Yanovski J A, Cutler G B
Section on Developmental Endocrinology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
Endocrinol Metab Clin North Am. 1994 Sep;23(3):487-509.
Glucocorticoids mainly act through binding to cytosolic receptors that translocate to the nucleus after ligand binding, and dimerize to affect gene transcription in multiple fashions. The liganded receptors may interact with DNA at specific glucocorticoid responsive-elements, may physically hinder the ability of other transcription-regulating proteins to interact with their own DNA response-elements, and may form intranuclear complexes with the transcription factor c-jun, thus changing the number of c-jun/c-fos heterodimers that bind at AP-1 sites. By these, and perhaps other, mechanisms, physiologic concentrations of glucocorticoids regulate normal tissue metabolism, and supraphysiologic concentrations cause Cushing's syndrome. Cushing's syndrome leaves virtually no body tissue untouched. Left untreated, it results in progressive adiposity, myopathy, dermopathy (atrophy, stria, purpura, and hirsutism), psychopathy, glucose intolerance, hypercholesterolemia, hypertension, atherosclerosis, immunosuppression, and, ultimately, death. The physiology underlying each of these effects of hypercortisolism has been reviewed. The differences in the presentation of Cushing's syndrome in children and adults have also been discussed. The goal of the clinician must be to identify individuals with Cushing's syndrome as early in the course of the disease as possible so as to avoid the devastating complications that result from prolonged hypercortisolism. In patients for whom screening tests are equivocal, or only intermittently elevated, it may be necessary to re-evaluate the patient over time to establish that the patient has hypercortisolism. Some clinical guidelines for which patients to screen for hypercortisolism have been presented. Once hypercortisolism is established, patients with mild hypercortisolism (urine free cortisol less than four-fold above the upper limit of normal) should undergo tests to differentiate true Cushing's syndrome from a pseudo-Cushing state.
糖皮质激素主要通过与胞质受体结合发挥作用,配体结合后这些受体易位至细胞核,并二聚化以多种方式影响基因转录。配体结合的受体可在特定的糖皮质激素反应元件处与DNA相互作用,可能在物理上阻碍其他转录调节蛋白与其自身DNA反应元件相互作用的能力,还可能与转录因子c-jun形成核内复合物,从而改变在AP-1位点结合的c-jun/c-fos异二聚体的数量。通过这些以及可能的其他机制,生理浓度的糖皮质激素调节正常组织代谢,而超生理浓度则导致库欣综合征。库欣综合征几乎累及身体的所有组织。若不治疗,会导致进行性肥胖、肌病、皮肤病(萎缩、条纹、紫癜和多毛症)、精神病变、葡萄糖不耐受、高胆固醇血症、高血压、动脉粥样硬化、免疫抑制,最终导致死亡。高皮质醇血症的每种效应背后的生理学机制已得到综述。儿童和成人库欣综合征表现的差异也已进行了讨论。临床医生的目标必须是在疾病过程中尽早识别出库欣综合征患者,以避免长期高皮质醇血症导致的毁灭性并发症。对于筛查试验结果不明确或仅间歇性升高的患者,可能有必要随时间重新评估患者以确定其患有高皮质醇血症。已提出了一些关于哪些患者应筛查高皮质醇血症的临床指南。一旦确诊为高皮质醇血症,轻度高皮质醇血症(尿游离皮质醇低于正常上限四倍以上)的患者应接受检查以区分真正的库欣综合征和假性库欣状态。