1. increased sensitivity to pain or enhanced intensity of pain sensation
hyperalgesia 片语
片语
secondary hyperalgesia继发性痛觉过敏
visceral hyperalgesia脏痛觉过敏
auditory hyperalgesia听觉性痛觉过敏
Inflammatory hyperalgesia炎性痛觉过敏
primary hyperalgesia痛觉过敏
mechanical hyperalgesia机械性痛敏
hyperalgesia score差值作为痛敏分数
thermal hyperalgesia热痛觉过敏
muscular hyperalgesia肌痛觉过敏
hyperalgesia 例句
英汉例句
Many researchers, therefore, have amelioration of hyperalgesia and allodynia foremost in their minds as they hunt for new analgesics.
因此,许多研究人员在寻求新的止痛药方时,都会把解除痛觉过敏及异位疼痛列入优先考量。
BACKGROUND: Chronic pain, including hyperalgesia and algesthesia paresthesia, is pathological phenomenons making the patients felt unendurable and lacking of clinical treatments.
背景:慢性痛包括痛觉过敏和痛觉感觉异常,是患者感到难以忍受和临床缺乏治疗手段的一种病理现象。
In clinic, pathological pain is one of the most frequently observed clinical symptoms, which is characterized by a persistent spontaneous pain, hyperalgesia and touch-evoked pain (allodynia).
临床病理性痛可表现为持续性的自发痛及伴有长时程持续性痛敏和触诱发痛现象。
Pain and hyperalgesia was caused by injury of tissue and peripheral nerves.
组织损伤及外周神经损伤后可导致痛及痛过敏。
Results Sprout number of DRG in experimental group rats decreased obviously and the symptom of hyperalgesia was improved as compared to control rats.
结果实验组大鼠drg内交感芽生明显减少,热痛过敏癥状被抑制。
RESULTS: Thermal hyperalgesia developed between Days 12 and 18 after cancer cell inoculation.
结果:热痛觉过敏在肿瘤细胞植入后的12-18天发生进展。
Objective to investigate the role of peripheral N-methyl-D-aspartate (NMDA) receptors in the long-term hyperalgesia induced by peripheral injection of formalin in rats.
目的观察外周n -甲基- D -天门冬氨酸(NMDA)受体对福尔·马林外周注射所致长时程痛敏的作用。
The behavior results showed that blocking peripheral 5-HT_(2A)receptors inhibited the thermal hyperalgesia in inflammatory and neuropathic pain.
行为学结果显示,阻断外周5-HT_(2A)受体能够明显抑制慢性炎癥及神经病理性痛引发的热痛觉过敏。
Preemptive analgesia is one of the analgesia measures which decreases the incidence of hyperalgesia and allodynia by reducing peripheral and central sensitization.
超前镇痛是通过防止外周和中枢敏化来降低伤害性刺激引起的痛觉过敏和痛觉异常的一种镇痛方法。
Conclusion Intrathecal FC can reduce the mechanical and heat hyperalgesia in mice with bone cancer pain, and the astrocytes may play a role in the nociceptive transmission at the spinal level.