Bellamy Julia R, Rubin Batsheva R, Zverovich Angelica, Zhou Yan, Contoreggi Natalina H, Gray Jason D, McEwen Bruce S, Kreek Mary Jeanne, Milner Teresa A
Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, 407 East 61st Street, New York, NY, 10065, United States.
The Laboratory of the Biology of Addictive Diseases, The Rockefeller University, 1230 York Avenue, New York, NY, 10065, United States.
Neurosci Lett. 2019 Nov 20;713:134514. doi: 10.1016/j.neulet.2019.134514. Epub 2019 Sep 24.
Following oxycodone conditioned place preference (CPP) in naïve female and male Sprague Dawley rats, delta- and mu-opioid receptors (DORs and MORs) redistribute in hippocampal CA3 pyramidal cells and GABAergic interneurons in a manner that would promote opioid-associative learning processes, particularly in females. MORs and DORs similarly redistribute in CA3 and hilar neurons following chronic immobilization stress (CIS) in females, but not males, essentially "priming" the opioid system for oxycodone-associative learning. Following CIS, only females acquire oxycodone CPP. The present study determined whether sex and CIS differentially affect the levels of phosphorylated MORs and DORs (pMORs and pDORs) in the hippocampus following oxycodone CPP as phosphorylation is important for opioid receptor internationalization and trafficking. In naïve oxycodone-injected (Oxy) female rats, the density of pMOR-immunoreactivity (ir) was increased in CA1 stratum oriens and CA3a,b strata lucidum and radiatum compared to saline-injected (Sal)-females. Additionally, the density of pDOR-ir increased in the pyramidal cell layer and stratum radiatum of CA2/3a in Oxy-males compared to Sal-males. In CIS females that acquire CPP, pDOR-ir levels were increased in the CA2/3a. These findings indicate only rats that acquire oxycodone CPP have activated MORs and DORs in the hippocampus but that the subregion containing activated opioid receptors differs in females and males. These results are consistent with previously observed sex differences in the hippocampal opioid system following Oxy-CPP.
在未接触过药物的雌性和雄性斯普拉格-道利大鼠中建立羟考酮条件性位置偏爱(CPP)后,δ-阿片受体和μ-阿片受体(DORs和MORs)在海马CA3锥体细胞和GABA能中间神经元中重新分布,其方式将促进阿片类药物关联学习过程,尤其是在雌性大鼠中。在雌性大鼠而非雄性大鼠中,慢性固定应激(CIS)后,MORs和DORs在CA3和门区神经元中类似地重新分布,这实际上为羟考酮关联学习“启动”了阿片系统。CIS后,只有雌性大鼠获得羟考酮CPP。本研究确定了性别和CIS是否对羟考酮CPP后海马中磷酸化MORs和DORs(pMORs和pDORs)的水平有不同影响,因为磷酸化对阿片受体的内化和运输很重要。在未接触过药物且注射羟考酮(Oxy)的雌性大鼠中,与注射生理盐水(Sal)的雌性大鼠相比,CA1层的原层以及CA3a、b层的透明层和辐射层中pMOR免疫反应性(ir)的密度增加。此外,与注射Sal的雄性大鼠相比,注射Oxy的雄性大鼠CA2/3a的锥体细胞层和辐射层中pDOR-ir的密度增加。在获得CPP的CIS雌性大鼠中,CA2/3a中的pDOR-ir水平升高。这些发现表明,只有获得羟考酮CPP的大鼠海马中的MORs和DORs被激活,但含有激活阿片受体的亚区域在雌性和雄性中有所不同。这些结果与先前观察到的Oxy-CPP后海马阿片系统中的性别差异一致。