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Tail-flick test response in 3 x Tg-AD mice at early and advanced stages of disease

机译:在疾病的早期和高级阶段,在3 x TG-AD小鼠中尾巴轻弹试验响应

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摘要

Despite the impact of pain in cognitive dysfunctions and affective disorders has been largely studied, the research that examines pain dimensions in cognitive impairment or dementia is still scarce. In patients with Alzheimer's disease (AD) and related dementias, management of pain is challenging. While the sensory-discriminative dimension of pain is preserved, the cognitive-evaluative and the affective-motivational pain dimensions are affected. Due to the complexity of the disease and the poor self-reports, pain is underdiagnosed and undertreated. In confluence with an impaired thermoregulatory behavior, the patients' ability to confront environmental stressors such as cold temperature can put them at risk of fatal accidental hypothermia. Here, 3xTg-AD mice demonstrate that the sensorial-discriminative threshold to a noxious cold stimulus, as measured by the latency of tail-flicking, was preserved at early and advances stages of disease (7 and 11 month-old, respectively) as compared to age-matched (adulthood and middle aged, respectively) non-transgenic mice (NTg). In both genotypes, the sensory deterioration and poor thermoregulatory behavior associated to age was observed as an increase of tail-flick response and poor sensorimotor performance. At both stages studied, 3xTg-AD mice exhibited BPSD (Behavioral and Psychological Symptoms of Dementia)-like alterations in the coiner, open-field, dark-light box and the T-maze tests. In the adult NTg mice, this nociceptive withdrawal response was correlated with copying with stress-related behaviors. This integrative behavioral profile was lost in both groups of 3xTg-AD mice and middle aged controls, suggesting derangements in their subjacent networks and the complex interplay between the pain dimensions in the elderly with dementia.
机译:尽管对认知功能障碍疼痛的影响,但在很大程度上研究了疼痛和情感障碍,但研究认知障碍或痴呆症疼痛尺寸的研究仍然稀缺。在阿尔茨海默病(AD)和相关痴呆症的患者中,疼痛的管理是挑战性的。虽然保留了疼痛的感官鉴别尺寸,但是认知评价和情感诱导疼痛尺寸受到影响。由于疾病的复杂性和贫困的自我报告,疼痛是不足的,并且患病。在汇合具有受损的热调节行为的情况下,患者面临寒冷温度等环境压力源的能力可以让它们面临致命意外体温过低的风险。这里,3xtg-AD小鼠表明,通过尾闪烁的潜伏量测量的有害冷刺激的感官鉴别阈值被保存在早期,并在比较方面预期疾病(7和11个月)的阶段以年龄匹配(成年和中年)非转基因小鼠(NTG)。在两个基因型中,观察到与年龄相关的感觉劣化和差的热调节行为作为尾部轻弹响应的增加和感觉电量差的性能。在研究的两个阶段,3XTG-AD小鼠表现出BPSD(痴呆的行为和心理症状) - 卷曲,开放场,暗灯箱和T型迷宫试验中的改变。在成虫小鼠中,这种伤害戒断反应与复制与应力相关的行为相关。这种综合行为概况在3XTG-AD小鼠和中年控制的两组中丢失,建议他们的亚洲网络中的紊乱以及老年人疼痛尺寸与痴呆症之间的疼痛尺寸之间的复杂相互作用。

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