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荷叶碱在强迫游泳试验中的抗抑郁样作用涉及小鼠的 5-羟色胺 1A(5-HT1A)受体。

Antidepressant-like effects of neferine in the forced swimming test involve the serotonin1A (5-HT1A) receptor in mice.

机构信息

Laboratory of Pharmacology, Department of Clinical Pharmacy, Yokohama College of Pharmacy, Matano-cho, Totsuka-ku, Yokohama, 245-0066, Japan.

出版信息

Eur J Pharmacol. 2010 May 25;634(1-3):62-7. doi: 10.1016/j.ejphar.2010.02.016. Epub 2010 Feb 20.

Abstract

The effects of neferine, an alkaloid of Nelumbo nucifera Gaertner embryos, on immobility in the forced swimming test, which is used to evaluate antidepressants, were investigated in mice. The administration of neferine from 25 to 100 mg/kg i.p. elicited anti-immobility effects in mice. The molecular dose effects of neferine in the forced swimming test were almost equal to those of the typical antidepressants maprotiline and imipramine. The involvement of the 5-HT receptor subtypes was also studied using 5-HT receptor antagonists. Anti-immobility effects of neferine are antagonized by the serotonin1A (5-HT1A) receptor antagonist, N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-(2-pyridinyl)cyclohexanecarboxamide (WAY 100635). However, the 5-HT1B receptor antagonist, 3-[3-(dimethylamino)propyl]-4-hydroxy-N-[4-(4-pyridinyl)phenyl] benzamide dihydrochloride (GR 55562), the 5-HT2 receptor antagonist, 6-methyl-1-(methylethyl)-ergoline-8beta-carboxylic acid 2-hydroxy-1-methylpropyl ester (LY 53857), the 5-HT3 receptor antagonist, ondansetron and the 5-HT4 receptor antagonist, 4-amino-5-chloro-2-methoxy-benzoic acid 2-(diethylamino)ethyl ester (SDZ 205,557) did not affect the anti-immobility effects of neferine. The anti-immobility effect of the selective 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetaralin (8-OH-DPAT) was also antagonized by WAY 100635. Furthermore, co-administration of subactive doses of neferine (10 mg/kg) and 8-OH-DPAT (0.1 mg/kg) produced synergistic antidepressant-like effects. These results suggest that neferine shows antidepressant-like effects in mice similar to typical antidepressants and that these effects are mediated by the 5-HT1A receptor. Therefore, the central effects of neferine are likely to be linked to serotonergic neurotransmission.

摘要

阿朴吗啡,一种从番荔枝科植物胚胎中提取的生物碱,被用于评估抗抑郁药的强迫游泳试验中,研究了其对不动性的影响。阿朴吗啡腹腔注射 25 至 100mg/kg 可引起小鼠抗不动性。阿朴吗啡在强迫游泳试验中的分子剂量效应几乎与典型抗抑郁药马普替林和丙咪嗪相同。使用 5-HT 受体拮抗剂还研究了 5-HT 受体亚型的参与。5-HT1A(5-HT1A)受体拮抗剂 N-[2-[4-(2-甲氧基苯基)-1-哌嗪基]乙基]-N-(2-吡啶基)环己烷甲酰胺(WAY 100635)拮抗阿朴吗啡的抗不动性作用。然而,5-HT1B 受体拮抗剂 3-[3-(二甲基氨基)丙基]-4-羟基-N-[4-(4-吡啶基)苯基]苯甲酰胺二盐酸盐(GR 55562),5-HT2 受体拮抗剂 6-甲基-1-(甲基乙基)-ergoline-8β-羧酸 2-羟基-1-甲基丙酯(LY 53857),5-HT3 受体拮抗剂昂丹司琼和 5-HT4 受体拮抗剂 4-氨基-5-氯-2-甲氧基苯甲酸 2-(二乙氨基)乙酯(SDZ 205,557)均不影响阿朴吗啡的抗不动性作用。选择性 5-HT1A 受体激动剂 8-羟基-2-(二正丙基氨基)四氢吖啶(8-OH-DPAT)的抗不动性作用也被 WAY 100635 拮抗。此外,亚有效剂量的阿朴吗啡(10mg/kg)和 8-OH-DPAT(0.1mg/kg)联合给药产生协同抗抑郁样作用。这些结果表明,阿朴吗啡在小鼠中表现出类似于典型抗抑郁药的抗抑郁样作用,这些作用是由 5-HT1A 受体介导的。因此,阿朴吗啡的中枢作用可能与 5-羟色胺能神经传递有关。

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