Kagitani F, Kimura A, Sato A, Suzuki A
Department of the Autonomic Nervous System, Tokyo Metropolitan Institute of Gerontology, Japan.
Neurosci Lett. 1996 Oct 18;217(2-3):109-12.
Somatic afferent regulation of splenic natural killer (NK) cell activity by hindpaw pinching has been proven, in anesthetized rats, to be a reflex response whose reflex center is in the brain and efferent arc is a splenic sympathetic nerve. Using central nervous system (CNS)-intact and acutely spinalized anesthetized rats, the present study aimed to examine the possibility of whether afferent stimulation (pinching) of the skin over the abdominal segments could influence cytotoxic activity of splenic NK cells and splenic sympathetic nerve activity at the spinal segmental level. In CNS-intact rats, pinching stimulation of the skin of the abdomen with surgical clamps for 30 min did not significantly change cytotoxic activity of splenic NK cells although splenic sympathetic nerve activity increased slightly. In acutely spinalized rats the same stimulation reduced cytotoxic activity of splenic NK cells and was accompanied by an intense reflex increase in splenic sympathetic nerve activity. It is concluded that the spinal cord is capable of producing propriospinally the reflex suppression of cytotoxic activity of splenic NK cells via reflex activation of the splenic sympathetic efferent nerve following stimulation to the abdominal segments whose afferent information enters the spinal cord at the same segments or segments overlapping the splenic sympathetic outflow. A possible mechanism of inhibition of this spinal reflex by inhibitory descending pathways is discussed.
在麻醉大鼠中已证实,通过后爪夹捏对脾脏自然杀伤(NK)细胞活性进行的躯体传入调节是一种反射反应,其反射中枢在脑内,传出弧为脾脏交感神经。本研究利用中枢神经系统(CNS)完整和急性脊髓横断的麻醉大鼠,旨在探讨腹部节段皮肤的传入刺激(夹捏)是否有可能在脊髓节段水平影响脾脏NK细胞的细胞毒性活性和脾脏交感神经活性。在CNS完整的大鼠中,用手术夹捏腹部皮肤30分钟,尽管脾脏交感神经活性略有增加,但脾脏NK细胞的细胞毒性活性没有显著变化。在急性脊髓横断的大鼠中,相同的刺激降低了脾脏NK细胞的细胞毒性活性,并伴有脾脏交感神经活性的强烈反射性增加。得出的结论是,脊髓能够通过对腹部节段的刺激后经脾脏交感传出神经的反射性激活,在脊髓内自主产生对脾脏NK细胞细胞毒性活性的反射性抑制,这些腹部节段的传入信息在与脾脏交感神经传出相同或重叠的节段进入脊髓。还讨论了抑制性下行通路对这种脊髓反射的抑制作用的可能机制。