• 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

8-羟基二苯丙氨酸(8-OH-DPAT)和达泊西汀对雄性大鼠射精过程中大脑基因表达的影响。

The effect of 8-OH-DPAT and dapoxetine on gene expression in the brain of male rats during ejaculation.

作者信息

Qin Xijun, Ma Xiaojun, Tu Dongping, Luo Zuliang, Huang Jie, Mo Changming

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100193, China.

Guangxi University of Chinese Medicine, Nanning 530200, China.

出版信息

Acta Pharm Sin B. 2017 May;7(3):381-389. doi: 10.1016/j.apsb.2016.11.004. Epub 2017 Mar 14.

DOI:10.1016/j.apsb.2016.11.004
PMID:28540176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5430880/
Abstract

The 5-HT receptor agonist 8-hydroxy-2-[di--propylamino] tetralin (8-OH-DPAT) promotes ejaculation of male rats, whereas dapoxetine delays this process. However, the gene expression profile of the brain at ejaculation following administrationof these two compounds has not been fully elucidated. In the present study, a transcriptomic BodyMap was generated by conducting mRNA-Seq on brain samples of male Sprague-Dawley rats. The study included four groups: pre-copulatory control (CK) group, ejaculation (EJ) group, 0.5 mg/kg 8-OH-DPAT-ejaculation group (DPAT), and 60 mg/kg dapoxetine-ejaculation (DAP) group. The resulting analysis generated an average of approximately 47 million sequence reads. Significant differences in the gene expression profiles of the aforementioned groups were observed in the EJ (257 genes), DPAT (349 genes) and the DAP (207 genes) compared with the control rats. The results indicate that the expression of and was significantly different after treatment with 8-OH-DPAT, whereas the expression of was significantly different after treatment with dapoxetine. Other genes, such as , and , exhibited significant differences in expression after the two treatments and are related to bladder cancer, renal cell carcinoma and sexual addiction. The present study reveals the basic pattern of gene expression that was activated at ejaculation in the presence of 8-OH-DPAT or dapoxetine, providing preliminary gene expression information during rat ejaculation.

摘要

5-羟色胺受体激动剂8-羟基-2-[二丙基氨基]四氢萘(8-OH-DPAT)可促进雄性大鼠射精,而达泊西汀则延迟这一过程。然而,这两种化合物给药后射精时大脑的基因表达谱尚未完全阐明。在本研究中,通过对雄性Sprague-Dawley大鼠的脑样本进行mRNA测序生成了转录组体图谱。该研究包括四组:交配前对照组(CK)、射精组(EJ)、0.5mg/kg 8-OH-DPAT射精组(DPAT)和60mg/kg达泊西汀射精组(DAP)。结果分析平均产生了约4700万个序列读数。与对照大鼠相比,在EJ组(257个基因)、DPAT组(349个基因)和DAP组(207个基因)中观察到上述组基因表达谱的显著差异。结果表明,8-OH-DPAT处理后,[具体基因1]和[具体基因2]的表达有显著差异,而达泊西汀处理后,[具体基因3]的表达有显著差异。其他基因,如[具体基因4]、[具体基因5]和[具体基因6],在两种处理后表达有显著差异,且与膀胱癌、肾细胞癌和性成瘾有关。本研究揭示了在8-OH-DPAT或达泊西汀存在下射精时激活的基因表达基本模式,提供了大鼠射精过程中的初步基因表达信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/9e8a70b21dc6/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/4c8a35816853/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/26d18b59d15c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/6038e09543ee/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/0c7b151e9547/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/fe6092e2df7f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/9e8a70b21dc6/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/4c8a35816853/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/26d18b59d15c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/6038e09543ee/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/0c7b151e9547/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/fe6092e2df7f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0eb/5430880/9e8a70b21dc6/gr5.jpg

相似文献

1
The effect of 8-OH-DPAT and dapoxetine on gene expression in the brain of male rats during ejaculation.8-羟基二苯丙氨酸(8-OH-DPAT)和达泊西汀对雄性大鼠射精过程中大脑基因表达的影响。
Acta Pharm Sin B. 2017 May;7(3):381-389. doi: 10.1016/j.apsb.2016.11.004. Epub 2017 Mar 14.
2
Region-selective inhibition of male rat sexual behavior and motor performance by localized forebrain 5-HT injections: a comparison with effects produced by 8-OH-DPAT.通过局部注射5-羟色胺对雄性大鼠性行为和运动能力进行区域选择性抑制:与8-羟基二丙胺基四氢萘产生的效果比较。
Behav Brain Res. 1991 Feb 28;42(2):169-80. doi: 10.1016/s0166-4328(05)80008-7.
3
Moderate role of oxytocin in the pro-ejaculatory effect of the 5-HT1A receptor agonist 8-OH-DPAT.催产素在5-羟色胺1A受体激动剂8-羟基二丙胺四乙酸促射精效应中的适度作用。
J Sex Med. 2015 Jan;12(1):17-28. doi: 10.1111/jsm.12742. Epub 2014 Oct 30.
4
The effects of idazoxan and 8-OH-DPAT on sexual behaviour and associated ultrasonic vocalizations in the rat.伊达唑新和8-羟基二苯丙氨酸对大鼠性行为及相关超声发声的影响。
Neurosci Biobehav Rev. 1991 Winter;15(4):505-15. doi: 10.1016/s0149-7634(05)80140-x.
5
The novel 5-HT1A receptor antagonist (S)-UH-301 antagonizes 8-OH-DPAT-induced effects on male as well as female rat copulatory behaviour.新型5-HT1A受体拮抗剂(S)-UH-301可拮抗8-OH-DPAT对雄性和雌性大鼠交配行为的影响。
Eur J Pharmacol. 1991 Sep 4;202(1):81-7. doi: 10.1016/0014-2999(91)90256-p.
6
D2-like receptors mediate the expulsion phase of ejaculation elicited by 8-hydroxy-2-(di-N-propylamino)tetralin in rats.D2样受体介导8-羟基-2-(二-N-丙基氨基)四氢萘诱发的大鼠射精排出期。
J Pharmacol Exp Ther. 2006 Feb;316(2):830-4. doi: 10.1124/jpet.105.092411. Epub 2005 Oct 12.
7
Profiles of brain central nervous system gene expression associated with ejaculation behavior in male rats.
Behav Brain Res. 2017 May 1;324:21-29. doi: 10.1016/j.bbr.2017.01.047. Epub 2017 Feb 4.
8
Testosterone is required for the stimulatory effects of 8-OH-DPAT on sexual behavior in castrated male rats.睾酮是8-OH-DPAT对去势雄性大鼠性行为产生刺激作用所必需的。
Eur J Pharmacol. 1993 Mar 23;233(2-3):187-92. doi: 10.1016/0014-2999(93)90049-n.
9
Partial antagonism of 8-OH-DPAT'S effects on male rat sexual behavior with a D2, but not a 5-HT1A, antagonist.用D2拮抗剂而非5-HT1A拮抗剂可部分拮抗8-OH-DPAT对雄性大鼠性行为的影响。
Brain Res. 1999 Feb 27;820(1-2):55-62. doi: 10.1016/s0006-8993(98)01331-6.
10
Demonstration of ejaculation-induced neural activity in the male rat brain using 5-HT1A agonist 8-OH-DPAT.使用5-羟色胺1A受体激动剂8-羟基二丙胺基四氢萘(8-OH-DPAT)证明雄性大鼠大脑中射精诱导的神经活动。
Physiol Behav. 1997 Oct;62(4):881-91. doi: 10.1016/s0031-9384(97)00258-8.

引用本文的文献

1
Dapoxetine prevents neuronal damage and improves functional outcomes in a model of ischemic stroke through the modulation of inflammation and oxidative stress.达泊西汀通过调节炎症和氧化应激预防缺血性脑卒中模型中的神经元损伤并改善其功能结局。
Naunyn Schmiedebergs Arch Pharmacol. 2024 Jan;397(1):253-266. doi: 10.1007/s00210-023-02601-7. Epub 2023 Jul 7.
2
: A Newly Discovered Gene Regulating Ejaculation Function.一个新发现的调控射精功能的基因。
Front Physiol. 2022 Feb 28;13:762272. doi: 10.3389/fphys.2022.762272. eCollection 2022.

本文引用的文献

1
Human INO80/YY1 chromatin remodeling complex transcriptionally regulates the BRCA2- and CDKN1A-interacting protein (BCCIP) in cells.人类INO80/YY1染色质重塑复合物在细胞中对BRCA2和CDKN1A相互作用蛋白(BCCIP)进行转录调控。
Protein Cell. 2016 Oct;7(10):749-760. doi: 10.1007/s13238-016-0306-1. Epub 2016 Aug 17.
2
Wnt3a suppresses Wnt/β-catenin signaling and cancer cell proliferation following serum deprivation.血清剥夺后,Wnt3a抑制Wnt/β-连环蛋白信号通路及癌细胞增殖。
Exp Cell Res. 2016 Feb 1;341(1):32-41. doi: 10.1016/j.yexcr.2015.11.025. Epub 2015 Nov 28.
3
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.
全基因组关联研究和小鼠表达数据确定,WNT3和WNT9b之间一个高度保守的32 kb基因间区域可能是孤立性典型膀胱外翻的易感位点。
Hum Mol Genet. 2014 Oct 15;23(20):5536-44. doi: 10.1093/hmg/ddu259. Epub 2014 May 22.
4
Neural mechanisms of sexual behavior in the male rat: emphasis on ejaculation-related circuits.雄性大鼠性行为的神经机制:重点关注射精相关回路。
Pharmacol Biochem Behav. 2014 Jun;121:170-83. doi: 10.1016/j.pbb.2013.12.017. Epub 2013 Dec 22.
5
Effects of 5-HT1A receptor stimulation on D1 receptor agonist-induced striatonigral activity and dyskinesia in hemiparkinsonian rats.5-HT1A 受体刺激对 D1 受体激动剂诱导的偏侧帕金森病大鼠纹状体苍白球活动和运动障碍的影响。
ACS Chem Neurosci. 2013 May 15;4(5):747-60. doi: 10.1021/cn300234z. Epub 2013 Apr 1.
6
Transcriptional mechanisms of drug addiction.药物成瘾的转录机制。
Clin Psychopharmacol Neurosci. 2012 Dec;10(3):136-43. doi: 10.9758/cpn.2012.10.3.136. Epub 2012 Dec 20.
7
Natural and drug rewards act on common neural plasticity mechanisms with ΔFosB as a key mediator.自然奖赏和药物奖赏通过共同的神经可塑性机制起作用,其中 ΔFosB 作为关键的中介。
J Neurosci. 2013 Feb 20;33(8):3434-42. doi: 10.1523/JNEUROSCI.4881-12.2013.
8
Effect of dapoxetine on ejaculatory performance and related brain neuronal activity in rapid ejaculator rats.达泊西汀对早泄大鼠射精性能及相关脑神经元活动的影响。
J Sex Med. 2012 Oct;9(10):2562-73. doi: 10.1111/j.1743-6109.2012.02884.x. Epub 2012 Aug 20.
9
Sex, drugs, and rock 'n' roll: hypothesizing common mesolimbic activation as a function of reward gene polymorphisms.性、药物和摇滚乐:假设奖赏基因多态性作为中脑边缘系统激活的共同功能。
J Psychoactive Drugs. 2012 Jan-Mar;44(1):38-55. doi: 10.1080/02791072.2012.662112.
10
Sex, drugs and gluttony: how the brain controls motivated behaviors.性、药物和暴食:大脑如何控制动机行为。
Physiol Behav. 2011 Jul 25;104(1):173-7. doi: 10.1016/j.physbeh.2011.04.057. Epub 2011 May 5.