Sakane T, Nakatsu M, Yamamoto A, Hashida M, Sezaki H, Yamashita S, Nadai T
Faculty of Pharmaceutical Sciences, Setsunan University, Osaka, Japan.
Pharm Res. 1991 Jun;8(6):683-9. doi: 10.1023/a:1015833513567.
Drug disposition in the brain was investigated by statistical moment analysis using an improved in situ brain perfusion technique. The right cerebral hemisphere of the rat was perfused in situ. The drug and inulin were injected into the right internal carotid artery as a rapid bolus and the venous outflow curve at the posterior facial vein was obtained. The infusion rate was adjusted to minimize the flow of perfusion fluid into the left hemisphere. The obtained disposition parameters were characteristics and considered to reflect the physicochemical properties of each drug. Antipyrine showed a small degree of initial uptake. Therefore, its apparent distribution volume (Vi) and apparent intrinsic clearance (CLint,i) were small. Diazepam showed large degrees of both influx and efflux and, thus, a large Vi. Water showed parameters intermediate between those of antipyrine and those of diazepam. Imipramine, desipramine, and propranolol showed a large CLint,i compared with those of the other drugs. The extraction ratio of propranolol significantly decreased with increasing concentrations of unlabeled propranolol in the perfusion fluid. These findings may be explained partly by the tissue binding of these drugs. In conclusion, the present method is useful for studying drug disposition in the brain.
采用改进的原位脑灌注技术,通过统计矩分析研究药物在脑内的处置情况。对大鼠的右大脑半球进行原位灌注。将药物和菊粉作为快速推注注入右颈内动脉,并获得面后静脉处的静脉流出曲线。调节灌注速率以使灌注液流入左半球的量最小化。所获得的处置参数具有特征性,被认为反映了每种药物的理化性质。安替比林的初始摄取程度较小。因此,其表观分布容积(Vi)和表观内在清除率(CLint,i)较小。地西泮的流入和流出程度均较大,因此Vi较大。水的参数介于安替比林和地西泮之间。与其他药物相比,丙咪嗪、去甲丙咪嗪和普萘洛尔的CLint,i较大。随着灌注液中未标记普萘洛尔浓度的增加,普萘洛尔的提取率显著降低。这些发现可能部分归因于这些药物的组织结合。总之,本方法对于研究药物在脑内的处置情况很有用。