Basal and IL-1 beta-stimulated cytokine and neuropeptide mRNA expression in brain regions of young and old Long-Evans rats

Young and old Long-Evans rats respond with fevers of equal magnitude and du ration to the brain administration of interleukin-la (IL-1 beta). Here, we characterized brain regional mRNA expression of cytokine and neuropeptide c omponents in response to the brain administration of IL-1 beta. We used spe cific and highly sensitive RNase protection assays to determine mRNA change s for IL-1 beta, IL-1 receptor type I (IL-1RI), IL-1R accessory proteins I and II (IL-1R AcP I and II), IL-1 receptor antagonist (IL-1Ra), transformin g growth factor-beta 1 (TGF-beta 1), glycoprotein 130 (gp 130), leptin rece ptor (OB-R), neuropeptide Y (NPY) and pro-opiomelanocortin (POMC) in the ce rebellum, parieto-frontal cortex, hippocampus, hypothalamus, and midbrain o f male young (3-5 months) and old (24-26 months) Long-Evans rats. In both y oung and old rats, IL-1 beta induced a significant up-regulation of cerebel lar IL-1Ra,IL-1RI, and TGF-beta 1 mRNAs; hippocampal TGF-beta 1 mRNA; hypot halamic IL-1 beta, IL-1Ra, TGF-beta 1, and gp 130 mRNAs; and midbrain IL-1 beta and TGF-beta 1 mRNAs. There were no age-related differences in any cyt okine mRNA levels under basal or IL-1 beta-stimulated conditions. Levels of hypothalamic POMC mRNA were different between age groups under basal and s timulated conditions. IL-1R AcP I and leptin receptor did not change in any brain region from either young or old rats,suggesting specificity of trans criptional changes. The data show that old Long-Evans rats are not defectiv e in their capacity to develop an appropriate cytokine response to the brai n administration of IL-1 beta. The implications of these findings for neuro immunological-neuroinflammatory and neurotoxic/neurodegenerative processes are discussed. (C) 1999 Elsevier Science B.V. All rights reserved.