Aston-Jones Gary, Smith Rachel J, Moorman David E, Richardson Kimberlei A
Department of Neurosciences, Medical University of South Carolina, Basic Science Building 403, 173 Ashley Avenue, MSC 510, Charleston, SC 29425-5100, USA.
Neuropharmacology. 2009;56 Suppl 1(Suppl 1):112-21. doi: 10.1016/j.neuropharm.2008.06.060. Epub 2008 Jul 4.
Orexins (also known as hypocretins) are recently discovered neuropeptides made exclusively in hypothalamic neurons that have been shown to be important in narcolepsy/cataplexy and arousal. Here, we conducted behavioral, anatomical and neurophysiological studies that show that a subset of these cells, located specifically in lateral hypothalamus (LH), are involved in reward processing and addictive behaviors. We found that Fos expression in LH orexin neurons varied in proportion to preference for morphine, cocaine or food. This relationship obtained both in drug naïve rats and in animals during protracted morphine withdrawal, when drug preference was elevated but food preference was decreased. Recent studies showed that LH orexin neurons that project to ventral tegmental area (VTA) have greater Fos induction in association with elevated morphine preference during protracted withdrawal than non-VTA-projecting orexin neurons, indicating that the VTA is an important site of action for orexin's role in reward processing. In addition, we found that stimulation of LH orexin neurons, or microinjection of orexin into VTA, reinstated an extinguished morphine preference. Most recently, using a self-administration paradigm we discovered that the Ox1 receptor antagonist SB-334867 (SB) blocks cocaine-seeking induced by discrete or contextual cues, but not by a priming injection of cocaine. Neurophysiological studies revealed that locally applied orexin often augmented responses of VTA dopamine (DA) neurons to activation of the medial prefrontal cortex (mPFC), consistent with the view that orexin facilitates activation of VTA DA neurons by stimulus-reward associations. We also recently showed that orexin in VTA is necessary for learning a morphine place preference. These findings are consistent with results from others showing that orexin facilitates glutamate-mediated responses, and is necessary for glutamate-dependent long-term potentiation, in VTA DA neurons. We surmise from these studies that LH orexin neurons play an important role in reward processing and addiction, and that LH orexin cells are an important input to VTA for behavioral effects associated with reward-paired stimuli.
食欲素(也称为下丘脑泌素)是最近发现的神经肽,仅在下丘脑神经元中产生,已被证明在发作性睡病/猝倒症和唤醒中起重要作用。在此,我们进行了行为、解剖和神经生理学研究,结果表明,这些细胞的一个子集,特别位于外侧下丘脑(LH),参与奖赏处理和成瘾行为。我们发现,LH食欲素神经元中的Fos表达与对吗啡、可卡因或食物的偏好成比例变化。这种关系在未接触过药物的大鼠以及处于长期吗啡戒断期的动物中均存在,此时药物偏好增加但食物偏好降低。最近的研究表明,投射到腹侧被盖区(VTA)的LH食欲素神经元在长期戒断期间与吗啡偏好升高相关的Fos诱导比非VTA投射的食欲素神经元更强,这表明VTA是食欲素在奖赏处理中发挥作用的重要作用位点。此外,我们发现刺激LH食欲素神经元,或将食欲素微量注射到VTA中,可恢复已消退的吗啡偏好。最近,我们使用自我给药范式发现,Ox1受体拮抗剂SB - 334867(SB)可阻断由离散或情境线索诱导的可卡因寻求行为,但不能阻断由可卡因引发注射诱导的行为。神经生理学研究表明,局部应用食欲素通常会增强VTA多巴胺(DA)神经元对内侧前额叶皮质(mPFC)激活的反应,这与食欲素通过刺激 - 奖赏关联促进VTA DA神经元激活的观点一致。我们最近还表明,VTA中的食欲素是学习吗啡位置偏好所必需的。这些发现与其他研究结果一致,即食欲素促进VTA DA神经元中谷氨酸介导的反应,并且是谷氨酸依赖性长时程增强所必需的。我们从这些研究中推测,LH食欲素神经元在奖赏处理和成瘾中起重要作用,并且LH食欲素细胞是VTA的重要输入,对与奖赏配对刺激相关的行为效应起作用。