TY - JOUR
T1 - Effects of propentofylline, a NGF synthesis stimulator, on alterations in muscarinic cholinergic receptors induced by basal forebrain lesion in rats
AU - Fuji, Kazuyuki
AU - Hiramatsu, Masayuki
AU - Hayashi, Saori
AU - Kameyama, Tsutomu
AU - Nabeshima, Toshitaka
N1 - Funding Information:
We are grateful to Nippon Hoechst Co. Ltd. (Tokyo, Japan) for the supply of propentofylline. This work was supported, in part, by a Grant from the Kimi Tokuda Memorial Foundation.
PY - 1993/2/5
Y1 - 1993/2/5
N2 - Basal forebrain (BF) lesions induced by ibotenic acid produced increases in the Bmax and Kd values of [3H]QNB binding sites in the frontal cortex, parietal cortex, and hippocampus. Twenty-eight-day successive administration of propentofylline (10 and 25 mg/kg, p.o.) significantly reduced the Kd values of [3H]QNB binding sites, to the levels of those in a sham group, in a dose-dependent manner. Moreover, propentofylline (25 mg/kg, p.o.) significantly reduced the Bmax value of [3H]QNB binding sites compared with that in a vehicle-treated BF-lesioned group. These results suggest that successive administration of propentofylline ameliorates changes in muscarinic cholinergic receptors through improving presynaptic cholinergic dysfunction.
AB - Basal forebrain (BF) lesions induced by ibotenic acid produced increases in the Bmax and Kd values of [3H]QNB binding sites in the frontal cortex, parietal cortex, and hippocampus. Twenty-eight-day successive administration of propentofylline (10 and 25 mg/kg, p.o.) significantly reduced the Kd values of [3H]QNB binding sites, to the levels of those in a sham group, in a dose-dependent manner. Moreover, propentofylline (25 mg/kg, p.o.) significantly reduced the Bmax value of [3H]QNB binding sites compared with that in a vehicle-treated BF-lesioned group. These results suggest that successive administration of propentofylline ameliorates changes in muscarinic cholinergic receptors through improving presynaptic cholinergic dysfunction.
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U2 - 10.1016/0304-3940(93)90117-4
DO - 10.1016/0304-3940(93)90117-4
M3 - Article
C2 - 8469410
AN - SCOPUS:0027208902
SN - 0304-3940
VL - 150
SP - 99
EP - 102
JO - Neuroscience Letters
JF - Neuroscience Letters
IS - 1
ER -