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[罗匹拉姆与地昔帕明治疗伴有严重抑郁症状住院患者的双盲研究初步结果]

[Preliminary results of a double-blind study between rolipram and desipramine in hospitalized patients with major depressive symptoms].

作者信息

Guiot-Goffioul F, Gerard-Vandenhove M A, Troisfontaines B, Breulet M, von Frenckell R, Bobon D

出版信息

Acta Psychiatr Belg. 1987 Mar-Apr;87(2):230-5.

PMID:3618273
Abstract

Rolipram facilitates the postsynaptic neurotransmission of NA through a completely new mechanism of action, namely, an inhibition of the inactivation of the second messenger (the cyclic AMP) by phosphodiesterase. In the present study, Rolipram is compared to a classical tricyclic antidepressant which facilitates the NA transmission through an inhibition of its presynaptic reuptake: Desipramine. Preliminary results on 12 Rolipram patients vs. 9 Desipramine patients indicate that Rolipram has an antidepressant potency comparable to Desipramine with less anticholinergic and hypotensive side effects. This study also illustrates that a 14-factor AMDP profile gives much more information than a single total score such as the Hamilton score.

摘要

咯利普兰通过一种全新的作用机制促进去甲肾上腺素(NA)的突触后神经传递,即抑制磷酸二酯酶对第二信使(环磷酸腺苷)的失活作用。在本研究中,将咯利普兰与一种经典的三环类抗抑郁药——通过抑制NA的突触前再摄取来促进NA传递的地昔帕明进行比较。12例服用咯利普兰的患者与9例服用地昔帕明的患者的初步结果表明,咯利普兰的抗抑郁效力与地昔帕明相当,且抗胆碱能和降压副作用较少。这项研究还表明,14项AMDP量表提供的信息比诸如汉密尔顿量表这样的单一总分要多得多。

相似文献

1
[Preliminary results of a double-blind study between rolipram and desipramine in hospitalized patients with major depressive symptoms].[罗匹拉姆与地昔帕明治疗伴有严重抑郁症状住院患者的双盲研究初步结果]
Acta Psychiatr Belg. 1987 Mar-Apr;87(2):230-5.
2
Is phosphodiesterase inhibition a new mechanism of antidepressant action? A double blind double-dummy study between rolipram and desipramine in hospitalized major and/or endogenous depressives.
Eur Arch Psychiatry Neurol Sci. 1988;238(1):2-6. doi: 10.1007/BF00381071.
3
Rolipram in major depressive disorder: results of a double-blind comparative study with imipramine.罗匹尼罗治疗重度抑郁症:与丙咪嗪的双盲对照研究结果
Pharmacopsychiatry. 1989 Jul;22(4):156-60. doi: 10.1055/s-2007-1014599.
4
Clinical and biochemical effects of the selective phosphodiesterase inhibitor rolipram in depressed inpatients controlled by determination of plasma level.通过测定血浆水平来控制的抑郁症住院患者中,选择性磷酸二酯酶抑制剂咯利普兰的临床和生化效应
Pharmacopsychiatry. 1988 Nov;21(6):378-9. doi: 10.1055/s-2007-1017016.
5
Results of a phase II study of the antidepressant effect of rolipram.咯利普兰抗抑郁作用的II期研究结果。
Pharmacopsychiatry. 1984 Nov;17(6):188-90. doi: 10.1055/s-2007-1017435.
6
The role of neuropharmacologic selectivity in antidepressant action: fluvoxamine versus desipramine.神经药理学选择性在抗抑郁作用中的角色:氟伏沙明与地昔帕明的对比
J Clin Psychiatry. 1990 Sep;51(9):367-72.
7
Controlled cross-over study of a 5-HT uptake inhibiting and an NA uptake inhibiting antidepressant.一项关于5-羟色胺摄取抑制型和去甲肾上腺素摄取抑制型抗抑郁药的对照交叉研究。
Acta Psychiatr Scand Suppl. 1981;290:244-55.
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Fluoxetine and desipramine in major depressive disorder.氟西汀和地昔帕明治疗重度抑郁症
J Clin Psychopharmacol. 1993 Oct;13(5):305-11.
9
Effects of rolipram, a phosphodiesterase 4 inhibitor, in combination with imipramine on depressive behavior, CRE-binding activity and BDNF level in learned helplessness rats.磷酸二酯酶4抑制剂咯利普兰与丙咪嗪联用对习得性无助大鼠抑郁行为、CRE结合活性及脑源性神经营养因子水平的影响
Eur J Pharmacol. 2004 Sep 13;498(1-3):135-42. doi: 10.1016/j.ejphar.2004.07.084.
10
In-patient major depression: is rolipram as effective as amitriptyline?住院重度抑郁症:咯利普兰与阿米替林疗效相同吗?
Eur J Clin Pharmacol. 1991;40(2):127-9. doi: 10.1007/BF00280065.

引用本文的文献

1
Is phosphodiesterase inhibition a new mechanism of antidepressant action? A double blind double-dummy study between rolipram and desipramine in hospitalized major and/or endogenous depressives.
Eur Arch Psychiatry Neurol Sci. 1988;238(1):2-6. doi: 10.1007/BF00381071.
2
Dysbalance of neuronal second messenger function in the aetiology of affective disorders: a pathophysiological concept hypothesising defects beyond first messenger receptors.情感障碍病因中神经元第二信使功能失衡:一种假设超出第一信使受体缺陷的病理生理概念。
J Neural Transm. 1989;75(1):21-9. doi: 10.1007/BF01250641.
3
Effects of the phosphodiesterase inhibitor rolipram on the acoustic startle response in rats.
Psychopharmacology (Berl). 1991;105(1):27-36. doi: 10.1007/BF02316860.