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潜在抗抑郁药UP 614-04与维洛沙嗪和丙咪嗪的药理学比较;行为学研究。

Pharmacological comparison of the potential antidepressant UP 614-04 with viloxazine and imipramine; behavioral studies.

作者信息

Meignen J, Grognet A, Deniard M J, Dalphrase F, Roux E, DeFeudis F V

出版信息

Gen Pharmacol. 1982;13(5):381-91. doi: 10.1016/0306-3623(82)90103-3.

DOI:10.1016/0306-3623(82)90103-3
PMID:6890919
Abstract
  1. Several behavioral tests were used to compare the pharmacological activity of the potential antidepressant UP 614-04 with those of viloxazine and imipramine. 2. Orally-administered UP 614-04, like viloxazine, reduced locomotor activity in mice, and, like viloxazine and imipramine, it antagonized the hypothermia or ptosis induced by reserpine or tetrabenazine and the hypothermia induced by a high dose of apomorphine. 3. UP 614-04 antagonized oxotremorine-induced hypothermia, and to a lesser extent, oxotremorine-induced tremors, indicating that it possesses some CNS anticholinergic activity. 4. Both imipramine and viloxazine were more potent than UP 614-04 in potentiating yohimbine toxicity in mice. 5. Orally-administered UP 614-04 potentiated d-amphetamine-induced stereotypy to a greater extent than viloxazine, but to a lesser extent than imipramine. 6. Intraperitoneally-injected UP 614-04 was much more potent than viloxazine in increasing tryptamine convulsive potential in rats, indicating that it might exert an inhibitory action on monoamine oxidase. 7. These results indicate that UP 614-04 has a behavioral profile that is consistent with an antidepressant action, but that it differs from imipramine and viloxazine.
摘要
  1. 采用了几种行为学测试来比较潜在抗抑郁药UP 614 - 04与维洛沙嗪和丙咪嗪的药理活性。2. 口服UP 614 - 04,与维洛沙嗪一样,可降低小鼠的运动活性,并且与维洛沙嗪和丙咪嗪一样,它能拮抗利血平或丁苯那嗪诱导的体温过低或眼睑下垂以及高剂量阿扑吗啡诱导的体温过低。3. UP 614 - 04可拮抗毒蕈碱诱导的体温过低,并且在较小程度上可拮抗毒蕈碱诱导的震颤,表明它具有一定的中枢神经系统抗胆碱能活性。4. 在增强小鼠育亨宾毒性方面,丙咪嗪和维洛沙嗪都比UP 614 - 04更有效。5. 口服UP 614 - 04比维洛沙嗪更能增强右旋苯丙胺诱导的刻板行为,但比丙咪嗪的作用程度小。6. 腹腔注射UP 614 - 04在增加大鼠色胺惊厥潜能方面比维洛沙嗪有效得多,表明它可能对单胺氧化酶发挥抑制作用。7. 这些结果表明,UP 614 - 04具有与抗抑郁作用一致的行为特征,但与丙咪嗪和维洛沙嗪不同。

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