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5-羟色胺1A受体在利血平处理小鼠的强迫游泳轮实验中的作用。

Role of 5-HT1A receptors in the forced swimming wheel test in reserpine-treated mice.

作者信息

Kasahara K, Nagatani T, Takao K, Hashimoto S

机构信息

First Lab. for Pharmacological Research, Asahi Chemical Industry Co., Ltd., Miyazaki, Japan.

出版信息

Life Sci. 1993;52(22):1741-9. doi: 10.1016/0024-3205(93)90462-c.

DOI:10.1016/0024-3205(93)90462-c
PMID:8492637
Abstract

The antidepressant-like effect of 8-hydroxy-2-(di-n-propylamino)tetralin(8-OH-DPAT), a selective 5-HT1A receptor agonist, was studied in the forced swimming wheel test in reserpine-treated mice. 8-OH-DPAT and the antidepressant imipramine, dose-dependently increased the number of turns of a water wheel made by mice. This effect of imipramine (30 mg/kg, i.p.) was enhanced by reserpine treatment 24 hr before the test. The effect of 8-OH-DPAT (0.3 mg/kg, i.p.) was also enhanced in reserpine-treated mice. This enhanced effect of 8-OH-DPAT was blocked by pretreatment with the 5-HT1A receptor antagonists, (-)-propranolol (3 mg/kg, i.p.) and NAN-190 (1 mg/kg, i.p.), but was not blocked by a beta-blocker, (-)-atenolol (3 mg/kg, i.p.). 8-OH-DPAT did not affect locomotor activity in the reserpinized mice and did not affect the reduction of monoamine content induced by reserpine. These results suggest that the effect of 8-OH-DPAT in increasing the number of turns of the wheel made by mice was exerted through a 5-HT1A receptor and that this effect did not reflect only changes in the locomotor activity of the mice.

摘要

在利血平处理的小鼠的强迫游泳轮试验中,研究了选择性5-羟色胺1A(5-HT1A)受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)的抗抑郁样作用。8-OH-DPAT和抗抑郁药丙咪嗪剂量依赖性地增加了小鼠转动水轮的次数。在试验前24小时用利血平处理可增强丙咪嗪(30毫克/千克,腹腔注射)的这种作用。在利血平处理的小鼠中,8-OH-DPAT(0.3毫克/千克,腹腔注射)的作用也增强。8-OH-DPAT的这种增强作用被5-HT1A受体拮抗剂(-)-普萘洛尔(3毫克/千克,腹腔注射)和NAN-190(1毫克/千克,腹腔注射)预处理所阻断,但不被β-阻滞剂(-)-阿替洛尔(3毫克/千克,腹腔注射)阻断。8-OH-DPAT不影响利血平化小鼠的运动活性,也不影响利血平诱导的单胺含量的降低。这些结果表明,8-OH-DPAT增加小鼠转动水轮次数的作用是通过5-HT1A受体发挥的,并且这种作用不仅仅反映了小鼠运动活性的变化。

相似文献

1
Role of 5-HT1A receptors in the forced swimming wheel test in reserpine-treated mice.5-羟色胺1A受体在利血平处理小鼠的强迫游泳轮实验中的作用。
Life Sci. 1993;52(22):1741-9. doi: 10.1016/0024-3205(93)90462-c.
2
Mediation of the antidepressant-like effect of 8-OH-DPAT in mice by postsynaptic 5-HT1A receptors.突触后5-HT1A受体介导8-OH-DPAT对小鼠的抗抑郁样作用。
Br J Pharmacol. 1993 Mar;108(3):669-77. doi: 10.1111/j.1476-5381.1993.tb12859.x.
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The role of 5-HT1A and 5-HT1B receptors in antidepressant drug actions in the mouse forced swimming test.5-HT1A和5-HT1B受体在小鼠强迫游泳试验中抗抑郁药物作用中的角色。
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Antidepressant-like properties of some serotonin receptor ligands and calcium channel antagonists measured with the forced swimming test in mice.用小鼠强迫游泳试验测定某些5-羟色胺受体配体和钙通道拮抗剂的抗抑郁样特性。
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8-Hydroxy-2-(di-n-propylamino)tetralin, a selective serotonin1A receptor agonist, reduces the immobility of rats in the forced swimming test by acting on the nucleus raphe dorsalis.
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Buspirone enhances immobility in the forced swim test in mice.丁螺环酮可增强小鼠强迫游泳试验中的不动时间。
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5-HT1A and alpha-2 adrenergic receptors mediate the hyperglycemic and hypoinsulinemic effects of 8-hydroxy-2-(di-n-propylamino)tetralin in the conscious rat.5-羟色胺1A受体和α-2肾上腺素能受体介导了8-羟基-2-(二正丙基氨基)四氢萘对清醒大鼠的高血糖和低胰岛素血症作用。
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The behavioural effects of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) in mice.8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)对小鼠的行为影响。
Eur J Pharmacol. 1988 Sep 23;154(3):299-304. doi: 10.1016/0014-2999(88)90205-1.
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[Behavioural effects of 8-OH-DPAT, a 5-HT1A agonist in rats and effects on the behaviour of antimanic drugs].[5-羟色胺1A受体激动剂8-OH-DPAT对大鼠的行为影响及对抗躁狂药物行为的影响]
Yakubutsu Seishin Kodo. 1987 Sep;7(3):383-92.
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5-HT(1A) receptor full agonist, 8-OH-DPAT, exerts antidepressant-like effects in the forced swim test in ACTH-treated rats.5-羟色胺(1A)受体完全激动剂8-羟基二丙基氨基四氢萘(8-OH-DPAT)在促肾上腺皮质激素(ACTH)处理的大鼠的强迫游泳试验中发挥类似抗抑郁的作用。
Eur J Pharmacol. 2003 Nov 14;481(1):75-7. doi: 10.1016/j.ejphar.2003.09.008.

引用本文的文献

1
Differential responsiveness of inbred strains of rats to antidepressants in the forced swimming test: are Wistar Kyoto rats an animal model of subsensitivity to antidepressants?大鼠近交系在强迫游泳试验中对抗抑郁药的反应差异:Wistar Kyoto大鼠是对抗抑郁药敏感性降低的动物模型吗?
Psychopharmacology (Berl). 1996 Jan;123(2):191-8. doi: 10.1007/BF02246177.