Romero-Sandoval Alfonso, Eisenach James C
Department of Anesthesiology and Center for the Study of Pharmacologic Plasticity in the Presence of Pain, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1009, USA.
Brain Behav Immun. 2007 Jul;21(5):569-80. doi: 10.1016/j.bbi.2006.09.001. Epub 2006 Oct 31.
Perineural alpha2-adrenoceptor activation relieves hypersensitivity induced by peripheral nerve injury or sciatic inflammatory neuritis. This effect is associated with a reduction in pro-inflammatory cytokines, as well as a reduction in local leukocyte number and their capacity to produce pro-inflammatory cytokines. Curiously, clonidine's antinociceptive effect appears with a 2-3-day delay after injection. Previous observations have shown that alpha-adrenoceptor activation induces apoptosis in leukocytes, which would reduce leukocyte number. Additionally, macrophage scavenging of apoptotic cells results in a shift to an anti-inflammatory phenotype, with expression of transforming growth factor (TGF)-beta1. We therefore examined the effects of perineural clonidine 24 h and 3 days after its injection on apoptosis, TGF-beta1 expression and lymphocyte and macrophage phenotype in acute sciatic inflammatory neuritis. Perineural clonidine reduced ipsilateral neuritis-induced hypersensitivity in a delayed manner (3 days after treatment), along with a reduction at this time in lymphocyte number and an increase in caspase-3 and TGF-beta1 expressing cells and macrophages co-expressing TGF-beta1 in the sciatic nerve. One day after injection clonidine treatment was associated with a reduction in lymphocytes and pro-inflammatory Th-1 cells as well as increased numbers of caspase-3 and TGF-beta1 expressing cells and macrophages co-expressing TGF-beta1 in sciatic nerve. Clonidine's effects were prevented by co-administration of an alpha2-adrenoceptor antagonist. These data suggest that alpha2-adrenoceptor activation in sciatic inflammatory neuritis increases local apoptosis and anti-inflammatory products early after treatment. This early effect likely underlies the delayed anti-inflammatory and anti-hypersensitivity effects of perineural clonidine in this setting.
神经周围α2 -肾上腺素能受体激活可减轻由周围神经损伤或坐骨神经炎性神经炎引起的超敏反应。这种效应与促炎细胞因子的减少有关,同时局部白细胞数量及其产生促炎细胞因子的能力也会降低。奇怪的是,可乐定的抗伤害感受作用在注射后2 - 3天出现延迟。先前的观察表明,α -肾上腺素能受体激活可诱导白细胞凋亡,从而减少白细胞数量。此外,巨噬细胞清除凋亡细胞会导致向抗炎表型转变,并伴有转化生长因子(TGF)-β1的表达。因此,我们研究了注射后24小时和3天神经周围可乐定对急性坐骨神经炎性神经炎中细胞凋亡、TGF-β1表达以及淋巴细胞和巨噬细胞表型的影响。神经周围可乐定以延迟方式(治疗后3天)减轻同侧神经炎诱导的超敏反应,同时此时坐骨神经中的淋巴细胞数量减少,而表达半胱天冬酶-3和TGF-β1的细胞以及共表达TGF-β1的巨噬细胞数量增加。注射可乐定治疗1天后,坐骨神经中的淋巴细胞和促炎Th-1细胞数量减少,而表达半胱天冬酶-3和TGF-β1的细胞以及共表达TGF-β1的巨噬细胞数量增加。α2 -肾上腺素能受体拮抗剂的共同给药可阻止可乐定的作用。这些数据表明,坐骨神经炎性神经炎中α2 -肾上腺素能受体激活在治疗后早期会增加局部细胞凋亡和抗炎产物。这种早期效应可能是神经周围可乐定在此情况下延迟的抗炎和抗超敏反应的基础。