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新型5-羟色胺1A受体激动剂5-[3-[((2S)-1,4-苯并二恶烷-2-基甲基)氨基]丙氧基]-1,3-苯并二恶烷盐酸盐(MKC-242)对小鼠攻击行为和埋大理石行为的影响

Effect of 5-[3-[((2S)-1,4-benzodioxan-2-ylmethyl)amino]propoxy]-1,3-benzodioxole HCl (MKC-242), a novel 5-HT1A-receptor agonist, on aggressive behavior and marble burying behavior in mice.

作者信息

Abe M, Nakai H, Tabata R, Saito K, Egawa M

机构信息

Pharmaceuticals Laboratory I, Yokohama Research Center, Mitsubishi Chemical Corporation, Japan.

出版信息

Jpn J Pharmacol. 1998 Mar;76(3):297-304. doi: 10.1254/jjp.76.297.

Abstract

Behavioral effects of 5-[3-[((2S)-1,4-benzodioxan-2-ylmethyl)amino]propoxy]-1,3-be nzodioxole HCl (MKC-242), a novel 5-HT1A-receptor agonist, were evaluated using animal models of anxiety and obsessive compulsive disorder and compared against reference compounds. MKC-242 suppressed foot shock-induced fighting behavior without loss of motor coordination in mice as the reference compounds did. The ED50 values of MKC-242, buspirone, tandospirone and diazepam were 1.7, 42, 80 and 2.0 mg/kg, p.o., respectively. The duration of the suppression of fighting by MKC-242 was longer than those of buspirone and tandospirone and comparable to that of diazepam. Similar results were also obtained with the water-lick conflict test in rats. The plasma concentration of MKC-242 in rats was much higher than the reported value of buspirone during 0.25-6 hr after oral administration. In addition, MKC-242 reduced marble burying behavior without reduction of motor activity. Fluoxetine, tandospirone and diazepam also reduced the behavior at non-sedative doses. These findings indicate that MKC-242 possesses a longer-lasting anxiolytic effect than azapirones. This might be due to the high concentration of the compound in plasma. In addition, it is also suggested that MKC-242 possesses an antiobsessional effect.

摘要

新型5-羟色胺1A受体激动剂5-[3-[((2S)-1,4-苯并二恶烷-2-基甲基)氨基]丙氧基]-1,3-苯并二恶烷盐酸盐(MKC-242)的行为效应,采用焦虑和强迫症动物模型进行评估,并与参比化合物进行比较。与参比化合物一样,MKC-242可抑制小鼠足部电击诱导的攻击行为,且不影响运动协调性。MKC-242、丁螺环酮、坦度螺酮和地西泮的口服半数有效剂量(ED50)分别为1.7、42、80和2.0mg/kg。MKC-242对攻击行为的抑制持续时间长于丁螺环酮和坦度螺酮,与地西泮相当。在大鼠水舔冲突试验中也得到了类似结果。口服给药后0.25至6小时内,大鼠体内MKC-242的血浆浓度远高于报道的丁螺环酮值。此外,MKC-242可减少埋大理石行为,且不降低运动活性。氟西汀、坦度螺酮和地西泮在非镇静剂量下也可减少该行为。这些发现表明,MKC-242具有比氮杂螺环酮类药物更持久的抗焦虑作用。这可能是由于该化合物在血浆中的高浓度所致。此外,还提示MKC-242具有抗强迫作用。

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