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Hypophysectomy does not prevent development of striatal dopamine receptor supersensitivity induced by repeated neuroleptic treatment.

作者信息

Jenner P, Rupniak N M, Hall M D, Dyer R, Leigh N, Marsden C D

出版信息

Eur J Pharmacol. 1981 Nov 19;76(1):31-6. doi: 10.1016/0014-2999(81)90006-6.

DOI:10.1016/0014-2999(81)90006-6
PMID:6119220
Abstract

Hruska et al. (1980) reported that hypophysectomy prevented the onset of dopamine receptor supersensitivity. We have repeated this investigation administering haloperidol (0.75 mg/day) or sulpiride (2 X 15 mg/day) or saline for 17 days, followed by a 3 day drug washout period, to sham-operated or hypophysectomised rats. Haloperidol or sulpiride pretreatment caused an enhancement of apomorphine-induced stereotyped behaviour and increased the number of specific striatal [3H]spiperone binding sites (Bmax) in both hypophysectomised and sham-operated animals compared to their respective saline controls. We conclude that hypophysectomy does not prevent the onset of striatal dopamine receptor supersensitivity induced by repeated neuroleptic treatment in the rat.

摘要

相似文献

1
Hypophysectomy does not prevent development of striatal dopamine receptor supersensitivity induced by repeated neuroleptic treatment.
Eur J Pharmacol. 1981 Nov 19;76(1):31-6. doi: 10.1016/0014-2999(81)90006-6.
2
Differential alterations in striatal dopamine receptor sensitivity induced by repeated administration of clinically equivalent doses of haloperidol, sulpiride or clozapine in rats.大鼠反复给予临床等效剂量的氟哌啶醇、舒必利或氯氮平所诱导的纹状体多巴胺受体敏感性的差异改变。
Psychopharmacology (Berl). 1984;84(4):512-9. doi: 10.1007/BF00431458.
3
Hypophysectomy may non-selectively alter pharmacokinetic parameters to enhance the ability of haloperidol to increase striatal dopamine receptor density in the rat.
Biochem Pharmacol. 1986 Oct 15;35(20):3501-6. doi: 10.1016/0006-2952(86)90618-0.
4
Changes in apomorphine-induced stereotypy as a result of subacute neuroleptic treatment correlates with increased D-2 receptors, but not with increases in D-1 receptors.亚急性抗精神病药物治疗导致的阿扑吗啡诱导的刻板行为变化与D-2受体增加相关,但与D-1受体增加无关。
Biochem Pharmacol. 1983 Oct 1;32(19):2921-7. doi: 10.1016/0006-2952(83)90397-0.
5
Differential effects of continuous administration for 1 year of haloperidol or sulpiride on striatal dopamine function in the rat.氟哌啶醇或舒必利连续给药1年对大鼠纹状体多巴胺功能的不同影响。
Psychopharmacology (Berl). 1984;84(4):503-11. doi: 10.1007/BF00431457.
6
Elevation of circulating prolactin concentrations may not cause striatal dopamine receptor supersensitivity.循环中催乳素浓度的升高可能不会导致纹状体多巴胺受体超敏反应。
Eur J Pharmacol. 1983 Sep 30;93(3-4):195-200. doi: 10.1016/0014-2999(83)90137-1.
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Repeated administration of sulpiride for three weeks produces behavioural and biochemical evidence for cerebral dopamine receptor supersensitivity.
Biochem Pharmacol. 1982 Feb 1;31(3):325-8. doi: 10.1016/0006-2952(82)90178-2.
8
Striatal dopamine receptor supersensitivity after long-term haloperidol treatment of hypophysectomized rats.
Braz J Med Biol Res. 1989;22(6):741-3.
9
Differential alteration of striatal D-1 and D-2 receptors induced by the long-term administration of haloperidol, sulpiride or clozapine to rats.长期给大鼠施用氟哌啶醇、舒必利或氯氮平所诱导的纹状体D-1和D-2受体的差异性改变。
Psychopharmacology Suppl. 1985;2:174-81. doi: 10.1007/978-3-642-70140-5_21.
10
Long-term adaptive changes in striatal dopamine function in response to chronic neuroleptic intake in rats.
J Neural Transm Suppl. 1983;18:205-12.

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