Ageing reveals the latent effects of early life stress on respiratory and metabolic function in female rats: Novel insights into the sex-specific origins of sleep apnoea.

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Danuzia Ambrozio-Marques, Loralie Mei Guay, Alicia A Koogler, Tim D Ostrowski, Richard Kinkead
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引用次数: 0

Abstract

Sleep apnoea (SA) is ∼2 times more prevalent in men than women. However, this changes at menopause as the occurrence of SA increases and matches that of men. Menopause is a natural process, but it remains unclear why SA emerges only in a subpopulation of ageing women. Early life stress has persistent and sex-specific effects on the brain. Since loss of ovarian hormones is commonly invoked to explain the emergence of various diseases in menopausal women, we tested the hypothesis that the impacts of early life stress on respiratory control remain latent until they reach old age. Newborn rats were either subjected to neonatal maternal separation (NMS; 3 h/day; postnatal days 3-12) or remained undisturbed (CTRL). Females were then raised under standard conditions until they reached adulthood (12-17 weeks), middle-age (35-40 weeks) or old age (60-65 weeks). Respiratory activity was measured with whole body plethysmography. Body weight and composition was assessed with nuclear magnetic resonance. NMS augmented the apnoea index; however, this effect was detected only in old females. Body mass index and the percentage of body fat increased progressively; these changes were enhanced by NMS and most notable in old females. We conclude that NMS compromises the ageing trajectory of female rats and leads to the development of a phenotype that shares many features reported in SA patients, including respiratory and metabolic dysfunction. Prior life experiences may be an important risk factor in the development of SA in ageing women.

衰老揭示了早期生活压力对雌性大鼠呼吸和代谢功能的潜在影响:睡眠呼吸暂停的性别特异性起源的新见解。
睡眠呼吸暂停(SA)在男性中的发病率是女性的2倍。然而,随着SA的发生增加,这种情况在更年期发生变化,与男性相同。更年期是一个自然过程,但尚不清楚为什么SA只出现在老年妇女的亚群中。早期的生活压力对大脑有持久的、性别特异性的影响。由于卵巢激素的丧失通常被用来解释更年期妇女各种疾病的出现,我们测试了早期生活压力对呼吸控制的影响直到她们进入老年时仍然是潜在的假设。新生大鼠接受新生儿母分离(NMS;3小时/天;出生后第3-12天)或保持不受干扰(CTRL)。然后在标准条件下饲养雌性,直到它们成年(12-17周)、中年(35-40周)或老年(60-65周)。用全身体积脉搏波仪测量呼吸活动。用核磁共振测定体重和身体成分。NMS提高了呼吸暂停指数;然而,这种影响只在老年女性中发现。体重指数和体脂率逐渐增加;NMS增强了这些变化,在老年女性中最为显著。我们的结论是,NMS损害了雌性大鼠的衰老轨迹,并导致了一种表型的发展,这种表型与SA患者的许多特征相同,包括呼吸和代谢功能障碍。既往生活经历可能是老年妇女SA发生的重要危险因素。
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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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