Hu Z, Yuri K, Ozawa H, Kawata M
Department of Anatomy and Neurobiology, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Japan.
Neuroscience. 1999;90(4):1185-95. doi: 10.1016/s0306-4522(98)00567-3.
To understand the effect of a chronic lack of endogenous glucocorticoids on glucocorticoid receptor levels, the changes of glucocorticoid receptor content in the rat forebrain five months after adrenalectomy were investigated. In the long-term adrenalectomized rats that showed a hormone deficiency and loss of glucocorticoid receptor immunoreactivity in the forebrain, an intraperitoneal injection of corticosterone was used to elevate the serum hormone levels and recover glucocorticoid receptor immunoreactivity in the forebrain. One hour later, when the blood corticosterone returned to the normal level, the recovery of glucocorticoid receptor immunoreactivity in the forebrain was examined by immunohistochemistry. Since the complete restoration of glucocorticoid receptor immunoreactivity was shown to depend on the presence of normal levels of both serum hormone and intracellular glucocorticoid receptors, the weak reappearance of glucocorticoid receptor immunoreactivity in any forebrain area of the long-term adrenalectomized rats that had normal serum corticosterone might reflect the low intracellular glucocorticoid receptor levels there. Our results revealed a weak reappearance of glucocorticoid receptor immunoreactivity in some forebrain areas of the long-term adrenalectomized rats after corticosterone treatment; the hippocampal granule cell layer and cerebral cortex in particular showed very weak recovery of glucocorticoid receptor immunoreactivity. Conversely, neurons in the CA1/CA2 subfields of the hippocampal pyramidal cell layer, immediately adjacent to the granule cell layer on the same brain section, exhibited a strong reappearance of glucocorticoid receptor immunoreactivity, to near normal levels. These results suggest that, five months after adrenalectomy, the intracellular glucocorticoid receptor content decreased in the rat granule cell layer and cerebral cortex. Therefore, the long-term lack of endogenous glucocorticoids after adrenalectomy might down-regulate but not up-regulate the intracellular glucocorticoid receptor level, and the presence of glucocorticoids is important for the continued synthesis of glucocorticoid receptors.
为了解内源性糖皮质激素长期缺乏对糖皮质激素受体水平的影响,研究了大鼠肾上腺切除术后五个月前脑糖皮质激素受体含量的变化。在长期肾上腺切除的大鼠中,前脑出现激素缺乏和糖皮质激素受体免疫反应性丧失,通过腹腔注射皮质酮来提高血清激素水平并恢复前脑的糖皮质激素受体免疫反应性。一小时后,当血液皮质酮恢复到正常水平时,通过免疫组织化学检查前脑糖皮质激素受体免疫反应性的恢复情况。由于糖皮质激素受体免疫反应性的完全恢复依赖于血清激素和细胞内糖皮质激素受体正常水平的存在,长期肾上腺切除且血清皮质酮正常的大鼠前脑任何区域中糖皮质激素受体免疫反应性的微弱重现可能反映了该区域细胞内糖皮质激素受体水平较低。我们的结果显示,长期肾上腺切除的大鼠经皮质酮治疗后,前脑某些区域出现了糖皮质激素受体免疫反应性的微弱重现;特别是海马颗粒细胞层和大脑皮层,糖皮质激素受体免疫反应性的恢复非常微弱。相反,在同一脑切片上紧邻颗粒细胞层的海马锥体细胞层CA1/CA2亚区的神经元,糖皮质激素受体免疫反应性强烈重现,接近正常水平。这些结果表明,肾上腺切除术后五个月,大鼠颗粒细胞层和大脑皮层中的细胞内糖皮质激素受体含量降低。因此,肾上腺切除术后内源性糖皮质激素的长期缺乏可能下调而非上调细胞内糖皮质激素受体水平,并且糖皮质激素的存在对于糖皮质激素受体的持续合成很重要。