nociceptive pain 中文意思是什麼

nociceptive pain 解釋
傷害性疼痛
  • nociceptive : adj. 疼痛的，致痛的；有疼痛反映的。
  • pain : n 1 痛，疼痛；（精神上的）痛苦，憂慮，煩悶，悲痛（opp pleasure）。2 〈古語〉罰，刑罰。3 〈pl 〉費...
  1. Not only the neurons but also the as in the rat brain play a very important role in the process of the peripheral nociceptive stimulation ; ? he newly - found eda may be the functional intercommunication ultrastructure between neurons and as, through which the as could modulate the neurons in the pain signal processing ; @ as might play an active and important role for modulation of pain through a new pathway from the peripheral afferent nerve to the as, then to neurons via electron - dense areas forming the glia - neuron s ignaling network

    光、電鏡水平發現as與神經元之間有多種途徑進行信息交流，新發現的eda有可能是神經元與as之間信息交流的結構之一。阻斷as與神經元間信息交流連接后，前者對外周組織4第四軍醫大學博士學位論文損傷所致疼痛的反應不受影響，而後者的反應明顯受到抑制，提示在非病理性疼痛反應中，膠質細胞對神經元具有主動調控作用。
  2. In addition, cortico - limbic pathways integrated nociceptive input with contextual information and memory to provide cognitive mediation of pain affect

    此外，皮質-邊緣通路整合傷害性刺激輸入並使之成為記憶，以起到影響疼痛的認知調停作用。
  3. According to behavioral studies in adult rats, intrathecal administration of nociceptin, anandamide and win - 55, 212 ( win - 2 ) ( cannabinoid receptor agonists ) produces an antinoceptive effect in versatile pain models including acute, tonic and chronic pain models ( see mogil & pasternak, 2001 ; pertwee, 2001 for review ). thus, it could be concluded that nociceptin - orll receptor and anandamide - cannabinoid receptor systems constitute an important part of endogenous antinociceptive system. however, cellular mechanisms underlying the actions of orl1 and cannabinoid receptors on nociceptive information transmission in the spinal cord are still unknown

    行為學研究也觀察到鞘內注入nociceptin和大麻受體的激動劑如win55 ， 212 - 2 （ win - 2 ） 、 anandamide等均可在多種痛模型上（包括急性痛、持續性痛和慢性痛模型等）產生明顯的抗傷害性作用（ seemogil pasternak ， 2001 ; pertwee ， 2001forreview ） ，由此可見nociceptin ?孤啡肽受體系統和anandamide ?大麻受體系統構成了內源性鎮痛系統的重要組成部分。
  4. By using the bee venom and other models of pain, they screened a novel anti - nociceptive drug with a distinct mechanism from opioids or nsaids ( patent acceptation no. 011 13738. 7 ) with high potentiality for clinical use

    （ 2 ）應用新的蜜蜂毒痛模型開展了臨床鎮痛新藥的篩選及其鎮痛機理研究，成功地篩選出一個臨床鎮痛新藥，獲得鎮痛新藥專利受理一項（ no
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