• 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

脑室内注射酪氨酰 -W-巨噬细胞移动抑制因子 -1(酪氨酰 -脯氨酰 -色氨酰 -甘氨酰胺)后,原癌基因FOS蛋白在脑中的表达。

Expression of the FOS proto-oncogene protein in brain after ICV administration of Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2).

作者信息

Gergen K A, Chang S L, Niu Y F, Kastin A J, Zadina J E

机构信息

VA Medical Center, New Orleans, LA 70146.

出版信息

Peptides. 1994;15(8):1505-11. doi: 10.1016/0196-9781(94)90130-9.

DOI:10.1016/0196-9781(94)90130-9
PMID:7700853
Abstract

Tyr-W-MIF-1 is a tetrapeptide recently isolated from brain that has opiate modulating activity. In this study, we used immunocytochemical (ICC) detection of FOS proto-oncogene protein to map brain areas activated by an ICV injection of Tyr-W-MIF-1 (200 micrograms). The analgesic effect of the peptide, which lasted 1 h, was confirmed in each rat with the tail flick test. FOS was activated in several limbic structures, including the cingulate and infralimbic cortex, nucleus accumbens, and central nucleus of the amygdala. FOS activation also occurred in several diencephalic nuclei, including the supraoptic, paraventricular, and periventricular nuclei of the hypothalamus, and the paraventricular nucleus of the thalamus. Several activated areas contained mu-opiate receptors. However, despite the known selectivity of Tyr-W-MIF-1 for mu receptors, FOS immunoreactivity was also induced in nuclei of the amygdala, hypothalamus, and thalamus, where concentrations of kappa receptors were high but those of mu and delta receptors were not detected. The results show that Tyr-W-MIF-1 induces FOS activation in several brain areas, including but not limited to, areas associated with nociception and stress-induced analgesia.

摘要

酪氨酰 - 色氨酸 - 甲硫氨酸 - 异亮氨酸 - 苯丙氨酸 - 1(Tyr-W-MIF-1)是一种最近从大脑中分离出来的具有阿片类调节活性的四肽。在本研究中,我们使用免疫细胞化学(ICC)检测FOS原癌基因蛋白,以绘制经脑室内注射Tyr-W-MIF-1(200微克)激活的脑区图谱。通过甩尾试验在每只大鼠中证实了该肽持续1小时的镇痛作用。FOS在几个边缘结构中被激活,包括扣带回和边缘下皮质、伏隔核以及杏仁核中央核。FOS激活也发生在几个间脑核中,包括下丘脑的视上核、室旁核和室周核以及丘脑的室旁核。几个激活区域含有μ-阿片受体。然而,尽管已知Tyr-W-MIF-1对μ受体具有选择性,但在杏仁核、下丘脑和丘脑的核中也诱导了FOS免疫反应性,其中κ受体浓度高,但未检测到μ和δ受体浓度。结果表明,Tyr-W-MIF-1在几个脑区诱导FOS激活,包括但不限于与伤害感受和应激诱导镇痛相关的区域。

相似文献

1
Expression of the FOS proto-oncogene protein in brain after ICV administration of Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2).脑室内注射酪氨酰 -W-巨噬细胞移动抑制因子 -1(酪氨酰 -脯氨酰 -色氨酰 -甘氨酰胺)后,原癌基因FOS蛋白在脑中的表达。
Peptides. 1994;15(8):1505-11. doi: 10.1016/0196-9781(94)90130-9.
2
Cyclic analogues of Tyr-W-MIF-1 with prolonged analgesic activity and potency comparable to DAMGO and morphine.具有延长镇痛活性且效力与DAMGO和吗啡相当的Tyr-W-MIF-1环类似物。
Peptides. 1994;15(8):1567-9. doi: 10.1016/0196-9781(94)90135-x.
3
A Tyr-W-MIF-1 analog containing D-Pro2 discriminates among antinociception in mice mediated by different classes of mu-opioid receptors.一种含有D-脯氨酸2的酪氨酸-W-巨噬细胞移动抑制因子-1类似物可区分小鼠中由不同类型的μ-阿片受体介导的抗伤害感受。
Eur J Pharmacol. 2007 Jun 1;563(1-3):109-16. doi: 10.1016/j.ejphar.2007.01.068. Epub 2007 Feb 8.
4
Binding of Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2) and related peptides to mu 1 and mu 2 opiate receptors.酪氨酸-W-巨噬细胞移动抑制因子-1(酪氨酸-脯氨酸-色氨酸-甘氨酸-氨基)及相关肽与μ1和μ2阿片受体的结合
Neurosci Lett. 1996 Aug 30;215(1):65-9. doi: 10.1016/s0304-3940(96)12928-1.
5
Tyr-W-MIF-1-induced conditioned place preference.
Peptides. 1999;20(4):479-84. doi: 10.1016/s0196-9781(99)00029-7.
6
Intrathecal Tyr-W-MIF-1 produces potent, naloxone-reversible analgesia modulated by alpha 2-adrenoceptors.鞘内注射酪氨酰-色氨酸-巨噬细胞移动抑制因子-1可产生强效的、纳洛酮可逆转的镇痛作用,该作用受α2肾上腺素能受体调节。
Eur J Pharmacol. 1996 Mar 18;298(3):235-9. doi: 10.1016/0014-2999(95)00823-3.
7
Prolonged analgesia after intracerebroventricular Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2).脑室内注射酪氨酰-色氨酰-巨噬细胞移动抑制因子-1(酪氨酰-脯氨酰-色氨酰-甘氨酰胺)后的延长镇痛作用
Neurosci Lett. 1993 Jun 11;155(2):220-2. doi: 10.1016/0304-3940(93)90712-t.
8
Mu, delta, and kappa opiate receptor binding of Tyr-MIF-1 and of Tyr-W-MIF-1, its active fragments, and two potent analogs.酪酪肽(Tyr-MIF-1)、酪色酪肽(Tyr-W-MIF-1)及其活性片段和两种有效类似物的μ、δ和κ阿片受体结合情况
Life Sci. 1994;55(24):PL461-6. doi: 10.1016/0024-3205(94)00533-8.
9
Analgesic effects of Tyr-W-MIF-1: a mixed mu2-opioid receptor agonist/mu1-opioid receptor antagonist.酪氨酰-色氨酸-巨噬细胞移动抑制因子-1(Tyr-W-MIF-1)的镇痛作用:一种混合的μ2阿片受体激动剂/μ1阿片受体拮抗剂
Eur J Pharmacol. 1996 Nov 28;316(1):33-8. doi: 10.1016/s0014-2999(96)00656-5.
10
Isolation of a novel tetrapeptide with opiate and antiopiate activity from human brain cortex: Tyr-Pro-Trp-Gly-NH2 (Tyr-W-MIF-1).从人脑海马皮质中分离出一种具有阿片样和抗阿片样活性的新型四肽:酪氨酰-脯氨酰-色氨酰-甘氨酰胺(酪氨酰-W-MIF-1)。
Peptides. 1992 Jul-Aug;13(4):623-31. doi: 10.1016/0196-9781(92)90165-y.