Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
Neural Plast. 2019 Mar 11;2019:2098083. doi: 10.1155/2019/2098083. eCollection 2019.
Although referred pain or hypersensitivity has been repeatedly reported in irritable bowel syndrome (IBS) patients and experimental colitis rodents, little is known about the neural mechanisms. Spinal long-term potentiation (LTP) of nociceptive synaptic transmission plays a critical role in the development of somatic hyperalgesia in chronic pain conditions. Herein, we sought to determine whether spinal LTP contributes to the referral hyperalgesia in colitis rats and particularly whether electroacupuncture (EA) is effective to alleviate somatic hyperalgesia via suppressing spinal LTP. Rats in the colitis group (induced by colonic infusion of 2,4,6-trinitrobenzenesulfonic acid, TNBS), instead of the control and vehicle groups, displayed evident focal inflammatory destruction of the distal colon accompanied not only with the sensitized visceromotor response (VMR) to noxious colorectal distension (CRD) but also with referral hindpaw hyperalgesia indicated by reduced mechanical and thermal withdrawal latencies. EA at Zusanli (ST36) and Shangjuxu (ST37) attenuated the severity of colonic inflammation, as well as the visceral hypersensitivity and referral hindpaw hyperalgesia in colitis rats. Intriguingly, the threshold of C-fiber-evoked field potentials (CFEFP) was significantly reduced and the spinal LTP was exaggerated in the colitis group, both of which were restored by EA treatment. Taken together, visceral hypersensitivity and referral hindpaw hyperalgesia coexist in TNBS-induced colitis rats, which might be attributed to the enhanced LTP of nociceptive synaptic transmission in the spinal dorsal horn. EA at ST36 and ST37 could relieve visceral hypersensitivity and, in particular, attenuate referral hindpaw hyperalgesia by suppressing the enhanced spinal LTP.
虽然在肠易激综合征(IBS)患者和实验性结肠炎大鼠中反复报道了牵涉痛或超敏反应,但对其神经机制知之甚少。伤害性突触传递的脊髓长时程增强(LTP)在慢性疼痛条件下躯体痛觉过敏的发展中起着关键作用。在此,我们试图确定脊髓 LTP 是否有助于结肠炎大鼠的牵涉性痛觉过敏,特别是电针(EA)是否通过抑制脊髓 LTP 有效缓解躯体痛觉过敏。在结肠炎组(通过结肠灌注 2,4,6-三硝基苯磺酸,TNBS 诱导)而不是对照组和载体组的大鼠中,表现出明显的远端结肠局灶性炎症破坏,不仅伴有对有害性结直肠扩张(CRD)的敏化内脏运动反应(VMR),而且还伴有牵涉性后足痛觉过敏,表现为机械和热缩足潜伏期降低。足三里(ST36)和上巨虚(ST37)的 EA 减弱了结肠炎症的严重程度,以及结肠炎大鼠的内脏高敏感性和牵涉性后足痛觉过敏。有趣的是,在结肠炎组中,C 纤维诱发的场电位(CFEFP)的阈值显着降低,并且脊髓 LTP 被夸大,这两者均通过 EA 治疗得到恢复。总之,在 TNBS 诱导的结肠炎大鼠中存在内脏高敏感性和牵涉性后足痛觉过敏,这可能归因于脊髓背角伤害性突触传递的 LTP 增强。ST36 和 ST37 的 EA 可以缓解内脏高敏感性,并且特别是通过抑制增强的脊髓 LTP 来减轻牵涉性后足痛觉过敏。