Li A J, Katafuchi T, Oda S, Hori T, Oomura Y
Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Brain Res. 1997 Feb 14;748(1-2):30-8. doi: 10.1016/s0006-8993(96)01283-8.
The effects of recombinant human interleukin-6 (rhIL-6) on long-term potentiation (LTP) induced in the Schaffer collateral/commissural-CA1 pathway were examined using rat hippocampal slices. Field excitatory postsynaptic potential was recorded in the stratum radiatum of the CA1 region. Ten-min applications of rhIL-6 (50-2000 U/ml), started 5 min before the tetanus, significantly inhibited the induction of LTP, and in high doses of rhIL-6 also inhibited short-term potentiation (over 200 U/ml) and post-tetanic potentiation (over 500 U/ml). The effects of rhIL-6 (500 U/ml) were completely abolished by the preincubation of the slices with monoclonal anti-IL-6 receptor antibody (16 microg/ml) for 2 h. Heat-inactivated rhIL-6 had no effect on the synaptic potentiation. RhIL-6 affected neither the previously established LTP nor the basal synaptic transmission. These findings indicated that rhIL-6 modulated synaptic potentiation through the IL-6 receptor-mediated process in the hippocampus, probably by affecting post- and presynaptic sites in the CA1 region. The possible mechanisms of the IL-6-induced suppression of the synaptic potentiation were discussed.
利用大鼠海马脑片,研究了重组人白细胞介素-6(rhIL-6)对在Schaffer侧支/联合-CA1通路诱导的长时程增强(LTP)的影响。在CA1区辐射层记录场兴奋性突触后电位。在强直刺激前5分钟开始应用10分钟的rhIL-6(50 - 2000 U/ml),显著抑制了LTP的诱导,并且在高剂量的rhIL-6时也抑制了短时程增强(超过200 U/ml)和强直后增强(超过500 U/ml)。用单克隆抗IL-6受体抗体(16 μg/ml)对脑片预孵育2小时,可完全消除rhIL-6(500 U/ml)的作用。热灭活的rhIL-6对突触增强无影响。rhIL-6既不影响先前建立的LTP,也不影响基础突触传递。这些发现表明,rhIL-6可能通过影响CA1区的突触后和突触前位点,在海马中通过IL-6受体介导的过程调节突触增强。讨论了IL-6诱导突触增强抑制的可能机制。