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硬膜外曲马多复合氟哌啶醇术后镇痛 被引量:1

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出处 《中国基层医药》 CAS 2003年第9期955-955,共1页 Chinese Journal of Primary Medicine and Pharmacy
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  • 1戴体俊.麻醉药理学.第2版.北京:人民卫生出版社,2007:44-45.
  • 2Raffa RB. A novel approach to the pharmacology of analgesics. Am J Med, 1996,101 (1A) :40s.
  • 3Markenson JA. Mechanisms of chronic pain. Am J Med, 1996,101 (1A) :6s.
  • 4J. S. HAN. The role of central catecholamine in acupuncture analgesic. Chinese medical journal. 1979 -92 ( 11 ) :793.
  • 5Walker JM, Bowen WD, Walker FO, et al. Sigma receptors : biology and function. Pharmacol Rev, 1990,42(4) :355-402.
  • 6Bowen WD, Moses EL, Tolentino PJ, et al. Metabolites of halo- peridol display preferential activity at - receptors compared to do- pamine D-2 receptors. Eur J Pharmacol, 1990,177(3) :111-118.
  • 7Jaen JC, Caprathe BW, Pugsley TA, et al. Evaluation of the effects of the enantiomers of reduced haloperidol, azapeml, and re- lated 4-amino-l-arylbutanols on dopamine and σ receptors. J Med Chem,1993, 36(24) :3929-3936.
  • 8Matsumoto RR, Pouw B. Correlation between neuroleptic binding to σ1 and σ2 receptors and acute dystonic reactions. Eur J Pharmacol,2000, 401 (2) :155-160.
  • 9Cendan CM, Pujahe JM, Portillo-Salido E, et al. Formalin-in- duced pain is reduced in σ1 receptor knockout mice. Eur J Pharmacol,2005, 511 (1) :73-74.
  • 10Chien CC, Pastemak GW. Selective antagonism of opioid analgesi- a by a sigma system. J Pharmacol Exp Ther, 1994, 271 (3) :1583- 1590.

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