Genest Sophie-Emmanuelle, Gulemetova Roumiana, Laforest Sylvie, Drolet Guy, Kinkead Richard
Centre de Recherche du Recherche Centre Hospitalier Universitaire de Québec, Université Laval, Québec City, QC, Canada.
J Physiol. 2004 Jan 15;554(Pt 2):543-57. doi: 10.1113/jphysiol.2003.052894. Epub 2003 Nov 21.
We tested the hypothesis that neonatal maternal separation (NMS), a form of stress that affects hypothalamo-pituitary-adrenal axis (HPA) function in adult rats, alters development of the respiratory control system. Pups subjected to NMS were placed in a temperature and humidity controlled incubator 3 h per day for 10 consecutive days (P3 to P12). Control pups were undisturbed. Once they reached adulthood (8-10 weeks old), rats were placed in a plethysmography chamber for measurement of ventilatory and cardiovascular parameters under normoxic and hypoxic conditions. Measurement of c-fos mRNA expression in the paraventricular nucleus of the hypothalamus (PVH) combined with plasma ACTH and corticosterone levels confirmed that NMS effectively disrupted HPA axis function in males. In males, baseline minute ventilation was not affected by NMS. In contrast, NMS females show a greater resting minute ventilation due to a larger tidal volume. The hypoxic ventilatory response of male NMS rats was 25% greater than controls, owing mainly to an increase in tidal volume response. This augmentation of the hypoxic ventilatory response was sex-specific also because NMS females show an attenuated minute ventilation increase. Baseline mean arterial blood pressure of male NMS rats was 20% higher than controls. NMS-related hypertension was not significant in females. The mechanisms underlying sex-specific disruption of cardio-respiratory control in NMS rats are unknown but may be a consequence of the neuroendocrine disruption associated with NMS. These data indicate that exposure to a non-respiratory stress during early life elicits significant plasticity of these homeostatic functions which persists until adulthood.
新生期母婴分离(NMS),一种影响成年大鼠下丘脑 - 垂体 - 肾上腺轴(HPA)功能的应激形式,会改变呼吸控制系统的发育。接受NMS的幼崽每天在温度和湿度可控的培养箱中放置3小时,连续10天(出生后第3天至第12天)。对照幼崽未受干扰。大鼠成年后(8 - 10周龄),将其置于体积描记室中,以测量常氧和低氧条件下的通气和心血管参数。下丘脑室旁核(PVH)中c - fos mRNA表达的测定结合血浆促肾上腺皮质激素(ACTH)和皮质酮水平证实,NMS有效地破坏了雄性大鼠的HPA轴功能。在雄性大鼠中,基础分钟通气量不受NMS影响。相比之下,NMS雌性大鼠由于潮气量较大,静息分钟通气量更大。雄性NMS大鼠的低氧通气反应比对照组高25%,主要是由于潮气量反应增加。这种低氧通气反应的增强也是性别特异性的,因为NMS雌性大鼠的分钟通气量增加减弱。雄性NMS大鼠的基础平均动脉血压比对照组高20%。NMS相关的高血压在雌性大鼠中不显著。NMS大鼠心肺控制性别特异性破坏的潜在机制尚不清楚,但可能是与NMS相关的神经内分泌破坏的结果。这些数据表明,生命早期暴露于非呼吸性应激会引发这些稳态功能的显著可塑性,这种可塑性会持续到成年期。