Vazquez Juan Francisco, Clement Hans-Willi, Sommer Olaf, Schulz Eberhard, van Calker Dietrich
Department of Child and Adolescent Psychiatry, University of Freiburg, Freiburg, Germany.
J Neurochem. 2008 May;105(3):904-9. doi: 10.1111/j.1471-4159.2007.05191.x. Epub 2007 Dec 15.
Both adenosine and interleukin-6 (IL-6) have been implicated in the pathophysiology of, e.g., epileptic seizures, traumatic brain injury, and affective disorders. Stimulation of adenosine A2B receptors on astrocytes in vitro leads to the increased synthesis and secretion of IL-6. We investigated whether or not activation of adenosine receptors evokes an increase of IL-6 release also in vivo. 5'-N-ethylcarboxamidoadenosine, a non-specific adenosine-agonist or vehicle was administered into the striatum of freely moving mice by reverse microdialysis. A statistical significant increase of the IL-6 concentration in the perfusate was detected already 60 min after 5'-N-ethylcarboxamidoadenosine administration. IL-6 increased progressively and reached a maximum after 240 min. This effect appears to be mediated through adenosine A2B receptors since it was counteracted by the specific A2B receptor antagonist MRS1706 but not by the specific A1 receptor antagonist DPCPX. We conclude that adenosine via activation of A2B receptors evokes IL-6 release also in vivo.
腺苷和白细胞介素-6(IL-6)均与例如癫痫发作、创伤性脑损伤和情感障碍的病理生理学有关。体外刺激星形胶质细胞上的腺苷A2B受体可导致IL-6的合成和分泌增加。我们研究了腺苷受体的激活在体内是否也会引起IL-6释放的增加。通过反向微透析将非特异性腺苷激动剂5'-N-乙基羧酰胺腺苷或赋形剂注入自由活动小鼠的纹状体。在给予5'-N-乙基羧酰胺腺苷后60分钟,即可检测到灌注液中IL-6浓度有统计学意义的显著增加。IL-6逐渐升高,并在240分钟后达到最大值。这种作用似乎是通过腺苷A2B受体介导的,因为它被特异性A2B受体拮抗剂MRS1706抵消,但未被特异性A1受体拮抗剂DPCPX抵消。我们得出结论,腺苷通过激活A2B受体在体内也会引起IL-6释放。