• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

5-羟色胺1A、5-羟色胺1B和5-羟色胺2受体激动剂在新生大鼠幼崽中引发不同的行为反应。

5-HT1A, 5-HT1B and 5-HT2 receptor agonists induce differential behavioral responses in neonatal rat pups.

作者信息

Kirstein C L, Spear L P

机构信息

Department of Psychology, SUNY-Binghamton, NY 13901.

出版信息

Eur J Pharmacol. 1988 Jun 10;150(3):339-45. doi: 10.1016/0014-2999(88)90016-7.

DOI:10.1016/0014-2999(88)90016-7
PMID:2970973
Abstract

Sprague-Dawley rat pups at 3-4 days prenatally were tested in both the absence and presence of milk following administration of various doses of either the 5-HT1A agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OHDPAT), the 5-HT1B agonist 1-(3-chlorophenyl)piperazine (mCPP), or the 5-HT2 agonist 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI). Administration of 8-OHDPAT decreased mouthing, increased probing and increased behavioral activation. Conversely, the 5-HT2 agonist DOI and the 5-HT1B agonist mCPP increased mouthing and decreased probing. mCPP and DOI differed in their effects on behavioral activation, with mCPP decreasing and DOI increasing this composite behavioral score. mCPP increased grooming, whereas DOI elicited a characteristic unusual positioning of the limbs. Thus it appears that 5-HT1A, 5-HT1B and 5-HT2 receptor subtypes are present in the neonate and elicit differential behavioral responses upon stimulation with selective agonists. Ontogenetic variations in the balance among these receptor subtypes during development may be related to the ontogenetic reversal that has been previously reported in the impact of serotonin manipulations on mouthing and suckling behavior during the neonatal to weanling age period.

摘要

在产前3 - 4天的斯普拉格-道利大鼠幼崽中,在给予不同剂量的5 - 羟色胺1A受体激动剂8 - 羟基-2 -(二正丙基氨基)四氢萘(8 - OHDPAT)、5 - 羟色胺1B受体激动剂1 -(3 - 氯苯基)哌嗪(mCPP)或5 - 羟色胺2受体激动剂1 -(2,5 - 二甲氧基-4 - 碘苯基)-2 - 氨基丙烷(DOI)后,分别在有无乳汁的情况下进行测试。给予8 - OHDPAT会减少口部动作、增加探究行为并增强行为激活。相反,5 - 羟色胺2受体激动剂DOI和5 - 羟色胺1B受体激动剂mCPP会增加口部动作并减少探究行为。mCPP和DOI对行为激活的影响不同,mCPP会降低而DOI会增加这种综合行为评分。mCPP增加梳理行为,而DOI会引发四肢的一种特征性异常姿势。因此,似乎5 - 羟色胺1A、5 - 羟色胺1B和5 - 羟色胺2受体亚型存在于新生儿中,并且在用选择性激动剂刺激时会引发不同的行为反应。在发育过程中这些受体亚型之间平衡的个体发生变化可能与先前报道的在新生儿到断奶期血清素操纵对口部动作和吸吮行为影响中的个体发生逆转有关。

相似文献

1
5-HT1A, 5-HT1B and 5-HT2 receptor agonists induce differential behavioral responses in neonatal rat pups.5-羟色胺1A、5-羟色胺1B和5-羟色胺2受体激动剂在新生大鼠幼崽中引发不同的行为反应。
Eur J Pharmacol. 1988 Jun 10;150(3):339-45. doi: 10.1016/0014-2999(88)90016-7.
2
5-HT1A, 5-HT1B and 5-HT2 receptor agonists induce differential behavioral responses in preweanling rat pups.
Eur J Pharmacol. 1990 Jun 21;182(1):9-17. doi: 10.1016/0014-2999(90)90488-r.
3
Behavioural profiles of putative 5-hydroxytryptamine receptor agonists and antagonists in developing rats.发育中大鼠体内假定的5-羟色胺受体激动剂和拮抗剂的行为特征
Neuropharmacology. 1989 Jun;28(6):635-42. doi: 10.1016/0028-3908(89)90143-3.
4
Agonist action at 5-HT1C receptors facilitates 5-HT1A receptor-mediated spontaneous tail-flicks in the rat.5-羟色胺1C受体的激动剂作用促进大鼠中5-羟色胺1A受体介导的自发甩尾。
Eur J Pharmacol. 1990 Nov 27;191(2):185-95. doi: 10.1016/0014-2999(90)94146-o.
5
5-hydroxytryptamine (5-HT)1A receptors and the tail-flick response. I. 8-hydroxy-2-(di-n-propylamino) tetralin HBr-induced spontaneous tail-flicks in the rat as an in vivo model of 5-HT1A receptor-mediated activity.5-羟色胺(5-HT)1A受体与甩尾反应。I. 8-羟基-2-(二正丙基氨基)四氢萘溴化氢诱导大鼠自发甩尾作为5-HT1A受体介导活性的体内模型。
J Pharmacol Exp Ther. 1991 Mar;256(3):973-82.
6
Facilitation of 8-OHDPAT-induced forepaw treading of rats by the 5-HT2 agonist DOI.
Eur J Pharmacol. 1989 Feb 14;161(1):45-51. doi: 10.1016/0014-2999(89)90178-7.
7
Behavioural evidence for functional interactions between 5-HT-receptor subtypes in rats and mice.大鼠和小鼠中5-羟色胺受体亚型之间功能相互作用的行为学证据。
Br J Pharmacol. 1990 Nov;101(3):667-73. doi: 10.1111/j.1476-5381.1990.tb14138.x.
8
The 5-HT2 receptor agonist 1-(2,5-dimethoxy-4-iodophenyl)2-aminopropane increases brain tryptophan levels in the rat.5-羟色胺2型受体激动剂1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷可提高大鼠大脑中的色氨酸水平。
Eur J Pharmacol. 1992 Apr 7;214(1):101-3. doi: 10.1016/0014-2999(92)90104-c.
9
Neonatal organizational effects of the 5-HT2 and 5-HT1A subsystems on adult behavior in the rat.5-羟色胺2和5-羟色胺1A子系统对大鼠成年行为的新生儿组织效应。
Pharmacol Biochem Behav. 1996 May;54(1):195-203. doi: 10.1016/0091-3057(95)02134-5.
10
The functional significance of neonatal 5,7-dihydroxytryptamine lesions in the rat: response to selective 5-HT1A and 5-HT2,1C agonists.
Brain Res Bull. 1990 Jun;24(6):747-53. doi: 10.1016/0361-9230(90)90134-l.

引用本文的文献

1
The role of 5-HT modulation in opioid withdrawal and neonatal opioid withdrawal syndrome: mechanisms and potential serotonergic targets.5-羟色胺调节在阿片类药物戒断及新生儿阿片类药物戒断综合征中的作用:机制及潜在的5-羟色胺能靶点
Expert Opin Investig Drugs. 2025 Jan-Feb;34(1-2):49-59. doi: 10.1080/13543784.2025.2462615. Epub 2025 Feb 8.
2
Low dose effects in psychopharmacology: ontogenetic considerations.精神药理学中的低剂量效应:个体发育方面的考量。
Nonlinearity Biol Toxicol Med. 2005 Jan;3(1):97-111. doi: 10.2201/nonlin.003.01.006.
3
Economical test methods for developmental neurobehavioral toxicity.
发育神经行为毒性的经济测试方法。
Environ Health Perspect. 1996 Apr;104 Suppl 2(Suppl 2):285-98. doi: 10.1289/ehp.96104s2285.
4
Ontogenetic transitions in the psychopharmacological response to serotonergic manipulations.对血清素能操作的心理药理学反应中的个体发生转变。
Psychopharmacology (Berl). 1988;96(2):161-8. doi: 10.1007/BF00177555.
5
ACTH-induced behaviors and their modulation by serotonergic agonists differ in neonatal and weanling rat pups.
Psychopharmacology (Berl). 1990;100(2):151-8. doi: 10.1007/BF02244398.