• 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

Characterization of a 3H-arginine8-vasopressin binding site in the cingulate gyrus of the rat pup.

作者信息

Szot P, Myers K M, Swank M, Dorsa D M

机构信息

Geriatric Research, Education and Clinical Center Veterans Affairs Medical Center, Seattle, WA 98108.

出版信息

Peptides. 1989 Nov-Dec;10(6):1231-7. doi: 10.1016/0196-9781(89)90017-x.

DOI:10.1016/0196-9781(89)90017-x
PMID:2622802
Abstract

Autoradiographic analysis of 1, 8, 16 and 26-day-old rat brains showed 3H-arginine8-vasopressin (3H-AVP) binding to the cingulate gyrus-dorsal hippocampus (CG) only in the 8-day-old rat brain. Saturation analysis of CG membranes prepared from pups (7-10 days) and adults (90 days) revealed a small but significant increase in binding site concentration in adults compared to pups. However, the Kd of the 3H-AVP binding site increased significantly with age. The Kd of 3H-AVP binding to pup CG membranes was 0.9 +/- 0.1 nM, while the adult CG was 5.7 +/- 1.0 nM. The pharmacological specificity of 3H-AVP binding sites in the pup and adult CG was similar, but differed markedly from the profile observed in adult septal membranes. The primary specificity difference between the pup CG and septum was the reduced potency of certain V1 receptor antagonists. In competition experiments the CG binding site showed a reduced affinity for the V1 antagonist, [d(CH2)5, Tyr(Me)]AVP. This reduced affinity for the V1 antagonist was also documented autoradiographically using 3H-[d(CH2)5, Tyr(Me)]AVP. The data suggest that the 3H-AVP binding site expressed in the pup CG is not identical to the V1 type receptor present in the periphery and brain of the adult rat.

摘要

相似文献

1
Characterization of a 3H-arginine8-vasopressin binding site in the cingulate gyrus of the rat pup.
Peptides. 1989 Nov-Dec;10(6):1231-7. doi: 10.1016/0196-9781(89)90017-x.
2
Direct identification of the rat hepatocyte arginine8 vasopressin receptor with a radiolabelled V1-selective antagonist.用放射性标记的V1选择性拮抗剂直接鉴定大鼠肝细胞精氨酸8血管加压素受体。
J Recept Res. 1989;9(1):1-18. doi: 10.3109/10799898909066041.
3
Interaction of a vasopressin antagonist with vasopressin receptors in the septum of the rat brain.一种血管加压素拮抗剂与大鼠脑隔区血管加压素受体的相互作用。
Synapse. 1988;2(3):205-11. doi: 10.1002/syn.890020306.
4
Hepatic vasopressin receptor: differential effects of divalent cations, guanine nucleotides, and N-ethylmaleimide on agonist and antagonist interactions with the V1 subtype receptor.肝血管加压素受体:二价阳离子、鸟嘌呤核苷酸和N-乙基马来酰亚胺对激动剂和拮抗剂与V1亚型受体相互作用的不同影响。
Endocrinology. 1988 Aug;123(2):922-31. doi: 10.1210/endo-123-2-922.
5
Characterization of a specific, high affinity [3H]arginine8 vasopressin-binding site on liver microsomes from different strains of rat and the role of magnesium.不同品系大鼠肝微粒体上特异性、高亲和力[³H]精氨酸⁸血管加压素结合位点的特性及镁的作用
Endocrinology. 1986 Mar;118(3):990-7. doi: 10.1210/endo-118-3-990.
6
Vasopressin (V1) receptor characteristics in rat aortic smooth muscle cells.大鼠主动脉平滑肌细胞中血管加压素(V1)受体的特性
Am J Physiol. 1991 Dec;261(6 Pt 2):H1927-36. doi: 10.1152/ajpheart.1991.261.6.H1927.
7
[125I]-[d(CH2)5, Sar7]AVP: a selective radioligand for V1 vasopressin receptors.
J Recept Res. 1989;9(1):27-41. doi: 10.3109/10799898909066043.
8
Vasopressin increases cytosolic free [Ca2+] in the neonatal rat cardiomyocyte. Evidence for V1 subtype receptors.
Circ Res. 1991 Jul;69(1):239-45. doi: 10.1161/01.res.69.1.239.
9
A novel radiolabeled vasopressin antagonist: [3H-Phe]-desGlyd(CH2)5D-Tyr(Et)VAVP, [3H]-SK&F 101926.一种新型放射性标记的血管加压素拮抗剂:[3H-苯丙氨酸]-去甘氨酰(CH2)5D-酪氨酸(乙基)血管加压素,[3H]-SK&F 101926。
Mol Pharmacol. 1987 Mar;31(3):267-72.
10
[3H]desGly-NH2(9)-d(CH2)5[D-Ileu2,Ileu4]AVP: an AVP V2 receptor antagonist radioligand.[3H]去甘氨酰胺(9)-d(CH2)5[D-异亮氨酸2,异亮氨酸4]精氨酸加压素:一种精氨酸加压素V2受体拮抗剂放射性配体。
Peptides. 1991 Nov-Dec;12(6):1195-200. doi: 10.1016/0196-9781(91)90194-t.

引用本文的文献

1
Modulation of parvalbumin interneuron number by developmentally transient neocortical vasopressin receptor 1a (V1aR).发育性短暂性新皮层血管加压素受体 1a(V1aR)对 parvalbumin 中间神经元数量的调节。
Neuroscience. 2012 Oct 11;222:20-8. doi: 10.1016/j.neuroscience.2012.07.025. Epub 2012 Jul 20.
2
Characterization of arginine vasopressin actions in human uterine artery: lack of role of the vascular endothelium.精氨酸加压素对人子宫动脉作用的特征:血管内皮的作用缺失
Br J Pharmacol. 1995 Aug;115(7):1295-301. doi: 10.1111/j.1476-5381.1995.tb15039.x.