Department of Animal Sciences, School of Environmental and Biological Sciences, Rutgers, The State University of New Jersey, New Brunswick, New Jersey, USA.
Behav Pharmacol. 2023 Oct 1;34(7):411-423. doi: 10.1097/FBP.0000000000000748. Epub 2023 Aug 15.
Sensorimotor gating disruptions have been noted in several psychiatric and neurodegenerative disorders. However, the involvement of sensorimotor gating processes in eating disorders has not been well characterized. Our objective was to examine the sensorimotor gating of the acoustic startle response following dietary-induced binge eating and high-fat diet (HFD) induced weight gain in male C57B/6J mice. Acute administration of the norepinephrine reuptake inhibitor, nisoxetine (0.5 and 5 mg/kg), and a dopamine reuptake inhibitor, GBR 12783 (1.6 and 16 mg/kg), were either given alone or in combination to assess norepinephrine and dopamine alterations, respectively. Male mice with repeated bouts of calorie restriction (Restrict) and with limited access to a sweetened fat food (Binge) demonstrated an escalation of intake over 2.5 weeks under standard chow conditions. Restrict Binge (RB) mice had a reduced startle response to the startle pulse (110 dB) compared with the Naive control group at 5 mg/kg nisoxetine. There was an overall effect of nisoxetine (0.5 and 5 mg/kg) to increase percent inhibition at pre-pulse (74 dB), %PP74. Under HFD conditions, the RB group did not demonstrate a binge-like eating phenotype. The RB group on HFD had a higher response to 74 dB with nisoxetine (5.0 mg/kg) compared with a combinational dose of nisoxetine (5.0 mg/kg) and GBR 12783 (1.6 mg/kg). These findings suggest that dietary conditions that promote binge-like eating can influence the central noradrenergic and dopaminergic controls of the acoustic startle response and potentially influence sensorimotor gating.
感觉运动门控障碍在几种精神和神经退行性疾病中都有发现。然而,感觉运动门控过程在进食障碍中的参与尚未得到很好的描述。我们的目的是研究饮食诱导的暴食和高脂肪饮食(HFD)诱导的雄性 C57B/6J 小鼠体重增加后,声刺激反应的感觉运动门控。单独给予去甲肾上腺素再摄取抑制剂去甲西汀(0.5 和 5mg/kg)和多巴胺再摄取抑制剂 GBR 12783(1.6 和 16mg/kg),或联合使用,分别评估去甲肾上腺素和多巴胺的变化。经过反复的热量限制(Restrict)和限制摄入含糖高脂肪食物(Binge)的雄性小鼠,在标准食物条件下,在 2.5 周内摄入量逐渐增加。与未处理的对照组相比,在 5mg/kg 去甲西汀时,Restrict Binge(RB)小鼠对起始脉冲(110dB)的起始反应降低。去甲西汀(0.5 和 5mg/kg)整体上增加了预脉冲(74dB)的抑制百分比,%PP74。在 HFD 条件下,RB 组没有表现出暴食样的进食表型。与去甲西汀(5.0mg/kg)和 GBR 12783(1.6mg/kg)联合剂量相比,RB 组在 HFD 下对 74dB 的反应更高。这些发现表明,促进暴食样进食的饮食条件可以影响声刺激反应的中枢去甲肾上腺素和多巴胺控制,并可能影响感觉运动门控。