Rotenstein Lisa S, Sheridan Margaret, Garg Rajesh, Adler Gail K
Harvard Medical School, Boston, Massachusetts, USA.
Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.
Obesity (Silver Spring). 2015 Jun;23(6):1136-42. doi: 10.1002/oby.21104. Epub 2015 May 9.
The hippocampus is crucial for paired-associate learning. Obesity is associated with increased mineralocorticoid receptor (MR) activity in peripheral and possibly central tissues, decreased hippocampal size in humans, and impaired hippocampal learning in rodents. The MR is expressed in hippocampal neurons, and MR blockade improves hippocampal learning in obese animals. The goal of the study was to determine whether MR blockade would modulate paired-associate learning in men and women with obesity.
Men and women ages 20-61 years with BMI between 30-45 kg/m(2) were randomly assigned to placebo (n = 11; 7 women) or 50 mg spironolactone daily (n = 12; 7 women) for six weeks. At baseline and post-treatment, subjects underwent a clinical and hormonal evaluation. They also underwent a computerized task that assesses paired-associate learning and has been shown by functional magnetic resonance imaging to activate the hippocampus.
In an ANCOVA model that adjusted for baseline paired-associate learning, age, and race, spironolactone treatment was associated with a significant (P = 0.043) improvement in hippocampal memory as compared to placebo treatment.
Our findings demonstrate, for the first time, that blocking MR with chronic, low-dose spironolactone treatment improves paired-associate learning in individuals with obesity, suggesting that MR activation contributes to hippocampal memory modulation in humans.
海马体对配对联想学习至关重要。肥胖与外周组织以及可能的中枢组织中盐皮质激素受体(MR)活性增加、人类海马体体积减小以及啮齿动物海马体学习受损有关。MR在海马体神经元中表达,阻断MR可改善肥胖动物的海马体学习能力。本研究的目的是确定阻断MR是否会调节肥胖男性和女性的配对联想学习。
将年龄在20 - 61岁、体重指数在30 - 45 kg/m²之间的男性和女性随机分为安慰剂组(n = 11;7名女性)或每日服用50 mg螺内酯组(n = 12;7名女性),为期六周。在基线和治疗后,受试者接受临床和激素评估。他们还进行了一项计算机化任务,该任务评估配对联想学习,并且功能磁共振成像已显示该任务可激活海马体。
在一个对基线配对联想学习、年龄和种族进行调整的协方差分析模型中,与安慰剂治疗相比,螺内酯治疗与海马体记忆显著改善(P = 0.043)相关。
我们的研究结果首次表明,长期低剂量螺内酯治疗阻断MR可改善肥胖个体的配对联想学习,提示MR激活在人类海马体记忆调节中起作用。