Nair Sunila G, Adams-Deutsch Tristan, Pickens Charles L, Smith Daniel G, Shaham Yavin
Behavioral Neuroscience Branch, NIDA/IRP/NIH/DHHS, 251 Bayview Blvd., Suite 200, Baltimore, MD 21224, USA.
Psychopharmacology (Berl). 2009 Jul;205(1):129-40. doi: 10.1007/s00213-009-1523-6. Epub 2009 Apr 2.
The melanin-concentrating hormone 1 (MCH1) receptors play an important role in home-cage food consumption in rodents, but their role in operant high-fat food-reinforced responding or reinstatement of food seeking in animal models is unknown. Here, we used the MCH1 receptor antagonist SNAP 94847 to explore these questions.
In experiment 1, we trained food-restricted rats (16 g/day of nutritionally balanced rodent diet) to lever press for high-fat (35%) pellets (3-h/day, every other day) for 14 sessions. We then tested the effect of SNAP 94847 (3-30 mg/kg, intraperitoneal (i.p.)) on food-reinforced operant responding. In experiments 2 and 3, we trained rats to lever press for the food pellets (9 to 14 3-h sessions) and subsequently extinguished the food-reinforced lever responding by removing the food (10 to 17 sessions). We then tested the effect of SNAP 94847 on reinstatement of food seeking induced by MCH (20 microg, intracerebroventricular), noncontingent delivery of three pellets during the first minute of the test session (pellet-priming), contingent tone-light cues previously associated with pellet delivery (cue), or the pharmacological stressor yohimbine (2 mg/kg, i.p.).
Systemic injections of SNAP 94847 decreased food-reinforced operant responding and MCH-induced reinstatement of food seeking. SNAP 94847 had no effect on pellet-priming-, cue-, or yohimbine-induced reinstatement.
Results indicate that MCH1 receptors are involved in food-reinforced operant responding but not in reinstatement induced by acute exposure to high-fat food, food cues, or the stress-like state induced by yohimbine. These results suggest that different mechanisms mediate food-reinforced operant responding and reinstatement of food seeking.
黑色素聚集激素1(MCH1)受体在啮齿动物笼内食物摄取中起重要作用,但其在动物模型中对操作性高脂食物强化反应或食物寻求恢复的作用尚不清楚。在此,我们使用MCH1受体拮抗剂SNAP 94847来探究这些问题。
在实验1中,我们训练食物受限的大鼠(每天16克营养均衡的啮齿动物饮食)每隔一天每天按压杠杆3小时以获取高脂(35%)颗粒饲料,共进行14次训练。然后我们测试了SNAP 94847(3 - 30毫克/千克,腹腔注射)对食物强化操作性反应的影响。在实验2和3中,我们训练大鼠按压杠杆获取颗粒饲料(9至14次3小时训练),随后通过移除食物来消除食物强化的杠杆反应(10至17次训练)。然后我们测试了SNAP 94847对由MCH(20微克,脑室内注射)、测试时段第一分钟非条件给予的三个颗粒饲料(颗粒启动)、先前与颗粒饲料给予相关的条件性声光提示(提示)或药理学应激源育亨宾(2毫克/千克,腹腔注射)诱导的食物寻求恢复的影响。
全身注射SNAP 94847降低了食物强化的操作性反应以及MCH诱导的食物寻求恢复。SNAP 94847对颗粒启动、提示或育亨宾诱导的恢复没有影响。
结果表明,MCH1受体参与食物强化的操作性反应,但不参与由急性暴露于高脂食物、食物提示或育亨宾诱导的应激样状态所引起的恢复。这些结果表明,不同机制介导食物强化的操作性反应和食物寻求的恢复。