Krukoff T L, MacTavish D, Jhamandas J H
Department of Cell Biology, Faculty of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Brain Res Mol Brain Res. 1999 Feb 19;65(1):70-9. doi: 10.1016/s0169-328x(98)00342-8.
To test the hypothesis that chronically elevated sympathetic drive is associated with hyperreactiveness of autonomic centers in the brain to stress, adult spontaneously hypertensive rats (SHRs) and two strains of normotensive rats (Wistar Kyoto [WKY] and Sprague Dawley [SD] rats) were acutely exposed to restraint stress; controls from each strain were not stressed. Brain sections were prepared for Fos immunohistochemistry to identify activated neurons in the paraventricular nucleus of the hypothalamus, Barrington's nucleus of the pons, nucleus of the tractus solitarius, and ventrolateral medulla, or for combined Fos immunohistochemistry and corticotropin-releasing factor (CRF) in situ hybridization in the paraventricular nucleus and Barrington's nucleus. Restraint led to increased activation of neurons in all nuclei. Strain differences were found only in the caudal and rostral paraventricular nucleus where restraint resulted in greater numbers of activated neurons in SHRs compared to either normotensive strain. Levels of CRF mRNA in Barrington's nucleus of unrestrained rats were similar among strains. After restraint, mRNA levels and double labeled neurons were increased in Barrington's nucleus of SHRs. In unstressed rats, CRF mRNA levels were elevated in some regions of the paraventricular nucleus in SHRs. After restraint, mRNA levels increased throughout the paraventricular nucleus of SHRs. Significantly greater numbers of double labeled neurons were found in the dorsolateral medial and ventral medial parvocellular paraventricular nucleus of stressed SHRs compared to WKY or SD rats. These data show that chronic elevation in sympathetic activity, present in SHRs, is associated with hyperreactiveness of the paraventricular and Barrington's nucleus including recruitment of neurons to express CRF, and may have important implications for the response of the hypothalamo-pituitary-adrenal axis during stress.
为了验证慢性交感神经驱动增强与大脑自主神经中枢对压力的高反应性相关这一假说,将成年自发性高血压大鼠(SHR)和两种正常血压大鼠品系(Wistar Kyoto [WKY]大鼠和Sprague Dawley [SD]大鼠)急性暴露于束缚应激;每个品系的对照组不施加应激。制备脑切片用于Fos免疫组织化学,以识别下丘脑室旁核、脑桥的巴林顿核、孤束核和延髓腹外侧的激活神经元,或用于室旁核和巴林顿核的Fos免疫组织化学与促肾上腺皮质激素释放因子(CRF)原位杂交联合检测。束缚导致所有核团中神经元的激活增加。仅在室旁核的尾侧和头侧发现品系差异,与任一正常血压品系相比,束缚导致SHR中激活神经元数量更多。未束缚大鼠的巴林顿核中CRF mRNA水平在各品系间相似。束缚后,SHR的巴林顿核中mRNA水平和双标神经元增加。在未施加应激的大鼠中,SHR室旁核的某些区域CRF mRNA水平升高。束缚后,SHR整个室旁核的mRNA水平增加。与WKY或SD大鼠相比,应激SHR的背外侧内侧和腹内侧小细胞室旁核中双标神经元数量显著更多。这些数据表明,SHR中存在的交感神经活动慢性增强与室旁核和巴林顿核的高反应性相关,包括募集神经元以表达CRF,并且可能对应激时下丘脑-垂体-肾上腺轴的反应具有重要意义。