Sirohi Sunil, Walker Brendan M
Laboratory of Alcoholism and Addictions Neuroscience, Department of Psychology, Washington State University, Pullman, Washington, USA.
Department of Integrative Physiology & Neuroscience, College of Veterinary Medicine, Washington State University, Pullman, Washington, USA.
J Neurochem. 2015 Nov;135(4):659-65. doi: 10.1111/jnc.13279. Epub 2015 Sep 11.
Opioid receptors can display spontaneous agonist-independent G-protein signaling (basal signaling/constitutive activity). While constitutive κ-opioid receptor (KOR) activity has been documented in vitro, it remains unknown if KORs are constitutively active in native systems. Using [(35) S] guanosine 5'-O-[gamma-thio] triphosphate coupling assay that measures receptor functional state, we identified the presence of medial prefrontal cortex KOR constitutive activity in young rats that declined with age. Furthermore, basal signaling showed an age-related decline and was insensitive to neutral opioid antagonist challenge. Collectively, the present data are first to demonstrate age-dependent alterations in the medial prefrontal cortex KOR constitutive activity in rats and changes in the constitutive activity of KORs can differentially impact KOR ligand efficacy. These data provide novel insights into the functional properties of the KOR system and warrant further consideration of KOR constitutive activity in normal and pathophysiological behavior. Opioid receptors exhibit agonist-independent constitutive activity; however, kappa-opioid receptor (KOR) constitutive activity has not been demonstrated in native systems. Our results confirm KOR constitutive activity in the medial prefrontal cortex (mPFC) that declines with age. With the ability to presynaptically inhibit multiple neurotransmitter systems in the mPFC, maturational or patho-logical alterations in constitutive activity could disrupt corticofugal glutamatergic pyramidal projection neurons mediating executive function. Regulation of KOR constitutive activity could serve as a therapeutic target to treat compromised executive function.
阿片受体可表现出非依赖激动剂的自发G蛋白信号传导(基础信号传导/组成性活性)。虽然组成性κ-阿片受体(KOR)活性已在体外得到证实,但KOR在天然系统中是否具有组成性活性仍不清楚。使用[(35)S]鸟苷5'-O-[γ-硫代]三磷酸偶联测定法来测量受体功能状态,我们发现在幼鼠内侧前额叶皮质中存在KOR组成性活性,且该活性随年龄增长而下降。此外,基础信号传导显示出与年龄相关的下降,并且对中性阿片拮抗剂的挑战不敏感。总的来说,目前的数据首次证明了大鼠内侧前额叶皮质KOR组成性活性随年龄的变化,并且KOR组成性活性的变化可不同程度地影响KOR配体的功效。这些数据为KOR系统的功能特性提供了新的见解,并值得在正常和病理生理行为中进一步考虑KOR的组成性活性。阿片受体表现出非依赖激动剂的组成性活性;然而,κ-阿片受体(KOR)的组成性活性尚未在天然系统中得到证实。我们的结果证实了内侧前额叶皮质(mPFC)中KOR的组成性活性随年龄下降。由于KOR能够在突触前抑制mPFC中的多种神经递质系统,组成性活性的成熟或病理改变可能会破坏介导执行功能的皮质离心谷氨酸能锥体投射神经元。调节KOR组成性活性可作为治疗受损执行功能的治疗靶点。