Perlstein R S, Mehta N R, Mougey E H, Whitnall M H, Neta R
Department of Experimental Hematology, Armed Forces Radiobiology Research Institute, Bethesda, Maryland 20889-5603.
Radiat Res. 1995 Mar;141(3):336-41.
Recombinant human interleukin-1 alpha (rhIL-1 alpha) has significant potential as a radioprotector and/or treatment for radiation-induced hematopoietic injury. Both IL-1 and whole-body ionizing irradiation acutely stimulate the hypothalamic-pituitary-adrenal axis. We therefore assessed the interaction of whole-body irradiation and rhIL-1 alpha in altering the functioning of the axis in mice. Specifically, we determined the adrenocorticotropin (ACTH) and corticosterone responses to rhIL-1 alpha administered just before and hours to days after whole-body or sham irradiation. Our results indicate that whole-body irradiation does not potentiate the rhIL-1 alpha-induced increase in ACTH levels at the doses used. In fact, the rhIL-1 alpha-induced increase in plasma ACTH is transiently impaired when the cytokine is administered 5 h after, but not 1 h before, exposure to whole-body irradiation. The ACTH response may be inhibited by elevated corticosterone levels after whole-body irradiation, or by other radiation-induced effects on the pituitary gland and hypothalamus.
重组人白细胞介素-1α(rhIL-1α)作为一种辐射防护剂和/或用于治疗辐射诱导的造血损伤具有巨大潜力。白细胞介素-1(IL-1)和全身电离辐射均可急性刺激下丘脑-垂体-肾上腺轴。因此,我们评估了全身照射与rhIL-1α在改变小鼠该轴功能方面的相互作用。具体而言,我们测定了在全身照射或假照射之前以及照射后数小时至数天给予rhIL-1α时促肾上腺皮质激素(ACTH)和皮质酮的反应。我们的结果表明,在所使用的剂量下,全身照射不会增强rhIL-1α诱导的ACTH水平升高。事实上,当在全身照射后5小时而非照射前1小时给予细胞因子时,rhIL-1α诱导的血浆ACTH升高会暂时受损。全身照射后升高的皮质酮水平或其他辐射对垂体和下丘脑的诱导效应可能会抑制ACTH反应。