Take S, Mori T, Katafuchi T, Hori T
Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Am J Physiol. 1993 Aug;265(2 Pt 2):R453-9. doi: 10.1152/ajpregu.1993.265.2.R453.
The brain has been known to produce high levels of interferon-alpha (IFN-alpha) during viral infections. We investigated the central and peripheral mechanisms of the brain IFN-alpha-induced suppression of natural killer (NK) cytotoxicity in the rat. The activity of NK cells in the spleen and the peripheral blood decreased 30-120 min after intracerebroventricular (icv) injection of recombinant human IFN-alpha of > 1,000 U but not after its intraperitoneal injection. This effect was antagonized by pretreatment with icv naltrexone (NLTX). Splenic denervation was observed to completely abolish the IFN-alpha-induced suppression of NK activity, whereas bilateral adrenalectomy did not. Furthermore, this immunosuppression was blocked by an icv injection of an antagonist of corticotropin-releasing factor (CRF), alpha-helical CRF-(9-41). The icv injection of CRF resulted in reduced NK activity, which was not affected by NLTX. The results suggest that brain IFN-alpha activates the CRF system through central opioid receptors and thereby suppresses the NK cytotoxicity predominantly through splenic sympathetic innervation.
已知在病毒感染期间大脑会产生高水平的α干扰素(IFN-α)。我们研究了大鼠脑中IFN-α诱导的自然杀伤(NK)细胞毒性抑制的中枢和外周机制。脑室内(icv)注射大于1000 U的重组人IFN-α后30 - 120分钟,脾脏和外周血中NK细胞的活性降低,但腹腔注射后未出现这种情况。预先经icv注射纳曲酮(NLTX)可拮抗这种作用。观察到脾脏去神经支配可完全消除IFN-α诱导的NK活性抑制,而双侧肾上腺切除术则无此作用。此外,icv注射促肾上腺皮质激素释放因子(CRF)拮抗剂α-螺旋CRF-(9 - 41)可阻断这种免疫抑制。icv注射CRF导致NK活性降低,这不受NLTX影响。结果表明,脑IFN-α通过中枢阿片受体激活CRF系统,从而主要通过脾脏交感神经支配抑制NK细胞毒性。