Chen X, Levine J D
Departments of Anatomy, Medicine and Oral and Maxillofacial Surgery, Division of Neuroscience, NIH Pain Center (University of California, San Francisco), C-522 Box 0440, University of California, San Francisco, CA 94143-0440, USA.
Neuroscience. 2003;121(4):1007-15. doi: 10.1016/s0306-4522(03)00486-x.
While enhanced nociceptor activity has been demonstrated in models of painful peripheral neuropathy, analyses of activity pattern, which could play a role in the symptoms experienced as well as help elucidate underlying mechanism, are still limited. We evaluated the pattern of C-fiber activity, in response to mechanical and chemical stimuli, in a rat model of diabetes induced by a pancreatic beta-cell toxin, streptozotocin (STZ). In diabetic rats the number of action potentials produced by threshold and suprathreshold (10 g) sustained (60 s) mechanical stimuli was elevated in approximately half of C-fibers. These high-firing C-fibers demonstrated a disproportionate increase in interspike intervals (ISIs) between 100 and 199 ms, compared with low-firing diabetic and control C-fibers. The co-efficient of variability (CV2), a frequency independent measure of ISI variability, was also greater in high-firing fibers, compared with control fibers. Unexpectedly, instantaneous frequency of the initial burst of activity during the first second was lower in high-firing fibers, even though the average frequency over the last 59 s was significantly higher. The number of action potentials evoked by a noxious chemical stimulus, 300 and 600 mM KCl, injected adjacent to the mechanical receptive field was also significantly increased in C-fibers from diabetic rats and mechanically high-firing fibers had more action potentials in response to KCl than control fibers and a disproportionate increase in ISIs between 100 and 199 ms for responses to chemical stimuli appeared only in mechanically high-firing C-fibers, compared with the mechanically low-firing diabetic or control C-fibers. There was, however, no corresponding change in CV2 or instantaneous frequency plots for the response to chemical stimulation in mechanically high-firing fibers, as there was in the response to mechanical stimulation. Our data demonstrate specific changes in firing pattern of high-firing C-fibers in the rat model of painful neuropathy produced by STZ-diabetes that might contribute to the symptoms experienced by patients.
虽然在疼痛性周围神经病变模型中已证实伤害感受器活性增强,但对活性模式的分析仍然有限,而这种活性模式可能在患者所经历的症状中发挥作用,并有助于阐明潜在机制。我们评估了在由胰腺β细胞毒素链脲佐菌素(STZ)诱导的糖尿病大鼠模型中,C纤维对机械和化学刺激的反应活性模式。在糖尿病大鼠中,大约一半的C纤维对阈值和阈上(10 g)持续(60 s)机械刺激产生的动作电位数量增加。与低放电的糖尿病和对照C纤维相比,这些高放电C纤维在100至199 ms之间的峰间间隔(ISI)增加不成比例。变异系数(CV2)是一种与频率无关的ISI变异性测量指标,与对照纤维相比,高放电纤维的CV2也更大。出乎意料的是,尽管在最后59 s的平均频率显著更高,但高放电纤维在最初1秒内活动爆发的瞬时频率较低。在机械感受野附近注射有害化学刺激物300和600 mM KCl诱发的动作电位数量在糖尿病大鼠的C纤维中也显著增加,并且与对照纤维相比,机械高放电纤维对KCl的反应有更多动作电位,对于化学刺激的反应,在100至199 ms之间的ISI增加不成比例仅出现在机械高放电C纤维中,与机械低放电的糖尿病或对照C纤维相比。然而,与对机械刺激的反应不同,机械高放电纤维对化学刺激的反应在CV2或瞬时频率图上没有相应变化。我们的数据表明,在由STZ诱导的糖尿病所致疼痛性神经病变大鼠模型中,高放电C纤维的放电模式发生了特定变化,这可能导致患者出现相应症状。