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5-羟色胺1A受体激动剂8-羟基二丙胺基四氢萘增加大鼠对美味湿软饲料和流质食物的摄入量。

The 5-HT1A agonist 8-OH-DPAT increases consumption of palatable wet mash and liquid diets in the rat.

作者信息

Dourish C T, Cooper S J, Gilbert F, Coughlan J, Iversen S D

机构信息

Merck Sharp and Dohme Research Laboratories, Neuroscience Research Centre, Harlow, Essex, UK.

出版信息

Psychopharmacology (Berl). 1988;94(1):58-63. doi: 10.1007/BF00735881.

DOI:10.1007/BF00735881
PMID:2964672
Abstract

The 5-HT1A agonist 8-OH-DPAT, at a dose of 30 micrograms/kg, enhanced the consumption of sweetened wet mash and sweetened milk in non-deprived rats. In partially satiated rats, sensitivity to the hyperphagic effect of 8-OH-DPAT on wet mash intake was substantially increased, so that the minimally effective dose was reduced to 3 micrograms/kg. Similarly, 8-OH-DPAT was more efficacious in increasing milk intake in satiated rats. Thus, 30 and 40 micrograms/kg 8-OH-DPAT produced a 4-fold increase of milk intake in completely satiated rats compared to a 2-fold increase in partially satiated animals at a dose of 30 micrograms/kg. The increased intake of liquid and wet mash diets observed after treatment with low doses of 8-OH-DPAT argues against the involvement of non-specific gnawing in the increased consumption of solid food produced by the drug. Rather, the data suggest that 8-OH-DPAT may specifically stimulate appetite by counteracting a tonic serotonergic inhibition of feeding. The present experiments also showed that 8-OH-DPAT attenuates fenfluramine-induced anorexia which is thought to depend on increased serotonergic neurotransmission.

摘要

5-羟色胺1A受体激动剂8-羟基二丙胺基四氢萘(8-OH-DPAT),剂量为30微克/千克时,可增加未禁食大鼠对加糖湿料和加糖牛奶的摄入量。在部分饱足的大鼠中,8-OH-DPAT对湿料摄入量的促食作用敏感性显著增加,以至于最小有效剂量降至3微克/千克。同样,8-OH-DPAT在增加饱足大鼠的牛奶摄入量方面更有效。因此,与30微克/千克剂量下部分饱足动物2倍的增加量相比,30微克/千克和40微克/千克的8-OH-DPAT可使完全饱足大鼠的牛奶摄入量增加4倍。低剂量8-OH-DPAT治疗后观察到的液体和湿料饮食摄入量增加,表明药物引起的固体食物摄入量增加并非由非特异性啃咬所致。相反,数据表明8-OH-DPAT可能通过抵消5-羟色胺对进食的紧张性抑制作用来特异性刺激食欲。本实验还表明,8-OH-DPAT可减轻芬氟拉明诱导的厌食症,这种厌食症被认为与5-羟色胺能神经传递增加有关。

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1
The 5-HT1A agonist 8-OH-DPAT increases consumption of palatable wet mash and liquid diets in the rat.5-羟色胺1A受体激动剂8-羟基二丙胺基四氢萘增加大鼠对美味湿软饲料和流质食物的摄入量。
Psychopharmacology (Berl). 1988;94(1):58-63. doi: 10.1007/BF00735881.
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3
Characteristics of feeding induced by the serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT).血清素激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)诱导的进食特征。
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Behavioural specificity of 8-OH-DPAT-induced feeding.8-羟基二丙基氨基四氢萘诱导进食的行为特异性。
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5
8-OH-DPAT elicits feeding and not chewing: evidence from liquid diet studies and a diet choice test.8-羟基二丙胺基四氢吡咯引发进食而非咀嚼:来自流食研究和饮食选择测试的证据。
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Hyperinsulinemia of the genetically obese (fa/fa) rat is decreased by a low dose of the 5-HT1A receptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT).低剂量的5-羟色胺1A受体激动剂8-羟基-2-(二正丙基氨基)四氢化萘(8-OH-DPAT)可降低遗传性肥胖(fa/fa)大鼠的高胰岛素血症。
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7
Low doses of the putative serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) elicit feeding in the rat.低剂量的假定血清素激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)会引发大鼠进食。
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8-Hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) elicits eating in free-feeding rats by acting on central serotonin neurons.
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Neurochemical and behavioural evidence for mediation of the hyperphagic action of 8-OH-DPAT by 5-HT cell body autoreceptors.5-羟色胺细胞体自身受体介导8-羟基二丙胺甲苯(8-OH-DPAT)食欲亢进作用的神经化学和行为学证据。
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Low doses of the 5-HT1A agonist 8-hydroxy-2-(di-n-propylamino)-tetralin (8-OH DPAT) increase ethanol intake.低剂量的5-羟色胺1A受体激动剂8-羟基-2-(二正丙基氨基)四氢化萘(8-OH DPAT)会增加乙醇摄入量。
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Effects of the novel anxiolytics gepirone, buspirone and ipsapirone on free feeding and on feeding induced by 8-OH-DPAT.新型抗焦虑药吉哌隆、丁螺环酮和伊沙匹隆对自由进食及8-羟基二丙胺诱发进食的影响。
Psychopharmacology (Berl). 1987;93(3):349-52. doi: 10.1007/BF00187255.
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Blockade of 8-OH-DPAT-induced feeding by dopamine antagonists.多巴胺拮抗剂对8-OH-DPAT诱导进食的阻断作用。
Psychopharmacology (Berl). 1989;99(3):402-8. doi: 10.1007/BF00445567.
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Selective reduction by serotonergic agents of hypertonic saline consumption in rats: evidence for possible 5-HT1C receptor mediation.血清素能药物对大鼠高渗盐水摄入量的选择性降低作用:5-HT1C受体介导的可能证据。
Psychopharmacology (Berl). 1989;99(2):196-201. doi: 10.1007/BF00442807.
8
Evidence that d-fenfluramine anorexia is mediated by 5-HT1 receptors.右旋芬氟拉明所致厌食由5-羟色胺1型受体介导的证据。
Psychopharmacology (Berl). 1989;97(2):213-8. doi: 10.1007/BF00442252.
9
Reversal of the anorectic effect of (+)-fenfluramine in the rat by the selective cholecystokinin receptor antagonist MK-329.选择性胆囊收缩素受体拮抗剂MK-329对大鼠体内(+)-芬氟拉明厌食作用的逆转
Br J Pharmacol. 1990 Jan;99(1):65-70. doi: 10.1111/j.1476-5381.1990.tb14655.x.
10
8-OH-DPAT specifically enhances feeding behaviour in mice: evidence from behavioural competition.8-羟基二丙基氨基四氢萘特异性增强小鼠的进食行为:来自行为竞争的证据。
Psychopharmacology (Berl). 1990;101(3):408-13. doi: 10.1007/BF02244062.
Eur J Pharmacol. 1983 May 20;90(1):151-3. doi: 10.1016/0014-2999(83)90230-3.
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Serotonin and appetite.血清素与食欲。
Neuropharmacology. 1984 Dec;23(12B):1537-51. doi: 10.1016/0028-3908(84)90098-4.
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Hyperphagic and anorectic effects of beta-carbolines in a palatable food consumption test: comparisons with triazolam and quazepam.β-咔啉在美味食物消费测试中的贪食和厌食作用:与三唑仑和夸西泮的比较
Eur J Pharmacol. 1986 Jan 29;120(3):257-65. doi: 10.1016/0014-2999(86)90466-8.
6
Low doses of the putative serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) elicit feeding in the rat.低剂量的假定血清素激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)会引发大鼠进食。
Psychopharmacology (Berl). 1985;86(1-2):197-204. doi: 10.1007/BF00431709.
7
Benzodiazepine receptor ligands and the consumption of a highly palatable diet in non-deprived male rats.苯二氮䓬受体配体与非饥饿雄性大鼠对高适口性饮食的消耗
Psychopharmacology (Berl). 1985;86(3):348-55. doi: 10.1007/BF00432227.
8
8-OH-DPAT elicits gnawing, and eating of solid but not liquid foods.8-羟基二丙胺基四氢萘引发啃咬以及对固体而非液体食物的进食行为。
Psychopharmacology (Berl). 1987;92(2):192-5. doi: 10.1007/BF00177914.
9
8-OH-DPAT-induced hyperphagia: its neural basis and possible therapeutic relevance.8-羟基二丙胺四乙酸诱导的食欲亢进:其神经基础及可能的治疗意义。
Appetite. 1986;7 Suppl:127-40. doi: 10.1016/s0195-6663(86)80058-7.
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Characteristics of feeding induced by the serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT).血清素激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)诱导的进食特征。
Brain Res Bull. 1985 Oct;15(4):377-84. doi: 10.1016/0361-9230(85)90005-x.