Weber Brittany C, Manfredo Heather N, Rinaman Linda
Department of Neuroscience, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
Behav Neurosci. 2009 Dec;123(6):1178-84. doi: 10.1037/a0017659.
Early life experience impacts emotional development in the infant. In rat pups, repeated, brief (i.e., 15 min) maternal separation (MS15) during the first 1-2 postnatal weeks has been shown to increase active maternal care and to reduce later anxiety-like behavior in the offspring. We hypothesized that the anxiolytic effect of MS15 is partly due to increased intestinal release of cholecystokinin (CCK) in rat pups as a result of increased maternal contact. We predicted that rats with a history of MS15 would display less anxiety in the elevated plus maze (EPMZ) and novelty-suppressed feeding (NSF) tests, as compared with nonseparated (NS) controls, and that the anxiolytic effect of MS15 would be attenuated in rats in which daily MS15 was accompanied by systemic administration of a CCK-1 receptor antagonist (i.e., devazepide). Treatment groups included NS control litters, litters exposed to MS15 from postnatal days (P)1-10, inclusive, and litters exposed to MS15 with concurrent subcutaneous injection of devazepide or vehicle. Litters were undisturbed after P10 and were weaned on P21. Subsets of adolescent males from each litter were tested in the EPMZ on P40-41, while others were tested for NSF on P50-52. As predicted, rats with a developmental history of MS15 displayed reduced anxiety-like behavior in the EPMZ and NSF tests. The anxiolytic effect of MS15 was preserved in vehicle-treated rats, but was reversed in devazepide-treated rats. These results support the view that endogenous CCK-1 receptor signaling in infants is a potential pathway through which maternal-pup interactions regulate the development and functional organization of emotional circuits that control anxiety-like behavior in the offspring.
早期生活经历会影响婴儿的情绪发展。在幼鼠中,出生后第1 - 2周内反复进行短暂(即15分钟)的母婴分离(MS15)已被证明会增加母性主动照料行为,并减少后代后期的焦虑样行为。我们推测,MS15的抗焦虑作用部分归因于幼鼠肠道中胆囊收缩素(CCK)释放增加,这是母鼠接触增加的结果。我们预测,与未分离(NS)的对照组相比,有MS15经历的大鼠在高架十字迷宫(EPMZ)和新奇抑制摄食(NSF)试验中表现出的焦虑会更少,并且在每日MS15同时伴有CCK - 1受体拮抗剂(即地伐西匹)全身给药的大鼠中,MS15的抗焦虑作用会减弱。治疗组包括NS对照窝、出生后第1天(P)至第10天(含)暴露于MS15的窝,以及暴露于MS15同时皮下注射地伐西匹或赋形剂的窝。P10之后各窝均不受干扰,并于P21断奶。每窝的一部分青春期雄性大鼠在P40 - 41接受EPMZ测试,而其他大鼠在P50 - 52接受NSF测试。如预测的那样,有MS15发育史的大鼠在EPMZ和NSF测试中表现出减少的焦虑样行为。MS15的抗焦虑作用在接受赋形剂治疗的大鼠中得以保留,但在接受地伐西匹治疗的大鼠中则相反。这些结果支持这样一种观点,即婴儿体内内源性CCK - 1受体信号传导是母婴互动调节控制后代焦虑样行为的情绪回路的发育和功能组织的潜在途径。