Peripheral corticotropin-releasing factor mediates the elevation of plasma IL-6 by immobilization stress in rats

被引:39
作者
Ando, T
Rivier, J
Yanaihara, H
Arimura, A [1 ]
机构
[1] Tulane Univ, Hebert Ctr, US Japan Biomed Res Labs, Belle Chasse, LA 70037 USA
[2] Salk Inst Biol Studies, Peptide Biol Lab, La Jolla, CA 92037 USA
关键词
neuroimmunomodulation; Astressin; D-Phe(12),Nle(21,38,) (CMe)-Me-alpha-Leu(37)]-anti-human rat corticotropin-releasing factor(12-41); urocortin; cytokine;
D O I
10.1152/ajpregu.1998.275.5.R1461
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We previously reported the elevation of plasma interleukin (IL)-6 activity in response to immobilization stress in rats. To investigate the role of peripheral corticotropin-releasing factor (CRF) in this response, we examined the effects of CRF antagonists on immobilization-induced IL-B response. Intravenous pretreatment with either [D-Phe(12),Nle(21,38),C(alpha)MeLeu(37)]-anti-human rat (h/r) CRF12-41 (1.5 mg/kg) or cyclo(30-33)[D-Phe(12), Nle(21,38), Glu(30),Lys(33)]-h/rCRF(12-41) (Astressin, 0.5 mg/kg) attenuated the IL-6 response to immobilization, which confirmed our previous finding that systemic administration of an antiserum against CRF blocked this response. In addition, an intraperitoneal injection of h/rCRF (100 mu g/kg) or rat urocortin (10 and 100 mu g/kg) increased the plasma IL-6 activity, mimicking the response to immobilization. An intravenous injection of h/rCRF (100 mu g/kg) also elevated plasma IL-6 in adrenalectomized rats. These findings suggest that peripheral CRF mediates the plasma IL-6 elevation in response to immobilization.
引用
收藏
页码:R1461 / R1467
页数:7
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