Björntorp P, Holm G, Rosmond R
Department of Heart and Lung Diseases, University of Gothenburg, Sahlgren's Hospital, Sweden.
Diabet Med. 1999 May;16(5):373-83. doi: 10.1046/j.1464-5491.1999.00067.x.
Type 2 diabetes mellitus (DM) develops when insulin resistance overcomes the capacity of compensatory insulin secretion. Insulin resistance may be induced via psychoneuroendocrine pathways, a possibility which has received little previous attention.
We have used salivary cortisol measurements to monitor the activity of the hypothalamic-pituitary-adrenal (HPA) axis, the major controller of hormones involved in the regulation of peripheral insulin sensitivity under everyday conditions. The influence of external challenges, as well as the sensitivity of feedback regulation, were followed in randomly selected middle-aged population samples.
In health there is a rhythmicity of cortisol secretion, with a high plasticity and efficient feedback control. In contrast, a group of subjects were identified with a flat, rigid day curve and poor feedback control, who showed consistent abnormalities in stress-related cortisol secretion, including inhibited secretions of sex steroids and growth hormone; insulin resistance; abdominal obesity; elevated leptin levels; hyperglycaemia; dyslipidaemia and hypertension with elevated heart rate. The endocrine abnormalities are probably responsible for the anthropometric and metabolic abnormalities. The circulatory perturbations seem to be induced by a parallel activation of the central sympathetic nervous system suggesting an 'hypothalamic arousal syndrome', gradually developing into an independent risk for disease. An associated cluster of environmental factors, including psychosocial and socio-economic stress, traits of depression and anxiety, alcohol consumption and smoking, all factors known to activate hypothalamic centres, has been identified. A polymorphism of the glucocorticoid receptor gene, with 13.7% homozygotes in the male Swedish population, parallels receptor dysfunction, and may be responsible for the associated insulin resistance, central obesity and hypertension.
This is the first detailed examination of psychoneuroendocrinological processes in the natural environment on a population basis in relation to somatic health. The results suggest that an hypothalamic arousal syndrome, with parallel activation of the HPA axis and the central sympathetic nervous system, is responsible for development of endocrine abnormalities, insulin resistance, central obesity, dyslipidaemia and hypertension, leading to frank disease, including Type 2 DM. We suggest that this syndrome is probably based on environmental pressures in genetically susceptible individuals.
当胰岛素抵抗超过代偿性胰岛素分泌能力时,2型糖尿病(DM)就会发生。胰岛素抵抗可能通过精神神经内分泌途径诱发,而这一可能性此前很少受到关注。
我们通过测量唾液皮质醇来监测下丘脑-垂体-肾上腺(HPA)轴的活性,HPA轴是日常条件下参与调节外周胰岛素敏感性的激素的主要调控者。在随机选取的中年人群样本中,跟踪外部挑战的影响以及反馈调节的敏感性。
在健康状态下,皮质醇分泌具有节律性,具有高可塑性和有效的反馈控制。相比之下,一组受试者的皮质醇日曲线平坦、僵硬,反馈控制不佳,他们在应激相关的皮质醇分泌方面表现出持续异常,包括性类固醇和生长激素分泌受抑制;胰岛素抵抗;腹部肥胖;瘦素水平升高;高血糖;血脂异常和心率升高的高血压。内分泌异常可能是人体测量和代谢异常的原因。循环系统紊乱似乎是由中枢交感神经系统的平行激活引起的,提示一种“下丘脑觉醒综合征”,逐渐发展为独立的疾病风险。已确定一组相关的环境因素,包括心理社会和社会经济压力、抑郁和焦虑特质、饮酒和吸烟,所有这些因素都已知会激活下丘脑中心。糖皮质激素受体基因的一种多态性,在瑞典男性人群中有13.7%的纯合子,与受体功能障碍平行,可能是相关胰岛素抵抗、中心性肥胖和高血压的原因。
这是首次在人群基础上,在自然环境中对与躯体健康相关的精神神经内分泌过程进行详细研究。结果表明,一种下丘脑觉醒综合征,伴有HPA轴和中枢交感神经系统的平行激活,是内分泌异常、胰岛素抵抗、中心性肥胖、血脂异常和高血压发展的原因,导致包括2型糖尿病在内的明显疾病。我们认为,这种综合征可能基于遗传易感个体中的环境压力。