Kristensen J D, Karlsten R, Gordh T
Department of Anaesthesiology and Intensive Care, University Hospital, Uppsala, Sweden.
Anesth Analg. 1994 May;78(5):925-31. doi: 10.1213/00000539-199405000-00016.
The N-methyl-D-aspartate (NMDA) receptor antagonist 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP), which produces antinociception in experimental animal models after spinal administration, may be of value in clinical pain treatment. Safety screening of drugs intended for spinal administration includes evaluation of the drug's effect on spinal cord blood flow (SCBF). In the present study, laser-Doppler flowmetry technique was used to assess SCBF in an experimental model using anesthetized, spontaneously breathing rats. Methodologic aspects of the experimental set-up were studied, and the effects on SCBF were evaluated after intrathecal (IT) administration of saline or CPP in a dose range of 1-100 nmol. The spontaneously breathing rats, anesthetized with enflurane/N2O had stable mean arterial blood pressure values throughout the study, and no difference was found in arterial blood gas values or acid-base status measured either before or after the 80-min observation period. A reproducible increase in SCBF of approximately 10% during an 80-min measuring period was found in saline-treated rats. The trauma of the IT injection procedure gave a disturbance in the registered SCBF that lasted less than 10 min. No difference was found in SCBF between rats injected IT with either saline or CPP in a dose range from 1 nmol, i.e., a pharmacologically active dose, to 100 nmol, i.e., a provocative dose 400-fold the smallest dose that produces antinociception. When acidic solutions were injected, the SCBF increased in inverse proportion to pH.(ABSTRACT TRUNCATED AT 250 WORDS)
N-甲基-D-天冬氨酸(NMDA)受体拮抗剂3-(2-羧基哌嗪-4-基)丙基-1-膦酸(CPP)在脊髓给药后可在实验动物模型中产生抗伤害感受作用,可能对临床疼痛治疗具有价值。用于脊髓给药的药物的安全性筛选包括评估药物对脊髓血流量(SCBF)的影响。在本研究中,激光多普勒血流仪技术用于在麻醉的自主呼吸大鼠实验模型中评估SCBF。研究了实验设置的方法学方面,并在鞘内(IT)注射生理盐水或剂量范围为1至100 nmol的CPP后评估对SCBF的影响。用恩氟烷/N₂O麻醉的自主呼吸大鼠在整个研究过程中平均动脉血压值稳定,在80分钟观察期之前或之后测量的动脉血气值或酸碱状态均未发现差异。在生理盐水处理的大鼠中,在80分钟的测量期内发现SCBF可重现性增加约10%。IT注射过程的创伤导致记录的SCBF出现干扰,持续时间不到10分钟。在IT注射剂量范围从1 nmol(即药理活性剂量)到100 nmol(即产生抗伤害感受的最小剂量的400倍激发剂量)的生理盐水或CPP的大鼠之间,SCBF未发现差异。当注射酸性溶液时,SCBF与pH成反比增加。(摘要截短于250字)