期刊
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
卷 100, 期 3, 页码 624-629出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbb.2011.11.004
关键词
alpha 7 nicotinic acetylcholine receptor; Serotonin reuptake inhibition; Antidepressant; Mouse forced swim test; Mouse tail suspension test
Emerging evidence points to an involvement of nicotinic acetylcholine receptors (nAChRs) in major depression. Nicotine improves symptoms of depression in humans and shows antidepressant-like effects in rodents. Monoamine release is facilitated by nAChR stimulation, and nicotine-evoked serotonin (5-HT) release has been shown to depend on alpha 7 nAChR activation. The alpha 7 nAChR agonist PNU-282987 shows no antidepressant-like activity when tested alone in the mouse forced swim (mFST) or tail suspension tests (mTST). However, in combination with a sub-active dose of the selective 5-HT reuptake inhibitor citalopram, inducing similar to 50% 5-HT reuptake inhibition, PNU-282987 has shown marked antidepressant-like effects in the mFST. SSR180711 is a recently described alpha 7 nAChR agonist that has shown antidepressant-like activity in the rat forced swim test. To address the possibility that 5-HT reuptake inhibition contributes to the antidepressant-like profile of SSR180711, we compared the behavioural and biochemical profiles of PNU-282987 and SSR180711. In the mFST and mTST, SSR180711 (3-30 mg/kg, s.c.) showed dose-dependent antidepressant-like activity, while PNU-282987 (3-30 mg/kg, s.c.) showed no significant effect. The ED50 to displace [H-3]alpha-bungarotoxin binding was 1.7 and 5.5 mg/kg for SSR180711 and PNU-282987, respectively, suggesting that both compounds produce near-maximal alpha 7 nAChR occupancy at the highest dose. While PNU-282987 did not affect ex vivo [H-3]5-HT uptake, SSR180711 inhibited [H-3]5-HT uptake with an ED50 of 30 mg/kg. This degree of inhibition is similar to that observed with a citalopram dose of similar to 2.4 mg/kg, a dose that is normally not active in the mFST or mTST. This suggests that the antidepressant-like activity of SSR180711 may involve partial 5-HT reuptake inhibition. SSR180711 therefore represents a compound displaying the synergistic effect of alpha 7 nAChR agonism combined with partial 5-HT reuptake inhibition previously described. The addition of alpha 7 nAChR agonism to classical monoamine-based mechanisms may represent a novel option for the improved treatment of major depression. (C) 2011 Elsevier Inc. All rights reserved.
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