抑制吗啡耐受的天然药物及其作用机制的研究进展
作者:何鑫;李轶聪;曾凡荣;
Author:
收稿日期: 年卷(期)页码:2018,33(04):-425-428
期刊名称:华西药学杂志
Journal Name:WEST CHINA JOURNAL OF PHARMACEUTICAL SCIENCES
关键字:吗啡耐受;阿片受体;神经胶质细胞;天然药物;芍药苷;白藜芦醇;氧化苦参碱;姜黄素
Key words:
基金项目:
中文摘要
以吗啡为代表的阿片类药物在急性与慢性疼痛的治疗中扮演着重要的角色,同时,大量此类药物的应用会导致吗啡耐受,降低镇痛效果的同时,常导致如痛觉过敏甚至药物成瘾等严重后果,近年来在寻找增强吗啡镇痛效果药物的同时,也在研究抑制阿片类药物的成瘾、耐受和痛觉过敏等不良反应的辅助治疗药物。文中综述了吗啡的镇痛机制与耐受成因及天然药物对吗啡耐受形成的影响。
参考文献
[1]Kissin I,Kerr CR,Smith LR.Assessment of anaesthetic action of morphine and fentanyl in rats[J].Can Anaesth Soc J,1983,30(6):623-628.
[2]Hutchinson MR,Coats BD,Lewis SS,et al.Proinflammatory cytokines oppose opioid-induced acute and chronic analgesia[J].Brain Behav Immun,2008,22(8):1178-1189.
[3]Mao J,Sung B,Ji RR,et al.Chronic morphine induces down regulation of spinal glutamate transporters:Implications in morphine tolerance and abnormal pain sensitivity[J].Neurosci,2002,22(18):8312-8323.
[4]Tai YH,Wang YH,Tsai RY,et al.Amitriptyline preserves morphine's antinociceptive effect by regulating the glutamate transporter GLAST and GLT-1 trafficking and excitatory amino acids concentration in morphine-tolerant rats[J].Pain,2007,129(3):343-354.
[5]Tawfik VL,Lacroix-Fralish ML,Bercury KK,et al.Induction of astrocyte differentiation by propentofylline increases glutamate transporter expression in vitro:Heterogeneity of the quiescent phenotype[J].GLIA,2006,54(3):193-203.
[6]Adler MW,Geller EB.Viewing chemokines as a third major system of communication in the brain[J].AAPS,2005,7(4):865-870.
[7]Bezzi P,Domercq M,Brambilla L,et al.CXCR4-activated astrocyte glutamate release via TNFalpha:Amplification by microglia triggers neurotoxicity[J].Nat Neurosci,2001,4(7):702-710.
[8]Chen X,Geller EB,Rogers TJ,et al.The chemokine CX3CL1/fractalkine interferes with the antinociceptive effect induced by opioid agonists in the periaqueductal grey of rats[J].Brain Res,2007,1153:52-57.
[9]Childers SR.Opioid receptor-coupled second messenger systems[J].Life Sci,1991,48(21):1991-2003.
[10]Dahl JB,Jeppesen IS,Jorgensen H,et al.Interaoperative and postoperative analgesic efficacy and adverse effects of intrathecal opioids in patients undergoing cesarean section with spinal anesthesia:A qualitative and quantitative systematic review of randomized controlled trials[J].Anesthesioligy,1999,91(6):1919.
[11]Nestler EJ.Molecular basis of long-term plasticity underlying addiction[J].Nat Rev Neurosci,2001,2(2):119-128.
[12]Dang UC,Christie MJ,Mechanisms of rapid opioid receptor desensitization,resensitization and tolerance in brain neurons[J].British J Pharmac,2012,165(6):1704-1716.
[13]Song P,Zhao ZQ.The involvement of glial cells in the development of morphine tolerance[J].Neurosci Res,2001,39(3):281-286.
[14]Raghavendra V,Tanga FY,Deleo JA.Attenuation of morphine tolerance,withdrawal-induced hyperalgesia,and associated spinal inflammatory immune responses by propentofylline in rats[J].Neuropsychopharmacology,2004,29(2):327-334.
[15]Juan YC,Tsai WJ,Lin YL,et al.The novel anti-hyperglycemic effect of paeonia ridix via the transcriptional suppression of phosphoenopyruvate carboxykinase(PEPCK)[J].Phytomedicine,2010,17:626-634.
[16]Chen L,Qi H,Jiang D,et al.The new use of an ancient remedy:A double-blinded randomized study on the treatment of rheumatoid arthritis[J].Am J Chin Med,2013,41:263-280.
[17]Tsai HY,Lin YT,Tsai CH,et al.Effects of paeoniflorin on the formalin-induced nociceptive behaviour in mice[J].J Ethnopharmacol 2001,75:267-271.
[18]Zhang XJ,Li Z,Leung WM,et al.The analgesic effect of paeoniflorin on neonatal maternal separation–induced visceral hyperalgesia in rats[J].J Pain,2008,9(6):497-505.
[19]HY Yu,D Mu,J Chen,et al.Suppressive effects of intrathecal paeoniflorin on bee venom-induced pain-related behaviors and spinal neuronal activation[J].Pharmacology,2011,88(3-4):159-166.
[20]Zhang Y,Li H,Huang M,et al.Paeoniflorin,a monoterpene glycoside,pretects the brain from creebral ischemic injury via inhibition of apoptosis[J].Am J Chin Med,2015,3:543-557.
[21]Jiang C,Xu L,et al.Selective suppression of microglial activation by paeoniflorin attenuates morphine tolerance[J].Eur J Pain,2015,19:908-919.
[22]宋扬,赵昱,曾凡荣,等.大鼠脊髓内大麻素CB2受体在芍药苷拮抗吗啡镇痛耐受中的作用[J].神经解剖学杂志,2016,32(5):635-640.
[23]Wang Y,Sun J,Chen L,et al.Effects of resveratrol on rat neurosteroid synthetic enzymes[J].Fitoterapia,2017,122:61
[24]Bobermin LD,Souza DO,Gon9alves CA,et al.Resveratrol prevents ammonia-induced mitochondrial dysfunction and cellular redox imbalance in C6 astroglial cells[J].Nutri Neurosci,2017,1.
[25]Silva AM,Oliveira MI,Sette L,et al.Resveratrol as a natural anti-tumor necrosis factor-alpha molecule:Implications to dendritic cells and their crosstalk with mesenchymal stromal cells[J].Plo S One,2014,9:e91406.
[26]Shen CH,Tsai RY,Shih MS,et al.Etanercept restores the antinociceptive effect of morphine and suppresses spinal neuroinflammation in morphine-tolerant rats[J].Anesth Analg,2011,112:45445-9.
[27]Perez-Severiano F,Bermudez-Ocana DY,Lopez-Sanchez P,et al.Spinal nerve ligation reduces nitric oxide synthase activity and expression:Effect of resveratrol[J].Pharmacol Biochem Behav,2008,90:742e7.
[28]Tsai RY,Wang JC,Chou KY,et al.Resveratrol reverses morphine-induced neuroinflammation in morphine-tolerant rats by reversal HDAC1 expression[J].Formosan Med Association,2015,115(6):445-454.
[29]Han Y,Jiang C,Tang J,et al.Resveratrol reduces morphine tolerance by inhibiting microglial activation via AMPK signalling[J].Eur J Pain,2014,18(10):1458-1470.
[30]Song H,Han Y.Activation of adenosine monophosphate-activated protein kinase suppresses neuroinflammation and ameliorates bone cancer pain:Involvement of inhibition on mitogen-activated protein kinase[J].Anesthesiology,2015,123(5):1170-1185.
[31]Zhang YY,Yi M,Huang YP.Oxymatrine ameliorates doxorubicininduced cardiotoxicity in rats[J].Cell Physiol Biochem,2017,43(2):626.
[32]Gorbett AD,Henderson G,Mcknight AT,et al.75 years of opioid research:The exciting but vain quest for the Holy Grail[J].Br J Pharmacol,2006,147:153-162.
[33]Li YW,Yue H,Xing YM,et al.Oxymatrine inhibits development of morphine-induced tolerance associated with decreased expression of P-glycoprotein in rats[J].Integr Cancer Ther,2010,9(2):213-218.
[34]Letrent SP,Pollack GM,Brouwer KR,et al.Effects of a potent and specific P-glycoprotein inhibitor on the blood-brain barrier distribution and antinociceptive effect of morphine in the rat[J].Drug Metab Dispos,1999,27:827-834.
[35]Aggarwal BB,Sung B.Pharmacological basis for the role of curcumin in chronic diseases:An age-old spice with modern targets[J].Trends Pharmacol Sci,2009,30:85-94.
[36]Agrawal SS,Gullaiya S,Dubey V,et al.Neurodegenerative shielding by curcumin and its derivatives on brain lesions induced by6-OHDA model of Parkinson's disease in albino wistar rats[J].Cardiovasc Psychiatry Neurol,2012:942-981.
[37]Zhou H,Beevers CS,Huang S.The targets of curcumin[J].Curr Drug Targets,2011,12(3):332-347.
[38]Zhao X,Xu Y,Zhao Q,et al.Curcumin exerts antinociceptive effects in a mouse model of neuropathic pain:Descending monoamine system and opioid receptors are differentially involved[J].Neuropharmacology,2012,62(2):843-854.
[39]Hu X,Huang F,Szymusiak M,et al.Curcumin attenuates opioid tolerance and dependence by inhibiting Ca2+/calmodulindependent protein kinaseⅡαactivity[J].Pharmacol Exp Ther,2015,3:420-428.
[40]Matsushita Y,Ueda H.Curcumin blocks chronic morphine analgesic tolerance and brain-derived neurotrophic factor upregulation[J].Neuroreport,2009,20(1):63-68.
[41]Lin J,Chen J,Lee Y,et al.Biphasic of curcumin on morphine tolerance:A preliminary evidence from cytokine/chemokine protein array analysis[J].Evid Based Complement Alternat Med,2011,2011:452153.
【关闭】