Selective localization of oxytocin receptors and vasopressin 1a receptors in the human brainstem

被引:34
|
作者
Freeman, Sara M. [1 ]
Smith, Aaron L. [2 ]
Goodman, Mark M. [3 ]
Bales, Karen L. [4 ]
机构
[1] Univ Calif Davis, Calif Natl Primate Res Ctr, One Shields Ave, Davis, CA 95616 USA
[2] Emory Univ, Yerkes Natl Primate Res Ctr, Ctr Translat Social Neurosci, Atlanta, GA 30322 USA
[3] Emory Univ, Ctr Syst Imaging, Dept Radiol & Imaging Sci, Atlanta, GA 30322 USA
[4] Univ Calif Davis, Dept Psychol, Davis, CA 95616 USA
关键词
Brainstem; receptor autoradiography; neuropeptides; spinal trigeminal nucleus; nucleus prepositus; UPPER SPINAL-CORD; BINDING-SITES; MESSENGER-RNA; MONTANE VOLES; NEUROANATOMICAL DISTRIBUTION; CEREBROSPINAL-FLUID; RAT-BRAIN; PRAIRIE; LIGAND; AUTORADIOGRAPHY;
D O I
10.1080/17470919.2016.1156570
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Intranasal oxytocin (OT) affects a suite of human social behaviors, including trust, eye contact, and emotion recognition. However, it is unclear where oxytocin receptors (OXTR) and the structurally related vasopressin 1a receptors (AVPR1a) are expressed in the human brain. We have previously described a reliable, pharmacologically informed receptor autoradiography protocol for visualizing these receptors in postmortem primate brain tissue. We used this technique in human brainstem tissue to identify the neural targets of OT and vasopressin. To determine binding selectivity of the OXTR radioligand and AVPR1a radioligand, sections were incubated in four conditions: radioligand alone, radioligand with the selective AVPR1a competitor SR49059, and radioligand with a low or high concentration of the selective OXTR competitor ALS-II-69. We found selective OXTR binding in the spinal trigeminal nucleus, a conserved region of OXTR expression in all primate species investigated to date. We found selective AVPR1a binding in the nucleus prepositus, an area implicated in eye gaze stabilization. The tissue's postmortem interval (PMI) was not correlated with either the specific or nonspecific binding of either radioligand, indicating that it will not likely be a factor in similar postmortem studies. This study provides critical data for future studies of OXTR and AVPR1a in human brain tissue.
引用
收藏
页码:113 / 123
页数:11
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