eliahu
PY - 1992/7/17
Y1 - 1992/7/17
N2 - The activities of various presynaptic cholinergic parameters were determined in hippocampal synaptosomes of rats 29 weeks after intracerebroventricular injection of ethylcholine aziridinium (AF64A) (3 nmol/2 μl/side) or vehicle (saline). Synaptosomes were preloaded with [3H]choline ([3H]Ch), treated with diisopropyl fluorophosphate to inhibit cholinesterase activity and then were assayed for their content of [3H]Ch and [3H]acetylcholine ([3H]ACh) and for their ability to synthesize and release [3H]ACh. In synaptosomes from AF64A-treated rats compared with synaptosomes from vehicle-treated rats we observed that: (i) specific uptake of [3H]ACh was reduced to 60% of control; (ii) residing [3H]ACh levels were 43% of control while residing [3H]Ch levels were 72% of control; (iii) basal and K+-induced [3H]ACh release were 77% and 73% of control, respectively; (iv) high K+-induced synthesis of [3H]ACh was only 9% of control; (v) but, choline acetyltransferase activity remained relatively high, being 80% of control. These results suggest that AF64A-induced cholinergic hypofunction is expressed by both loss of some cholinergic neurons and impairment in the functioning of the spared neurons.
AB - The activities of various presynaptic cholinergic parameters were determined in hippocampal synaptosomes of rats 29 weeks after intracerebroventricular injection of ethylcholine aziridinium (AF64A) (3 nmol/2 μl/side) or vehicle (saline). Synaptosomes were preloaded with [3H]choline ([3H]Ch), treated with diisopropyl fluorophosphate to inhibit cholinesterase activity and then were assayed for their content of [3H]Ch and [3H]acetylcholine ([3H]ACh) and for their ability to synthesize and release [3H]ACh. In synaptosomes from AF64A-treated rats compared with synaptosomes from vehicle-treated rats we observed that: (i) specific uptake of [3H]ACh was reduced to 60% of control; (ii) residing [3H]ACh levels were 43% of control while residing [3H]Ch levels were 72% of control; (iii) basal and K+-induced [3H]ACh release were 77% and 73% of control, respectively; (iv) high K+-induced synthesis of [3H]ACh was only 9% of control; (v) but, choline acetyltransferase activity remained relatively high, being 80% of control. These results suggest that AF64A-induced cholinergic hypofunction is expressed by both loss of some cholinergic neurons and impairment in the functioning of the spared neurons.
KW - AF64A
KW - Acetylcholine release
KW - Acetylcholine synthesis
KW - Cholinergic dysfunction
KW - Cholinergic toxicity
UR - http://www.scopus.com/inward/record.url?scp=0026713637&partnerID=8YFLogxK
U2 - 10.1016/0006-8993(92)91386-S
DO - 10.1016/0006-8993(92)91386-S
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AN - SCOPUS:0026713637
SN - 0006-8993
VL - 586
SP - 148
EP - 151
JO - Brain Research
JF - Brain Research
IS - 1
ER -