Livestock Behavior Research Unit, USDA-ARS, West Lafayette, IN 47906, United States.
Behav Brain Res. 2013 Sep 15;253:290-6. doi: 10.1016/j.bbr.2013.07.043. Epub 2013 Aug 1.
Serotonin (5-HT) acts as a neurogenic compound in the developing brain; however serotonin altering drugs such as SSRIs are often prescribed to pregnant and lactating mothers. Early agonism of 5-HT receptors could alter the development of serotonergic circuitry, altering neurotransmission and behaviors mediated by 5-HT signaling, including memory, fear and aggression. This study was designed to investigate the effects of early serotonin agonism on later behaviors. An extremely aggressive White leghorn strain (15I5) was used in the study. The chicks were injected with 5-MT (a serotonin agonist) at 2.5mg/kg (low dose), 10mg/kg (high dose) or saline (control) on the day of hatch and a second dose 24h later (n=9/sex/trt). Chicks' fear response and memory were tested at 2 weeks of age. In the fear test, chicks were subjected to a social isolation test for 20min, time to first vocalization and numbers of vocalizations were recorded. In the memory test, chicks were placed in a running wheel and presented with an imprinted object (white box with a red light) and a similar shaped novel object (blue box with a white light), respectively. The distance traveled in the wheel toward each object was measured. At 10 weeks of age birds were tested for aggression and concentrations of catecholamines were determined from the raphe nucleus and hypothalamus by HPLC (n=12). Expression of 5-HT1A and 5-HT1B receptor genes were measured by RT-PCR. Both high and low dose chicks tended to have shorter latency to first vocalization and a greater number of vocalizations compared with control chicks. Memory test showed that chicks from all groups traveled a similar distance toward a familiar object. However, control chicks walked the least toward a novel object, low dose chicks tended to walk further, and high dose chicks walked significantly further for a novel object. In aggression tests, both high and low dose males exhibited greater frequency of aggressive behaviors compared to controls, while no difference in aggression was evident in the females. Norepinephrine concentrations were also reduced in the low dose birds in the hypothalamus and in the raphe nucleus. Serotonin concentrations tended to be lower only in the both hypothalamus and raphe nucleus of the low dose birds. 5-HT1A expression was greatest in the hypothalamus and raphe nucleus of low dose birds. The agonism of the serotonin system during neural development of birds genetically predisposed to aggression alters both the dopaminergic and serotonergic systems further increasing their aggressiveness.
血清素(5-HT)在发育中的大脑中充当神经递质;然而,SSRIs 等改变血清素的药物经常被开给怀孕和哺乳期的母亲。5-HT 受体的早期激动可能会改变血清素能回路的发育,改变 5-HT 信号介导的神经传递和行为,包括记忆、恐惧和攻击。这项研究旨在调查早期血清素激动对后期行为的影响。使用一种非常具有攻击性的白来航鸡(15I5)进行研究。小鸡在孵化当天以 2.5mg/kg(低剂量)、10mg/kg(高剂量)或生理盐水(对照)注射 5-MT(一种血清素激动剂),24 小时后再注射第二剂(n=9/性别/处理)。小鸡的恐惧反应和记忆在 2 周龄时进行测试。在恐惧测试中,小鸡进行 20 分钟的社会隔离测试,记录第一次发声的时间和发声次数。在记忆测试中,小鸡被放置在跑步轮中,并分别呈现一个被印上的物体(带有红光的白色盒子)和一个类似形状的新物体(带有白光的蓝色盒子)。测量轮子向每个物体行驶的距离。在 10 周龄时,通过 HPLC(n=12)从中缝核和下丘脑测定儿茶酚胺的浓度,对鸟类进行攻击性测试。通过 RT-PCR 测量 5-HT1A 和 5-HT1B 受体基因的表达。与对照小鸡相比,高剂量和低剂量小鸡的第一次发声潜伏期较短,发声次数较多。记忆测试显示,所有组的小鸡都朝着熟悉的物体行驶相似的距离。然而,对照小鸡朝着新物体走的距离最短,低剂量小鸡倾向于走得更远,高剂量小鸡则明显朝着新物体走得更远。在攻击性测试中,高剂量和低剂量雄性小鸡的攻击性行为频率均高于对照组,而雌性小鸡则没有明显差异。低剂量鸟类下丘脑和中缝核中的去甲肾上腺素浓度也降低。低剂量鸟类下丘脑和中缝核中的血清素浓度也趋于降低。5-HT1A 表达在低剂量鸟类的下丘脑和中缝核中最高。在具有攻击性遗传倾向的鸟类的神经发育过程中,血清素系统的激动作用改变了多巴胺能和血清素能系统,进一步增加了它们的攻击性。