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断奶前发育过程中大鼠听觉惊吓反应的5-羟色胺能调节

Serotonergic modulation of the acoustic startle response in rats during preweaning development.

作者信息

Sheets L P, Cook L L, Reiter L W

机构信息

Neurotoxicology Division, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711.

出版信息

Pharmacol Biochem Behav. 1989 Jun;33(2):415-22. doi: 10.1016/0091-3057(89)90524-8.

DOI:10.1016/0091-3057(89)90524-8
PMID:2530591
Abstract

The involvement of serotonin (5-HT) in modulating the acoustic startle response (ASR) is well established in adult rats, but 5-HT involvement during the preweaning period, when 5-HT neurons undergo extensive development, has not previously been described. Three 5-HT receptor subtypes are reported to modulate the ASR in adult rats: 5-HT1A and 5-HT2 receptor agonists facilitate the ASR, whereas 5-HT1B agonists decrease the response. In the present study, the effects of 5-HT agonists and generalized 5-HT depletion on the ASR were studied in preweanling animals, using independent groups of Long-Evans rats tested on postnatal day (PND) 13, 17 and 21. 8-Hydroxy-2-(di-n-propylamino) tetralin (8OHDPAT, 62-1000 micrograms/kg), a 5-HT1A receptor agonist, and 5-methoxy-N,N-dimethyl tryptamine (MeODMT, 2-4 mg/kg), a nonselective 5-HT agonist, had no effect on PND 13 and then increased the ASR on PND 17 and 21. The 5-HT2 receptor antagonists cyproheptadine (5 mg/kg) and ketanserin (5 mg/kg) blocked the effect of MeODMT at both ages, providing some evidence that MeODMT increased the ASR through 5-HT2 receptors. 1-(m-Chlorophenyl) piperazine (mCPP, 1-5 mg/kg), a 5-HT1B agonist, had no effect on ASR amplitude on PND 13 or 17 and then produced a dose-related decrease in the response on PND 21. Generalized depletion of 5-HT by 80-90% in whole-brain and spinal cord, using p-chlorophenylalanine (PCPA, 300 mg/kg 24 hr prior to testing), did not alter ASR amplitude at any age.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

血清素(5-羟色胺,5-HT)参与调节成年大鼠的听觉惊吓反应(ASR),这一点已得到充分证实,但在离乳前期,即5-HT神经元经历广泛发育的时期,5-HT的参与情况此前尚未见报道。据报道,三种5-HT受体亚型可调节成年大鼠的ASR:5-HT1A和5-HT2受体激动剂可促进ASR,而5-HT1B激动剂则会降低反应。在本研究中,使用独立分组的Long-Evans大鼠,在出生后第13、17和21天进行测试,研究了5-HT激动剂和全身性5-HT耗竭对离乳前动物ASR的影响。5-HT1A受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8OHDPAT,62-1000微克/千克)和非选择性5-HT激动剂5-甲氧基-N,N-二甲基色胺(MeODMT,2-4毫克/千克)在出生后第13天对ASR无影响,而在出生后第17天和21天则增加了ASR。5-HT2受体拮抗剂赛庚啶(5毫克/千克)和酮色林(5毫克/千克)在两个年龄段均阻断了MeODMT的作用,这为MeODMT通过5-HT2受体增加ASR提供了一些证据。5-HT1B激动剂1-(间氯苯基)哌嗪(mCPP,1-5毫克/千克)在出生后第13天或17天对ASR幅度无影响,而在出生后第21天则产生了与剂量相关的反应降低。在测试前24小时使用对氯苯丙氨酸(PCPA,300毫克/千克)使全脑和脊髓中的5-HT普遍耗竭80-90%,在任何年龄段均未改变ASR幅度。(摘要截选至250字)

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