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Anti-nociceptive Effect of Patchouli Alcohol: Involving Attenuation of Cyclooxygenase 2 and Modulation of Mu-Opioid Receptor 被引量:3
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作者 YU Xuan WANG Xin-pei +5 位作者 YAN Xiao-jin JIANG Jing-fei LEI Fan XING Dong-ming GUO Yue-ying DU Li-jun 《Chinese Journal of Integrative Medicine》 SCIE CAS CSCD 2019年第6期454-461,共8页
Objective: To explore the anti-nociceptive effect of patchouli alcohol(PA), the essential oil isolated from Pogostemon cablin(Blanco) Bent, and determine the mechanism in molecular levels. Methods: The acetic acid-ind... Objective: To explore the anti-nociceptive effect of patchouli alcohol(PA), the essential oil isolated from Pogostemon cablin(Blanco) Bent, and determine the mechanism in molecular levels. Methods: The acetic acid-induced writhing test and formalin-induced plantar injection test in mice were employed to con?rm the effect in vivo. Intracellular calcium ion was imaged to verify PA on mu-opioid receptor(MOR). Cyclooxygenase 2(COX2)and MOR of mouse brain were expressed for determination of PA’s target. Cellular experiments were carried out to find out COX2 and MOR expression induced by PA. Results: PA significantly reduced latency period of visceral pain and writhing induced by acetic acid saline solution(P<0.01) and allodynia after intra-plantar formalin(P<0.01) in mice. PA also up-regulated COX2 mRNA and protein(P<0.05) with a down-regulation of MOR(P<0.05) both in in vivo and in vitro experiments, which devote to the analgesic effect of PA. A decrease in the intracellular calcium level(P<0.05) induced by PA may play an important role in its anti-nociceptive effect.PA showed the characters of enhancing the MOR expression and reducing the intracellular calcium ion similar to opioid effect. Conclusions: Both COX2 and MOR are involved in the mechanism of PA’s anti-nociceptive effect,and the up-regulation of the receptor expression and the inhibition of intracellular calcium are a new perspective to PA’s effect on MOR. 展开更多
关键词 Chinese MEDICI ne patchouli ALCOHOL an algesic EFFECT mu-opioid receptor cyclooxyge nase 2
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非甾体类抗炎药抗肿瘤机制研究新进展 被引量:1
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作者 徐振宇 高建平 孙颖浩 《世界肿瘤杂志》 2005年第2期144-147,165,共5页
近年来研究发现,非甾体类抗炎药(NSAID)有与抗炎作用无关的抗肿瘤功能:长期服用阿斯匹林或其他NSAID可降低结直肠癌、食管癌、胃癌、胰腺癌等消化道肿瘤的发病率,关于NSAID具体的抗肿瘤机制众说纷纭,一般认为NSAID作为环氧合酶-2抑... 近年来研究发现,非甾体类抗炎药(NSAID)有与抗炎作用无关的抗肿瘤功能:长期服用阿斯匹林或其他NSAID可降低结直肠癌、食管癌、胃癌、胰腺癌等消化道肿瘤的发病率,关于NSAID具体的抗肿瘤机制众说纷纭,一般认为NSAID作为环氧合酶-2抑制剂,对于抑制肿瘤的生长有重要的作用。最新的研究发现,其抑制肿瘤的活性可能与其调节RECK基因的表达有关,本文就其可能的作用机制作一综述。 展开更多
关键词 非甾体类抗炎药 环氧化物酶(cyclooxyg—enase COX) RECK基因
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